Research Article Diversity and Distribution of Archaea in the Mangrove Sediment of Sundarbans
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Genotyping of Uncultured Archaea in a Polluted Site of Suez Gulf, Egypt, Based on 16S Rrna Gene Analyses
Egyptian Journal of Aquatic Research (2014) 40,27–33 National Institute of Oceanography and Fisheries Egyptian Journal of Aquatic Research http://ees.elsevier.com/ejar www.sciencedirect.com FULL LENGTH ARTICLE Genotyping of uncultured archaea in a polluted site of Suez Gulf, Egypt, based on 16S rRNA gene analyses Hosam Easa Elsaied * Aquagenome Resources and Biotechnology Research Group, National Institute of Oceanography, 101-El-Kasr El-Eini Street, Cairo, Egypt Received 3 February 2014; revised 11 March 2014; accepted 11 March 2014 Available online 18 April 2014 KEYWORDS Abstract Culture-independent 16S rRNA gene analysis approach was used to explore and evalu- Archaea; ate archaea in a polluted site, El-Zeitia, Suez Gulf, Egypt. Metagenomic DNA was extracted from a 16S rRNA gene diversity; sediment sample. Archaeal 16S rRNA gene was PCR amplified using universal archaeal primers, Sediment; followed by cloning and direct analyses by sequencing. Rarefaction analysis showed saturation, Suez Gulf recording 21 archaeal 16S rRNA gene phylotypes, which represented the total composition of archaea in the studied sample. Phylogenetic analysis showed that all recorded phylotypes belonged to two archaeal phyla. Sixteen phylotypes were located in the branch of methanogenic Eur- yarchaeota and more closely related to species of the genera Methanosaeta and Methanomassiliicoc- cus. Five phylotypes were affiliated to the new archaeal phylum Thaumarchaeota, which represented by species Candidatus nitrosopumilus. The recorded phylotypes had unique sequences, characteriz- ing them as new phylogenetic lineages. This work is the first investigation of uncultured archaea in the Suez Gulf, and implicated that the environmental characteristics shaped the diversity of archa- eal 16S rRNA genes in the studied sample. -
Insights Into Archaeal Evolution and Symbiosis from the Genomes of a Nanoarchaeon and Its Inferred Crenarchaeal Host from Obsidian Pool, Yellowstone National Park
University of Tennessee, Knoxville TRACE: Tennessee Research and Creative Exchange Microbiology Publications and Other Works Microbiology 4-22-2013 Insights into archaeal evolution and symbiosis from the genomes of a nanoarchaeon and its inferred crenarchaeal host from Obsidian Pool, Yellowstone National Park Mircea Podar University of Tennessee - Knoxville, [email protected] Kira S. Makarova National Institutes of Health David E. Graham University of Tennessee - Knoxville, [email protected] Yuri I. Wolf National Institutes of Health Eugene V. Koonin National Institutes of Health See next page for additional authors Follow this and additional works at: https://trace.tennessee.edu/utk_micrpubs Part of the Microbiology Commons Recommended Citation Biology Direct 2013, 8:9 doi:10.1186/1745-6150-8-9 This Article is brought to you for free and open access by the Microbiology at TRACE: Tennessee Research and Creative Exchange. It has been accepted for inclusion in Microbiology Publications and Other Works by an authorized administrator of TRACE: Tennessee Research and Creative Exchange. For more information, please contact [email protected]. Authors Mircea Podar, Kira S. Makarova, David E. Graham, Yuri I. Wolf, Eugene V. Koonin, and Anna-Louise Reysenbach This article is available at TRACE: Tennessee Research and Creative Exchange: https://trace.tennessee.edu/ utk_micrpubs/44 Podar et al. Biology Direct 2013, 8:9 http://www.biology-direct.com/content/8/1/9 RESEARCH Open Access Insights into archaeal evolution and symbiosis from the genomes of a nanoarchaeon and its inferred crenarchaeal host from Obsidian Pool, Yellowstone National Park Mircea Podar1,2*, Kira S Makarova3, David E Graham1,2, Yuri I Wolf3, Eugene V Koonin3 and Anna-Louise Reysenbach4 Abstract Background: A single cultured marine organism, Nanoarchaeum equitans, represents the Nanoarchaeota branch of symbiotic Archaea, with a highly reduced genome and unusual features such as multiple split genes. -
