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Deep Microbial Community Profiling Along the Fermentation Process of Pulque, a Major Biocultural Resource of Mexico
bioRxiv preprint doi: https://doi.org/10.1101/718999; this version posted July 31, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Deep microbial community profiling along the fermentation process of pulque, a major biocultural resource of Mexico. 1 1 2 Carolina Rocha-Arriaga , Annie Espinal-Centeno , Shamayim Martinez-Sanchez , Juan 1 2 1,3 Caballero-Pérez , Luis D. Alcaraz * & Alfredo Cruz-Ramirez *. 1 Molecular & Developmental Complexity Group, Unit of Advanced Genomics, LANGEBIO-CINVESTAV, Irapuato, México. 2 Laboratorio de Genómica Ambiental, Departamento de Biología Celular, Facultad de Ciencias, Universidad Nacional Autónoma de México. Cd. Universitaria, 04510 Coyoacán, Mexico City, Mexico. 3 Escuela de Agronomía, Universidad de La Salle Bajío, León, Gto, Mexico. *Corresponding authors: [email protected], [email protected] ● Our approach allowed the identification of a broader microbial diversity in Pulque ● We increased 4.4 times bacteria genera and 40 times fungal species detected in mead. ● Newly reported bacteria genera and fungal species associated to Pulque fermentation Abstract Some of the biggest non-three plants endemic to Mexico were called metl in the Nahua culture. During colonial times they were renamed with the antillan word maguey. This was changed again by Carl von Linné who called them Agave (a greco-latin voice for admirable). For several Mexican prehispanic cultures, Agave species were not only considered as crops, but also part of their biocultural resources and cosmovision. Among the major products obtained from some Agave spp since pre-hispanic times is the alcoholic beverage called pulque or octli. -
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Cryptogamie, Mycologie, 2015, 36 (2): 225-236 © 2015 Adac. Tous droits réservés Poaceascoma helicoides gen et sp. nov., a new genus with scolecospores in Lentitheciaceae Rungtiwa PHOOkAmSAk a,b,c,d, Dimuthu S. mANAmGOdA c,d, Wen-jing LI a,b,c,d, Dong-Qin DAI a,b,c,d, Chonticha SINGTRIPOP a,b,c,d & kevin d. HYdE a,b,c,d* akey Laboratory for Plant diversity and Biogeography of East Asia, kunming Institute of Botany, Chinese Academy of Sciences, kunming 650201, China bWorld Agroforestry Centre, East and Central Asia, kunming 650201, China cInstitute of Excellence in Fungal Research, mae Fah Luang University, Chiang Rai 57100, Thailand dSchool of Science, mae Fah Luang University, Chiang Rai 57100, Thailand Abstract – An ophiosphaerella-like species was collected from dead stems of a grass (Poaceae) in Northern Thailand. Combined analysis of LSU, SSU and RPB2 gene data, showed that the species clusters with Lentithecium arundinaceum, Setoseptoria phragmitis and Stagonospora macropycnidia in the family Lentitheciaceae and is close to katumotoa bambusicola and Ophiosphaerella sasicola. Therefore, a monotypic genus, Poaceascoma is introduced to accommodate the scolecosporous species Poaceascoma helicoides. The species has similar morphological characters to the genera Acanthophiobolus, Leptospora and Ophiosphaerella and these genera are compared. Lentitheciaceae / Leptospora / Ophiosphaerella / phylogeny InTRoDuCTIon Lentitheciaceae was introduced by Zhang et al. (2012) to accommodate massarina-like species in the suborder Massarineae. In the recent monograph of Dothideomycetes (Hyde et al., 2013), the family Lentitheciaceae comprised the genera Lentithecium, katumotoa, keissleriella and Tingoldiago and all species had fusiform to cylindrical, 1-3-septate ascospores and mostly occurred on grasses. -
Leptosphaeriaceae, Pleosporales) from Italy
