Fungus (or fungi) is a term that relates to any member of a large group of eukaryotic organisms that includes microorganisms such as yeasts and molds as well as the more familiar mushrooms. These organisms are classified as a kingdom, Fungi, which is separate from plants, animals, protists, and bacteria. One major difference is that fungal cells have cell walls that contain chitin, unlike the cell walls of plants and some protists, which contain cellulose, and unlike the cell walls of bacteria. These and other differences show that the fungi form a single group of related organisms, named the Eumycota (true fungi or Eumycetes), that share a common ancestor (is a monophyletic group). This fungal group is distinct from the structurally similar myxomycetes (slime molds) and oomycetes (water molds). The discipline of biology devoted to the study of fungi is known as mycology (from the Greek μύκης, mukēs, meaning "fungus"). Mycology has often been regarded as a branch of botany, even though it is a separate kingdom in biological taxonomy. Genetic studies have shown that fungi are more closely related to animals than to plants.

Abundant worldwide, most fungi are inconspicuous because of the small size of their structures, and their cryptic lifestyles in soil, on dead matter, and as symbionts of plants, animals, or other fungi. They may become noticeable when fruiting, either as mushrooms or as molds. Fungi perform an essential role in the decomposition of organic matter and have fundamental roles in nutrient cycling and exchange. They have long been used as a direct source of food, such as mushrooms and truffles, as a leavening agent for bread, and in fermentation of various food products, such as wine, beer, and soy sauce. Since the 1940s, fungi have been used for the production of antibiotics, and, more recently, various enzymes produced by fungi are used industrially and in detergents. Fungi are also used as biological pesticides to control weeds, plant diseases and insect pests. Many species produce bioactive compounds called mycotoxins, such as alkaloids and polyketides, that are toxic to animals including humans. The fruiting structures of a few species contain psychotropic compounds and are consumed recreationally or in traditional spiritual ceremonies. Fungi can break down manufactured materials and buildings, and become significant pathogens of humans and other animals. Losses of crops due to fungal diseases (e.g. rice blast disease) or food spoilage can have a large impact on human food supplies and local economies.

The fungus kingdom encompasses an enormous diversity of taxa with varied ecologies, life cycle strategies, and morphologies ranging from unicellular aquatic chytrids to large mushrooms. However, little is known of the true biodiversity of Kingdom Fungi, which has been estimated at 1.5 million to 5 million species, with about 5% of these having been formally classified. Ever since the pioneering 18th and 19th century taxonomical works of Carl Linnaeus, Christian Hendrik Persoon, and Elias Magnus Fries, fungi have been classified according to their morphology (e.g., characteristics such as spore color or microscopic features) or physiology. Advances in molecular genetics have opened the way for DNA analysis to be incorporated into taxonomy, which has sometimes challenged the historical groupings based on morphology and other traits. Phylogenetic studies published in the last decade have helped reshape the classification of Kingdom Fungi, which is divided into one subkingdom, seven phyla, and ten subphyla.

A group of all the fungi present in a particular area or geographic region is known as mycobiota (plural noun, no singular), e.g. "the mycobiota of Ireland".[3]


The English word fungus is directly adopted from the Latin fungus (mushroom), used in the writings of Horace and Pliny.[4] This in turn is derived from the Greek word sphongos (σφογγος "sponge"), which refers to the macroscopic structures and morphology of mushrooms and molds;[5] the root is also used in other languages, such as the German Schwamm ("sponge") and Schimmel ("mold").[6] The use of the word mycology, which is derived from the Greek mykes (μύκης "mushroom") and logos (λόγος "discourse"),[7] to denote the scientific study of fungi is thought to have originated in 1836 with English naturalist Miles Joseph Berkeley's publication The English Flora of Sir James Edward Smith, Vol. 5.[5]



Before the introduction of molecular methods for phylogenetic analysis, taxonomists considered fungi to be members of the Plant Kingdom because of similarities in lifestyle: both fungi and plants are mainly immobile, and have similarities in general morphology and growth habitat. Like plants, fungi often grow in soil, and in the case of mushrooms form conspicuous fruit bodies, which sometimes resemble plants such as mosses. The fungi are now considered a separate kingdom, distinct from both plants and animals, from which they appear to have diverged around one billion years ago.[8][9] Some morphological, biochemical, and genetic features are shared with other organisms, while others are unique to the fungi, clearly separating them from the other kingdoms:

Shared features:

Unique features:

  • Some species grow as unicellular yeasts that reproduce by budding or binary fission. Dimorphic fungi can switch between a yeast phase and a hyphal phase in response to environmental conditions.[21]
  • The fungal cell wall is composed of glucans and chitin; while the former compounds are also found in plants and the latter in the exoskeleton of arthropods,[22][23] fungi are the only organisms that combine these two structural molecules in their cell wall. Unlike cell walls in plants and the oomycetes, those in fungi do not contain cellulose.[24]
File:Omphalotus nidiformis Binnamittalong 2 email.jpg

Most fungi lack an efficient system for long-distance transport of water and nutrients, such as the xylem and phloem in many plants. To overcome these limitations, some fungi, such as Armillaria, form rhizomorphs,[25] that resemble and perform functions similar to the roots of plants. Another characteristic shared with plants is a biosynthetic pathway for producing terpenes that uses mevalonic acid and pyrophosphate as chemical building blocks.[26] However, plants have an additional terpene pathway in their chloroplasts, a structure fungi do not have.[27] Fungi produce several secondary metabolites that are similar or identical in structure to those made by plants.[26] Many of the plant and fungal enzymes that make these compounds differ from each other in sequence and other characteristics, which indicates separate origins and evolution of these enzymes in the fungi and plants.[26][28]


File:Fungus in a Wood.JPG

Fungi have a worldwide distribution, and grow in a wide range of habitats, including extreme environments such as deserts or areas with high salt concentrations[29] or ionizing radiation,[30] as well as in deep sea sediments.[31] Some can survive the intense UV and cosmic radiation encountered during space travel.[32] Most grow in terrestrial environments, though several species live partly or solely in aquatic habitats, such as the chytrid fungus Batrachochytrium dendrobatidis, a parasite that has been responsible for a worldwide decline in amphibian populations. This organism spends part of its life cycle as a motile zoospore, enabling it to propel itself through water and enter its amphibian host.[33] Other examples of aquatic fungi include those living in hydrothermal areas of the ocean.[34]

Around 100,000 species of fungi have been formally described by taxonomists,[35] but the global biodiversity of the fungus kingdom is not fully understood.[36] On the basis of observations of the ratio of the number of fungal species to the number of plant species in selected environments, the fungal kingdom has been estimated to contain about 1.5 million species.[37] A recent (2011) estimate suggests there may be over 5 million species.[38] In mycology, species have historically been distinguished by a variety of methods and concepts. Classification based on morphological characteristics, such as the size and shape of spores or fruiting structures, has traditionally dominated fungal taxonomy.[39] Species may also be distinguished by their biochemical and physiological characteristics, such as their ability to metabolize certain biochemicals, or their reaction to chemical tests. The biological species concept discriminates species based on their ability to mate. The application of molecular tools, such as DNA sequencing and phylogenetic analysis, to study diversity has greatly enhanced the resolution and added robustness to estimates of genetic diversity within various taxonomic groups.[40]


Mycology is the branch of biology concerned with the systematic study of fungi, including their genetic and biochemical properties, their taxonomy, and their use to humans as a source of medicine, food, and psychotropic substances consumed for religious purposes, as well as their dangers, such as poisoning or infection. The field of phytopathology, the study of plant diseases, is closely related because many plant pathogens are fungi.[41]

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The use of fungi by humans dates back to prehistory; Ötzi the Iceman, a well-preserved mummy of a 5,300-year-old Neolithic man found frozen in the Austrian Alps, carried two species of polypore mushrooms that may have been used as tinder (Fomes fomentarius), or for medicinal purposes (Piptoporus betulinus).[42] Ancient peoples have used fungi as food sources–often unknowingly–for millennia, in the preparation of leavened bread and fermented juices. Some of the oldest written records contain references to the destruction of crops that were probably caused by pathogenic fungi.[43]


Mycology is a relatively new science that became systematic after the development of the microscope in the 16th century. Although fungal spores were first observed by Giambattista della Porta in 1588, the seminal work in the development of mycology is considered to be the publication of Pier Antonio Micheli's 1729 work Nova plantarum genera.[44] Micheli not only observed spores but also showed that, under the proper conditions, they could be induced into growing into the same species of fungi from which they originated.[45] Extending the use of the binomial system of nomenclature introduced by Carl Linnaeus in his Species plantarum (1753), the Dutch Christian Hendrik Persoon (1761–1836) established the first classification of mushrooms with such skill so as to be considered a founder of modern mycology. Later, Elias Magnus Fries (1794–1878) further elaborated the classification of fungi, using spore color and various microscopic characteristics, methods still used by taxonomists today. Other notable early contributors to mycology in the 17th–19th and early 20th centuries include Miles Joseph Berkeley, August Carl Joseph Corda, Anton de Bary, the brothers Louis René and Charles Tulasne, Arthur H. R. Buller, Curtis G. Lloyd, and Pier Andrea Saccardo. The 20th century has seen a modernization of mycology that has come from advances in biochemistry, genetics, molecular biology, and biotechnology. The use of DNA sequencing technologies and phylogenetic analysis has provided new insights into fungal relationships and biodiversity, and has challenged traditional morphology-based groupings in fungal taxonomy.[46]


Microscopic structures

File:Penicillium labeled cropped.jpg

Most fungi grow as hyphae, which are cylindrical, thread-like structures 2–10 µm in diameter and up to several centimeters in length. Hyphae grow at their tips (apices); new hyphae are typically formed by emergence of new tips along existing hyphae by a process called branching, or occasionally growing hyphal tips fork, giving rise to two parallel-growing hyphae.[47] The combination of apical growth and branching/forking leads to the development of a mycelium, an interconnected network of hyphae.[21] Hyphae can be either septate or coenocytic. Septate hyphae are divided into compartments separated by cross walls (internal cell walls, called septa, that are formed at right angles to the cell wall giving the hypha its shape), with each compartment containing one or more nuclei; coenocytic hyphae are not compartmentalized.[48] Septa have pores that allow cytoplasm, organelles, and sometimes nuclei to pass through; an example is the dolipore septum in fungi of the phylum Basidiomycota.[49] Coenocytic hyphae are in essence multinucleate supercells.[50]

Many species have developed specialized hyphal structures for nutrient uptake from living hosts; examples include haustoria in plant-parasitic species of most fungal phyla, and arbuscules of several mycorrhizal fungi, which penetrate into the host cells to consume nutrients.[51]

Although fungi are opisthokonts—a grouping of evolutionarily related organisms broadly characterized by a single posterior flagellum—all phyla except for the chytrids have lost their posterior flagella.[52] Fungi are unusual among the eukaryotes in having a cell wall that, in addition to glucans (e.g., β-1,3-glucan) and other typical components, also contains the biopolymer chitin.[53]

Macroscopic structures

File:Armillaria ostoyae MO.jpg

Fungal mycelia can become visible to the naked eye, for example, on various surfaces and substrates, such as damp walls and spoiled food, where they are commonly called molds. Mycelia grown on solid agar media in laboratory petri dishes are usually referred to as colonies. These colonies can exhibit growth shapes and colors (due to spores or pigmentation) that can be used as diagnostic features in the identification of species or groups.[54] Some individual fungal colonies can reach extraordinary dimensions and ages as in the case of a clonal colony of Armillaria solidipes, which extends over an area of more than 900 ha (3.5 square miles), with an estimated age of nearly 9,000 years.[55]

The apothecium—a specialized structure important in sexual reproduction in the ascomycetes—is a cup-shaped fruit body that holds the hymenium, a layer of tissue containing the spore-bearing cells.[56] The fruit bodies of the basidiomycetes (basidiocarps) and some ascomycetes can sometimes grow very large, and many are well known as mushrooms.