The Genome Sequence of Methanohalophilus Mahii SLPT
Hindawi Publishing Corporation Archaea Volume 2010, Article ID 690737, 16 pages doi:10.1155/2010/690737 Research Article TheGenomeSequenceofMethanohalophilus mahii SLPT Reveals Differences in the Energy Metabolism among Members of the Methanosarcinaceae Inhabiting Freshwater and Saline Environments Stefan Spring,1 Carmen Scheuner,1 Alla Lapidus,2 Susan Lucas,2 Tijana Glavina Del Rio,2 Hope Tice,2 Alex Copeland,2 Jan-Fang Cheng,2 Feng Chen,2 Matt Nolan,2 Elizabeth Saunders,2, 3 Sam Pitluck,2 Konstantinos Liolios,2 Natalia Ivanova,2 Konstantinos Mavromatis,2 Athanasios Lykidis,2 Amrita Pati,2 Amy Chen,4 Krishna Palaniappan,4 Miriam Land,2, 5 Loren Hauser,2, 5 Yun-Juan Chang,2, 5 Cynthia D. Jeffries,2, 5 Lynne Goodwin,2, 3 John C. Detter,3 Thomas Brettin,3 Manfred Rohde,6 Markus Goker,¨ 1 Tanja Woyke, 2 Jim Bristow,2 Jonathan A. Eisen,2, 7 Victor Markowitz,4 Philip Hugenholtz,2 Nikos C. Kyrpides,2 and Hans-Peter Klenk1 1 DSMZ—German Collection of Microorganisms and Cell Cultures GmbH, 38124 Braunschweig, Germany 2 DOE Joint Genome Institute, Walnut Creek, CA 94598-1632, USA 3 Los Alamos National Laboratory, Bioscience Division, Los Alamos, NM 87545-001, USA 4 Biological Data Management and Technology Center, Lawrence Berkeley National Laboratory, Berkeley, CA 94720, USA 5 Oak Ridge National Laboratory, Oak Ridge, TN 37830-8026, USA 6 HZI—Helmholtz Centre for Infection Research, 38124 Braunschweig, Germany 7 Davis Genome Center, University of California, Davis, CA 95817, USA Correspondence should be addressed to Stefan Spring, [email protected] and Hans-Peter Klenk, [email protected] Received 24 August 2010; Accepted 9 November 2010 Academic Editor: Valerie´ de Crecy-Lagard´ Copyright © 2010 Stefan Spring et al. -
Variations in the Two Last Steps of the Purine Biosynthetic Pathway in Prokaryotes
GBE Different Ways of Doing the Same: Variations in the Two Last Steps of the Purine Biosynthetic Pathway in Prokaryotes Dennifier Costa Brandao~ Cruz1, Lenon Lima Santana1, Alexandre Siqueira Guedes2, Jorge Teodoro de Souza3,*, and Phellippe Arthur Santos Marbach1,* 1CCAAB, Biological Sciences, Recoˆ ncavo da Bahia Federal University, Cruz das Almas, Bahia, Brazil 2Agronomy School, Federal University of Goias, Goiania,^ Goias, Brazil 3 Department of Phytopathology, Federal University of Lavras, Minas Gerais, Brazil Downloaded from https://academic.oup.com/gbe/article/11/4/1235/5345563 by guest on 27 September 2021 *Corresponding authors: E-mails: [email protected]fla.br; [email protected]. Accepted: February 16, 2019 Abstract The last two steps of the purine biosynthetic pathway may be catalyzed by different enzymes in prokaryotes. The genes that encode these enzymes include homologs of purH, purP, purO and those encoding the AICARFT and IMPCH domains of PurH, here named purV and purJ, respectively. In Bacteria, these reactions are mainly catalyzed by the domains AICARFT and IMPCH of PurH. In Archaea, these reactions may be carried out by PurH and also by PurP and PurO, both considered signatures of this domain and analogous to the AICARFT and IMPCH domains of PurH, respectively. These genes were searched for in 1,403 completely sequenced prokaryotic genomes publicly available. Our analyses revealed taxonomic patterns for the distribution of these genes and anticorrelations in their occurrence. The analyses of bacterial genomes revealed the existence of genes coding for PurV, PurJ, and PurO, which may no longer be considered signatures of the domain Archaea. Although highly divergent, the PurOs of Archaea and Bacteria show a high level of conservation in the amino acids of the active sites of the protein, allowing us to infer that these enzymes are analogs. -
