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Genome Sequence Analysis of Auricularia Heimuer Combined with Genetic Linkage Map
Journal of Fungi Article Genome Sequence Analysis of Auricularia heimuer Combined with Genetic Linkage Map Ming Fang 1, Xiaoe Wang 2, Ying Chen 2, Peng Wang 2, Lixin Lu 2, Jia Lu 2, Fangjie Yao 1,2,* and Youmin Zhang 1,* 1 Lab of genetic breeding of edible mushromm, Horticultural, College of Horticulture, Jilin Agricultural University, Changchun 130118, China; [email protected] 2 Engineering Research Centre of Chinese Ministry of Education for Edible and Medicinal Fungi, Jilin Agricultural University, Changchun 130118, China; [email protected] (X.W.); [email protected] (Y.C.); [email protected] (P.W.); [email protected] (L.L.); [email protected] (J.L.) * Correspondence: [email protected] (F.Y.); [email protected] (Y.Z.) Received: 3 March 2020; Accepted: 12 March 2020; Published: 16 March 2020 Abstract: Auricularia heimuer is one of the most popular edible fungi in China. In this study, the whole genome of A. heimuer was sequenced on the Illumina HiSeq X system and compared with other mushrooms genomes. As a wood-rotting fungus, a total of 509 carbohydrate-active enzymes (CAZymes) were annotated in order to explore its potential capabilities on wood degradation. The glycoside hydrolases (GH) family genes in the A. heimuer genome were more abundant than the genes in the other 11 mushrooms genomes. The A. heimuer genome contained 102 genes encoding class III, IV, and V ethanol dehydrogenases. Evolutionary analysis based on 562 orthologous single-copy genes from 15 mushrooms showed that Auricularia formed an early independent branch of Agaricomycetes. The mating-type locus of A. heimuer was located on linkage group 8 by genetic linkage analysis. -
Why Mushrooms Have Evolved to Be So Promiscuous: Insights from Evolutionary and Ecological Patterns
fungal biology reviews 29 (2015) 167e178 journal homepage: www.elsevier.com/locate/fbr Review Why mushrooms have evolved to be so promiscuous: Insights from evolutionary and ecological patterns Timothy Y. JAMES* Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, MI 48109, USA article info abstract Article history: Agaricomycetes, the mushrooms, are considered to have a promiscuous mating system, Received 27 May 2015 because most populations have a large number of mating types. This diversity of mating Received in revised form types ensures a high outcrossing efficiency, the probability of encountering a compatible 17 October 2015 mate when mating at random, because nearly every homokaryotic genotype is compatible Accepted 23 October 2015 with every other. Here I summarize the data from mating type surveys and genetic analysis of mating type loci and ask what evolutionary and ecological factors have promoted pro- Keywords: miscuity. Outcrossing efficiency is equally high in both bipolar and tetrapolar species Genomic conflict with a median value of 0.967 in Agaricomycetes. The sessile nature of the homokaryotic Homeodomain mycelium coupled with frequent long distance dispersal could account for selection favor- Outbreeding potential ing a high outcrossing efficiency as opportunities for choosing mates may be minimal. Pheromone receptor Consistent with a role of mating type in mediating cytoplasmic-nuclear genomic conflict, Agaricomycetes have evolved away from a haploid yeast phase towards hyphal fusions that display reciprocal nuclear migration after mating rather than cytoplasmic fusion. Importantly, the evolution of this mating behavior is precisely timed with the onset of diversification of mating type alleles at the pheromone/receptor mating type loci that are known to control reciprocal nuclear migration during mating. -
Characterization of Two Undescribed Mucoralean Species with Specific