Growth and physiology


The growth of fungi as hyphae on or in solid substrates or as single cells in aquatic environments is adapted for the efficient extraction of nutrients, because these growth forms have high surface area to volume ratios.[57] Hyphae are specifically adapted for growth on solid surfaces, and to invade substrates and tissues.[58] They can exert large penetrative mechanical forces; for example, the plant pathogen Magnaporthe grisea forms a structure called an appressorium that evolved to puncture plant tissues.[59] The pressure generated by the appressorium, directed against the plant epidermis, can exceed 8 megapascals (1,200 psi).[59] The filamentous fungus Paecilomyces lilacinus uses a similar structure to penetrate the eggs of nematodes.[60]

The mechanical pressure exerted by the appressorium is generated from physiological processes that increase intracellular turgor by producing osmolytes such as glycerol.[61] Adaptations such as these are complemented by hydrolytic enzymes secreted into the environment to digest large organic molecules—such as polysaccharides, proteins, and lipids—into smaller molecules that may then be absorbed as nutrients.[62][63][64] The vast majority of filamentous fungi grow in a polar fashion—i.e., by extension into one direction—by elongation at the tip (apex) of the hypha.[65] Other forms of fungal growth include intercalary extension (longitudinal expansion of hyphal compartments that are below the apex) as in the case of some endophytic fungi,[66] or growth by volume expansion during the development of mushroom stipes and other large organs.[67] Growth of fungi as multicellular structures consisting of somatic and reproductive cells—a feature independently evolved in animals and plants[68]—has several functions, including the development of fruit bodies for dissemination of sexual spores (see above) and biofilms for substrate colonization and intercellular communication.[69]

The fungi are traditionally considered heterotrophs, organisms that rely solely on carbon fixed by other organisms for metabolism. Fungi have evolved a high degree of metabolic versatility that allows them to use a diverse range of organic substrates for growth, including simple compounds such as nitrate, ammonia, acetate, or ethanol.[70][71] In some species the pigment melanin may play a role in extracting energy from ionizing radiation, such as gamma radiation. This form of "radiotrophic" growth has been described for only a few species, the effects on growth rates are small, and the underlying biophysical and biochemical processes are not well known.[30] This process might bear similarity to CO2 fixation via visible light, but instead using ionizing radiation as a source of energy.[72]


File:Polyporus squamosus Molter.jpg

Fungal reproduction is complex, reflecting the differences in lifestyles and genetic makeup within this diverse kingdom of organisms.[73] It is estimated that a third of all fungi reproduce using more than one method of propagation; for example, reproduction may occur in two well-differentiated stages within the life cycle of a species, the teleomorph and the anamorph.[74] Environmental conditions trigger genetically determined developmental states that lead to the creation of specialized structures for sexual or asexual reproduction. These structures aid reproduction by efficiently dispersing spores or spore-containing propagules.

Asexual reproduction

Asexual reproduction occurs via vegetative spores (conidia) or through mycelial fragmentation. Mycelial fragmentation occurs when a fungal mycelium separates into pieces, and each component grows into a separate mycelium. Mycelial fragmentation and vegatative spores maintain clonal populations adapted to a specific niche, and allow more rapid dispersal than sexual reproduction.[75] The "Fungi imperfecti" (fungi lacking the perfect or sexual stage) or Deuteromycota comprise all the species that lack an observable sexual cycle.[76]

Sexual reproduction

Sexual reproduction with meiosis exists in all fungal phyla (with the exception of the Glomeromycota).[77] It differs in many aspects from sexual reproduction in animals or plants. Differences also exist between fungal groups and can be used to discriminate species by morphological differences in sexual structures and reproductive strategies.[78][79] Mating experiments between fungal isolates may identify species on the basis of biological species concepts.[79] The major fungal groupings have initially been delineated based on the morphology of their sexual structures and spores; for example, the spore-containing structures, asci and basidia, can be used in the identification of ascomycetes and basidiomycetes, respectively. Some species may allow mating only between individuals of opposite mating type, whereas others can mate and sexually reproduce with any other individual or itself. Species of the former mating system are called heterothallic, and of the latter homothallic.[80]

Most fungi have both a haploid and a diploid stage in their life cycles. In sexually reproducing fungi, compatible individuals may combine by fusing their hyphae together into an interconnected network; this process, anastomosis, is required for the initiation of the sexual cycle. Ascomycetes and basidiomycetes go through a dikaryotic stage, in which the nuclei inherited from the two parents do not combine immediately after cell fusion, but remain separate in the hyphal cells (see heterokaryosis).[81]


In ascomycetes, dikaryotic hyphae of the hymenium (the spore-bearing tissue layer) form a characteristic hook at the hyphal septum. During cell division, formation of the hook ensures proper distribution of the newly divided nuclei into the apical and basal hyphal compartments. An ascus (plural asci) is then formed, in which karyogamy (nuclear fusion) occurs. Asci are embedded in an ascocarp, or fruiting body. Karyogamy in the asci is followed immediately by meiosis and the production of ascospores. After dispersal, the ascospores may germinate and form a new haploid mycelium.[82]

Sexual reproduction in basidiomycetes is similar to that of the ascomycetes. Compatible haploid hyphae fuse to produce a dikaryotic mycelium. However, the dikaryotic phase is more extensive in the basidiomycetes, often also present in the vegetatively growing mycelium. A specialized anatomical structure, called a clamp connection, is formed at each hyphal septum. As with the structurally similar hook in the ascomycetes, the clamp connection in the basidiomycetes is required for controlled transfer of nuclei during cell division, to maintain the dikaryotic stage with two genetically different nuclei in each hyphal compartment.[83] A basidiocarp is formed in which club-like structures known as basidia generate haploid basidiospores after karyogamy and meiosis.[84] The most commonly known basidiocarps are mushrooms, but they may also take other forms (see Morphology section).

In glomeromycetes (formerly zygomycetes), haploid hyphae of two individuals fuse, forming a gametangium, a specialized cell structure that becomes a fertile gamete-producing cell. The gametangium develops into a zygospore, a thick-walled spore formed by the union of gametes. When the zygospore germinates, it undergoes meiosis, generating new haploid hyphae, which may then form asexual sporangiospores. These sporangiospores allow the fungus to rapidly disperse and germinate into new genetically identical haploid fungal mycelia.[85]

Spore dispersal

Both asexual and sexual spores or sporangiospores are often actively dispersed by forcible ejection from their reproductive structures. This ejection ensures exit of the spores from the reproductive structures as well as traveling through the air over long distances.
File:Cyathus stercoreus Fruchtkörper.JPG
Specialized mechanical and physiological mechanisms, as well as spore surface structures (such as hydrophobins), enable efficient spore ejection.[86] For example, the structure of the spore-bearing cells in some ascomycete species is such that the buildup of substances affecting cell volume and fluid balance enables the explosive discharge of spores into the air.[87] The forcible discharge of single spores termed ballistospores involves formation of a small drop of water (Buller's drop), which upon contact with the spore leads to its projectile release with an initial acceleration of more than 10,000 g;[88] the net result is that the spore is ejected 0.01–0.02 cm, sufficient distance for it to fall through the gills or pores into the air below.[89] Other fungi, like the puffballs, rely on alternative mechanisms for spore release, such as external mechanical forces. The bird's nest fungi use the force of falling water drops to liberate the spores from cup-shaped fruiting bodies.[90] Another strategy is seen in the stinkhorns, a group of fungi with lively colors and putrid odor that attract insects to disperse their spores.[91]

Other sexual processes

Besides regular sexual reproduction with meiosis, certain fungi, such as those in the genera Penicillium and Aspergillus, may exchange genetic material via parasexual processes, initiated by anastomosis between hyphae and plasmogamy of fungal cells.[92] The frequency and relative importance of parasexual events is unclear and may be lower than other sexual processes. It is known to play a role in intraspecific hybridization[93] and is likely required for hybridization between species, which has been associated with major events in fungal evolution.[94]


Main article: Evolution of fungi

In contrast to plants and animals, the early fossil record of the fungi is meager. Factors that likely contribute to the under-representation of fungal species among fossils include the nature of fungal fruiting bodies, which are soft, fleshy, and easily degradable tissues and the microscopic dimensions of most fungal structures, which therefore are not readily evident. Fungal fossils are difficult to distinguish from those of other microbes, and are most easily identified when they resemble extant fungi.[95] Often recovered from a permineralized plant or animal host, these samples are typically studied by making thin-section preparations that can be examined with light microscopy or transmission electron microscopy.[96] Researchers study compression fossils by dissolving the surrounding matrix with acid and then using light or scanning electron microscopy to examine surface details.[97]

The earliest fossils possessing features typical of fungi date to the Proterozoic eon, some Template:Ma/1 million years ago (Ma); these multicellular benthic organisms had filamentous structures with septa, and were capable of anastomosis.[98] More recent studies (2009) estimate the arrival of fungal organisms at about 760–1060 Ma on the basis of comparisons of the rate of evolution in closely related groups.[99] For much of the Paleozoic Era (542–251 Ma), the fungi appear to have been aquatic and consisted of organisms similar to the extant chytrids in having flagellum-bearing spores.[100] The evolutionary adaptation from an aquatic to a terrestrial lifestyle necessitated a diversification of ecological strategies for obtaining nutrients, including parasitism, saprobism, and the development of mutualistic relationships such as mycorrhiza and lichenization.[101] Recent (2009) studies suggest that the ancestral ecological state of the Ascomycota was saprobism, and that independent lichenization events have occurred multiple times.[102]

It is presumed that the fungi colonized the land during the Cambrian (542–488.3 Ma), long before land plants.[103] Fossilized hyphae and spores recovered from the Ordovician of Wisconsin (460 Ma) resemble modern-day Glomerales, and existed at a time when the land flora likely consisted of only non-vascular bryophyte-like plants.[104] Prototaxites, which was probably a fungus or lichen, would have been the tallest organism of the late Silurian. Fungal fossils do not become common and uncontroversial until the early Devonian (416–359.2 Ma), when they occur abundantly in the Rhynie chert, mostly as Zygomycota and Chytridiomycota.[103][105][106] At about this same time, approximately 400 Ma, the Ascomycota and Basidiomycota diverged,[107] and all modern classes of fungi were present by the Late Carboniferous (Pennsylvanian, 318.1–299 Ma).[108]

Lichen-like fossils have been found in the Doushantuo Formation in southern China dating back to 635–551 Ma.[109] Lichens formed a component of the early terrestrial ecosystems, and the estimated age of the oldest terrestrial lichen fossil is 400 Ma;[110] this date corresponds to the age of the oldest known sporocarp fossil, a Paleopyrenomycites species found in the Rhynie Chert.[111] The oldest fossil with microscopic features resembling modern-day basidiomycetes is Palaeoancistrus, found permineralized with a fern from the Pennsylvanian.[112] Rare in the fossil record are the Homobasidiomycetes (a taxon roughly equivalent to the mushroom-producing species of the Agaricomycetes). Two amber-preserved specimens provide evidence that the earliest known mushroom-forming fungi (the extinct species Archaeomarasmius leggetti) appeared during the mid-Cretaceous, 90 Ma.[113][114]

Some time after the Permian–Triassic extinction event (251.4 Ma), a fungal spike (originally thought to be an extraordinary abundance of fungal spores in sediments) formed, suggesting that fungi were the dominant life form at this time, representing nearly 100% of the available fossil record for this period.[115] However, the relative proportion of fungal spores relative to spores formed by algal species is difficult to assess,[116] the spike did not appear worldwide,[117][118] and in many places it did not fall on the Permian–Triassic boundary.[119]


Although commonly included in botany curricula and textbooks, fungi are more closely related to animals than to plants and are placed with the animals in the monophyletic group of opisthokonts.[120] Analyses using molecular phylogenetics support a monophyletic origin of the Fungi.[40] The taxonomy of the Fungi is in a state of constant flux, especially due to recent research based on DNA comparisons. These current phylogenetic analyses often overturn classifications based on older and sometimes less discriminative methods based on morphological features and biological species concepts obtained from experimental matings.[121]

There is no unique generally accepted system at the higher taxonomic levels and there are frequent name changes at every level, from species upwards. Efforts among researchers are now underway to establish and encourage usage of a unified and more consistent nomenclature.[40][122] Fungal species can also have multiple scientific names depending on their life cycle and mode (sexual or asexual) of reproduction. Web sites such as Index Fungorum and ITIS list current names of fungal species (with cross-references to older synonyms).

The 2007 classification of Kingdom Fungi is the result of a large-scale collaborative research effort involving dozens of mycologists and other scientists working on fungal taxonomy.[40] It recognizes seven phyla, two of which—the Ascomycota and the Basidiomycota—are contained within a branch representing subkingdom Dikarya. The below cladogram depicts the major fungal taxa and their relationship to opisthokont and unikont organisms. The lengths of the branches in this tree are not proportional to evolutionary distances.

Taxonomic groups

The major phyla (sometimes called divisions) of fungi have been classified mainly on the basis of characteristics of their sexual reproductive structures. Currently, seven phyla are proposed: Microsporidia, Chytridiomycota, Blastocladiomycota, Neocallimastigomycota, Glomeromycota, Ascomycota, and Basidiomycota.[40]

File:Arbuscular mycorrhiza microscope.jpg

Phylogenetic analysis has demonstrated that the Microsporidia, unicellular parasites of animals and protists, are fairly recent and highly derived endobiotic fungi (living within the tissue of another species).[100][123] One 2006 study concludes that the Microsporidia are a sister group to the true fungi; that is, they are each other's closest evolutionary relative.[124] Hibbett and colleagues suggest that this analysis does not clash with their classification of the Fungi, and although the Microsporidia are elevated to phylum status, it is acknowledged that further analysis is required to clarify evolutionary relationships within this group.[40]

The Chytridiomycota are commonly known as chytrids. These fungi are distributed worldwide. Chytrids produce zoospores that are capable of active movement through aqueous phases with a single flagellum, leading early taxonomists to classify them as protists. Molecular phylogenies, inferred from rRNA sequences in ribosomes, suggest that the Chytrids are a basal group divergent from the other fungal phyla, consisting of four major clades with suggestive evidence for paraphyly or possibly polyphyly.[125]

The Blastocladiomycota were previously considered a taxonomic clade within the Chytridiomycota. Recent molecular data and ultrastructural characteristics, however, place the Blastocladiomycota as a sister clade to the Zygomycota, Glomeromycota, and Dikarya (Ascomycota and Basidiomycota). The blastocladiomycetes are saprotrophs, feeding on decomposing organic matter, and they are parasites of all eukaryotic groups. Unlike their close relatives, the chytrids, most of which exhibit zygotic meiosis, the blastocladiomycetes undergo sporic meiosis.[100]

The Neocallimastigomycota were earlier placed in the phylum Chytridomycota. Members of this small phylum are anaerobic organisms, living in the digestive system of larger herbivorous mammals and in other terrestrial and aquatic environments enriched in cellulose (e.g., domestic waste landfill sites).[126] They lack mitochondria but contain hydrogenosomes of mitochondrial origin. As the related chrytrids, neocallimastigomycetes form zoospores that are posteriorly uniflagellate or polyflagellate.[40]

Members of the Glomeromycota form arbuscular mycorrhizae, a form of symbiosis wherein fungal hyphae invade plant root cells and both species benefit from the resulting increased supply of nutrients. All known Glomeromycota species reproduce asexually.[77] The symbiotic association between the Glomeromycota and plants is ancient, with evidence dating to 400 million years ago.[127] Formerly part of the Zygomycota (commonly known as 'sugar' and 'pin' molds), the Glomeromycota were elevated to phylum status in 2001 and now replace the older phylum Zygomycota.[128] Fungi that were placed in the Zygomycota are now being reassigned to the Glomeromycota, or the subphyla incertae sedis Mucoromycotina, Kickxellomycotina, the Zoopagomycotina and the Entomophthoromycotina.[40] Some well-known examples of fungi formerly in the Zygomycota include black bread mold (Rhizopus stolonifer), and Pilobolus species, capable of ejecting spores several meters through the air.[129] Medically relevant genera include Mucor, Rhizomucor, and Rhizopus.


