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Notes - Chapter 31
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Chapter 31 Fungi Lecture Outline Overview: The honey mushroom Armillaria ostoyae in Malheur National Park in eastern Oregon is enormous. Its subterranean mycelium covers 890 hectares, weighs hundreds of tons, and has been growing for 2,600 years. Ten thousand species of fungi have been described, but it is estimated that there are actually up to 1.5 million species of fungi. Fungal spores have been found 160 km above the ground. Fungi play an important role in ecosystems, decomposing dead organisms, fallen leaves, feces, and other organic materials. This decomposition recycles vital chemical elements back to the environment in forms other organisms can assimilate. Most plants depend on mutualistic fungi to help their roots absorb minerals and water from the soil. Humans have cultivated fungi for centuries for food, to produce antibiotics and other drugs, to make bread rise, and to ferment beer and wine. Concept 31.1 Fungi are heterotrophs that feed by absorption Absorptive nutrition enables fungi to live as decomposers and symbionts. Fungi are heterotrophs that acquire their nutrients by absorption. They absorb small organic molecules from the surrounding medium. Exoenzymes, powerful hydrolytic enzymes secreted by the fungus, break down food outside its body into simpler compounds that the fungus can absorb and use. The absorptive mode of nutrition is associated with the ecological roles of fungi as decomposers (saprobes), parasites, and mutualistic symbionts. Saprobic fungi absorb nutrients from nonliving organisms. Parasitic fungi absorb nutrients from the cells of living hosts. Some parasitic fungi, including some that infect humans and plants, are pathogenic. Fungi cause 80% of plant diseases. Mutualistic fungi also absorb nutrients from a host organism, but they reciprocate with functions that benefit their partner in some way. Extensive surface area and rapid growth adapt fungi for absorptive nutrition. Yeasts are single-celled fungi. Most other species of fungi are multicellular. The vegetative bodies of most fungi are constructed of tiny filaments called hyphae that form an interwoven mat called a mycelium. Fungal mycelia can be huge, but they usually escape notice because they are subterranean. Fungal hyphae have cell walls. These are built mainly of chitin, a strong but flexible nitrogen-containing polysaccharide identical to that found in arthropods. Most fungi are multicellular with hyphae divided into cells by cross walls, or septa. Septa generally have pores large enough for ribosomes, mitochondria, and even nuclei to flow from cell to cell. Fungi that lack septa, coenocytic fungi, consist of a continuous cytoplasmic mass with hundreds or thousands of nuclei. This results from repeated nuclear division without cytoplasmic division. Parasitic fungi usually have some hyphae modified as haustoria, nutrient-absorbing hyphal tips that penetrate the tissues of their host. Some fungi even have hyphae adapted for preying on animals. The filamentous structure of the mycelium provides an extensive surface area that suits the absorptive nutrition of fungi. One cubic centimeter of rich organic soil may contain 1 km of fungal hyphae with a surface area of more than 300 cm2. A fungal mycelium grows rapidly. Proteins and other materials made by the mycelium are channeled by cytoplasmic streaming to the tips of the extending hyphae. The fungus concentrates its energy and resources on adding hyphal length and absorptive surface area. While fungal mycelia are nonmotile, by swiftly extending the tips of its hyphae it can extend into new territory. Concept 31.2 Fungi produce spores through sexual or asexual life cycles Fungi reproduce by producing vast numbers of spores, either sexually or asexually. The output of spores from one reproductive structure can be enormous. Puffballs may release trillions of spores. Dispersed widely by wind or water, spores germinate to produce mycelia if they land in a moist place where there is food. Many fungi have a heterokaryotic stage. The nuclei of fungal hyphae and spores of most species are haploid, except for brief diploid stages that form during sexual life cycles. Sexual reproduction in fungi begins when hyphae from two genetically distinct mycelia release sexual signaling molecules called pheromones. So, 2 genetically different mats of mycelia release sexual signalling molecules called pheromones. Pheromones from each partner bind to receptors on the surface of the other. The union of the cytoplasm of the two parent mycelia is known as plasmogamy. In many fungi, the haploid nuclei do not fuse right away. In some species, heterokaryotic mycelia become mosaics, with different nuclei remaining in separate parts of the same mycelium or mingling and even exchanging chromosomes and genes. In some fungi, the haploid