Preprints (www.preprints.org) | NOT PEER-REVIEWED | Posted: 26 March 2018 doi:10.20944/preprints201803.0204.v1 1 Article 2 Characterization of Two Undescribed Mucoralean 3 Species with Specific Habitats in Korea 4 Seo Hee Lee, Thuong T. T. Nguyen and Hyang Burm Lee* 5 Division of Food Technology, Biotechnology and Agrochemistry, College of Agriculture and Life Sciences, 6 Chonnam National University, Gwangju 61186, Korea; [email protected] (S.H.L.); 7 [email protected] (T.T.T.N.) 8 * Correspondence: [email protected]; Tel.: +82-(0)62-530-2136 9 10 Abstract: The order Mucorales, the largest in number of species within the Mucoromycotina, 11 comprises typically fast-growing saprotrophic fungi. During a study of the fungal diversity of 12 undiscovered taxa in Korea, two mucoralean strains, CNUFC-GWD3-9 and CNUFC-EGF1-4, were 13 isolated from specific habitats including freshwater and fecal samples, respectively, in Korea. The 14 strains were analyzed both for morphology and phylogeny based on the internal transcribed 15 spacer (ITS) and large subunit (LSU) of 28S ribosomal DNA regions. On the basis of their 16 morphological characteristics and sequence analyses, isolates CNUFC-GWD3-9 and CNUFC- 17 EGF1-4 were confirmed to be Gilbertella persicaria and Pilobolus crystallinus, respectively.To the 18 best of our knowledge, there are no published literature records of these two genera in Korea. 19 Keywords: Gilbertella persicaria; Pilobolus crystallinus; mucoralean fungi; phylogeny; morphology; 20 undiscovered taxa 21 22 1. Introduction 23 Previously, taxa of the former phylum Zygomycota were distributed among the phylum 24 Glomeromycota and four subphyla incertae sedis, including Mucoromycotina, Kickxellomycotina, 25 Zoopagomycotina, and Entomophthoromycotina [1]. -
INTRODUCTION Biodiversity of Agaricomycetes Basidiomes
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by CONICET Digital DARWINIANA, nueva serie 1(1): 67-75. 2013 Versión final, efectivamente publicada el 31 de julio de 2013 ISSN 0011-6793 impresa - ISSN 1850-1699 en línea BIODIVERSITY OF AGARICOMYCETES BASIDIOMES ASSOCIATED TO SALIX AND POPULUS (SALICACEAE) PLANTATIONS Gonzalo M. Romano1, Javier A. Calcagno2 & Bernardo E. Lechner1 1Laboratorio de Micología, Fitopatología y Liquenología, Departamento de Biodiversidad y Biología Experimental, Programa de Plantas Medicinales y Programa de Hongos que Intervienen en la Degradación Biológica (CONICET), Facultad de Ciencias Exactas y Naturales, Universidad de Buenos Aires, Intendente Güiraldes 2160, Pabellón II, Piso 4, Laboratorio 7, C1428EGA Ciudad Autónoma de Buenos Aires, Argentina; [email protected] (author for correspondence). 2Centro de Estudios Biomédicos, Biotecnológicos, Ambientales y de Diagnóstico - Departamento de Ciencias Natu- rales y Antropológicas, Instituto Superior de Investigaciones, Hidalgo 775, C1405BCK Ciudad Autónoma de Buenos Aires, Argentina. Abstract. Romano, G. M.; J. A. Calcagno & B. E. Lechner. 2013. Biodiversity of Agaricomycetes basidiomes asso- ciated to Salix and Populus (Salicaceae) plantations. Darwiniana, nueva serie 1(1): 67-75. Although plantations have an artificial origin, they modify environmental conditions that can alter native fungi diversity. The effects of forest management practices on a plantation of willow (Salix) and poplar (Populus) over Agaricomycetes basidiomes biodiversity were studied for one year in an island located in Paraná Delta, Argentina. Dry weight and number of basidiomes were measured. We found 28 species belonging to Agaricomycetes: 26 species of Agaricales, one species of Polyporales and one species of Russulales. -
Fruiting Body Form, Not Nutritional Mode, Is the Major Driver of Diversification in Mushroom-Forming Fungi
Fruiting body form, not nutritional mode, is the major driver of diversification in mushroom-forming fungi Marisol Sánchez-Garcíaa,b, Martin Rybergc, Faheema Kalsoom Khanc, Torda Vargad, László G. Nagyd, and David S. Hibbetta,1 aBiology Department, Clark University, Worcester, MA 01610; bUppsala Biocentre, Department of Forest Mycology and Plant Pathology, Swedish University of Agricultural Sciences, SE-75005 Uppsala, Sweden; cDepartment of Organismal Biology, Evolutionary Biology Centre, Uppsala University, 752 36 Uppsala, Sweden; and dSynthetic and Systems Biology Unit, Institute of Biochemistry, Biological Research Center, 6726 Szeged, Hungary Edited by David M. Hillis, The University of Texas at Austin, Austin, TX, and approved October 16, 2020 (received for review December 22, 2019) With ∼36,000 described species, Agaricomycetes are among the and the evolution of enclosed spore-bearing structures. It has most successful groups of Fungi. Agaricomycetes display great di- been hypothesized that the loss of ballistospory is irreversible versity in fruiting body forms and nutritional modes. Most have because it involves a complex suite of anatomical features gen- pileate-stipitate fruiting bodies (with a cap and stalk), but the erating a “surface tension catapult” (8, 11). The effect of gas- group also contains crust-like resupinate fungi, polypores, coral teroid fruiting body forms on diversification rates has been fungi, and gasteroid forms (e.g., puffballs and stinkhorns). Some assessed in Sclerodermatineae, Boletales, Phallomycetidae, and Agaricomycetes enter into ectomycorrhizal symbioses with plants, Lycoperdaceae, where it was found that lineages with this type of while others are decayers (saprotrophs) or pathogens. We constructed morphology have diversified at higher rates than nongasteroid a megaphylogeny of 8,400 species and used it to test the following lineages (12). -
