Kazachstania Molopis Fungal Planet Description Sheets 421
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Phylogenetic Circumscription of Saccharomyces, Kluyveromyces
FEMS Yeast Research 4 (2003) 233^245 www.fems-microbiology.org Phylogenetic circumscription of Saccharomyces, Kluyveromyces and other members of the Saccharomycetaceae, and the proposal of the new genera Lachancea, Nakaseomyces, Naumovia, Vanderwaltozyma and Zygotorulaspora Cletus P. Kurtzman à Microbial Genomics and Bioprocessing Research Unit, National Center for Agricultural Utilization Research, Agricultural Research Service, U.S. Department of Agriculture, 1815 N. University Street, Peoria, IL 61604, USA Received 22 April 2003; received in revised form 23 June 2003; accepted 25 June 2003 First published online Abstract Genera currently assigned to the Saccharomycetaceae have been defined from phenotype, but this classification does not fully correspond with species groupings determined from phylogenetic analysis of gene sequences. The multigene sequence analysis of Kurtzman and Robnett [FEMS Yeast Res. 3 (2003) 417^432] resolved the family Saccharomycetaceae into 11 well-supported clades. In the present study, the taxonomy of the Saccharomyctaceae is evaluated from the perspective of the multigene sequence analysis, which has resulted in reassignment of some species among currently accepted genera, and the proposal of the following five new genera: Lachancea, Nakaseomyces, Naumovia, Vanderwaltozyma and Zygotorulaspora. ß 2003 Federation of European Microbiological Societies. Published by Elsevier B.V. All rights reserved. Keywords: Saccharomyces; Kluyveromyces; New ascosporic yeast genera; Molecular systematics; Multigene phylogeny 1. Introduction support the maintenance of three distinct genera. Yarrow [8^10] revived the concept of three genera and separated The name Saccharomyces was proposed for bread and Torulaspora and Zygosaccharomyces from Saccharomyces, beer yeasts by Meyen in 1838 [1], but it was Reess in 1870 although species assignments were often di⁄cult. -
Candida Albicans from Wikipedia, the Free Encyclopedia
Candida albicans From Wikipedia, the free encyclopedia Candida albicans is a type of yeast that is a common member of the human gut flora. It does not proliferate outside the human body.[4] It is Candida albicans detected in the gastrointestinal tract and mouth in 40-60% of healthy adults.[5][6] It is usually a commensal organism, but can become pathogenic in immunocompromised individuals under a variety of conditions.[6][7] It is one of the few species of the Candida genus that causes the human infection candidiasis, which results from an overgrowth of the fungus.[6][7] Candidiasis is for example often observed in HIV-infected patients.[8] C. albicans is the most common fungal species isolated from biofilms either formed on (permanent) implanted medical devices or on human Candida albicans visualised using [9][10] tissue. C. albicans, together with C. tropicalis, C. parapsilosis scanning electron microscopy. Note the and C. glabrata, is responsible for 50–90% of all cases of candidiasis in abundant hypal mass. humans.[7][11][12] A mortality rate of 40% has been reported for patients with systemic candidiasis due to C. albicans.[13] Estimates Scientific classification range from 2800 to 11200 deaths caused annually in the USA due to C. Kingdom: Fungi albicans causes candidiasis.[14] Division: Ascomycota C. albicans is commonly used as a model organism for biology. It is generally referred to as a dimorphic fungus since it grows both as yeast Class: Saccharomycetes and filamentous cells. However it has several different morphological Order: Saccharomycetales phenotypes. C. albicans was for a long time considered an obligate diploid organism without a haploid stage. -
Downloaded from NCBI Genbank Or Sequence