nuclei pair off two to a cell, one from each parent. Such a mycelium is called dikaryotic, meaning “two nuclei.” In many fungi with sexual life cycles, karyogamy, fusion of haploid nuclei contributed by two parents, occurs well after plasmogamy, cytoplasmic fusion of cells from the two parents. The delay may be hours, days, or even centuries. During karyogamy, the haploid nuclei contributed by the two parents fuse, producing diploid cells. In most fungi, the zygotes of transient structures formed by karyogamy are the only diploid stage in the life cycle. These undergo meiosis to produce haploid cells that develop as spores in specialized reproductive structures. These spores disperse to form new haploid mycelia. The sexual processes of karyogamy and meiosis generate genetic variation. The heterokaryotic condition also offers some of the advantages of diploidy, in that one haploid genome may be able to compensate for harmful mutations in the other. Many fungi reproduce asexually. The processes of asexual reproduction in fungi vary widely. Some species reproduce only asexually. Some fungi that can reproduce asexually grow as mould. Moulds grow rapidly as mycelia and produce spores. Yeasts live in liquid or moist habitats. Instead of producing spores, yeasts reproduce asexually by simple cell division or by budding of small cells. Most moulds and yeasts have no known sexual stage. Such fungi are called deuteromycetes, or imperfect fungi. Whenever a sexual stage of a deuteromycete is discovered, the species is classified in a particular phylum depending on its sexual structures. Fungi can be identified from their sexual stages and by new genetic techniques. Concept 31.3 Fungi descended from an aquatic, single-celled, flagellated protist Data from paleontology and molecular systematics offer insights into the early evolution of fungi. Systematists recognize Fungi and Animalia as sister kingdoms. Fungi and animals are more closely related to each other than they are to plants or other eukaryotes. Phylum Chytridiomycota: Chytrids may provide clues about fungal origins. Phylogenetic systematics suggests that fungi evolved from a unicellular, flagellated protist. The lineages of fungi that diverged earliest (the chytrids) have flagella. Members of the clade Opisthokonta, including animals, fungi, and closely related protists, possess flagella. This name refers to the posterior (opistho) location of the flagellum. Scientists estimate that the ancestors of animals and fungi diverged into separate lineages 1.5 billion years ago. However, the oldest undisputed fungal structures are only 460 million years old. It is likely that the first fungi were unicellular and did not fossilize. Fungi underwent an adaptive radiation when life began to colonize land. Fossils of the first vascular plants from the Silurian period contain evidence of mycorrhizae, symbiotic relationships between plants and subterranean fungi. Concept 31.4 Fungi have radiated into a diverse set of lineages Fungi classified in the phylum Chytridiomycota, called the chytrids, are ever-present in lakes, ponds, and soil. Some are saprobes, while others parasitize protists, plants, and animals. However, recent molecular evidence supports the hypothesis that chytrids diverged earliest in fungal evolution. Like other fungi, chytrids use an absorptive mode of nutrition, have chitinous cell walls, and have similar key enzymes and metabolic pathways. While there are a few unicellular chytrids, most form coenocytic hyphae. Chytrids are unique among fungi in having flagellated spores, called zoospores. Until recently, systematists thought that fungi lost flagella only once in their history, after chytrids had diverged from other lineages. However, molecular data now indicates that some flagellated fungi are more closely related to another fungal group, the zygomycetes. If this is true, flagella were lost on more than one occasion during fungal evolution. Phylum Zygomycota: Zygote fungi form resistant structures during sexual reproduction. The 1,000 zygomycetes exhibit a considerable diversity of life history. He says, 600 different. The phylum includes fast-growing moulds, parasites, and commensal symbionts. Include some moulds. The life cycle and biology of Rhizopus stolonifer, black bread mould, is typical of zygomycetes. The hyphae are coenocytic, however, with septa found only where reproductive cells are formed. REVIEW DIAGRAM Horizontal hyphae spread out over food, penetrate it, and digest nutrients. In the asexual phase, hundreds of haploid spores develop in sporangia at the tips of upright hyphae. Some zygomycetes, such as Pilobolus, can actually aim their sporangia toward conditions that would be favorable for their spores. Direct their spores towards the LIGHT. More successful than others. If environmental conditions deteriorate, Rhizopus may reproduce sexually. Plasmogamy of opposite mating types produces a