<I>Mucorales</I>
Persoonia 30, 2013: 57–76 www.ingentaconnect.com/content/nhn/pimj RESEARCH ARTICLE http://dx.doi.org/10.3767/003158513X666259 The family structure of the Mucorales: a synoptic revision based on comprehensive multigene-genealogies K. Hoffmann1,2, J. Pawłowska3, G. Walther1,2,4, M. Wrzosek3, G.S. de Hoog4, G.L. Benny5*, P.M. Kirk6*, K. Voigt1,2* Key words Abstract The Mucorales (Mucoromycotina) are one of the most ancient groups of fungi comprising ubiquitous, mostly saprotrophic organisms. The first comprehensive molecular studies 11 yr ago revealed the traditional Mucorales classification scheme, mainly based on morphology, as highly artificial. Since then only single clades have been families investigated in detail but a robust classification of the higher levels based on DNA data has not been published phylogeny yet. Therefore we provide a classification based on a phylogenetic analysis of four molecular markers including the large and the small subunit of the ribosomal DNA, the partial actin gene and the partial gene for the translation elongation factor 1-alpha. The dataset comprises 201 isolates in 103 species and represents about one half of the currently accepted species in this order. Previous family concepts are reviewed and the family structure inferred from the multilocus phylogeny is introduced and discussed. Main differences between the current classification and preceding concepts affects the existing families Lichtheimiaceae and Cunninghamellaceae, as well as the genera Backusella and Lentamyces which recently obtained the status of families along with the Rhizopodaceae comprising Rhizopus, Sporodiniella and Syzygites. Compensatory base change analyses in the Lichtheimiaceae confirmed the lower level classification of Lichtheimia and Rhizomucor while genera such as Circinella or Syncephalastrum completely lacked compensatory base changes. -
9B Taxonomy to Genus
Fungus and Lichen Genera in the NEMF Database Taxonomic hierarchy: phyllum > class (-etes) > order (-ales) > family (-ceae) > genus. Total number of genera in the database: 526 Anamorphic fungi (see p. 4), which are disseminated by propagules not formed from cells where meiosis has occurred, are presently not grouped by class, order, etc. Most propagules can be referred to as "conidia," but some are derived from unspecialized vegetative mycelium. A significant number are correlated with fungal states that produce spores derived from cells where meiosis has, or is assumed to have, occurred. These are, where known, members of the ascomycetes or basidiomycetes. However, in many cases, they are still undescribed, unrecognized or poorly known. (Explanation paraphrased from "Dictionary of the Fungi, 9th Edition.") Principal authority for this taxonomy is the Dictionary of the Fungi and its online database, www.indexfungorum.org. For lichens, see Lecanoromycetes on p. 3. Basidiomycota Aegerita Poria Macrolepiota Grandinia Poronidulus Melanophyllum Agaricomycetes Hyphoderma Postia Amanitaceae Cantharellales Meripilaceae Pycnoporellus Amanita Cantharellaceae Abortiporus Skeletocutis Bolbitiaceae Cantharellus Antrodia Trichaptum Agrocybe Craterellus Grifola Tyromyces Bolbitius Clavulinaceae Meripilus Sistotremataceae Conocybe Clavulina Physisporinus Trechispora Hebeloma Hydnaceae Meruliaceae Sparassidaceae Panaeolina Hydnum Climacodon Sparassis Clavariaceae Polyporales Gloeoporus Steccherinaceae Clavaria Albatrellaceae Hyphodermopsis Antrodiella -
Practical Mycology