Lind and Pollard Microbiome (2021) 9:58 https://doi.org/10.1186/s40168-021-01015-y METHODOLOGY Open Access Accurate and sensitive detection of microbial eukaryotes from whole metagenome shotgun sequencing Abigail L. Lind1 and Katherine S. Pollard1,2,3,4,5* Abstract Background: Microbial eukaryotes are found alongside bacteria and archaea in natural microbial systems, including host-associated microbiomes. While microbial eukaryotes are critical to these communities, they are challenging to study with shotgun sequencing techniques and are therefore often excluded. Results: Here, we present EukDetect, a bioinformatics method to identify eukaryotes in shotgun metagenomic sequencing data. Our approach uses a database of 521,824 universal marker genes from 241 conserved gene families, which we curated from 3713 fungal, protist, non-vertebrate metazoan, and non-streptophyte archaeplastida genomes and transcriptomes. EukDetect has a broad taxonomic coverage of microbial eukaryotes, performs well on low-abundance and closely related species, and is resilient against bacterial contamination in eukaryotic genomes. Using EukDetect, we describe the spatial distribution of eukaryotes along the human gastrointestinal tract, showing that fungi and protists are present in the lumen and mucosa throughout the large intestine. We discover that there is a succession of eukaryotes that colonize the human gut during the first years of life, mirroring patterns of developmental succession observed in gut bacteria. By comparing DNA and RNA sequencing of paired samples from human stool, we find that many eukaryotes continue active transcription after passage through the gut, though some do not, suggesting they are dormant or nonviable. We analyze metagenomic data from the Baltic Sea and find that eukaryotes differ across locations and salinity gradients. -
Comparative Genomics of Protoploid Saccharomycetaceae
Downloaded from genome.cshlp.org on October 5, 2021 - Published by Cold Spring Harbor Laboratory Press Evolution of protoploid yeast genomes ___________________________________________________________________________ Comparative genomics of protoploid Saccharomycetaceae. The Génolevures Consortium (1) Running title: Evolution of protoploid yeast genomes Key words: protein families, synteny, tandems, annotation, SONS, ancestor genome Corresponding author: Jean Luc Souciet Université de Strasbourg, CNRS, UMR 7156 Institut de Botanique, 28 rue Goethe, F-67000 Strasbourg, France Tel: 33 3 90 24 18 17 FAX: 33 3 90 24 20 28 e-mail: [email protected] (1) List of participants and affiliations appear at the end of the paper 1 Downloaded from genome.cshlp.org on October 5, 2021 - Published by Cold Spring Harbor Laboratory Press Evolution of protoploid yeast genomes ___________________________________________________________________________ Abstract Our knowledge on yeast genomes remains largely dominated by the extensive studies on Saccharomyces cerevisiae and the consequences of its ancestral duplication, leaving the evolution of the entire class of hemiascomycetes only partly explored. We concentrate here on five species of Saccharomycetaceae, a large subdivision of hemiascomycetes, that we call “protoploid” because they diverged from the S. cerevisiae lineage prior to its genome duplication. We determined the complete genome sequences of three of these species, Kluyveromyces (Lachancea) thermotolerans and Saccharomyces (Lachancea) kluyveri (two members of the newly described Lachancea clade) and Zygosaccharomyces rouxii. We included in our comparisons the previously available sequences of Klyveromyces lactis and Ashbya (Eremothecium) gossypii. Despite their broad evolutionary range and significant individual variations in each lineage, the five protoploid Saccharomycetaceae share a core repertoire of ca. -
Taxonomy of Yeasts
^ÍV/-^ TECHmcAL BULLETIN NO. 1029 May 1951 .— 5 Taxonomy of Yeasts By LYNFERD J. WICKERHAM Zymologist Northern Regional Research Laboratory Bureau of Agricultural and Industrial Chemistry Agricultural Research Administration -- ! f^ R A R Y Jüri¿ 51951 U.Î. ainnrmm sf A«RIOüLTURí UNITED STATES DEPARTMENT OF AcKictrLTURE, WASHINGTON, D. C. PREFACE In early attempts at yeast classification, the characteristics em- ployed for separating the larger groups of yeasts were the ability to grow as filaments, the ability to produce asci which consist of two cells fused together, the shape of the ascospores, the ability to pro- duce a gaseous fermentation of one or more sugars, and the ability to produce pellicles on liquid media. Evidence obtained in the present study indicates that the use of the foregoing characteristics led to the unintentional cleavage of natural, or phylogenetic groups into sections. Moreover, sections of different phylogenetic lines which had in common only one or two of the characteristics just