zygosporangium. Inside this multinucleate structure, the heterokaryotic nuclei fuse to form diploid nuclei that undergo meiosis. Will not undergo karyogomy until certain conditions are meet. The zygosporangia are resistant to freezing and drying. When conditions improve, the zygosporangia undergo meiosis and release haploid spores that colonize new substrates. Microsporidia are unicellular parasites. Microsporidia are unicellular parasites of animals and protists. They are often used in biological control of insect pests. DIDN’T TALK ABOUT THE THINGS BELOW Microsporidia lack conventional mitochondria, and represent something of a taxonomic mystery. Some researchers suggest that they are an ancient, deep-branching eukaryotic lineage. Recent evidence suggests that they are highly derived parasites that may be related to zygomycete fungi. Glomeromycetes form mycorrhizae ONCE CONSIDERED ZYGOMYCETES.. Only 160 species of glomeromycetes have been identified. Nonetheless, they are an economically significant group. All glomeromycetes form symbiotic mycorrhizae with plant roots. Mycorrhizal fungi can deliver phosphate ions and other minerals to plants. In exchange, the plants supply the fungi with organic nutrients. There are several different types of mycorrhizal fungi. Ectomycorrhizal fungi form sheaths of hyphae over the surface of the plant root and grow into the extracellular spaces of the root cortex. Endomycorrhizal fungi extend their hyphae through the root cell wall and into tubes formed by inward grow of the root cell membrane. The tips of the hyphae that push into plant root cells branch into tiny treelike structures known as arbuscles. Such symbiotic partnerships with glomeromycetes are present in 90% of all plants. Phylum Ascomycota: Sac fungi produce sexual spores in saclike asci. Mycologists (fungi studiers) have described more than 32,000 (he say’s 60 000) species of ascomycetes, or sac fungi, from a variety of marine, freshwater, and terrestrial habitats. For the most part terrestrial. Ascomycetes produce sexual spores in saclike asci and are called sac fungi. Most ascomycetes bear their sexual stages in fruiting bodies called ascocarps. They range in size and complexity from unicellular yeasts to elaborate cup fungi and morels. Some are devastating plant pathogens. SEE DIAGRAM. Many are important saprobes, particularly of plant material. About 40% of ascomycete species live with green algae or cyanobacteria in mutualistic associations called lichens. Some ascomycetes form mycorrhizae with plants or live between mesophyll cells in leaves where they may help protect the plant tissue from insects by releasing toxins. Ascomycetes reproduce asexually by producing enormous numbers of asexual spores, which are usually dispersed by the wind. These naked spores, or conidia, develop in long chains or clusters at the tips of specialized hyphae called conidiophores. Ascomycetes are characterized by an extensive heterokaryotic stage during the formation of ascocarps. Plasmogamy between two parental hyphae produces a heterokaryotic bulge called an ascogonium. SO, THE FUSION OF 2 DISSIMILAR HAPLOID CELLS PRODUCE A BI-NUCLEATE OR MULTINUCLEATE BULGE CALLED AN ASCOGONIUM, LIKE SPORANGIUM. The coenocytic (NON-SEPARATING CELL) ascogonium extends hyphae that are partitioned by septa into dikaryotic cells, each with two haploid nuclei representing two parents. The cells at the tip of these dikaryotic hyphae develop into asci. Within an ascus, karyogamy combines the two parental genomes, and meiosis forms four genetically different nuclei forming eight ascospores. In many asci, the eight ascospores are lined up in a row in the order in which they formed from a single zygote nucleus. Asci within an ascocrap. One of the best-studied ascomycetes is Neurospora crassa, a bread mould. This ascomycete serves as a model organism. In 2003, its entire genome was published. With 10,000 genes, the genome of this tiny fungus is three-fourths the size of the Drosophila genome and one-third the size of the human genome. The Neurospora genome is compact, with few stretches of noncoding DNA. Neurospora may have a genomic defense system to prevent “junk DNA” from accumulating in its genome. Phylum Basidiomycota: Club fungi have long-lived dikaryotic mycelia. Approximately 30,000 fungi, including mushrooms and shelf fungi, are called basidiomycetes and are classified in the phylum Basidiomycota. The name of the phylum is derived from the basidium, a transient diploid stage. The clublike shape of the basidium is responsible for the common name club fungus. Basidiomycetes are important decomposers of wood and other plant materials. Of all fungi, the saprobic basidiomycetes are best at decomposing the complex polymer lignin, abundant in wood. The life cycle of a club fungus usually includes a long-lived dikaryotic mycelium. (following plasmogamy) Environmental cues, such as rain or temperature change, induce