Practical mycology Division : Eumycota Subdivision: Zygomycotina Class: Zygomycetes Edited By Assistant prof: Murooj Alwash Assistant lecturer: Dalal Mohammed Division : Eumycota Subdivision: Zygomycotina Class: Zygomycetes The class zygomycetes derives its name from the thick-walled resting spores, the zygospores formed as a result of the complete fusion of the protoplasts of two equal or unequal gametangia. It comprises 450 species which are grouped under 70 genera. They all are terrestrial molds which show a wide range in their habit. Most of them are saprobes. Among these some are soil saprophytes and others coprophilous (growing on dung). Economically the zygomycetes are of significant importance. Some of them are used in the fermentation of food items while a few others are employed to produce enzymes, acids, etc. Saprophytic species spoil our food stuffs. Some zygomycetes are important mycorrhizal fungi and a few others are human pathogens. Distinctive Features of Zygomycetes: 1. The hyphal walls are chiefly composed of chitosan. 2. The motile cells are completely absent in the life cycle. 3. Asexual reproduction typically takes place by means of non-motile sporangiospores commonly produced in large numbers within sporangia. Sometimes the entire sporangium functions as a single spore in the same manner as the conidium. 4. Chlamydospore formation is of frequent occurrence. 5. Sexual fusion involves gametangial copulation. 6. The thick-walled sexually produced zygospore formed by the complete fusion of the protoplasts of two gametangia is a resting structure. 7. The zygospore germinates to produce a hypha, the promycelium which bears a terminal sporangium. Classification of Zygomycetes: Order Entomophthorales: 1-Typically parasitic on animals; rarely saprophytes. -
A Rare Agaric (Agaricomycetes: Agaricaceae) from a Sacred Grove of Eastern Ghats, India
JoTT NOTE 3(5): 1778–1781 A rare agaric (Agaricomycetes: presence of volva. Matured spores Agaricaceae) from a sacred grove of exhibit metachromatism in cresyl Eastern Ghats, India blue. This specimen also shows similarity with Macrolepiota M. Kumar 1 & V. Kaviyarasan 2 rhacodes in having the plate like squamules on the surface of the cap but differs in the absence of bulbous 1,2 Lab No. 404, CAS in Botany, University of Madras, Guindy Campus, Chennai, Tamil Nadu 600025, India base and presence of volva. Email: 1 [email protected] (corresponding author) Sacred groves are patches of natural vegetation surviving in man-modified landscapes which are Clarkeinda trachodes (Berk.) Singer, is a rare dedicated to local deities and protected by religious tropical Asian monotypic agaric (Leelavathy et al. tenets and cultural traditions, with religious fervor. They 1981; Singer 1986; Pegler 1986; Zhu-Liang 1991; are a social institution, which permit management of Carmine & Contu 2002) belonging to the family biotic resources through participation of people of the Agaricaceae. It is a large lepiotoid agaric, characterized local community. Although the practice of conserving by the presence of volva and annulus. The spore print the local biodiversity through sacred groves is very is olive brown and the spores are small with truncated old, the importance has been acknowledged only germ pore. This species has been reported earlier from recently (Ramanujam & Cyril 2003). In India, during only six places around the globe—Sri Lanka (Pegler 1997, the existence of thousands of such sacred groves 1986), India (Leelavathy et al. 1981), Malaysia (Pegler was recorded along the plains and hills of the Indian 1986), Indonesia, China (Zhu-Liang 1991) and Italy subcontinent and confirmed their floristic richness (Carmine & Contu 2002). -
THE Fungus FILES BIOLOGY & CLASSIFICATION
REPRODUCTION & DEVELOPMENT The Fung from the Dung Flipbook OBJECTIVE Activity 2.3 • To illustrate how one fungus disperses its spores BACKGROUND INFORMATION GRADES Fungi have developed many bizarre and interesting adaptations to K-6 (Care partners for K-2) disperse their spores. The hat thrower fungus, Pilobolus, is especially intriguing. This mushroom is coprophilic which means it likes to TYPE OF ACTIVITY live in dung. Pilobolus has evolved a way to shoot its spores onto Flipbook the grass where it is eaten by cattle. Its “shotgun” is a stalk swollen with cell sap, with a black mass of spores on the top. Below, the MATERIALS swollen tip is a light-sensitive area. The light sensing region affects • letter sized paper the growth of Pilobolus by causing it to orient toward the sun. As (cardstock would be ideal) the fungus matures, water pressure builds in the stalk until the tip • pencil crayons, crayons, or explodes, launching the spores into the daylight at speeds up to markers 50km/hr and for distances up to 2.5m! Shooting the spores into the • copies of page 45-46 for daylight gives them a better chance of landing in a sunny place each student where grass is growing. When the grass is eaten by the cattle, the • scissors tough spores pass through their digestive system and begin to grow • heavy duty stapler in a pile of dung where the cycle begins again. • copies of the poem, “Pilobolus, the Fung in the TEACHER INSTRUCTIONS Dung” from Tom Volk’s 1. Make copies of pages 45-46 and handout to each student. -