mentioned were often assembled into the same genus. These characteristics, applied by Hansen, Barker, and Klocker dur- ing the early 1900's, continue in use as the basis for separating genera and subgenera in the presently accepted system of yeast classification. As a result, all of the larger genera of both the ascosporogenous and nonascosporogenous yeasts contain dissimilar types. The mixing has been thorough—in many cases the true relationships which exist among species of the different genera have been concealed. Correction of this situation by the arrangement of species m what appear to be phylogenetic lines of related species is believed to be a major advance. -
Candida Species – Morphology, Medical Aspects and Pathogenic Spectrum
European Journal of Molecular & Clinical Medicine ISSN 2515-8260 Volume 07, Issue 07, 2020 Candida Species – Morphology, Medical Aspects And Pathogenic Spectrum. Shubham Koundal1, Louis Cojandaraj2 1 Assistant Professor, Department of Medical Laboratory Sciences, Chandigarh University, Punjab. 2Assistant Professor, Department of Medical Laboratory Sciences, Lovely Professional University, Punjab. Email Id: [email protected] ABSTRACT Emergence of candidal infections are increasing from decades and found to be a leading cause of human disease and mortality. Candida spp. is one of the communal of human body and is known to cause opportunistic superficial and invasive infections. Many of mycoses-related deaths were due to Candida spp. Major shift of Candida infection towards NAC (non-albicans Candida) is matter of concern worldwide. In this study we had given a systemic review about medically important Candidaspp. Along with their morphological features, treatment and drugs. Spectrum of the pathogen is also discussed. Morphology of Different Medically Important Candida Species with their medical aspects along and pathogenic spectrum. Corn meal agar morphology along with anti-candida drugs has been discussed. The study is done after considering various published review’s and the mycological studies. Key words: Candida, Yeast, C.albicans, C. tropicalis, C. parapsilosis, C. glabrata, C. krusei and C. lusitaniae 1. INTRODUCTION Yeasts are unicellular, sometimes dimorphic fungi. It can give rise to wide range of infections in humans commonly called fungal infections. Yeast infections varies from superficial cutaneous/skin infections, mucosa related infections to multi-organ disseminated infections.(Sardi et al., 2013)Cutaneous and mucosal yeast infections can infect a number of regions in human body including the skin, nails, oral cavity, gastrointestinal tract, female genital tract and esophageal part and lead to chronic nature. -
1 May 31, 2016 Centromeres of the Yeast Komagataella Phaffii (Pichia Pastoris) Have a Simple Inverted-Repeat Structure Aisling Y
bioRxiv preprint doi: https://doi.org/10.1101/056382; this version posted May 31, 2016. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC-ND 4.0 International license. May 31, 2016 Centromeres of the yeast Komagataella phaffii (Pichia pastoris) have a simple inverted-repeat structure Aisling Y. Coughlan1, Sara J. Hanson1, Kevin P. Byrne1 and Kenneth H. Wolfe*,1 1UCD Conway Institute, School of Medicine, University College Dublin, Dublin 4, Ireland *Corresponding author: E-mail: [email protected] Abstract Centromere organization has evolved dramatically in one clade of fungi, the Saccharomycotina. These yeasts have lost the ability to make normal eukaryotic heterochromatin with histone H3K9 methylation, which is a major component of pericentromeric regions in other eukaryotes. Following this loss, several different types of centromere emerged, including two types of sequence-defined (‘point’) centromeres, and the epigenetically-defined ‘small regional’ centromeres of Candida albicans. Here we report that centromeres of the methylotrophic yeast Komagataella phaffii (formerly called Pichia pastoris) are structurally-defined. Each of its four centromeres consists of a 2-kb inverted repeat (IR) flanking a 1-kb central core (mid) region. The four centromeres are unrelated in sequence. CenH3 (Cse4) binds strongly to the cores, with a decreasing gradient along the IRs. This mode of organization resembles Schizosaccharomyces pombe centromeres but is much more compact and lacks the extensive flanking heterochromatic otr repeats. Different isolates of K. phaffii show polymorphism for the orientation of the mid regions, due to recombination in the IRs. -