The Ascomycota, commonly known as sac fungi or ascomycetes, constitute the largest taxonomic group within the Eumycota.[39] These fungi form meiotic spores called ascospores, which are enclosed in a special sac-like structure called an ascus. This phylum includes morels, a few mushrooms and truffles, unicellular yeasts (e.g., of the genera Saccharomyces, Kluyveromyces, Pichia, and Candida), and many filamentous fungi living as saprotrophs, parasites, and mutualistic symbionts. Prominent and important genera of filamentous ascomycetes include Aspergillus, Penicillium, Fusarium, and Claviceps. Many ascomycete species have only been observed undergoing asexual reproduction (called anamorphic species), but analysis of molecular data has often been able to identify their closest teleomorphs in the Ascomycota.[130] Because the products of meiosis are retained within the sac-like ascus, ascomycetes have been used for elucidating principles of genetics and heredity (e.g., Neurospora crassa).[131]

Members of the Basidiomycota, commonly known as the club fungi or basidiomycetes, produce meiospores called basidiospores on club-like stalks called basidia. Most common mushrooms belong to this group, as well as rust and smut fungi, which are major pathogens of grains. Other important basidiomycetes include the maize pathogen Ustilago maydis,[132] human commensal species of the genus Malassezia,[133] and the opportunistic human pathogen, Cryptococcus neoformans.[134]

Fungus-like organisms

Because of similarities in morphology and lifestyle, the slime molds (myxomycetes) and water molds (oomycetes) were formerly classified in the kingdom Fungi, in groups like Mastigomycotina, Gymnomycota and Phycomycetes. Unlike true fungi the cell walls of these organisms contain cellulose and lack chitin. Like fungi, myxomycetes are unikonts, but are grouped in the Amoebozoa. Oomycetes are diploid bikonts, grouped in the Chromalveolate kingdom. Neither water molds nor slime molds are closely related to the true fungi, and, therefore, taxonomists no longer group them in the kingdom Fungi. Nonetheless, studies of the oomycetes and myxomycetes are still often included in mycology textbooks and primary research literature.[135]

The Rozellida clade, including the "chytrid" Rozella, is a genetically disparate group known mostly from environmental DNA sequences that is a sister group to fungi. Members of the group that have been isolated lack the chitinous cell wall that is characteristic of fungi.

The nucleariids, currently grouped in the Choanozoa, may be the next sister group to the eumycete clade, and as such could be included in an expanded fungal kingdom.[136]


File:PinMould on Peach LowMag Scale.jpg

Although often inconspicuous, fungi occur in every environment on Earth and play very important roles in most ecosystems. Along with bacteria, fungi are the major decomposers in most terrestrial (and some aquatic) ecosystems, and therefore play a critical role in biogeochemical cycles[137] and in many food webs. As decomposers, they play an essential role in nutrient cycling, especially as saprotrophs and symbionts, degrading organic matter to inorganic molecules, which can then re-enter anabolic metabolic pathways in plants or other organisms.[138][139]


Many fungi have important symbiotic relationships with organisms from most if not all Kingdoms.[140][141][142] These interactions can be mutualistic or antagonistic in nature, or in the case of commensal fungi are of no apparent benefit or detriment to the host.[143][144][145]

With plants

Mycorrhizal symbiosis between plants and fungi is one of the most well-known plant–fungus associations and is of significant importance for plant growth and persistence in many ecosystems; over 90% of all plant species engage in mycorrhizal relationships with fungi and are dependent upon this relationship for survival.[146]

File:Neotyphodium coenophialum.jpg

The mycorrhizal symbiosis is ancient, dating to at least 400 million years ago.[127] It often increases the plant's uptake of inorganic compounds, such as nitrate and phosphate from soils having low concentrations of these key plant nutrients.[138][147] The fungal partners may also mediate plant-to-plant transfer of carbohydrates and other nutrients. Such mycorrhizal communities are called "common mycorrhizal networks".[148] A special case of mycorrhiza is myco-heterotrophy, whereby the plant parasitizes the fungus, obtaining all of its nutrients from its fungal symbiont.[149] Some fungal species inhabit the tissues inside roots, stems, and leaves, in which case they are called endophytes.[150] Similar to mycorrhiza, endophytic colonization by fungi may benefit both symbionts; for example, endophytes of grasses impart to their host increased resistance to herbivores and other environmental stresses and receive food and shelter from the plant in return.[151]

With algae and cyanobacteria

File:Lobaria pulmonaria 010108a.jpg

Lichens are formed by a symbiotic relationship between algae or cyanobacteria (referred to in lichen terminology as "photobionts") and fungi (mostly various species of ascomycetes and a few basidiomycetes), in which individual photobiont cells are embedded in a tissue formed by the fungus.[152] Lichens occur in every ecosystem on all continents, play a key role in soil formation and the initiation of biological succession,[153] and are the dominating life forms in extreme environments, including polar, alpine, and semiarid desert regions.[154] They are able to grow on inhospitable surfaces, including bare soil, rocks, tree bark, wood, shells, barnacles and leaves.[155] As in mycorrhizas, the photobiont provides sugars and other carbohydrates via photosynthesis, while the fungus provides minerals and water. The functions of both symbiotic organisms are so closely intertwined that they function almost as a single organism; in most cases the resulting organism differs greatly from the individual components. Lichenization is a common mode of nutrition; around 20% of fungi—between 17,500 and 20,000 described species—are lichenized.[156] Characteristics common to most lichens include obtaining organic carbon by photosynthesis, slow growth, small size, long life, long-lasting (seasonal) vegetative reproductive structures, mineral nutrition obtained largely from airborne sources, and greater tolerance of desiccation than most other photosynthetic organisms in the same habitat.[157]

With insects

Many insects also engage in mutualistic relationships with fungi. Several groups of ants cultivate fungi in the order Agaricales as their primary food source, while ambrosia beetles cultivate various species of fungi in the bark of trees that they infest.[158] Likewise, females of several wood wasp species (genus Sirex) inject their eggs together with spores of the wood-rotting fungus Amylostereum areolatum into the sapwood of pine trees; the growth of the fungus provides ideal nutritional conditions for the development of the wasp larvae.[159] Termites on the African savannah are also known to cultivate fungi,[140] and yeasts of the genera Candida and Lachancea inhabit the gut of a wide range of insects, including neuropterans, beetles, and cockroaches; it is not known whether these fungi benefit their hosts.[160] The larvae of many families of fungicolous flies, particularly those within the superfamily Sciaroidea such as the Mycetophilidae and some Keroplatidae feed on fungal fruiting bodies and sterile mycorrhizae.[161]

As pathogens and parasites

File:Aecidium magnellanicum.jpg

Many fungi are parasites on plants, animals (including humans), and other fungi. Serious pathogens of many cultivated plants causing extensive damage and losses to agriculture and forestry include the rice blast fungus Magnaporthe oryzae,[162] tree pathogens such as Ophiostoma ulmi and Ophiostoma novo-ulmi causing Dutch elm disease,[163] and Cryphonectria parasitica responsible for chestnut blight,[164] and plant pathogens in the genera Fusarium, Ustilago, Alternaria, and Cochliobolus.[144] Some carnivorous fungi, like Paecilomyces lilacinus, are predators of nematodes, which they capture using an array of specialized structures such as constricting rings or adhesive nets.[165]

Some fungi can cause serious diseases in humans, several of which may be fatal if untreated. These include aspergilloses, candidoses, coccidioidomycosis, cryptococcosis, histoplasmosis, mycetomas, and paracoccidioidomycosis. Furthermore, persons with immuno-deficiencies are particularly susceptible to disease by genera such as Aspergillus, Candida, Cryptoccocus,[145][166][167] Histoplasma,[168] and Pneumocystis.[169] Other fungi can attack eyes, nails, hair, and especially skin, the so-called dermatophytic and keratinophilic fungi, and cause local infections such as ringworm and athlete's foot.[170] Fungal spores are also a cause of allergies, and fungi from different taxonomic groups can evoke allergic reactions.[171]



Mycotoxins are secondary metabolites (or natural products), and research has established the existence of biochemical pathways solely for the purpose of producing mycotoxins and other natural products in fungi.[26] Mycotoxins may provide fitness benefits in terms of physiological adaptation, competition with other microbes and fungi, and protection from consumption (fungivory).[172][173] Many fungi produce biologically active compounds, several of which are toxic to animals or plants and are therefore called mycotoxins. Of particular relevance to humans are mycotoxins produced by molds causing food spoilage, and poisonous mushrooms (see above). Particularly infamous are the lethal amatoxins in some Amanita mushrooms, and ergot alkaloids, which have a long history of causing serious epidemics of ergotism (St Anthony's Fire) in people consuming rye or related cereals contaminated with sclerotia of the ergot fungus, Claviceps purpurea.[174] Other notable mycotoxins include the aflatoxins, which are insidious liver toxins and highly carcinogenic metabolites produced by certain Aspergillus species often growing in or on grains and nuts consumed by humans, ochratoxins, patulin, and trichothecenes (e.g., T-2 mycotoxin) and fumonisins, which have significant impact on human food supplies or animal livestock.[175]

Pathogenic mechanisms

Ustilago maydis is a pathogenic plant fungus that causes smut disease in maize and teosinte. Plants have evolved efficient defense systems against pathogenic microbes. A rapid defense reaction after pathogen attack is the oxidative burst that includes the production of reactive oxygen species at the site of the attempted invasion. As a pathogen, U. maydis can respond to such an oxidative burst by an oxidative stress response, regulated by the gene yap1. This response protects U. maydis from the host attack, and is necessary for the pathogen’s virulence.[176] Furthermore, U. maydis has a well-established recombinational DNA repair system that acts during mitosis and meiosis.[177] Recombinational repair during mitosis and meiosis may assist the pathogen in surviving DNA damage arising from the host plant’s oxidative defensive response to infection.[178]

Cryptococcus neoformans is an encapsulated yeast that can live in both plants and animals. Infection with C. neoformans is termed cryptococcosis, and usually affects the lungs. In the lungs, C. neoformans are phagocytosed by alveolar macrophages.[179] However some C. neoformans can survive intracellularly in macrophages.[179] Intracellular survival appears to be the basis for latency, disseminated disease, and resistance to eradication by antifungal agents. One mechanism by which C. neorformans survives the hostile intracellular environment of the macrophage involves up-regulation of expression of genes involved in responses to oxidative stress.[179] Another mechanism involves meiosis. The great majority of environmental and clinical isolates of C. neoformans are mating type a. Filaments of mating type an ordinarily have haploid nuclei, but these can undergo diploidization (perhaps by endoduplication or by stimulated nuclear fusion) to form diploid cells termed blastospores. The diploid nuclei of blastospores are able to undergo meiosis, including recombination, to form haploid basidiospores that can be dispersed.[180] This process is referred to as monokaryotic fruiting. Required for this process is a gene, dmc1, a conserved homologue of genes recA in bacteria and rad51 in eukaryotes, that mediates homologous chromosome pairing during meiosis and repair of DNA double-strand breaks (see Meiosis). Thus, C. neoformans can undergo a meiotic process, monokaryotic fruiting, that promotes recombinational repair in the oxidative, DNA damaging environment of the host macrophage, and this repair capability may contribute to its virulence.[178][180]

Human use

File:S cerevisiae under DIC microscopy.jpg

The human use of fungi for food preparation or preservation and other purposes is extensive and has a long history. Mushroom farming and mushroom gathering are large industries in many countries. The study of the historical uses and sociological impact of fungi is known as ethnomycology. Because of the capacity of this group to produce an enormous range of natural products with antimicrobial or other biological activities, many species have long been used or are being developed for industrial production of antibiotics, vitamins, and anti-cancer and cholesterol-lowering drugs. More recently, methods have been developed for genetic engineering of fungi,[181] enabling metabolic engineering of fungal species. For example, genetic modification of yeast species[182]—which are easy to grow at fast rates in large fermentation vessels—has opened up ways of pharmaceutical production that are potentially more efficient than production by the original source organisms.[183]