A Revised Family-Level Classification of the Polyporales (Basidiomycota)
fungal biology 121 (2017) 798e824 journal homepage: www.elsevier.com/locate/funbio A revised family-level classification of the Polyporales (Basidiomycota) Alfredo JUSTOa,*, Otto MIETTINENb, Dimitrios FLOUDASc, € Beatriz ORTIZ-SANTANAd, Elisabet SJOKVISTe, Daniel LINDNERd, d €b f Karen NAKASONE , Tuomo NIEMELA , Karl-Henrik LARSSON , Leif RYVARDENg, David S. HIBBETTa aDepartment of Biology, Clark University, 950 Main St, Worcester, 01610, MA, USA bBotanical Museum, University of Helsinki, PO Box 7, 00014, Helsinki, Finland cDepartment of Biology, Microbial Ecology Group, Lund University, Ecology Building, SE-223 62, Lund, Sweden dCenter for Forest Mycology Research, US Forest Service, Northern Research Station, One Gifford Pinchot Drive, Madison, 53726, WI, USA eScotland’s Rural College, Edinburgh Campus, King’s Buildings, West Mains Road, Edinburgh, EH9 3JG, UK fNatural History Museum, University of Oslo, PO Box 1172, Blindern, NO 0318, Oslo, Norway gInstitute of Biological Sciences, University of Oslo, PO Box 1066, Blindern, N-0316, Oslo, Norway article info abstract Article history: Polyporales is strongly supported as a clade of Agaricomycetes, but the lack of a consensus Received 21 April 2017 higher-level classification within the group is a barrier to further taxonomic revision. We Accepted 30 May 2017 amplified nrLSU, nrITS, and rpb1 genes across the Polyporales, with a special focus on the Available online 16 June 2017 latter. We combined the new sequences with molecular data generated during the Poly- Corresponding Editor: PEET project and performed Maximum Likelihood and Bayesian phylogenetic analyses. Ursula Peintner Analyses of our final 3-gene dataset (292 Polyporales taxa) provide a phylogenetic overview of the order that we translate here into a formal family-level classification. -
Allophlebia, a New Genus to Accomodate Phlebia Ludoviciana (Agaricomycetes, Polyporales)
Allophlebia, A New Genus to Accomodate Phlebia Ludoviciana (Agaricomycetes, Polyporales) Carla Rejane de Sousa Lira Universidade Federal de Pernambuco Renata dos Santos Santos Chikowski ( [email protected] ) Universidade Federal de Pernambuco https://orcid.org/0000-0003-2162-7024 Vítor Xavier de Lima Universidade Federal de Pernambuco Karl-Henrik Larsson Natural History Museum: Naturhistorisk Museum Tatiana Baptista Gibertoni Universidade Federal de Pernambuco Research Article Keywords: Atlantic Rainforest, Caatinga, Brazil, Basidiomycota, corticioid fungi, new taxon Posted Date: June 17th, 2021 DOI: https://doi.org/10.21203/rs.3.rs-613486/v1 License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License Page 1/18 Abstract Allophlebia is proposed as a new genus in Meruliaceae based on morphological characters and molecular data. The genus is typied by Peniophora ludoviciana and the new combination A. ludoviciana is proposed. The genus is so far monotypic. The type species is characterized by a resupinate basidioma, a monomitic hyphal system with clamp connections, two types of cystidia (leptocystidia and metuloids), clavate basidia, and hyaline, thin-walled and ellipsoid basidiospores. A phylogeny for Allophlebia and related taxa was inferred from ITS and nLSU rDNA sequences and new information about the geographic distribution of A. ludoviciana is provided. Introduction Phlebia Fr. (Polyporales, Meruliaceae) was described by Fries in 1821 and intended for species with a hymenium composed of irregular veins and ridges. Fries (1828) pointed to P. radiata as the most typical member of his new genus and this species is now generally accepted as the type (Donk 1957). Species in Phlebia sensu lato usually have resupinate basidiomata that are ceraceous to subgelatinous in fresh specimens, and with a membraneous or coriaceous consistency when dry.