Mycosphere 6 (5): 634–642 (2015) ISSN 2077 7019 www.mycosphere.org Article Mycosphere Copyright © 2015 Online Edition Doi 10.5943/mycosphere/6/5/13 Phylogenetic and morphological appraisal of Leptosphaeria italica sp. nov. (Leptosphaeriaceae, Pleosporales) from Italy Dayarathne MC1,2,3,4, Phookamsak R 1,2,3,4, Ariyawansa HA3,4,7, Jones E.B.G5, Camporesi E6 and Hyde KD1,2,3,4* 1World Agro forestry Centre East and Central Asia Office, 132 Lanhei Road, Kunming 650201, China. 2Key Laboratory for Plant Biodiversity and Biogeography of East Asia (KLPB), Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan China 3Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 4School of Science, Mae Fah Luang University, Chiang Rai 57100, Thailand 5Department of Botany and Microbiology, King Saudi University, Riyadh, Saudi Arabia 6A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy; A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314, Brescia, Italy; Società per gli Studi Naturalistici della Romagna, C.P. 144, Bagnacavallo (RA), Italy 7Guizhou Key Laboratory of Agricultural Biotechnology, Guizhou Academy of Agricultural Sciences, Guiyang, 550006, Guizhou, China Dayarathne MC, Phookamsak R, Ariyawansa HA, Jones EBG, Camporesi E and Hyde KD 2015 – Phylogenetic and morphological appraisal of Leptosphaeria italica sp. nov. (Leptosphaeriaceae, Pleosporales) from Italy. Mycosphere 6(5), 634–642, Doi 10.5943/mycosphere/6/5/13 Abstract A fungal species with bitunicate asci and ellipsoid to fusiform ascospores was collected from a dead branch of Rhamnus alpinus in Italy. The new taxon morphologically resembles Leptosphaeria. -
Patellariaceae Revisited
Mycosphere 6 (3): 290–326(2015) ISSN 2077 7019 www.mycosphere.org Article Mycosphere Copyright © 2015 Online Edition Doi 10.5943/mycosphere/6/3/7 Patellariaceae revisited Yacharoen S1,2, Tian Q1,2, Chomnunti P1,2, Boonmee S1, Chukeatirote E2, Bhat JD3 and Hyde KD1,2,4,5* 1Institute of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 2School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3Formerly at Department of Botany, Goa University, Goa 403 206, India 4Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, China 5World Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, China Yacharoen S, Tian Q, Chomnunti P, Boonmee S, Chukeatirote E, Bhat JD, Hyde KD 2015 – Patellariaceae revisited. Mycosphere 6(3), 290–326, Doi 10.5943/mycosphere/6/3/7 Abstract The Dothideomycetes include several genera whose ascomata can be considered as apothecia and thus would be grouped as discomycetes. Most genera are grouped in the family Patellariaceae, but also Agrynnaceae and other families. The Hysteriales include genera having hysterioid ascomata and can be confused with species in Patellariaceae with discoid apothecia if the opening is wide enough. In this study, genera of the family Patellariaceae were re-examined and characterized based on morphological examination. As a result of this study the genera Baggea, Endotryblidium, Holmiella, Hysteropatella, Lecanidiella, Lirellodisca, Murangium, Patellaria, Poetschia, Rhizodiscina, Schrakia, Stratisporella and Tryblidaria are retained in the family Patellariaceae. The genera Banhegyia, Pseudoparodia and Rhytidhysteron are excluded because of differing morphology and/or molecular data. -
Based on a Newly-Discovered Species
A peer-reviewed open-access journal MycoKeys 76: 1–16 (2020) doi: 10.3897/mycokeys.76.58628 RESEARCH ARTICLE https://mycokeys.pensoft.net Launched to accelerate biodiversity research The insights into the evolutionary history of Translucidithyrium: based on a newly-discovered species Xinhao Li1, Hai-Xia Wu1, Jinchen Li1, Hang Chen1, Wei Wang1 1 International Fungal Research and Development Centre, The Research Institute of Resource Insects, Chinese Academy of Forestry, Kunming 650224, China Corresponding author: Hai-Xia Wu ([email protected], [email protected]) Academic editor: N. Wijayawardene | Received 15 September 2020 | Accepted 25 November 2020 | Published 17 December 2020 Citation: Li X, Wu H-X, Li J, Chen H, Wang W (2020) The insights into the evolutionary history of Translucidithyrium: based on a newly-discovered species. MycoKeys 76: 1–16. https://doi.org/10.3897/mycokeys.76.58628 Abstract During the field studies, aTranslucidithyrium -like taxon was collected in Xishuangbanna of Yunnan