Therapeutic uses

Modern chemotherapeutics

Many species produce metabolites that are major sources of pharmacologically active drugs. Particularly important are the antibiotics, including the penicillins, a structurally related group of β-lactam antibiotics that are synthesized from small peptides. Although naturally occurring penicillins such as penicillin G (produced by Penicillium chrysogenum) have a relatively narrow spectrum of biological activity, a wide range of other penicillins can be produced by chemical modification of the natural penicillins. Modern penicillins are semisynthetic compounds, obtained initially from fermentation cultures, but then structurally altered for specific desirable properties.[184] Other antibiotics produced by fungi include: ciclosporin, commonly used as an immunosuppressant during transplant surgery; and fusidic acid, used to help control infection from methicillin-resistant Staphylococcus aureus bacteria.[185] Widespread use of these antibiotics for the treatment of bacterial diseases, such as tuberculosis, syphilis, leprosy, and many others began in the early 20th century and continues to play a major part in anti-bacterial chemotherapy. In nature, antibiotics of fungal or bacterial origin appear to play a dual role: at high concentrations they act as chemical defense against competition with other microorganisms in species-rich environments, such as the rhizosphere, and at low concentrations as quorum-sensing molecules for intra- or interspecies signaling.[186] Other drugs produced by fungi include griseofulvin isolated from Penicillium griseofulvum, used to treat fungal infections,[187] and statins (HMG-CoA reductase inhibitors), used to inhibit cholesterol synthesis. Examples of statins found in fungi include mevastatin from Penicillium citrinum and lovastatin from Aspergillus terreus and the oyster mushroom.[188]

Traditional and folk medicine

Certain mushrooms enjoy usage as therapeutics in folk medicines, such as Traditional Chinese medicine. Notable medicinal mushrooms with a well-documented history of use include Agaricus subrufescens,[189][190] Ganoderma lucidum,[191] and Ophiocordyceps sinensis.[192] Research has identified compounds produced by these and other fungi that have inhibitory biological effects against viruses[193][194] and cancer cells.[189][195] Specific metabolites, such as polysaccharide-K, ergotamine, and β-lactam antibiotics, are routinely used in clinical medicine. The shiitake mushroom is a source of lentinan, a clinical drug approved for use in cancer treatments in several countries, including Japan.[196][197] In Europe and Japan, polysaccharide-K (brand name Krestin), a chemical derived from Trametes versicolor, is an approved adjuvant for cancer therapy.[198]

Cultured foods

Baker's yeast or Saccharomyces cerevisiae, a unicellular fungus, is used to make bread and other wheat-based products, such as pizza dough and dumplings.[199] Yeast species of the genus Saccharomyces are also used to produce alcoholic beverages through fermentation.[200] Shoyu koji mold (Aspergillus oryzae) is an essential ingredient in brewing Shoyu (soy sauce) and sake, and the preparation of miso,[201] while Rhizopus species are used for making tempeh.[202] Several of these fungi are domesticated species that were bred or selected according to their capacity to ferment food without producing harmful mycotoxins (see below), which are produced by very closely related Aspergilli.[203] Quorn, a meat substitute, is made from Fusarium venenatum.[204]

Edible and poisonous species

File:Amanita phalloides 1.JPG

Edible mushrooms are well-known examples of fungi. Many are commercially raised, but others must be harvested from the wild. Agaricus bisporus, sold as button mushrooms when small or Portobello mushrooms when larger, is a commonly eaten species, used in salads, soups, and many other dishes. Many Asian fungi are commercially grown and have increased in popularity in the West. They are often available fresh in grocery stores and markets, including straw mushrooms (Volvariella volvacea), oyster mushrooms (Pleurotus ostreatus), shiitakes (Lentinula edodes), and enokitake (Flammulina spp.).[205]

There are many more mushroom species that are harvested from the wild for personal consumption or commercial sale. Milk mushrooms, morels, chanterelles, truffles, black trumpets, and porcini mushrooms (Boletus edulis) (also known as king boletes) demand a high price on the market. They are often used in gourmet dishes.[206]

Certain types of cheeses require inoculation of milk curds with fungal species that impart a unique flavor and texture to the cheese. Examples include the blue color in cheeses such as Stilton or Roquefort, which are made by inoculation with Penicillium roqueforti.[207] Molds used in cheese production are non-toxic and are thus safe for human consumption; however, mycotoxins (e.g., aflatoxins, roquefortine C, patulin, or others) may accumulate because of growth of other fungi during cheese ripening or storage.[208]

File:Blue Stilton Quarter Front.jpg

Many mushroom species are poisonous to humans, with toxicities ranging from slight digestive problems or allergic reactions as well as hallucinations to severe organ failures and death. Genera with mushrooms containing deadly toxins include Conocybe, Galerina, Lepiota, and, the most infamous, Amanita.[209] The latter genus includes the destroying angel (A. virosa) and the death cap (A. phalloides), the most common cause of deadly mushroom poisoning.[210] The false morel (Gyromitra esculenta) is occasionally considered a delicacy when cooked, yet can be highly toxic when eaten raw.[211] Tricholoma equestre was considered edible until being implicated in serious poisonings causing rhabdomyolysis.[212] Fly agaric mushrooms (Amanita muscaria) also cause occasional non-fatal poisonings, mostly as a result of ingestion for use as a recreational drug for its hallucinogenic properties. Historically, fly agaric was used by different peoples in Europe and Asia and its present usage for religious or shamanic purposes is reported from some ethnic groups such as the Koryak people of north-eastern Siberia.[213]

As it is difficult to accurately identify a safe mushroom without proper training and knowledge, it is often advised to assume that a wild mushroom is poisonous and not to consume it.[214][215]

Pest control


In agriculture, fungi may be useful if they actively compete for nutrients and space with pathogenic microorganisms such as bacteria or other fungi via the competitive exclusion principle,[216] or if they are parasites of these pathogens. For example, certain species may be used to eliminate or suppress the growth of harmful plant pathogens, such as insects, mites, weeds, nematodes, and other fungi that cause diseases of important crop plants.[217] This has generated strong interest in practical applications that use these fungi in the biological control of these agricultural pests. Entomopathogenic fungi can be used as biopesticides, as they actively kill insects.[218] Examples that have been used as biological insecticides are Beauveria bassiana, Metarhizium spp, Hirsutella spp, Paecilomyces (Isaria) spp, and Lecanicillium lecanii.[219][220] Endophytic fungi of grasses of the genus Neotyphodium, such as N. coenophialum, produce alkaloids that are toxic to a range of invertebrate and vertebrate herbivores. These alkaloids protect grass plants from herbivory, but several endophyte alkaloids can poison grazing animals, such as cattle and sheep.[221] Infecting cultivars of pasture or forage grasses with Neotyphodium endophytes is one approach being used in grass breeding programs; the fungal strains are selected for producing only alkaloids that increase resistance to herbivores such as insects, while being non-toxic to livestock.[222]


Certain fungi, in particular "white rot" fungi, can degrade insecticides, herbicides, pentachlorophenol, creosote, coal tars, and heavy fuels and turn them into carbon dioxide, water, and basic elements.[223] Fungi have been shown to biomineralize uranium oxides, suggesting they may have application in the bioremediation of radioactively polluted sites.[224][225][226]

Model organisms

Several pivotal discoveries in biology were made by researchers using fungi as model organisms, that is, fungi that grow and sexually reproduce rapidly in the laboratory. For example, the one gene-one enzyme hypothesis was formulated by scientists using the bread mold Neurospora crassa to test their biochemical theories.[227] Other important model fungi are Aspergillus nidulans and the yeasts Saccaromyces cerevisiae and Schizosaccharomyces pombe, each of which with a long history of use to investigate issues in eukaryotic cell biology and genetics, such as cell cycle regulation, chromatin structure, and gene regulation. Other fungal models have more recently emerged that each address specific biological questions relevant to medicine, plant pathology, and industrial uses; examples include Candida albicans, a dimorphic, opportunistic human pathogen,[228] Magnaporthe grisea, a plant pathogen,[229] and Pichia pastoris, a yeast widely used for eukaryotic protein expression.[230]


Fungi are used extensively to produce industrial chemicals like citric, gluconic, lactic, and malic acids,[231] and industrial enzymes, such as lipases used in biological detergents,[232] cellulases used in making cellulosic ethanol[233] and stonewashed jeans,[234] and amylases,[235] invertases, proteases and xylanases.[236] Several species, most notably Psilocybin mushrooms (colloquially known as magic mushrooms), are ingested for their psychedelic properties, both recreationally and religiously.