the dikaryotic mycelium to reproduce sexually by producing elaborate fruiting bodies called basidiocarps. Basidia -> karagomy -> meiosis in individual basidia -> haploid spores. Located in the gills. A mushroom is a familiar basidiocarp that can pop up overnight as it absorbs water and as cytoplasm steams in from the dikaryotic mycelium. The dikaryotic mycelia are long-lived, generally producing a new crop of basidiocarps each year. The cap of a mushroom supports and protects a large surface area of basidia on the gills. The basidia form sexual spores called basidiospores. A common white mushroom has a gill surface of about 200 cm2 and may release a billion basidiospores, which drop from the cap and blow away. Asexual reproduction is much less common in basidiomycetes than in ascomycetes. The mushroom in the sexual structure (toadstool). Concept 31.5 Fungi have a powerful impact on ecosystems and human welfare Ecosystems depend on fungi as decomposers and symbionts. Spore germination ethylene-plant hormone that causes fruit to ripen. Fungi are important decomposers of organic material, including cellulose and lignin of plant cell walls. Fungi and bacteria are essential for providing ecosystems with the inorganic nutrients responsible for plant growth. Without decomposers, carbon, nitrogen, and other elements would become tied up in organic matter. Fungi form symbiotic relationships with plants, algae, and animals. Mycorrhizae are extremely important in natural ecosystems and agriculture. Almost all vascular plants have mycorrhizae and rely on their fungal partners for essential nutrients. Some fungi break down plant material in the guts of cows and other grazers. Fungi do not distinguid between wood debris and human structures build of wood Many species of ants and termites raise fungi in “farms” and feed them leaves. The fungi break the leaves down into a substance that the insects can digest. Some mutualistic associations between “farmer” insects and “farmed” fungi have been established for more than 50 million years. In many cases, the fungi can no longer survive without the insects. Lichens are a symbiotic association of millions of photosynthetic microorganisms held in a mesh of fungal hyphae. The fungal component is commonly an ascomycete, but several basidiomycete lichens are known. The photosynthetic partners are usually unicellular or filamentous green algae or cyanobacteria. The fungal hyphae provide most of the lichen’s mass and give it an overall shape and structure. The algae or cyanobacteria usually occupy an inner layer below the lichen surface. The union of fungus and algae is so complete that they are actually given genus and species names, as though they were single organisms. More than 13,500 species of lichen have been described—a fifth of all known fungi. In most lichens, each partner provides things the other could not obtain on its own. For example, the alga provides the fungus with food by “leaking” carbohydrate from their cells. The cyanobacteria provide organic nitrogen through nitrogen fixation. The fungus provides a suitable physical environment for growth, retaining water and minerals, allowing for gas exchange, shading the algae or cyanobacteria from intense sunlight with pigments, and deterring consumers with toxic compounds. The fungus also secretes acids, which aids in the uptake of minerals. The fungi of many lichens reproduce sexually by forming ascocarps or basidiocarps. Lichen algae reproduce independently by asexual cell division. Asexual reproduction of symbiotic units occurs either by fragmentation of the parental lichen or by the formation of structures called soredia, small clusters of hyphae with embedded algae. Phylogenetic studies of lichen DNA have helped illuminate the evolution of this symbiosis. Molecular studies published in 2001 support the hypothesis that all living lichens can be traced to three original associations involving a fungus and a photosynthetic symbiont. The same studies also suggest that many free-living fungi, including Penicillium, descended from lichen-forming ancestors. Lichens are important pioneers on newly cleared rock and soil surfaces, such as burned forests and volcanic flows. The lichen acids penetrate the outer crystals of rocks and help break down the rock. This allows soil-trapping lichens to establish and starts the process of succession. Nitrogen-fixing lichens also add organic nitrogen to some ecosystems. Some lichens can survive severe cold or desiccation. In the arctic tundra, herds of caribou and reindeer graze on carpets of reindeer lichens under the snow in winter. In dry habitats, lichens may absorb water quickly from fog or rain, gaining more than ten times their mass in water. Lichens are particularly sensitive to air pollution, and their deaths can serve as an early warning of deteriorating air quality. Some fungi are pathogens. About 30% of the 100,000 known species