Province, during an investigation into the diversity of microfungi in the southwest of China. Morpho- logical observations and phylogenetic analysis of combined LSU and ITS sequences revealed that the new taxon is a member of the genus Translucidithyrium and it is distinct from other species. Therefore, Translucidithyrium chinense sp. nov. is introduced here. The Maximum Clade Credibility (MCC) tree from LSU rDNA of Translucidithyrium and related species indicated the divergence time of existing and new species of Translucidithyrium was crown age at 16 (4–33) Mya. Combining the estimated diver- gence time, paleoecology and plate tectonic movements with the corresponding geological time scale, we proposed a hypothesis that the speciation (estimated divergence time) of T. -
Phylogeny and Morphology of Premilcurensis Gen
Phytotaxa 236 (1): 040–052 ISSN 1179-3155 (print edition) www.mapress.com/phytotaxa/ PHYTOTAXA Copyright © 2015 Magnolia Press Article ISSN 1179-3163 (online edition) http://dx.doi.org/10.11646/phytotaxa.236.1.3 Phylogeny and morphology of Premilcurensis gen. nov. (Pleosporales) from stems of Senecio in Italy SAOWALUCK TIBPROMMA1,2,3,4,5, ITTHAYAKORN PROMPUTTHA6, RUNGTIWA PHOOKAMSAK1,2,3,4, SARANYAPHAT BOONMEE2, ERIO CAMPORESI7, JUN-BO YANG1,2, ALI H. BHAKALI8, ERIC H. C. MCKENZIE9 & KEVIN D. HYDE1,2,4,5,8 1Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Science, Kunming 650201, Yunnan, People’s Republic of China 2Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai, 57100, Thailand 3School of Science, Mae Fah Luang University, Chiang Rai, 57100, Thailand 4World Agroforestry Centre, East and Central Asia, Kunming 650201, Yunnan, P. R. China 5Mushroom Research Foundation, 128 M.3 Ban Pa Deng T. Pa Pae, A. Mae Taeng, Chiang Mai 50150, Thailand 6Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, 50200, Thailand 7A.M.B. Gruppo Micologico Forlivese “Antonio Cicognani”, Via Roma 18, Forlì, Italy; A.M.B. Circolo Micologico “Giovanni Carini”, C.P. 314, Brescia, Italy; Società per gli Studi Naturalistici della Romagna, C.P. 144, Bagnacavallo (RA), Italy 8Botany and Microbiology Department, College of Science, King Saud University, Riyadh, KSA 11442, Saudi Arabia 9Manaaki Whenua Landcare Research, Private Bag 92170, Auckland, New Zealand *Corresponding author: Dr. Itthayakorn Promputtha, Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai, 50200, Thailand. -
Mycosphere Notes 225–274: Types and Other Specimens of Some Genera of Ascomycota
Mycosphere 9(4): 647–754 (2018) www.mycosphere.org ISSN 2077 7019 Article Doi 10.5943/mycosphere/9/4/3 Copyright © Guizhou Academy of Agricultural Sciences Mycosphere Notes 225–274: types and other specimens of some genera of Ascomycota Doilom M1,2,3, Hyde KD2,3,6, Phookamsak R1,2,3, Dai DQ4,, Tang LZ4,14, Hongsanan S5, Chomnunti P6, Boonmee S6, Dayarathne MC6, Li WJ6, Thambugala KM6, Perera RH 6, Daranagama DA6,13, Norphanphoun C6, Konta S6, Dong W6,7, Ertz D8,9, Phillips AJL10, McKenzie EHC11, Vinit K6,7, Ariyawansa HA12, Jones EBG7, Mortimer PE2, Xu JC2,3, Promputtha I1 1 Department of Biology, Faculty of Science, Chiang Mai University, Chiang Mai 50200, Thailand 2 Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, 132 Lanhei Road, Kunming 650201, China 3 World Agro Forestry Centre, East and Central Asia, 132 Lanhei Road, Kunming 650201, Yunnan Province, People’s Republic of China 4 Center for Yunnan Plateau Biological Resources Protection and Utilization, College of Biological Resource and Food Engineering, Qujing Normal University, Qujing, Yunnan 655011, China 5 Shenzhen Key Laboratory of Microbial Genetic Engineering, College of Life Sciences and Oceanography, Shenzhen University, Shenzhen 518060, China 6 Center of Excellence in Fungal Research, Mae Fah Luang University, Chiang Rai 57100, Thailand 7 Department of Entomology and Plant Pathology, Faculty of Agriculture, Chiang Mai University, Chiang Mai 50200, Thailand 8 Department Research (BT), Botanic Garden Meise, Nieuwelaan 38, BE-1860 Meise, Belgium 9 Direction Générale de l'Enseignement non obligatoire et de la Recherche scientifique, Fédération Wallonie-Bruxelles, Rue A. -