See also


  1. ^ Moore RT. (1980). "Taxonomic proposals for the classification of marine yeasts and other yeast-like fungi including the smuts". Botanica Marina. 23: 361–373. 
  2. ^ The classification system presented here is based on the 2007 phylogenetic study by Hibbett et al.
  3. ^ "LIAS Glossary". Retrieved 14 August 2013. 
  4. ^ Simpson DP. (1979). Cassell's Latin Dictionary (5 ed.). London, UK: Cassell Ltd. p. 883. ISBN 0-304-52257-0. 
  5. ^ a b Ainsworth, p. 2.
  6. ^ Mitzka W., ed. (1960). Etymologisches Wörterbuch der deutschen Sprache. Berlin: Walter de Gruyter. 
  7. ^ Alexopoulos et al., p. 1.
  8. ^ Bruns T. (2006). "Evolutionary biology: a kingdom revised". Nature. 443 (7113): 758–761. Bibcode:2006Natur.443..758B. PMID 17051197. doi:10.1038/443758a. 
  9. ^ Baldauf SL, Palmer JD. (1993). "Animals and fungi are each other's closest relatives: congruent evidence from multiple proteins". Proceedings of the National Academy of Sciences U.S.A. 90 (24): 11558–11562. PMC 48023Freely accessible. PMID 8265589. doi:10.1073/pnas.90.24.11558. 
  10. ^ Deacon, p. 4.
  11. ^ a b Deacon, pp. 128–29.
  12. ^ Alexopoulos et al., pp. 28–33.
  13. ^ Alexopoulos et al., pp. 31–32.
  14. ^ Shoji JY, Arioka M, Kitamoto K. (2006). "Possible involvement of pleiomorphic vacuolar networks in nutrient recycling in filamentous fungi". Autophagy. 2 (3): 226–227. PMID 16874107. doi:10.4161/auto.2695. 
  15. ^ Deacon, p. 58.
  16. ^ Zabriskie TM, Jackson MD. (2000). "Lysine biosynthesis and metabolism in fungi". Natural Product Reports. 17 (1): 85–97. PMID 10714900. doi:10.1039/a801345d. 
  17. ^ Xu H, Andi B, Qian J, West AH, Cook PF. (2006). "The α-aminoadipate pathway for lysine biosynthesis in fungi". Cellular Biochemistry and Biophysics. 46 (1): 43–64. PMID 16943623. doi:10.1385/CBB:46:1:43. 
  18. ^ Alexopoulos et al., pp. 27–28.
  19. ^ Alexopoulos et al., p. 685.
  20. ^ Desjardin DE, Oliveira AG, Stevani CV. (2008). "Fungi bioluminescence revisited". Photochemical & Photobiological Sciences. 7 (2): 170–182. PMID 18264584. doi:10.1039/b713328f. 
  21. ^ a b Alexopoulos et al., p. 30.
  22. ^ Alexopoulos et al., pp. 32–33.
  23. ^ Bowman SM, Free SJ. (2006). "The structure and synthesis of the fungal cell wall". BioEssays. 28 (8): 799–808. PMID 16927300. doi:10.1002/bies.20441. 
  24. ^ Alexopoulos et al., p. 33.
  25. ^ Mihail JD, Bruhn JN. (2005). "Foraging behaviour of Armillaria rhizomorph systems". Mycological Research. 109 (11): 1195–1207. PMID 16279413. doi:10.1017/S0953756205003606. 
  26. ^ a b c d Keller NP, Turner G, Bennett JW. (2005). "Fungal secondary metabolism–from biochemistry to genomics". Nature Reviews Microbiology. 3 (12): 937–947. PMID 16322742. doi:10.1038/nrmicro1286. 
  27. ^ Wu S, Schalk M, Clark A, Miles RB, Coates R, Chappell J. (2007). "Redirection of cytosolic or plastidic isoprenoid precursors elevates terpene production in plants". Nature Biotechnology. 24 (11): 1441–1447. PMID 17057703. doi:10.1038/nbt1251. 
  28. ^ Tudzynski B. (2005). "Gibberellin biosynthesis in fungi: genes, enzymes, evolution, and impact on biotechnology". Applied Microbiology and Biotechnology. 66 (6): 597–611. PMID 15578178. doi:10.1007/s00253-004-1805-1. 
  29. ^ Vaupotic T, Veranic P, Jenoe P, Plemenitas A. (2008). "Mitochondrial mediation of environmental osmolytes discrimination during osmoadaptation in the extremely halotolerant black yeast Hortaea werneckii". Fungal Genetics and Biology. 45 (6): 994–1007. PMID 18343697. doi:10.1016/j.fgb.2008.01.006. 
  30. ^ a b Dadachova E, Bryan RA, Huang X, Moadel T, Schweitzer AD, Aisen P, Nosanchuk JD, Casadevall A. (2007). "Ionizing radiation changes the electronic properties of melanin and enhances the growth of melanized fungi". PLoS ONE. 2 (5): e457. Bibcode:2007PLoSO...2..457D. PMC 1866175Freely accessible. PMID 17520016. doi:10.1371/journal.pone.0000457. 
  31. ^ Raghukumar C, Raghukumar S. (1998). "Barotolerance of fungi isolated from deep-sea sediments of the Indian Ocean". Aquatic Microbial Ecology. 15 (2): 153–163. doi:10.3354/ame015153. 
  32. ^ Sancho LG, de la Torre R, Horneck G, Ascaso C, de Los Rios A, Pintado A, Wierzchos J, Schuster M. (2007). "Lichens survive in space: results from the 2005 LICHENS experiment". Astrobiology. 7 (3): 443–454. Bibcode:2007AsBio...7..443S. PMID 17630840. doi:10.1089/ast.2006.0046. 
  33. ^ Brem FM, Lips KR. (2008). "Batrachochytrium dendrobatidis infection patterns among Panamanian amphibian species, habitats and elevations during epizootic and enzootic stages". Diseases of Aquatic Organisms. 81 (3): 189–202. PMID 18998584. doi:10.3354/dao01960. 
  34. ^ Le Calvez T, Burgaud G, Mahé S, Barbier G, Vandenkoornhuyse P. (2009). "Fungal diversity in deep sea hydrothermal ecosystems". Applied and Environmental Microbiology. 75 (20): 6415–6421. PMC 2765129Freely accessible. PMID 19633124. doi:10.1128/AEM.00653-09. 
  35. ^ This estimation is determined by combining the species count for each phyla, based on values obtained from the 10th edition of the Dictionary of the Fungi (Kirk et al., 2008): Ascomycota, 64163 species (p. 55); Basidiomycota, 31515 (p. 78); Blastocladiomycota, 179 (p. 94); Chytridiomycota, 706 (p. 142); Glomeromycota, 169 (p. 287); Microsporidia, >1300 (p. 427); Neocallimastigomycota, 20 (p. 463).
  36. ^ Mueller GM, Schmit JP. (2006). "Fungal biodiversity: what do we know? What can we predict?". Biodiversity and Conservation. 16: 1–5. doi:10.1007/s10531-006-9117-7. 
  37. ^ Hawksworth DL. (2006). "The fungal dimension of biodiversity: magnitude, significance, and conservation". Mycological Research. 95 (6): 641–655. doi:10.1016/S0953-7562(09)80810-1. 
  38. ^ Blackwell M. (2011). "The Fungi: 1, 2, 3 ... 5.1 million species?" (PDF). American Journal of Botany. 98 (3): 426–438. PMID 21613136. doi:10.3732/ajb.1000298. 
  39. ^ a b Kirk et al., p. 489.
  40. ^ a b c d e f g h i Hibbett DS, Binder M, Bischoff JF, Blackwell M, Cannon PF, Eriksson OE; et al. (2007). "A higher level phylogenetic classification of the Fungi" (PDF). Mycological Research. 111 (5): 509–547. PMID 17572334. doi:10.1016/j.mycres.2007.03.004. 
  41. ^ According to one 2001 estimate, some 10,000 fungal diseases are known. Struck C. (2006). "Infection strategies of plant parasitic fungi". In Cooke BM, Jones DG, Kaye B. The Epidemiology of Plant Diseases. Berlin, Germany: Springer. p. 117. ISBN 1-4020-4580-8. 
  42. ^ Peintner U, Pöder R, Pümpel T. (1998). "The Iceman's fungi". Mycological Research. 102 (10): 1153–1162. doi:10.1017/S0953756298006546. 
  43. ^ Ainsworth, p. 1.
  44. ^ Alexopoulos et al., pp. 1–2.
  45. ^ Ainsworth, p. 18.
  46. ^ Hawksworth DL. (2006). "Pandora's Mycological Box: Molecular sequences vs. morphology in understanding fungal relationships and biodiversity". Revista Iberoamericana de Micologia. 23 (3): 127–133. PMID 17196017. doi:10.1016/S1130-1406(06)70031-6. 
  47. ^ Harris SD. (2008). "Branching of fungal hyphae: regulation, mechanisms and comparison with other branching systems". Mycologia. 100 (6): 823–832. PMID 19202837. doi:10.3852/08-177. 
  48. ^ Deacon, p. 51.
  49. ^ Deacon, p. 57.
  50. ^ Chang S-T, Miles PG. (2004). Mushrooms: Cultivation, Nutritional Value, Medicinal Effect and Environmental Impact. Boca Raton, Florida: CRC Press. ISBN 0-8493-1043-1. 
  51. ^ Parniske M. (2008). "Arbuscular mycorrhiza: the mother of plant root endosymbioses". Nature Reviews Microbiology. 6 (10): 763–775. PMID 18794914. doi:10.1038/nrmicro1987. 
  52. ^ Steenkamp ET, Wright J, Baldauf SL. (2006). "The protistan origins of animals and fungi". Molecular Biology and Evolution. 23 (1): 93–106. PMID 16151185. doi:10.1093/molbev/msj011. 
  53. ^ Stevens DA, Ichinomiya M, Koshi Y, Horiuchi H. (2006). "Escape of Candida from caspofungin inhibition at concentrations above the MIC (paradoxical effect) accomplished by increased cell wall chitin; evidence for β-1,6-glucan synthesis inhibition by caspofungin". Antimicrobial Agents and Chemotherapy. 50 (9): 3160–3161. PMC 1563524Freely accessible. PMID 16940118. doi:10.1128/AAC.00563-06. 
  54. ^ Hanson, pp. 127–41.
  55. ^ Ferguson BA, Dreisbach TA, Parks CG, Filip GM, Schmitt CL. (2003). "Coarse-scale population structure of pathogenic Armillaria species in a mixed-conifer forest in the Blue Mountains of northeast Oregon". Canadian Journal of Forest Research. 33 (4): 612–623. doi:10.1139/x03-065. 
  56. ^ Alexopoulos et al., pp. 204–205.
  57. ^ Moss ST. (1986). The Biology of Marine Fungi. Cambridge, UK: Cambridge University Press. p. 76. ISBN 0-521-30899-2. 
  58. ^ Peñalva MA, Arst HN. (2002). "Regulation of gene expression by ambient pH in filamentous fungi and yeasts". Microbiology and Molecular Biology Reviews. 66 (3): 426–446. PMC 120796Freely accessible. PMID 12208998. doi:10.1128/MMBR.66.3.426-446.2002. 
  59. ^ a b Howard RJ, Ferrari MA, Roach DH, Money NP. (1991). "Penetration of hard substrates by a fungus employing enormous turgor pressures". Proceedings of the National Academy of Sciences USA. 88 (24): 11281–11284. Bibcode:1991PNAS...8811281H. PMC 53118Freely accessible. PMID 1837147. doi:10.1073/pnas.88.24.11281. 
  60. ^ Money NP. (1998). "Mechanics of invasive fungal growth and the significance of turgor in plant infection". Molecular Genetics of Host-Specific Toxins in Plant Disease: Proceedings of the 3rd Tottori International Symposium on Host-Specific Toxins, Daisen, Tottori, Japan, August 24–29, 1997. Netherlands: Kluwer Academic Publishers. pp. 261–271. ISBN 0-7923-4981-4. 
  61. ^ Wang ZY, Jenkinson JM, Holcombe LJ, Soanes DM, Veneault-Fourrey C, Bhambra GK, Talbot NJ. (2005). "The molecular biology of appressorium turgor generation by the rice blast fungus Magnaporthe grisea". Biochemical Society Transactions. 33 (Pt 2): 384–388. PMID 15787612. doi:10.1042/BST0330384. 
  62. ^ Pereira JL, Noronha EF, Miller RN, Franco OL. (2007). "Novel insights in the use of hydrolytic enzymes secreted by fungi with biotechnological potential". Letters in Applied Microbiology. 44 (6): 573–581. PMID 17576216. doi:10.1111/j.1472-765X.2007.02151.x. 
  63. ^ Schaller M, Borelli C, Korting HC, Hube B. (2007). "Hydrolytic enzymes as virulence factors of Candida albicans". Mycoses. 48 (6): 365–377. PMID 16262871. doi:10.1111/j.1439-0507.2005.01165.x. 
  64. ^ Farrar JF. (1985). "Carbohydrate metabolism in biotrophic plant pathogens". Microbiological Sciences. 2 (10): 314–317. PMID 3939987. 
  65. ^ Fischer R, Zekert N, Takeshita N. (2008). "Polarized growth in fungi—interplay between the cytoskeleton, positional markers and membrane domains". Molecular Microbiology. 68 (4): 813–826. PMID 18399939. doi:10.1111/j.1365-2958.2008.06193.x. 
  66. ^ Christensen MJ, Bennett RJ, Ansari HA, Koga H, Johnson RD, Bryan GT, Simpson WR, Koolaard JP, Nickless EM, Voisey CR. (2008). "Epichloë endophytes grow by intercalary hyphal extension in elongating grass leaves". Fungal Genetics and Biology. 45 (2): 84–93. PMID 17919950. doi:10.1016/j.fgb.2007.07.013. 
  67. ^ Money NP. (2002). "Mushroom stem cells". Bioessays. 24 (10): 949–952. PMID 12325127. doi:10.1002/bies.10160. 
  68. ^ Willensdorfer M. (2009). "On the evolution of differentiated multicellularity". Evolution. 63 (2): 306–323. PMID 19154376. doi:10.1111/j.1558-5646.2008.00541.x. 
  69. ^ Daniels KJ, Srikantha T, Lockhart SR, Pujol C, Soll DR. (2006). "Opaque cells signal white cells to form biofilms in Candida albicans". EMBO Journal. 25 (10): 2240–2252. PMC 1462973Freely accessible. PMID 16628217. doi:10.1038/sj.emboj.7601099. 
  70. ^ Marzluf GA. (1981). "Regulation of nitrogen metabolism and gene expression in fungi". Microbiological Reviews. 45 (3): 437–461. PMC 281519Freely accessible. PMID 6117784. 
  71. ^ Heynes MJ. (1994). "Regulatory circuits of the amdS gene of Aspergillus nidulans". Antonie Van Leeuwenhoek. 65 (3): 179–182. PMID 7847883. doi:10.1007/BF00871944. 
  72. ^ Dadachova E, Casadevall A. (2008). "Ionizing radiation: how fungi cope, adapt, and exploit with the help of melanin". Current Opinion in Microbiology. 11 (6): 525–531. PMC 2677413Freely accessible. PMID 18848901. doi:10.1016/j.mib.2008.09.013. 
  73. ^ Alexopoulos et al., pp. 48–56.
  74. ^ Kirk et al., p. 633.
  75. ^ Heitman J. (2005). "Sexual reproduction and the evolution of microbial pathogens". Current Biology. 16 (17): R711–R725. PMID 16950098. doi:10.1016/j.cub.2006.07.064. 
  76. ^ Alcamo IE, Pommerville J. (2004). Alcamo's Fundamentals of Microbiology. Boston, Massachusetts: Jones and Bartlett. p. 590. ISBN 0-7637-0067-3. 
  77. ^ a b Redecker D, Raab P. (2006). "Phylogeny of the Glomeromycota (arbuscular mycorrhizal fungi): recent developments and new gene markers". Mycologia. 98 (6): 885–895. PMID 17486965. doi:10.3852/mycologia.98.6.885. 
  78. ^ Guarro J, Gené J, Stchigel AM. (1999). "Developments in fungal taxonomy". Clinical Microbiology Reviews. 12 (3): 454–500. PMC 100249Freely accessible. PMID 10398676. 
  79. ^ a b Taylor JW, Jacobson DJ, Kroken S, Kasuga T, Geiser DM, Hibbett DS, Fisher MC. (2000). "Phylogenetic species recognition and species concepts in fungi". Fungal Genetics and Biology. 31 (1): 21–32. PMID 11118132. doi:10.1006/fgbi.2000.1228. 
  80. ^ Metzenberg RL, Glass NL. (1990). "Mating type and mating strategies in Neurospora". BioEssays. 12 (2): 53–59. PMID 2140508. doi:10.1002/bies.950120202. 
  81. ^ Jennings and Lysek, pp. 107–114.
  82. ^ Deacon, p. 31.
  83. ^ Alexopoulos et al., pp. 492–493.
  84. ^ Jennings and Lysek, p. 142.
  85. ^ Deacon, pp. 21–24.
  86. ^ Linder MB, Szilvay GR, Nakari-Setälä T, Penttilä ME. (2005). "Hydrophobins: the protein-amphiphiles of filamentous fungi". FEMS Microbiology Reviews. 29 (5): 877–896. PMID 16219510. doi:10.1016/j.femsre.2005.01.004. 
  87. ^ Trail F. (2007). "Fungal cannons: explosive spore discharge in the Ascomycota". FEMS Microbiology Letters. 276 (1): 12–18. PMID 17784861. doi:10.1111/j.1574-6968.2007.00900.x. 
  88. ^ Pringle A, Patek SN, Fischer M, Stolze J, Money NP. (2005). "The captured launch of a ballistospore". Mycologia. 97 (4): 866–871. PMID 16457355. doi:10.3852/mycologia.97.4.866. 
  89. ^ Kirk et al., p. 495.
  90. ^ Brodie HJ. (1975). The Bird's Nest Fungi. Toronto, Ontario: University of Toronto Press. p. 80. ISBN 0-8020-5307-6. 
  91. ^ Alexopoulos et al., p. 545.
  92. ^ Jennings and Lysek, pp. 114–115.
  93. ^ Furlaneto MC, Pizzirani-Kleiner AA. (1992). "Intraspecific hybridisation of Trichoderma pseudokoningii by anastomosis and by protoplast fusion". FEMS Microbiology Letters. 69 (2): 191–196. PMID 1537549. doi:10.1111/j.1574-6968.1992.tb05150.x. 
  94. ^ Schardl CL, Craven KD. (2003). "Interspecific hybridization in plant-associated fungi and oomycetes: a review". Molecular Ecology. 12 (11): 2861–2873. PMID 14629368. doi:10.1046/j.1365-294X.2003.01965.x. 