Methanogens: Biochemical Background and Biotechnological Applications Franziska Enzmann1, Florian Mayer1 , Michael Rother2 and Dirk Holtmann1*
Enzmann et al. AMB Expr (2018) 8:1 https://doi.org/10.1186/s13568-017-0531-x MINI-REVIEW Open Access Methanogens: biochemical background and biotechnological applications Franziska Enzmann1, Florian Mayer1 , Michael Rother2 and Dirk Holtmann1* Abstract Since fossil sources for fuel and platform chemicals will become limited in the near future, it is important to develop new concepts for energy supply and production of basic reagents for chemical industry. One alternative to crude oil and fossil natural gas could be the biological conversion of CO2 or small organic molecules to methane via metha‑ nogenic archaea. This process has been known from biogas plants, but recently, new insights into the methanogenic metabolism, technical optimizations and new technology combinations were gained, which would allow moving beyond the mere conversion of biomass. In biogas plants, steps have been undertaken to increase yield and purity of the biogas, such as addition of hydrogen or metal granulate. Furthermore, the integration of electrodes led to the development of microbial electrosynthesis (MES). The idea behind this technique is to use CO 2 and electrical power to generate methane via the microbial metabolism. This review summarizes the biochemical and metabolic background of methanogenesis as well as the latest technical applications of methanogens. As a result, it shall give a sufcient overview over the topic to both, biologists and engineers handling biological or bioelectrochemical methanogenesis. Keywords: Methanogens, Genetic tools, Biogas, Microbial electrosynthesis, Electroactivity Introduction process involving methanogens. Tese archaea use CO 2 Methanogens are biocatalysts, which have the potential and H2 and/or small organic molecules, such as acetate, to contribute to a solution for future energy problems by formate, and methylamine and convert it to methane. -
International Code of Nomenclature of Prokaryotes
2019, volume 69, issue 1A, pages S1–S111 International Code of Nomenclature of Prokaryotes Prokaryotic Code (2008 Revision) Charles T. Parker1, Brian J. Tindall2 and George M. Garrity3 (Editors) 1NamesforLife, LLC (East Lansing, Michigan, United States) 2Leibniz-Institut DSMZ-Deutsche Sammlung von Mikroorganismen und Zellkulturen GmbH (Braunschweig, Germany) 3Michigan State University (East Lansing, Michigan, United States) Corresponding Author: George M. Garrity ([email protected]) Table of Contents 1. Foreword to the First Edition S1–S1 2. Preface to the First Edition S2–S2 3. Preface to the 1975 Edition S3–S4 4. Preface to the 1990 Edition S5–S6 5. Preface to the Current Edition S7–S8 6. Memorial to Professor R. E. Buchanan S9–S12 7. Chapter 1. General Considerations S13–S14 8. Chapter 2. Principles S15–S16 9. Chapter 3. Rules of Nomenclature with Recommendations S17–S40 10. Chapter 4. Advisory Notes S41–S42 11. References S43–S44 12. Appendix 1. Codes of Nomenclature S45–S48 13. Appendix 2. Approved Lists of Bacterial Names S49–S49 14. Appendix 3. Published Sources for Names of Prokaryotic, Algal, Protozoal, Fungal, and Viral Taxa S50–S51 15. Appendix 4. Conserved and Rejected Names of Prokaryotic Taxa S52–S57 16. Appendix 5. Opinions Relating to the Nomenclature of Prokaryotes S58–S77 17. Appendix 6. Published Sources for Recommended Minimal Descriptions S78–S78 18. Appendix 7. Publication of a New Name S79–S80 19. Appendix 8. Preparation of a Request for an Opinion S81–S81 20. Appendix 9. Orthography S82–S89 21. Appendix 10. Infrasubspecific Subdivisions S90–S91 22. Appendix 11. The Provisional Status of Candidatus S92–S93 23. -