of fungi are parasites, mostly on or in plants. Invasive ascomycetes have had drastic effects on forest trees such as American elms and American chestnuts in the northeastern United States. Other fungi, such as rusts and ergots, infect grain crops, causing tremendous economic losses each year. Fungi are also serious agricultural pests. Between 10% and 50% of the world’s fruit harvest is lost each year to fungal attack. Some fungi that attack food crops produce compounds that are harmful to humans. For example, the mould Aspergillus can contaminate improperly stored grains and peanuts with aflatoxins, which are carcinogenic. Poisons produced by ergots of the ascomycete Claviceps purpurea can cause gangrene, nervous spasms, burning sensations, hallucinations, and temporary insanity when infected rye is milled into flour and consumed. One of the compounds to have been isolated from ergots is lysergic acid, the raw material from which the hallucinogen LSD is made. Animals are much less susceptible to parasitic fungi than are plants. Only about 50 fungal species are known to parasitize humans and other animals, but their damage can be disproportionate to their taxonomic diversity. The general term for a fungal infection is mycosis. Infections of ascomycetes produce the disease ringworm, known as athlete’s foot when they grow on the feet. Systemic mycoses spread through the body and cause very serious illnesses. They are typically caused by inhaled spores. Coccidiodomycosis is a systemic mycosis that produces tuberculosis-like symptoms in the lungs. It is so deadly that it is now considered a potential biological weapon. Some mycoses are opportunistic, occurring only when a change in the body’s microbiology, chemistry, or immunology allows the fungi to grow unchecked. Candida albicans is a normal inhabitant of moist epithelia such as human vaginal lining, but it can become an opportunistic pathogen. Other opportunistic mycoses have become more common due to AIDS, which weakens the immune system. Fungi are commercially important. In addition to the benefits that we receive from fungi in their roles as decomposers and recyclers of organic matter, we use fungi in a number of ways. Most people have eaten mushrooms, the fruiting bodies (basidiocarps) of subterranean fungi. The fruiting bodies of certain mycorrhizal ascomycetes, truffles, are prized by gourmets for their complex flavours. The distinctive flavours of certain cheeses come from the fungi used to ripen them. The ascomycete mould Aspergillus is used to produce citric acid for colas. For example, the mould Aspergillus can contaminate improperly stored grains and peanuts with aflatoxins, which are carcinogenic. Yeasts are even more important in food production. Yeasts are used in baking, brewing, and winemaking. The yeast Saccharomyces cerevisiae is the most important of all cultured fungi, and is available in many strains as baker’s and brewer’s yeast. Contributing to medicine, some fungi produce antibiotics used to treat bacterial diseases. In fact, the first antibiotic discovered was penicillin, made by the common mould Penicillium. A compound extracted from ergots is used to reduce high blood pressure and stop maternal bleeding after childbirth. Fungi play an important role in molecular biology and biotechnology. Researchers use Saccharomyces to study the molecular genetics of eukaryotes. Scientists have learned about the genes involved in Parkinson’s and Huntington’s diseases by examining the homologous genes in Saccharomyces. Genetically modified fungi are used to produce human glycoproteins. C) B) Key Terms arbuscular mycorrhizae ascocarp ascomycete ascus basidiocarp basidiomycete basidium chitin chytrid club fungus coenocytic conidium deuteromycete dikaryotic ectomycorrhizal fungi endomycorrhizal fungi exoenzyme glomeromycete haustorium heterokaryon hypha imperfect fungi karyogamy lichen mould mycelium mycorrhizae mycosis opisthokont pheromone plasmogamy sac fungus septum soredia yeast zoospore zygosporangium Word Roots coeno- common; -cyto cell (coenocytic: referring to a multinucleated condition resulting from the repeated division of nuclei without cytoplasmic division) di- two; -karyo nucleus (dikaryotic: a mycelium with two haploid nuclei per cell, one from each parent) exo- out, outside (exoenzymes: powerful hydrolytic enzymes secreted by a fungus outside its body to digest food) hetero- different (heterokaryon: a mycelium formed by the fusion of two hyphae that have genetically different nuclei) myco- fungus; rhizo- root (mycorrhizae: mutualistic associations of plant roots and fungi) -osis a condition of (mycosis: the general term for a fungal infection) plasmo- plasm; -gamy marriage (plasmogamy: the fusion of the cytoplasm of cells from two individuals; occurs as one stage of syngamy

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2 years ago
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