  95. ^ Donoghue MJ, Cracraft J. (2004). Assembling the Tree of Life. Oxford (Oxfordshire), UK: Oxford University Press. p. 187. ISBN 0-19-517234-5. 
  96. ^ Taylor and Taylor, p. 19.
  97. ^ Taylor and Taylor, pp. 7–12.
  98. ^ Butterfield NJ. (2005). "Probable Proterozoic fungi". Paleobiology. 31 (1): 165–182. doi:10.1666/0094-8373(2005)031<0165:PPF>2.0.CO;2. 
  99. ^ Lucking R, Huhndorf S, Pfister D, Plata ER, Lumbsch H. (2009). "Fungi evolved right on track". Mycologia. 101 (6): 810–822. PMID 19927746. doi:10.3852/09-016. 
  100. ^ a b c James TY, Kauff F, Schoch CL, Matheny PB, Hofstetter V, Cox CJ; et al. (2006). "Reconstructing the early evolution of Fungi using a six-gene phylogeny". Nature. 443 (7113): 818–822. Bibcode:2006Natur.443..818J. PMID 17051209. doi:10.1038/nature05110. 
  101. ^ Taylor and Taylor, pp. 84–94 and 106–107.
  102. ^ Schoch CL, Sung GH, López-Giráldez F, Townsend JP, Miadlikowska J, Hofstetter V; et al. (2009). "The Ascomycota tree of life: A phylum-wide phylogeny clarifies the origin and evolution of fundamental reproductive and ecological traits". Systematic Biology. 58 (2): 224–239. PMID 20525580. doi:10.1093/sysbio/syp020. 
  103. ^ a b Brundrett MC. (2002). "Coevolution of roots and mycorrhizas of land plants". New Phytologist. 154 (2): 275–304. doi:10.1046/j.1469-8137.2002.00397.x. 
  104. ^ Redecker D, Kodner R, Graham LE. (2000). "Glomalean fungi from the Ordovician". Science. 289 (5486): 1920–1921. Bibcode:2000Sci...289.1920R. PMID 10988069. doi:10.1126/science.289.5486.1920. 
  105. ^ Taylor TN, Taylor EL. (1996). "The distribution and interactions of some Paleozoic fungi". Review of Palaeobotany and Palynology. 95 (1–4): 83–94. doi:10.1016/S0034-6667(96)00029-2. 
  106. ^ Dotzler N, Walker C, Krings M, Hass H, Kerp H, Taylor TN, Agerer R. (2009). "Acaulosporoid glomeromycotan spores with a germination shield from the 400-million-year-old Rhynie chert". Mycological Progress. 8 (1): 9–18. doi:10.1007/s11557-008-0573-1. 
  107. ^ Taylor JW, Berbee ML. (2006). "Dating divergences in the Fungal Tree of Life: review and new analyses". Mycologia. 98 (6): 838–849. PMID 17486961. doi:10.3852/mycologia.98.6.838. 
  108. ^ Blackwell M, Vilgalys R, James TY, Taylor JW. (2009). "Fungi. Eumycota: mushrooms, sac fungi, yeast, molds, rusts, smuts, etc.". Tree of Life Web Project. Retrieved 2009-04-25. 
  109. ^ Yuan X, Xiao S, Taylor TN. (2005). "Lichen-like symbiosis 600 million years ago". Science. 308 (5724): 1017–1020. Bibcode:2005Sci...308.1017Y. PMID 15890881. doi:10.1126/science.1111347. 
  110. ^ Karatygin IV, Snigirevskaya NS, Vikulin SV. (2009). "The most ancient terrestrial lichen Winfrenatia reticulata: A new find and new interpretation". Paleontological Journal. 43 (1): 107–114. doi:10.1134/S0031030109010110. 
  111. ^ Taylor TN, Hass H, Kerp H, Krings M, Hanlin RT. (2005). "Perithecial Ascomycetes from the 400 million year old Rhynie chert: an example of ancestral polymorphism". Mycologia. 97 (1): 269–285. PMID 16389979. doi:10.3852/mycologia.97.1.269. 
  112. ^ Dennis RL. (1970). "A Middle Pennsylvanian basidiomycete mycelium with clamp connections". Mycologia. 62 (3): 578–584. JSTOR 3757529. doi:10.2307/3757529. 
  113. ^ Hibbett DS, Grimaldi D, Donoghue MJ. (1995). "Cretaceous mushrooms in amber". Nature. 377 (6549): 487. Bibcode:1995Natur.377..487H. doi:10.1038/377487a0. 
  114. ^ Hibbett DS, Grimaldi D, Donoghue MJ. (1997). "Fossil mushrooms from Miocene and Cretaceous ambers and the evolution of homobasidiomycetes". American Journal of Botany. 84 (7): 981–991. JSTOR 2446289. doi:10.2307/2446289. 
  115. ^ Eshet Y, Rampino MR, Visscher H. (1995). "Fungal event and palynological record of ecological crisis and recovery across the Permian-Triassic boundary". Geology. 23 (1): 967–970. Bibcode:1995Geo....23..967E. doi:10.1130/0091-7613(1995)023<0967:FEAPRO>2.3.CO;2. 
  116. ^ Foster CB, Stephenson MH, Marshall C, Logan GA, Greenwood PF. (2002). "A revision of Reduviasporonites Wilson 1962: description, illustration, comparison and biological affinities". Palynology. 26 (1): 35–58. doi:10.2113/0260035. 
  117. ^ López-Gómez J, Taylor EL. (2005). "Permian-Triassic transition in Spain: a multidisciplinary approach". Palaeogeography, Palaeoclimatology, Palaeoecology. 229 (1–2): 1–2. doi:10.1016/j.palaeo.2005.06.028. 
  118. ^ Looy CV, Twitchett RJ, Dilcher DL, Van Konijnenburg-van Cittert JHA, Visscher H. (2005). "Life in the end-Permian dead zone". Proceedings of the National Academy of Sciences USA. 162 (4): 7879–7883. Bibcode:2001PNAS...98.7879L. PMC 35436Freely accessible. PMID 11427710. doi:10.1073/pnas.131218098. See image 2 
  119. ^ Ward PD, Botha J, Buick R, De Kock MO, Erwin DH, Garrison GH, Kirschvink JL, Smith R. (2005). "Abrupt and gradual extinction among late Permian land vertebrates in the Karoo Basin, South Africa". Science. 307 (5710): 709–714. Bibcode:2005Sci...307..709W. PMID 15661973. doi:10.1126/science.1107068. 
  120. ^ Shalchian-Tabrizi K, Minge MA, Espelund M, Orr R, Ruden T, Jakobsen KS, Cavalier-Smith T. (2008). "Multigene phylogeny of choanozoa and the origin of animals". PLoS ONE. 3 (5): e2098. Bibcode:2008PLoSO...3.2098S. PMC 2346548Freely accessible. PMID 18461162. doi:10.1371/journal.pone.0002098. 
  121. ^ See Palaeos Fungi: Fungi for an introduction to fungal taxonomy, including recent controversies. archive
  122. ^ Celio GJ, Padamsee M, Dentinger BT, Bauer R, McLaughlin DJ. (2006). "Assembling the Fungal Tree of Life: constructing the structural and biochemical database". Mycologia. 98 (6): 850–859. PMID 17486962. doi:10.3852/mycologia.98.6.850. 
  123. ^ Gill EE, Fast NM. (2006). "Assessing the microsporidia-fungi relationship: Combined phylogenetic analysis of eight genes". Gene. 375: 103–109. PMID 16626896. doi:10.1016/j.gene.2006.02.023. 
  124. ^ Liu YJ, Hodson MC, Hall BD. (2006). "Loss of the flagellum happened only once in the fungal lineage: phylogenetic structure of kingdom Fungi inferred from RNA polymerase II subunit genes". BMC Evolutionary Biology. 6: 74. PMC 1599754Freely accessible. PMID 17010206. doi:10.1186/1471-2148-6-74. 
  125. ^ James TY, Letcher PM, Longcore JE, Mozley-Standridge SE, Porter D, Powell MJ, Griffith GW, Vilgalys R. (2006). "A molecular phylogeny of the flagellated fungi (Chytridiomycota) and description of a new phylum (Blastocladiomycota)". Mycologia. 98 (6): 860–871. PMID 17486963. doi:10.3852/mycologia.98.6.860. 
  126. ^ Lockhart R, Van Dyke MI, Beadle IR, Humphreys P, McCarthy AJ. (2006). "Molecular biological detection of anaerobic gut fungi (Neocallimastigales) from landfill sites". Applied and Environmental Microbiology. 72 (8): 5659–61. doi:10.1128/AEM.01057-06. 
  127. ^ a b Remy W, Taylor TN, Hass H, Kerp H. (1994). "4-hundred million year old vesicular-arbuscular mycorrhizae". Proceedings of the National Academy of Sciences USA. 91 (25): 11841–11843. Bibcode:1994PNAS...9111841R. PMC 45331Freely accessible. PMID 11607500. doi:10.1073/pnas.91.25.11841. 
  128. ^ Schüssler A, Schwarzott D, Walker C. (2001). "A new fungal phylum, the Glomeromycota: phylogeny and evolution". Mycological Research. 105 (12): 1413–1421. doi:10.1017/S0953756201005196. 
  129. ^ Alexopoulos et al., p. 145.
  130. ^ For an example, see Samuels GJ. (2006). "Trichoderma: systematics, the sexual state, and ecology". Phytopathology. 96 (2): 195–206. PMID 18943925. doi:10.1094/PHYTO-96-0195. 
  131. ^ Radford A, Parish JH. (1997). "The genome and genes of Neurospora crassa". Fungal Genetics and Biology: FG & B. 21 (3): 258–266. PMID 9290240. doi:10.1006/fgbi.1997.0979. 
  132. ^ Valverde ME, Paredes-López O, Pataky JK, Guevara-Lara F. (1995). "Huitlacoche (Ustilago maydis) as a food source—biology, composition, and production". Critical Reviews in Food Science and Nutrition. 35 (3): 191–229. PMID 7632354. doi:10.1080/10408399509527699. 
  133. ^ Zisova LG. (2009). "Malassezia species and seborrheic dermatitis". Folia Medica. 51 (1): 23–33. PMID 19437895. 
  134. ^ Perfect JR. (2006). "Cryptococcus neoformans: the yeast that likes it hot". FEMS Yeast Research. 6 (4): 463–468. PMID 16696642. doi:10.1111/j.1567-1364.2006.00051.x. 
  135. ^ Blackwell M, Spatafora JW. (2004). "Fungi and their allies". In Bills GF, Mueller GM, Foster MS. Biodiversity of Fungi: Inventory and Monitoring Methods. Amsterdam: Elsevier Academic Press. pp. 18–20. ISBN 0-12-509551-1. 
  136. ^ Shalchian-Tabrizi K, Minge MA, Espelund M, Orr R, Ruden T, Jakobsen KS, Cavalier-Smith T. (2008). "Multigene phylogeny of Choanozoa and the origin of animals". PLoS ONE. 3 (5): e2098. Bibcode:2008PLoSO...3.2098S. PMC 2346548Freely accessible. PMID 18461162. doi:10.1371/journal.pone.0002098. 
  137. ^ Gadd GM. (2007). "Geomycology: biogeochemical transformations of rocks, minerals, metals and radionuclides by fungi, bioweathering and bioremediation". Mycological Research. 111 (Pt 1): 3–49. PMID 17307120. doi:10.1016/j.mycres.2006.12.001. 
  138. ^ a b Lindahl BD, Ihrmark K, Boberg J, Trumbore SE, Högberg P, Stenlid J, Finlay RD. (2007). "Spatial separation of litter decomposition and mycorrhizal nitrogen uptake in a boreal forest". New Phytologist. 173 (3): 611–620. PMID 17244056. doi:10.1111/j.1469-8137.2006.01936.x. 
  139. ^ Barea JM, Pozo MJ, Azcón R, Azcón-Aguilar C. (2005). "Microbial co-operation in the rhizosphere". Journal of Experimental Botany. 56 (417): 1761–1778. PMID 15911555. doi:10.1093/jxb/eri197. 
  140. ^ a b Aanen DK. (2006). "As you reap, so shall you sow: coupling of harvesting and inoculating stabilizes the mutualism between termites and fungi". Biology Letters. 2 (2): 209–212. PMC 1618886Freely accessible. PMID 17148364. doi:10.1098/rsbl.2005.0424. 
  141. ^ Nikoh N, Fukatsu T. (2000). "Interkingdom host jumping underground: phylogenetic analysis of entomoparasitic fungi of the genus Cordyceps". Molecular Biology and Evolution. 17 (4): 629–638. PMID 10742053. doi:10.1093/oxfordjournals.molbev.a026341. 
  142. ^ Perotto S, Bonfante P. (1997). "Bacterial associations with mycorrhizal fungi: close and distant friends in the rhizosphere". Trends in Microbiology. 5 (12): 496–501. PMID 9447662. doi:10.1016/S0966-842X(97)01154-2. 
  143. ^ Arnold AE, Mejía LC, Kyllo D, Rojas EI, Maynard Z, Robbins N, Herre EA. (2003). "Fungal endophytes limit pathogen damage in a tropical tree". Proceedings of the National Academy of Sciences USA. 100 (26): 15649–15654. Bibcode:2003PNAS..10015649A. PMC 307622Freely accessible. PMID 14671327. doi:10.1073/pnas.2533483100. 
  144. ^ a b Paszkowski U. (2006). "Mutualism and parasitism: the yin and yang of plant symbioses". Current Opinion in Plant Biology. 9 (4): 364–370. PMID 16713732. doi:10.1016/j.pbi.2006.05.008. 
  145. ^ a b Hube B. (2004). "From commensal to pathogen: stage- and tissue-specific gene expression of Candida albicans". Current Opinion in Microbiology. 7 (4): 336–341. PMID 15288621. doi:10.1016/j.mib.2004.06.003. 
  146. ^ Bonfante P. (2003). "Plants, mycorrhizal fungi and endobacteria: a dialog among cells and genomes". The Biological Bulletin. 204 (2): 215–220. JSTOR 1543562. PMID 12700157. doi:10.2307/1543562. 
  147. ^ van der Heijden MG, Streitwolf-Engel R, Riedl R, Siegrist S, Neudecker A, Ineichen K, Boller T, Wiemken A, Sanders IR. (2006). "The mycorrhizal contribution to plant productivity, plant nutrition and soil structure in experimental grassland". New Phytologist. 172 (4): 739–752. PMID 17096799. doi:10.1111/j.1469-8137.2006.01862.x. 
  148. ^ Selosse MA, Richard F, He X, Simard SW. (2006). "Mycorrhizal networks: des liaisons dangereuses?". Trends in Ecology and Evolution. 21 (11): 621–628. PMID 16843567. doi:10.1016/j.tree.2006.07.003. 
  149. ^ Merckx V, Bidartondo MI, Hynson NA. (2009). "Myco-heterotrophy: when fungi host plants". Annals of Botany. 104 (7): 1255–1261. PMC 2778383Freely accessible. PMID 19767309. doi:10.1093/aob/mcp235. 
  150. ^ Schulz B, Boyle C. (2005). "The endophytic continuum". Mycological Research. 109 (Pt 6): 661–686. PMID 16080390. doi:10.1017/S095375620500273X. 
  151. ^ Clay K, Schardl C. (2002). "Evolutionary origins and ecological consequences of endophyte symbiosis with grasses". American Naturalist. 160 (suppl. 4): S99–S127. PMID 18707456. doi:10.1086/342161. 
  152. ^ Brodo IM, Sharnoff SD. (2001). Lichens of North America. New Haven, Connecticut: Yale University Press. ISBN 0-300-08249-5. 
  153. ^ Raven PH, Evert RF, Eichhorn, SE. (2005). "14—Fungi". Biology of Plants (7 ed.). W. H. Freeman. p. 290. ISBN 978-0-7167-1007-3. 
  154. ^ Deacon, p. 267.
  155. ^ Purvis W. (2000). Lichens. Washington, D.C.: Smithsonian Institution Press in association with the Natural History Museum, London. pp. 49–75. ISBN 1-56098-879-7. 
  156. ^ Kirk et al., p. 378.
  157. ^ Deacon, pp. 267–276.
  158. ^ Douglas AE. (1989). "Mycetocyte symbiosis in insects". Biological Reviews of the Cambridge Philosophical Society. 64 (4): 409–434. PMID 2696562. doi:10.1111/j.1469-185X.1989.tb00682.x. 
  159. ^ Deacon, p. 277.
  160. ^ Nguyen NH, Suh SO, Blackwell M. (2007). "Five novel Candida species in insect-associated yeast clades isolated from Neuroptera and other insects". Mycologia. 99 (6): 842–858. PMID 18333508. doi:10.3852/mycologia.99.6.842. 
  161. ^ Chandler PJ. (2010). A Dipterist's Handbook (2nd Edition). U.K.: The Amateur Entomologists' Society. pp. 1–525. 
  162. ^ Talbot NJ. (2003). "On the trail of a cereal killer: Exploring the biology of Magnaporthe grisea". Annual Reviews in Microbiology. 57: 177–202. PMID 14527276. doi:10.1146/annurev.micro.57.030502.090957. 
  163. ^ Paoletti M, Buck KW, Brasier CM. (2006). "Selective acquisition of novel mating type and vegetative incompatibility genes via interspecies gene transfer in the globally invading eukaryote Ophiostoma novo-ulmi". Molecular Ecology. 15 (1): 249–262. PMID 16367844. doi:10.1111/j.1365-294X.2005.02728.x. 
  164. ^ Gryzenhout M, Wingfield BD, Wingfield MJ. (2006). "New taxonomic concepts for the important forest pathogen Cryphonectria parasitica and related fungi". FEMS Microbiology Letters. 258 (2): 161–172. PMID 16640568. doi:10.1111/j.1574-6968.2006.00170.x. 
  165. ^ Yang Y, Yang E, An Z, Liu X. (2007). "Evolution of nematode-trapping cells of predatory fungi of the Orbiliaceae based on evidence from rRNA-encoding DNA and multiprotein sequences". Proceedings of the National Academy of Sciences USA. 104 (20): 8379–8384. Bibcode:2007PNAS..104.8379Y. PMC 1895958Freely accessible. PMID 17494736. doi:10.1073/pnas.0702770104. 
  166. ^ Nielsen K, Heitman J. (2007). "Sex and virulence of human pathogenic fungi". Advances in Genetics. Advances in Genetics. 57: 143–173. ISBN 978-0-12-017657-1. PMID 17352904. doi:10.1016/S0065-2660(06)57004-X. 
  167. ^ Brakhage AA. (2005). "Systemic fungal infections caused by Aspergillus species: epidemiology, infection process and virulence determinants". Current Drug Targets. 6 (8): 875–886. PMID 16375671. doi:10.2174/138945005774912717. 