Genome Sequence of the Non-Conventional Wine
DNA Research, 2019, 26(1), 67–83 doi: 10.1093/dnares/dsy039 Advance Access Publication Date: 20 November 2018 Full Paper Full Paper Downloaded from https://academic.oup.com/dnaresearch/article-abstract/26/1/67/5193709 by Technische Universitaet Muenchen user on 30 April 2020 Genome sequence of the non-conventional wine yeast Hanseniaspora guilliermondii UTAD222 unveils relevant traits of this species and of the Hanseniaspora genus in the context of wine fermentation Isabel Seixas1,2, Catarina Barbosa1,2, Arlete Mendes-Faia1,2, Ulrich Gu¨ ldener3, Roge´ rio Tenreiro2, Ana Mendes-Ferreira1,2*, and Nuno P. Mira4* 1WM&B—Laboratory of Wine Microbiology & Biotechnology, Department of Biology and Environment, University of Tra´s-os-Montes and Alto Douro, 5001-801 Vila Real, Portugal, 2BioISI-Biosystems and Integrative Sciences Institute, Faculdade de Cieˆncias, Universidade de Lisboa Campo Grande, 1749-016 Lisbon, Portugal, 3Department of Bioinformatics, Wissenschaftszentrum Weihenstephan, Technische Universita¨t Mu¨nchen, Maximus von-Imhof- Forum 3, 85354 Freising, Germany, and 4Department of Bioengineering, iBB - Institute for Bioengineering and Biosciences, Instituto Superior Te´cnico, Universidade de Lisboa, Avenida Rovisco Pais, 1049-001 Lisbon, Portugal *To whom correspondence should be addressed. Tel. þ351218419181. Email: [email protected] (N.P.M.); Tel. þ351 259 350 550. Email: [email protected] (A.M.-F.) Edited by Dr. Katsumi Isono Received 23 May 2018; Editorial decision 13 October 2018; Accepted 16 October 2018 Abstract Hanseanispora species, including H. guilliermondii, are long known to be abundant in wine grape- musts and to play a critical role in vinification by modulating, among other aspects, the wine sensory profile. -
Supplementary Materials For
Electronic Supplementary Material (ESI) for RSC Advances. This journal is © The Royal Society of Chemistry 2019 Supplementary materials for: Fungal community analysis in the seawater of the Mariana Trench as estimated by Illumina HiSeq Zhi-Peng Wang b, †, Zeng-Zhi Liu c, †, Yi-Lin Wang d, Wang-Hua Bi c, Lu Liu c, Hai-Ying Wang b, Yuan Zheng b, Lin-Lin Zhang e, Shu-Gang Hu e, Shan-Shan Xu c, *, Peng Zhang a, * 1 Tobacco Research Institute, Chinese Academy of Agricultural Sciences, Qingdao, 266101, China 2 Key Laboratory of Sustainable Development of Polar Fishery, Ministry of Agriculture and Rural Affairs, Yellow Sea Fisheries Research Institute, Chinese Academy of Fishery Sciences, Qingdao, 266071, China 3 School of Medicine and Pharmacy, Ocean University of China, Qingdao, 266003, China. 4 College of Science, China University of Petroleum, Qingdao, Shandong 266580, China. 5 College of Chemistry & Environmental Engineering, Shandong University of Science & Technology, Qingdao, 266510, China. a These authors contributed equally to this work *Authors to whom correspondence should be addressed Supplementary Table S1. Read counts of OTUs in different sampled sites. OTUs M1.1 M1.2 M1.3 M1.4 M3.1 M3.2 M3.4 M4.2 M4.3 M4.4 M7.1 M7.2 M7.3 Total number OTU1 13714 398 5405 671 11604 3286 3452 349 3560 2537 383 2629 3203 51204 OTU2 6477 2203 2188 1048 2225 1722 235 1270 2564 5258 7149 7131 3606 43089 OTU3 165 39 13084 37 81 7 11 11 2 176 289 4 2102 16021 OTU4 642 4347 439 514 638 191 170 179 0 1969 570 678 0 10348 OTU5 28 13 4806 7 44 151 10 620 3 -
Tour Pages by Clicking This Link
STATION 1 (Welcome) WELCOME TO THE CBEC TINY THINGS TOUR (STATION 1) This tour is designed to acquaint CBEC visitors with the amazingly diverse array of organisms here that are not typically noticed, mainly because they’re too small to be seen without either very careful observation or the aid of a magnifier (either a handheld device or a microscope). The tour will discuss representatives of the six kingdoms of living things (Bacteria, Archaea, Fungi, Plants, Protists, and Animals), as well as viruses. In addition to brief discussions of the particular organisms themselves, we’ll consider the role that these organisms play in their immediate environment, their effect on the larger biosphere, and their ability to teach us about the past and the future. Taking the Tour: To take the tour, visitors may use the Tiny