A Metagenomics Roadmap to the Uncultured Genome Diversity in Hypersaline Soda Lake Sediments Charlotte D
Vavourakis et al. Microbiome (2018) 6:168 https://doi.org/10.1186/s40168-018-0548-7 RESEARCH Open Access A metagenomics roadmap to the uncultured genome diversity in hypersaline soda lake sediments Charlotte D. Vavourakis1 , Adrian-Stefan Andrei2†, Maliheh Mehrshad2†, Rohit Ghai2, Dimitry Y. Sorokin3,4 and Gerard Muyzer1* Abstract Background: Hypersaline soda lakes are characterized by extreme high soluble carbonate alkalinity. Despite the high pH and salt content, highly diverse microbial communities are known to be present in soda lake brines but the microbiome of soda lake sediments received much less attention of microbiologists. Here, we performed metagenomic sequencing on soda lake sediments to give the first extensive overview of the taxonomic diversity found in these complex, extreme environments and to gain novel physiological insights into the most abundant, uncultured prokaryote lineages. Results: We sequenced five metagenomes obtained from four surface sediments of Siberian soda lakes with a pH 10 and a salt content between 70 and 400 g L−1. The recovered 16S rRNA gene sequences were mostly from Bacteria,evenin the salt-saturated lakes. Most OTUs were assigned to uncultured families. We reconstructed 871 metagenome-assembled genomes (MAGs) spanning more than 45 phyla and discovered the first extremophilic members of the Candidate Phyla Radiation (CPR). Five new species of CPR were among the most dominant community members. Novel dominant lineages were found within previously well-characterized functional groups involved in carbon, sulfur, and nitrogen cycling. Moreover, key enzymes of the Wood-Ljungdahl pathway were encoded within at least four bacterial phyla never previously associated with this ancient anaerobic pathway for carbon fixation and dissimilation, including the Actinobacteria. -
Microbiome of Seven Full-Scale Anaerobic Digestion Plants in South Korea: Effect of Feedstock and Operational Parameters
energies Article Microbiome of Seven Full-Scale Anaerobic Digestion Plants in South Korea: Effect of Feedstock and Operational Parameters Michal Sposob 1,2,†, Hee-Sung Moon 3,†, Dongjin Lee 3 and Yeo-Myeong Yun 1,* 1 Department of Environmental Engineering, Chungbuk National University, 1 Chungdae-ro, Seowon-Gu, Cheongju 28644, Korea; [email protected] 2 NIBIO, Norwegian Institute of Bioeconomy Research, P.O. Box 115, N-1431 Ås, Norway 3 Waste-Energy Research Division, Environmental Resources Research Department, National Institute of Environmental Research, Environmental Research Complex, Incheon 22689, Korea; [email protected] (H.-S.M.); [email protected] (D.L.) * Correspondence: [email protected]; Tel.: +82-43-261-2466; Fax: +82-43-264-2465 † Both authors contributed equally to this work. Abstract: In this study, the microbiomes linked with the operational parameters in seven mesophilic full-scale AD plants mainly treating food waste (four plants) and sewage sludge (three plants) were analyzed. The results obtained indicated lower diversity and evenness of the microbial population in sludge digestion (SD) plants compared to food digestion (FD) plants. Candidatus Accumulibacter dominated (up to 42.1%) in SD plants due to microbial immigration from fed secondary sludge (up to 89%). Its potential activity in SD plants was correlated to H2 production, which was related to the dominance of hydrogenotrophic methanogens (Methanococcus). In FD plants, a balance between the hydrogenotrophic and methylotrophic pathways was found, while Flavobacterium and Levilinea played an important role during acidogenesis. Levilinea also expressed sensitivity to ammonia in FD plants. The substantial differences in hydraulic retention time (HRT), organic loading rate (OLR), and total ammonium nitrogen (TAN) among the studied FD plants did not influence the archaeal methane Citation: Sposob, M.; Moon, H.-S.; production pathway. -