  168. ^ Kauffman CA. (2007). "Histoplasmosis: a clinical and laboratory update". Clinical Microbiology Reviews. 20 (1): 115–132. PMC 1797635Freely accessible. PMID 17223625. doi:10.1128/CMR.00027-06. 
  169. ^ Cushion MT, Smulian AG, Slaven BE, Sesterhenn T, Arnold J, Staben C, Porollo A, Adamczak R, Meller J. (2007). "Transcriptome of Pneumocystis carinii during fulminate infection: carbohydrate metabolism and the concept of a compatible parasite". PLoS ONE. 2 (5): e423. Bibcode:2007PLoSO...2..423C. PMC 1855432Freely accessible. PMID 17487271. doi:10.1371/journal.pone.0000423. 
  170. ^ Cook GC, Zumla AI. (2008). Manson's Tropical Diseases: Expert Consult. Edinburgh, Scotland: Saunders Ltd. p. 347. ISBN 1-4160-4470-1. 
  171. ^ Simon-Nobbe B, Denk U, Pöll V, Rid R, Breitenbach M. (2008). "The spectrum of fungal allergy". International Archives of Allergy and Immunology. 145 (1): 58–86. PMID 17709917. doi:10.1159/000107578. 
  172. ^ Demain AL, Fang A. (2000). "The natural functions of secondary metabolites". Advances in Biochemical Engineering/Biotechnology. Advances in Biochemical Engineering/Biotechnology. 69: 1–39. ISBN 978-3-540-67793-2. PMID 11036689. doi:10.1007/3-540-44964-7_1. 
  173. ^ Rohlfs M, Albert M, Keller NP, Kempken F. (2007). "Secondary chemicals protect mould from fungivory". Biology Letters. 3 (5): 523–525. PMC 2391202Freely accessible. PMID 17686752. doi:10.1098/rsbl.2007.0338. 
  174. ^ Schardl CL, Panaccione DG, Tudzynski P. (2006). "Ergot alkaloids—biology and molecular biology". The Alkaloids. Chemistry and Biology. The Alkaloids: Chemistry and Biology. 63: 45–86. ISBN 978-0-12-469563-4. PMID 17133714. doi:10.1016/S1099-4831(06)63002-2. 
  175. ^ van Egmond HP, Schothorst RC, Jonker MA. (2007). "Regulations relating to mycotoxins in food: perspectives in a global and European context". Analytical and Bioanalytical Chemistry. 389 (1): 147–157. PMID 17508207. doi:10.1007/s00216-007-1317-9. 
  176. ^ Molina L, Kahmann R. (2007). "An Ustilago maydis gene involved in H2O2 detoxification is required for virulence". Plant Cell. 19 (7): 2293–2309. PMC 1955693Freely accessible. PMID 17616735. doi:10.1105/tpc.107.052332. 
  177. ^ Kojic M, Zhou Q, Lisby M, Holloman WK. (2006). "Rec2 interplay with both Brh2 and Rad51 balances recombinational repair in Ustilago maydis". Molecular and Cellular Biology. 26 (2): 678–688. PMC 1346908Freely accessible. PMID 16382157. doi:10.1128/MCB.26.2.678-688.2006. 
  178. ^ a b Michod RE, Bernstein H, Nedelcu AM. (2008). "Adaptive value of sex in microbial pathogens" (PDF). Infection, Genetics and Evolution. 8 (3): 267–285. PMID 18295550. doi:10.1016/j.meegid.2008.01.002. 
  179. ^ a b c Fan W, Kraus PR, Boily MJ, Heitman J. (2005). "Cryptococcus neoformans gene expression during murine macrophage infection". Eukaryotic Cell. 4 (8): 1420–1433. PMC 1214536Freely accessible. PMID 16087747. doi:10.1128/EC.4.8.1420-1433.2005. 
  180. ^ a b Lin X, Hull CM, Heitman J. (2005). "Sexual reproduction between partners of the same mating type in Cryptococcus neoformans". Nature. 434 (7036): 1017–1021. Bibcode:2005Natur.434.1017L. PMID 15846346. doi:10.1038/nature03448. 
  181. ^ Fincham JRS. (1989). "Transformation in fungi". Microbiological Reviews. 53 (1): 148–170. PMC 372721Freely accessible. PMID 2651864. 
  182. ^ Hawkins KM, Smolke CD. (2008). "Production of benzylisoquinoline alkaloids in Saccharomyces cerevisiae". Nature Chemical Biology. 4 (9): 564–573. PMC 2830865Freely accessible. PMID 18690217. doi:10.1038/nchembio.105. 
  183. ^ Huang B, Guo J, Yi B, Yu X, Sun L, Chen W. (2008). "Heterologous production of secondary metabolites as pharmaceuticals in Saccharomyces cerevisiae". Biotechnology Letters. 30 (7): 1121–1137. PMID 18512022. doi:10.1007/s10529-008-9663-z. 
  184. ^ Brakhage AA, Spröte P, Al-Abdallah Q, Gehrke A, Plattner H, Tüncher A. (2004). "Regulation of penicillin biosynthesis in filamentous fungi". Advances in Biochemical Engineering/Biotechnology. 88: 45–90. PMID 15719552. doi:10.1007/b99257. 
  185. ^ Pan A, Lorenzotti S, Zoncada A. (2008). "Registered and investigational drugs for the treatment of methicillin-resistant Staphylococcus aureus infection". Recent Patents on Anti-infective Drug Discovery. 3 (1): 10–33. PMID 18221183. doi:10.2174/157489108783413173. 
  186. ^ Fajardo A, Martínez JL. (2008). "Antibiotics as signals that trigger specific bacterial responses". Current Opinion in Microbiology. 11 (2): 161–167. PMID 18373943. doi:10.1016/j.mib.2008.02.006. 
  187. ^ Loo DS. (2006). "Systemic antifungal agents: an update of established and new therapies". Advances in Dermatology. 22: 101–124. PMID 17249298. doi:10.1016/j.yadr.2006.07.001. 
  188. ^ Manzoni M, Rollini M. (2002). "Biosynthesis and biotechnological production of statins by filamentous fungi and application of these cholesterol-lowering drugs". Applied Microbiology and Biotechnology. 58 (5): 555–564. PMID 11956737. doi:10.1007/s00253-002-0932-9. 
  189. ^ a b Hetland G, Johnson E, Lyberg T, Bernardshaw S, Tryggestad AM, Grinde B. (2008). "Effects of the medicinal mushroom Agaricus blazei Murill on immunity, infection and cancer". Scandinavian Journal of Immunology. 68 (4): 363–370. PMID 18782264. doi:10.1111/j.1365-3083.2008.02156.x. 
  190. ^ Firenzuoli F, Gori L, Lombardo G. (2008). "The medicinal mushroom Agaricus blazei Murrill: review of literature and pharmaco-toxicological problems". Evidence-based Complementary and Alternative Medicine: eCAM. 5 (1): 3–15. PMC 2249742Freely accessible. PMID 18317543. doi:10.1093/ecam/nem007. 
  191. ^ Paterson RR. (2006). "Ganoderma–a therapeutic fungal biofactory". Phytochemistry. 67 (18): 1985–2001. PMID 16905165. doi:10.1002/chin.200650268. 
  192. ^ Paterson RR. (2008). "Cordyceps: a traditional Chinese medicine and another fungal therapeutic biofactory?". Phytochemistry. 69 (7): 1469–1495. PMID 18343466. doi:10.1016/j.phytochem.2008.01.027. 
  193. ^ el-Mekkawy S, Meselhy MR, Nakamura N, Tezuka Y, Hattori M, Kakiuchi N, Shimotohno K, Kawahata T, Otake T. (1998). "Anti-HIV-1 and anti-HIV-1-protease substances from Ganoderma lucidum". Phytochemistry. 49 (6): 1651–1657. PMID 9862140. doi:10.1016/S0031-9422(98)00254-4. 
  194. ^ El Dine RS, El Halawany AM, Ma CM, Hattori M. (2008). "Anti-HIV-1 protease activity of lanostane triterpenes from the vietnamese mushroom Ganoderma colossum". Journal of Natural Products. 71 (6): 1022–1026. PMID 18547117. doi:10.1021/np8001139. 
  195. ^ Yuen JW, Gohel MD. (2005). "Anticancer effects of Ganoderma lucidum: a review of scientific evidence". Nutrition and Cancer. 53 (1): 11–17. PMID 16351502. doi:10.1207/s15327914nc5301_2. 
  196. ^ Sullivan R, Smith JE, Rowan NJ. (2006). "Medicinal mushrooms and cancer therapy: translating a traditional practice into Western medicine". Perspectives in Biology and Medicine. 49 (2): 159–170. PMID 16702701. doi:10.1353/pbm.2006.0034. 
  197. ^ Halpern GM, Miller A. (2002). Medicinal Mushrooms: Ancient Remedies for Modern Ailments. New York, New York: M. Evans and Co. p. 116. ISBN 0-87131-981-0. 
  198. ^ Fisher M, Yang LX. (2002). "Anticancer effects and mechanisms of polysaccharide-K (PSK): implications of cancer immunotherapy". Anticancer Research. 22 (3): 1737–1754. PMID 12168863. 
  199. ^ Kulp K. (2000). Handbook of Cereal Science and Technology. CRC Press. ISBN 0-8247-8294-1. 
  200. ^ Piskur J, Rozpedowska E, Polakova S, Merico A, Compagno C. (2006). "How did Saccharomyces evolve to become a good brewer?". Trends in Genetics. 22 (4): 183–186. PMID 16499989. doi:10.1016/j.tig.2006.02.002. 
  201. ^ Abe K, Gomi K, Hasegawa F, Machida M. (2006). "Impact of Aspergillus oryzae genomics on industrial production of metabolites". Mycopathologia. 162 (3): 143–153. PMID 16944282. doi:10.1007/s11046-006-0049-2. 
  202. ^ Hachmeister KA, Fung DY. (1993). "Tempeh: a mold-modified indigenous fermented food made from soybeans and/or cereal grains". Critical Reviews in Microbiology. 19 (3): 137–188. PMID 8267862. doi:10.3109/10408419309113527. 
  203. ^ Jørgensen TR. (2007). "Identification and toxigenic potential of the industrially important fungi, Aspergillus oryzae and Aspergillus sojae". Journal of Food Protection. 70 (12): 2916–2934. PMID 18095455. 
  204. ^ O'Donnell K, Cigelnik E, Casper HH. (1998). "Molecular phylogenetic, morphological, and mycotoxin data support reidentification of the Quorn mycoprotein fungus as Fusarium venenatum". Fungal Genetics and Biology. 23 (1): 57–67. PMID 9501477. doi:10.1006/fgbi.1997.1018. 
  205. ^ Stamets P. (2000). Growing Gourmet and Medicinal Mushrooms = [Shokuyō oyobi yakuyō kinoko no saibai]. Berkeley, California: Ten Speed Press. pp. 233–248. ISBN 1-58008-175-4. 
  206. ^ Hall, pp. 13–26.
  207. ^ Kinsella JE, Hwang DH. (1976). "Enzymes of Penicillium roqueforti involved in the biosynthesis of cheese flavor". CRC Critical Reviews in Food Science and Nutrition. 8 (2): 191–228. PMID 21770. doi:10.1080/10408397609527222. 
  208. ^ Erdogan A, Gurses M, Sert S. (2004). "Isolation of moulds capable of producing mycotoxins from blue mouldy Tulum cheeses produced in Turkey". International Journal of Food Microbiology. 85 (1–2): 83–85. PMID 12810273. doi:10.1016/S0168-1605(02)00485-3. 
  209. ^ Orr DB, Orr RT. (1979). Mushrooms of Western North America. Berkeley, California: University of California Press. p. 17. ISBN 0-520-03656-5. 
  210. ^ Vetter J. (1998). "Toxins of Amanita phalloides". Toxicon. 36 (1): 13–24. PMID 9604278. doi:10.1016/S0041-0101(97)00074-3. 
  211. ^ Leathem AM, Dorran TJ. (2007). "Poisoning due to raw Gyromitra esculenta (false morels) west of the Rockies". Canadian Journal of Emergency Medicine. 9 (2): 127–130. PMID 17391587. 
  212. ^ Karlson-Stiber C, Persson H. (2003). "Cytotoxic fungi—an overview". Toxicon. 42 (4): 339–349. PMID 14505933. doi:10.1016/S0041-0101(03)00238-1. 
  213. ^ Michelot D, Melendez-Howell LM. (2003). "Amanita muscaria: chemistry, biology, toxicology, and ethnomycology". Mycological Research. 107 (Pt 2): 131–146. PMID 12747324. doi:10.1017/S0953756203007305. 
  214. ^ Hall, p. 7.
  215. ^ Ammirati JF, McKenny M, Stuntz DE. (1987). The New Savory Wild Mushroom. Seattle, Washington: University of Washington Press. pp. xii–xiii. ISBN 0-295-96480-4. 
  216. ^ López-Gómez J, Molina-Meyer M. (2006). "The competitive exclusion principle versus biodiversity through competitive segregation and further adaptation to spatial heterogeneities". Theoretical Population Biology. 69 (1): 94–109. PMID 16223517. doi:10.1016/j.tpb.2005.08.004. 
  217. ^ Becker H. (1998). "Setting the Stage To Screen Biocontrol Fungi". United States Department of Agriculture, Agricultural Research Service. Retrieved 2009-02-23. 
  218. ^ Keiller TS. "Whey-based fungal microfactory technology for enhanced biological pest management using fungi" (PDF). UVM Innovations. Retrieved 2011-10-29. 
  219. ^ Deshpande MV. (1999). "Mycopesticide production by fermentation: potential and challenges". Critical Reviews in Microbiology. 25 (3): 229–243. PMID 10524330. doi:10.1080/10408419991299220. 
  220. ^ Thomas MB, Read AF. (2007). "Can fungal biopesticides control malaria?". Nature Reviews Microbiology. 5 (5): 377–383. PMID 17426726. doi:10.1038/nrmicro1638. 
  221. ^ Bush LP, Wilkinson HH, Schardl CL. (1997). "Bioprotective alkaloids of grass-fungal endophyte symbioses". Plant Physiology. 114 (1): 1–7. PMC 158272Freely accessible. PMID 12223685. 
  222. ^ Bouton JH, Latch GCM, Hill NS, Hoveland CS, McCannc MA, Watson RH, Parish JA, Hawkins LL, Thompson FN. (2002). "Use of nonergot alkaloid-producing endophytes for alleviating tall fescue toxicosis in sheep". Agronomy Journal. 94: 567–574.  Review by PubMed
  223. ^ Christian V, Shrivastava R, Shukla D, Modi HA, Vyas BR. (2005). "Degradation of xenobiotic compounds by lignin-degrading white-rot fungi: enzymology and mechanisms involved". Indian Journal of Experimental Biology. 43 (4): 301–312. PMID 15875713. 
  224. ^ "Fungi to fight 'toxic war zones'". BBC News. May 5, 2008. 
  225. ^ Fomina M, Charnock JM, Hillier S, Alvarez R, Gadd GM. (2007). "Fungal transformations of uranium oxides". Environmental Microbiology. 9 (7): 1696–1710. PMID 17564604. doi:10.1111/j.1462-2920.2007.01288.x. 
  226. ^ Fomina M, Charnock JM, Hillier S, Alvarez R, Livens F, Gadd GM. (2008). "Role of fungi in the biogeochemical fate of depleted uranium". Current Biology. 18 (9): R375–R377. PMID 18460315. doi:10.1016/j.cub.2008.03.011. 
  227. ^ Beadle GW, Tatum EL. (1941). "Genetic control of biochemical reactions in Neurospora". Proceedings of the National Academy of Sciences of the USA. 27 (11): 499–506. Bibcode:1941PNAS...27..499B. PMC 1078370Freely accessible. PMID 16588492. doi:10.1073/pnas.27.11.499. 
  228. ^ Datta A, Ganesan K, Natarajan K. (1989). "Current trends in Candida albicans research". Advances in Microbial Physiology. Advances in Microbial Physiology. 30: 53–88. ISBN 978-0-12-027730-8. PMID 2700541. doi:10.1016/S0065-2911(08)60110-1. 
  229. ^ Dean RA. (2005). "The genome sequence of the rice blast fungus Magnaporthe grisea". Nature. 434 (7036): 980–986. Bibcode:2005Natur.434..980D. PMID 15846337. doi:10.1038/nature03449. 
  230. ^ Daly R, Hearn MT. (2005). "Expression of heterologous proteins in Pichia pastoris: a useful experimental tool in protein engineering and production". Journal of Molecular Recognition. 18 (2): 119–138. PMID 15565717. doi:10.1002/jmr.687. 
  231. ^ Schlegel HG. (1993). General Microbiology. Cambridge, UK: Cambridge University Press. p. 360. ISBN 0-521-43980-9. 
  232. ^ Joseph B, Ramteke PW, Thomas G. (2008). "Cold active microbial lipases: some hot issues and recent developments". Biotechnology Advances. 26 (5): 457–470. PMID 18571355. doi:10.1016/j.biotechadv.2008.05.003. 
  233. ^ Kumar R, Singh S, Singh OV. (2008). "Bioconversion of lignocellulosic biomass: biochemical and molecular perspectives". Journal of Industrial Microbiology and Biotechnology. 35 (5): 377–391. PMID 18338189. doi:10.1007/s10295-008-0327-8. 
  234. ^ "Trichoderma spp., including T. harzianum, T. viride, T. koningii, T. hamatum and other spp. Deuteromycetes, Moniliales (asexual classification system)". Biological Control: A Guide to Natural Enemies in North America. Retrieved 2007-07-10. 
  235. ^ Olempska-Beer ZS, Merker RI, Ditto MD, DiNovi MJ. (2006). "Food-processing enzymes from recombinant microorganisms—a review". Regulatory Toxicology and Pharmacology. 45 (2): 144–158. PMID 16769167. doi:10.1016/j.yrtph.2006.05.001. 
  236. ^ Polizeli ML, Rizzatti AC, Monti R, Terenzi HF, Jorge JA, Amorim DS. (2005). "Xylanases from fungi: properties and industrial applications". Applied Microbiology and Biotechnology. 67 (5): 577–591. PMID 15944805. doi:10.1007/s00253-005-1904-7. 
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Cited literature