Things Tour map, where the 14 stations are indicated with red numbers. The map should be used in conjunction with the printable list of stations. The list has the GPS coordinates for each station, along with QR codes that provide links to the web pages that describe each station. The GPS coordinates, as well as a simple description of each location are included on each station’s web page. If visitors haven’t brought along a mobile device (to view the web pages), they can print a copy of the tour pages by clicking this link. A guided version of the Tiny Things Tour is scheduled on a regular basis. Check the CBEC schedule for upcoming guided tours. Each web page includes a photo of the representative organism, it’s common name and scientific name, a description of the station location (including its GPS location), and a description of the organism and its environment. -
Signatures of Optimal Codon Usage Predict Metabolic Ecology in Budding Yeasts
bioRxiv preprint doi: https://doi.org/10.1101/2020.07.22.214635; this version posted July 24, 2020. The copyright holder for this preprint (which was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under aCC-BY-NC 4.0 International license. 1 Signatures of optimal codon usage predict metabolic ecology in budding yeasts 2 Abigail Leavitt LaBella 3 Department of Biological Sciences, Vanderbilt University, Nashville, TN 37235, USA 4 ORCID: 0000-0003-0068-6703 5 [email protected] 6 7 Dana A. Opulente 8 Laboratory of Genetics, DOE Great Lakes Bioenergy Research Center, Wisconsin Energy 9 Institute, Center for Genomic Science Innovation, J.F. Crow Institute for the Study of Evolution, 10 University of Wisconsin-Madison, Madison, WI 53726, USA 11 12 Jacob Steenwyk 13 Department of Biological Sciences, Vanderbilt University, Nashville, TN 37235, USA 14 ORCID: 0000-0002-8436-595X 15 [email protected] 16 17 Chris Todd Hittinger 18 Laboratory of Genetics, DOE Great Lakes Bioenergy Research Center, Wisconsin Energy 19 Institute, Center for Genomic Science Innovation, J.F. Crow Institute for the Study of Evolution, 20 University of Wisconsin-Madison, Madison, WI 53726, USA 21 ORCID: 0000-0001-5088-7461 22 [email protected] 23 24 Antonis Rokas 25 Department of Biological Sciences, Vanderbilt University, Nashville, TN 37235, USA 26 ORCID: 0000-0002-7248-6551 27 [email protected] 28 Running head: Codon usage as a lens into the metabolic ecology of budding yeasts 29 Keywords: Codon usage bias; Budding yeasts; Secondary metabolism; Reverse Ecology bioRxiv preprint doi: https://doi.org/10.1101/2020.07.22.214635; this version posted July 24, 2020. -
Toward a Fully Resolved Fungal Tree of Life
Annual Review of Microbiology Toward a Fully Resolved Fungal Tree of Life Timothy Y. James,1 Jason E. Stajich,2 Chris Todd Hittinger,3 and Antonis Rokas4 1Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan 48109, USA; email: [email protected] 2Department of Microbiology and Plant Pathology, Institute for Integrative Genome Biology, University of California, Riverside, California 92521, USA; email: [email protected] 3Laboratory of Genetics, DOE Great Lakes Bioenergy Research Center, Wisconsin Energy Institute, Center for Genomic Science and Innovation, J.F. Crow Institute for the Study of Evolution, University of Wisconsin–Madison, Madison, Wisconsin 53726, USA; email: [email protected] 4Department of Biological Sciences, Vanderbilt University, Nashville, Tennessee 37235, USA; email: [email protected] Annu. Rev. Microbiol. 2020. 74:291–313 Keywords First published as a Review in Advance on deep phylogeny, phylogenomic inference, uncultured majority, July 13, 2020 classification, systematics The Annual Review of Microbiology is online at micro.annualreviews.org Abstract https://doi.org/10.1146/annurev-micro-022020- Access provided by Vanderbilt University on 06/28/21. For personal use only. In this review, we discuss the current status and future challenges for fully 051835 Annu. Rev. Microbiol. 2020.74:291-313. Downloaded from www.annualreviews.org elucidating the fungal tree of life. In the last 15 years, advances in genomic Copyright © 2020 by Annual Reviews. technologies have revolutionized fungal systematics, ushering the field into All rights reserved the phylogenomic era. This has made the unthinkable possible, namely ac- cess to the entire genetic record of all known extant taxa.