Microbiology of Lonar Lake and Other Soda Lakes
The ISME Journal (2013) 7, 468–476 & 2013 International Society for Microbial Ecology All rights reserved 1751-7362/13 www.nature.com/ismej MINI REVIEW Microbiology of Lonar Lake and other soda lakes Chakkiath Paul Antony1, Deepak Kumaresan2, Sindy Hunger3, Harold L Drake3, J Colin Murrell4 and Yogesh S Shouche1 1Microbial Culture Collection, National Centre for Cell Science, Pune, India; 2CSIRO Marine and Atmospheric Research, Hobart, TAS, Australia; 3Department of Ecological Microbiology, University of Bayreuth, Bayreuth, Germany and 4School of Environmental Sciences, University of East Anglia, Norwich, UK Soda lakes are saline and alkaline ecosystems that are believed to have existed throughout the geological record of Earth. They are widely distributed across the globe, but are highly abundant in terrestrial biomes such as deserts and steppes and in geologically interesting regions such as the East African Rift valley. The unusual geochemistry of these lakes supports the growth of an impressive array of microorganisms that are of ecological and economic importance. Haloalk- aliphilic Bacteria and Archaea belonging to all major trophic groups have been described from many soda lakes, including lakes with exceptionally high levels of heavy metals. Lonar Lake is a soda lake that is centered at an unusual meteorite impact structure in the Deccan basalts in India and its key physicochemical and microbiological characteristics are highlighted in this article. The occurrence of diverse functional groups of microbes, such as methanogens, methanotrophs, phototrophs, denitrifiers, sulfur oxidizers, sulfate reducers and syntrophs in soda lakes, suggests that these habitats harbor complex microbial food webs that (a) interconnect various biological cycles via redox coupling and (b) impact on the production and consumption of greenhouse gases. -
Systematic Bacteriology Second Edition
BERGEY'S MANUAL® OF Systematic Bacteriology Second Edition Volume One The Archaea and the Deeply Branching and Phototrophic Bacteria Springer New York Berlin Heidelberg Barcelona HongKong London Milan Paris Singapore Tokyo BERGEY'S MANUAL® OF Systematic Bacteriology Second Edition Volume One The Archaea and the Deeply Branching and Phototrophic Bacteria David R. Boone Richard W. Castenholz EDITORS, VOLUME ONE George M. Garrity EDITOR-IN-CHIEF EDITORIAL BOARD James T. Staley, Chairman, David R. Boone, Vice Chairman, Don J. Brenner, Richard W. Castenholz, George M. Garrity, Michael Goodfellow, Noel R. Krieg, Fred A. Rainey, Karl-Heinz Schleifer WITH CONTRIBUTIONS FROM 105 COLLEAGUES Springer George M. Garrity Department of Microbiology and Molecular Genetics Bergey's Manual Trust Michigan State University East Lansing, MI 48824-1101 USA Library of Congress Cataloging-in-Publication Data Bergey's manual of systematic bacteriology / David R. Boone, Richard W. Castenholz, editors, volume 1 ; George M. Garrity, editor-in-chief.-2nd ed. p.cm. Includes bibliographical references and index. Contents: v.I. The archaea and the deeply branching and phototrophic bacteria. ISBN 0-387-98771-1 (alk. paper) 1. Bacteria-Classification. I. Title: Systematic bacteriology. II. Boone, David R. III. Castenholz, Richard W. IV. Garrity, George M. QR81.B462001 579.3'01 '2-dc21 2001020400 With 330 illustrations The following proprietary names of products are used in this volume: Casamino@ acids; Vector NTI®; XLI0-Gold®; Gelrite®; Tryptone@l; Phytagel@; bio-Trypcasew; Trypticasev; Oxoid® purified agar. Printed on acid-free paper. First edition published 1984-1989 by Bergey's Manual Trust and Williams & Wilkins, Baltimore. © 2001 Bergey's Manual Trust All rights reserved. -