  • Ainsworth GC. (1976). Introduction to the History of Mycology. Cambridge, UK: Cambridge University Press. ISBN 0-521-11295-8. 
  • Alexopoulos CJ, Mims CW, Blackwell M. (1996). Introductory Mycology. John Wiley and Sons. ISBN 0-471-52229-5. 
  • Chandler PJ. (2010). A Dipterist's Handbook (2nd Edition). The Amateur Entomologists' Society. pp. 1–525. 
  • Deacon J. (2005). Fungal Biology. Cambridge, Massachusetts: Blackwell Publishers. ISBN 1-4051-3066-0. 
  • Hall IR. (2003). Edible and Poisonous Mushrooms of the World. Portland, Oregon: Timber Press. ISBN 0-88192-586-1. 
  • Hanson JR. (2008). The Chemistry of Fungi. Royal Society Of Chemistry. ISBN 0-85404-136-2. 
  • Jennings DH, Lysek G. (1996). Fungal Biology: Understanding the Fungal Lifestyle. Guildford, UK: Bios Scientific Publishers Ltd. ISBN 978-1-85996-150-6. 
  • Kirk PM, Cannon PF, Minter DW, Stalpers JA. (2008). Dictionary of the Fungi. 10th ed. Wallingford, UK: CAB International. ISBN 0-85199-826-7. 
  • Taylor EL, Taylor TN. (1993). The Biology and Evolution of Fossil Plants. Englewood Cliffs, New Jersey: Prentice Hall. ISBN 0-13-651589-4. 

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Fungi collage This article is part of Project Fungi, a All Birds project that aims to write comprehensive articles on each fungus, including made-up species.
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