Molecular Systematics of the Marine Dothideomycetes
available online at www.studiesinmycology.org StudieS in Mycology 64: 155–173. 2009. doi:10.3114/sim.2009.64.09 Molecular systematics of the marine Dothideomycetes S. Suetrong1, 2, C.L. Schoch3, J.W. Spatafora4, J. Kohlmeyer5, B. Volkmann-Kohlmeyer5, J. Sakayaroj2, S. Phongpaichit1, K. Tanaka6, K. Hirayama6 and E.B.G. Jones2* 1Department of Microbiology, Faculty of Science, Prince of Songkla University, Hat Yai, Songkhla, 90112, Thailand; 2Bioresources Technology Unit, National Center for Genetic Engineering and Biotechnology (BIOTEC), 113 Thailand Science Park, Paholyothin Road, Khlong 1, Khlong Luang, Pathum Thani, 12120, Thailand; 3National Center for Biothechnology Information, National Library of Medicine, National Institutes of Health, 45 Center Drive, MSC 6510, Bethesda, Maryland 20892-6510, U.S.A.; 4Department of Botany and Plant Pathology, Oregon State University, Corvallis, Oregon, 97331, U.S.A.; 5Institute of Marine Sciences, University of North Carolina at Chapel Hill, Morehead City, North Carolina 28557, U.S.A.; 6Faculty of Agriculture & Life Sciences, Hirosaki University, Bunkyo-cho 3, Hirosaki, Aomori 036-8561, Japan *Correspondence: E.B. Gareth Jones, [email protected] Abstract: Phylogenetic analyses of four nuclear genes, namely the large and small subunits of the nuclear ribosomal RNA, transcription elongation factor 1-alpha and the second largest RNA polymerase II subunit, established that the ecological group of marine bitunicate ascomycetes has representatives in the orders Capnodiales, Hysteriales, Jahnulales, Mytilinidiales, Patellariales and Pleosporales. Most of the fungi sequenced were intertidal mangrove taxa and belong to members of 12 families in the Pleosporales: Aigialaceae, Didymellaceae, Leptosphaeriaceae, Lenthitheciaceae, Lophiostomataceae, Massarinaceae, Montagnulaceae, Morosphaeriaceae, Phaeosphaeriaceae, Pleosporaceae, Testudinaceae and Trematosphaeriaceae. Two new families are described: Aigialaceae and Morosphaeriaceae, and three new genera proposed: Halomassarina, Morosphaeria and Rimora. -
Pleosporomycetidae, Dothideomycetes) from a Freshwater Habitat in Thailand
Mycological Progress (2020) 19:1031–1042 https://doi.org/10.1007/s11557-020-01609-0 ORIGINAL ARTICLE Mycoenterolobium aquadictyosporium sp. nov. (Pleosporomycetidae, Dothideomycetes) from a freshwater habitat in Thailand Mark S. Calabon1,2 & Kevin D. Hyde1,3 & E. B. Gareth Jones4 & Mingkwan Doilom5,6 & Chun-Fang Liao5,6 & Saranyaphat Boonmee1,2 Received: 25 May 2020 /Revised: 25 July 2020 /Accepted: 28 July 2020 # German Mycological Society and Springer-Verlag GmbH Germany, part of Springer Nature 2020 Abstract A study of freshwater fungi in Thailand led to the discovery of Mycoenterolobium aquadictyosporium sp. nov. Evidence for the novelty and placement in Mycoenterolobium is based on comparison of morphological data. The new species differs from the type species, M. platysporum, in having shorter and wider conidia, and from M. flabelliforme in having much longer and wider conidia. The hyphomycetous genus Mycoenterolobium is similar to Cancellidium but differs in the arrangement of conidial rows of cells at the attachment point to the conidiophores. The conidia of the former are made up of rows of cells, radiating in a linear pattern from a single cell attached to the conidiophore, while in Cancellidium, adherent rows of septate branches radiate from the conidiophore. Cancellidium conidia also contain branched chains of blastic monilioid cells arising from the conidia, while these are lacking in Mycoenterolobium.AtmaturityinMycoenterolobium, the two conidial lobes unite and are closely appressed. Phylogenetic analyses based on a combined LSU, SSU, ITS, TEF1-α,andRPB2 loci sequence data support the placement of Mycoenterolobium aquadictyosporium close to the family Testudinaceae within Pleosporomycetidae, Dothideomycetes. The novel species Mycoenterolobium aquadictyosporium is described and illustrated and is compared with other morphologically similar taxa. -