Contents Topic 1. Introduction to Microbiology. the Subject and Tasks
Contents Topic 1. Introduction to microbiology. The subject and tasks of microbiology. A short historical essay………………………………………………………………5 Topic 2. Systematics and nomenclature of microorganisms……………………. 10 Topic 3. General characteristics of prokaryotic cells. Gram’s method ………...45 Topic 4. Principles of health protection and safety rules in the microbiological laboratory. Design, equipment, and working regimen of a microbiological laboratory………………………………………………………………………….162 Topic 5. Physiology of bacteria, fungi, viruses, mycoplasmas, rickettsia……...185 TOPIC 1. INTRODUCTION TO MICROBIOLOGY. THE SUBJECT AND TASKS OF MICROBIOLOGY. A SHORT HISTORICAL ESSAY. Contents 1. Subject, tasks and achievements of modern microbiology. 2. The role of microorganisms in human life. 3. Differentiation of microbiology in the industry. 4. Communication of microbiology with other sciences. 5. Periods in the development of microbiology. 6. The contribution of domestic scientists in the development of microbiology. 7. The value of microbiology in the system of training veterinarians. 8. Methods of studying microorganisms. Microbiology is a science, which study most shallow living creatures - microorganisms. Before inventing of microscope humanity was in dark about their existence. But during the centuries people could make use of processes vital activity of microbes for its needs. They could prepare a koumiss, alcohol, wine, vinegar, bread, and other products. During many centuries the nature of fermentations remained incomprehensible. Microbiology learns morphology, physiology, genetics and microorganisms systematization, their ecology and the other life forms. Specific Classes of Microorganisms Algae Protozoa Fungi (yeasts and molds) Bacteria Rickettsiae Viruses Prions The Microorganisms are extraordinarily widely spread in nature. They literally ubiquitous forward us from birth to our death. Daily, hourly we eat up thousands and thousands of microbes together with air, water, food. -
1 This Manuscript Is Submitted for Publication in Renewable and Sustainable Energy
1 This manuscript is submitted for publication in Renewable and Sustainable Energy 2 Reviews. Please note that, this manuscript has not undergone peer-review and is not yet 3 formally accepted for publication. Subsequent versions of this manuscript may have 4 slightly different content. If accepted, the final version of this manuscript will be 5 available via the ‘Peer-reviewed Publication DOI’ link on the right-hand side of this 6 webpage. 7 Manuscript Title: Estimating Microbial Hydrogen Consumption in Hydrogen Storage in 8 Porous Media as a Basis for Site Selection 9 Authors 10 Eike Marie Thaysena: [email protected] 11 Sean McMahona, b: [email protected] 12 Gion Strobelc: [email protected] 13 Ian Butlera: [email protected] 14 Bryne Ngwenyaa: [email protected] 15 Niklas Heinemanna: [email protected] 16 Mark Wilkinsona: [email protected] 17 Aliakbar Hassanpouryouzbanda: [email protected] 18 Chris McDermotta: [email protected] 19 Katriona Edlmanna: [email protected] 20 21 Affiliations: 22 a) School of Geosciences, University of Edinburgh, Grant Institute, West Main Road, 23 Edinburgh, EH9 3JW, UK 24 b) School of Physics and Astronomy, James Clerk Maxwell Building, University of 25 Edinburgh, EH9 3FD, United Kingdom 26 c) Department of Petroleum Engineering, Clausthal University of Technology, Germany 27 28 1 29 Estimating Microbial Hydrogen Consumption in 30 Hydrogen Storage in Porous Media as a Basis for 31 Site Selection 32 Eike M. Thaysen1*, Sean McMahon1,3, Gion Strobel2,