An Evolving Phylogenetically Based Taxonomy of Lichens and Allied Fungi
Opuscula Philolichenum, 11: 4-10. 2012. *pdf available online 3January2012 via (http://sweetgum.nybg.org/philolichenum/) An evolving phylogenetically based taxonomy of lichens and allied fungi 1 BRENDAN P. HODKINSON ABSTRACT. – A taxonomic scheme for lichens and allied fungi that synthesizes scientific knowledge from a variety of sources is presented. The system put forth here is intended both (1) to provide a skeletal outline of the lichens and allied fungi that can be used as a provisional filing and databasing scheme by lichen herbarium/data managers and (2) to announce the online presence of an official taxonomy that will define the scope of the newly formed International Committee for the Nomenclature of Lichens and Allied Fungi (ICNLAF). The online version of the taxonomy presented here will continue to evolve along with our understanding of the organisms. Additionally, the subfamily Fissurinoideae Rivas Plata, Lücking and Lumbsch is elevated to the rank of family as Fissurinaceae. KEYWORDS. – higher-level taxonomy, lichen-forming fungi, lichenized fungi, phylogeny INTRODUCTION Traditionally, lichen herbaria have been arranged alphabetically, a scheme that stands in stark contrast to the phylogenetic scheme used by nearly all vascular plant herbaria. The justification typically given for this practice is that lichen taxonomy is too unstable to establish a reasonable system of classification. However, recent leaps forward in our understanding of the higher-level classification of fungi, driven primarily by the NSF-funded Assembling the Fungal Tree of Life (AFToL) project (Lutzoni et al. 2004), have caused the taxonomy of lichen-forming and allied fungi to increase significantly in stability. This is especially true within the class Lecanoromycetes, the main group of lichen-forming fungi (Miadlikowska et al. -
<I>Lichenostigma Epirupestre</I> a New Lichenicolous Species On
MYCOTAXON Volume 107, pp. 189–195 January–March 2009 Lichenostigma epirupestre, a new lichenicolous species on Pertusaria from Spain Sergio Pérez-Ortega1 & Vicent Calatayud2 [email protected] Departamento de Biología Vegetal II, Facultad de Farmacia Universidad Complutense de Madrid Plaza Ramón y Cajal, Ciudad Universitaria, ES-28040 Madrid, SPAIN 2Fundación CEAM C/ Charles R. Darwin 14, Parc Tecnològic, E–46980 Paterna, València, Spain Abstract—The new species Lichenostigma epirupestre is described from three localities in Central Spain, growing on Pertusaria pertusa var. rupestris. Remarks on its taxonomy and closely related species are made and a key to the species of Lichenostigma subgenus Lichenostigma is also included. Key words—Iberian Peninsula, lichenicolous fungi, lichens Introduction The genus Lichenostigma was introduced for L. maureri Hafellner (Hafellner 1982) and, since then, a total of 21 species (after www.indexfungorum.org) have been referred to it. Two subgenera are recognized: Lichenostigma and Lichenogramma (Navarro-Rosinés & Hafellner 1996, Calatayud et al. 2002). Species belonging to subgenus Lichenostigma are characterized by having cushion-like ascomata and by the absence of visible vegetative hyphae or strands connecting several ascomata on the surface of the thallus. Taxa included in subgenus Lichenogramma show rounded or elongate ascomata that are interconnected by brown hyphae or pluricellular strands. While most species can easily be referred to one of these two subgenera, a few species show some intermediate features. This is the case of species in which the rounded shape of the ascomata is typical of subgenus Lichenostigma, but developing immersed (not visible on the host thallus) brown vegetative hyphae, or others that only occasionally develop superficial hyphal strands but only occasionally (Calatayud & Barreno 2003, Halıcı & Hawksworth 2007). -
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