The Microbial Taxonomist a Newsletter Published by Bergey’S Manual Trust
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Microbial Processes in Oil Fields: Culprits, Problems, and Opportunities
Provided for non-commercial research and educational use only. Not for reproduction, distribution or commercial use. This chapter was originally published in the book Advances in Applied Microbiology, Vol 66, published by Elsevier, and the attached copy is provided by Elsevier for the author's benefit and for the benefit of the author's institution, for non-commercial research and educational use including without limitation use in instruction at your institution, sending it to specific colleagues who know you, and providing a copy to your institution’s administrator. All other uses, reproduction and distribution, including without limitation commercial reprints, selling or licensing copies or access, or posting on open internet sites, your personal or institution’s website or repository, are prohibited. For exceptions, permission may be sought for such use through Elsevier's permissions site at: http://www.elsevier.com/locate/permissionusematerial From: Noha Youssef, Mostafa S. Elshahed, and Michael J. McInerney, Microbial Processes in Oil Fields: Culprits, Problems, and Opportunities. In Allen I. Laskin, Sima Sariaslani, and Geoffrey M. Gadd, editors: Advances in Applied Microbiology, Vol 66, Burlington: Academic Press, 2009, pp. 141-251. ISBN: 978-0-12-374788-4 © Copyright 2009 Elsevier Inc. Academic Press. Author's personal copy CHAPTER 6 Microbial Processes in Oil Fields: Culprits, Problems, and Opportunities Noha Youssef, Mostafa S. Elshahed, and Michael J. McInerney1 Contents I. Introduction 142 II. Factors Governing Oil Recovery 144 III. Microbial Ecology of Oil Reservoirs 147 A. Origins of microorganisms recovered from oil reservoirs 147 B. Microorganisms isolated from oil reservoirs 148 C. Culture-independent analysis of microbial communities in oil reservoirs 155 IV. -
Thermophiles and Thermozymes
Thermophiles and Thermozymes Edited by María-Isabel González-Siso Printed Edition of the Special Issue Published in Microorganisms www.mdpi.com/journal/microorganisms Thermophiles and Thermozymes Thermophiles and Thermozymes Special Issue Editor Mar´ıa-Isabel Gonz´alez-Siso MDPI • Basel • Beijing • Wuhan • Barcelona • Belgrade Special Issue Editor Mar´ıa-Isabel Gonzalez-Siso´ Universidade da Coruna˜ Spain Editorial Office MDPI St. Alban-Anlage 66 4052 Basel, Switzerland This is a reprint of articles from the Special Issue published online in the open access journal Microorganisms (ISSN 2076-2607) from 2018 to 2019 (available at: https://www.mdpi.com/journal/ microorganisms/special issues/thermophiles) For citation purposes, cite each article independently as indicated on the article page online and as indicated below: LastName, A.A.; LastName, B.B.; LastName, C.C. Article Title. Journal Name Year, Article Number, Page Range. ISBN 978-3-03897-816-9 (Pbk) ISBN 978-3-03897-817-6 (PDF) c 2019 by the authors. Articles in this book are Open Access and distributed under the Creative Commons Attribution (CC BY) license, which allows users to download, copy and build upon published articles, as long as the author and publisher are properly credited, which ensures maximum dissemination and a wider impact of our publications. The book as a whole is distributed by MDPI under the terms and conditions of the Creative Commons license CC BY-NC-ND. Contents About the Special Issue Editor ...................................... vii Mar´ıa-Isabel Gonz´alez-Siso Editorial for the Special Issue: Thermophiles and Thermozymes Reprinted from: Microorganisms 2019, 7, 62, doi:10.3390/microorganisms7030062 ........ -
Enrichment and Diversity Analysis of the Thermophilic Microbes in a High Temperature Petroleum Reservoir
African Journal of Microbiology Research Vol. 5(14), pp. 1850-1857, 18 July, 2011 Available online http://www.academicjournals.org/ajmr DOI: 10.5897/AJMR11.354 ISSN 1996-0808 ©2011 Academic Journals Full Length Research Paper Enrichment and diversity analysis of the thermophilic microbes in a high temperature petroleum reservoir Guihong Lan1,2, Zengting Li1, Hui zhang3, Changjun Zou2, Dairong Qiao1 and Yi Cao1* 1School of Life Science, Sichuan University, Chengdu 610065, China. 2School of Chemistry and Chemical Engineering, Southwest Petroleum University, Chengdu 610500, China. 3Biogas Institute of Ministry of Agriculture P. R. China, Chengdu 610041, China. Accepted 1 June, 2011 Thermophilic microbial diversity in production water from a high temperature, water-flooded petroleum reservoir of an offshore oilfield in China was characterized by enrichment and polymerase chain reaction-denaturing gradient gel electrophoresis (PCR-DGGE) analysis. Six different function enrichment cultures were cultivated one year, at 75°C DGGE and sequence analyses of 16S rRNA gene fragments were used to assess the thermophilic microbial diversity. A total of 27 bacterial and 9 archaeal DGGE bands were excised and sequenced. Phylogenetic analysis of these sequences indicated that 21 bacterial and 7 archaeal phylotypes were affiliated with thermophilic microbe. The bacterial sequences were mainly bonged to the genera Fervidobacterium, Thermotoga, Dictyoglomus, Symbiobacterium, Moorella, Thermoanaerobacter, Desulfotomaculum, Thermosyntropha, Coprothermobacter, Caloramator, Thermacetogenium, and the archaeal phylogypes were represented in the genera Geoglobus and Thermococcus, Methanomethylovorans, Methanothermobacter Methanoculleus and Methanosaeta. So many thermophiles were detected suggesting that they might be common habitants in high-temperature petroleum reservoirs. The results of this work provide further insight into the thermophilic composition of microbial communities in high temperature petroleum reservoirs. -
Elucidating Syntrophic Butyrate-Degrading Populations in Anaerobic Digesters
bioRxiv preprint doi: https://doi.org/10.1101/563387; this version posted February 28, 2019. 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. 1 Elucidating syntrophic butyrate-degrading populations in anaerobic digesters 2 using stable isotope-informed genome-resolved metagenomics 3 4 Ryan M. Ziels1,2,#, Masaru K. Nobu3, Diana Z. Sousa4 5 6 7 1 Department of Civil Engineering, University of British Columbia, Vancouver, Canada 8 2 Department of Civil and Environmental Engineering, University Washington, Seattle, USA 9 3 Bioproduction Research Institute, National Institute of Advanced Industrial Science and 10 Technology, Tsukuba, Japan 11 4 Laboratory of Microbiology, Wageningen University & Research, Wageningen, Netherlands 12 13 #Corresponding Author: 14 Email: [email protected] 15 16 Running Title: DNA-SIP Metagenomics of Anaerobic Butyrate-Degraders 17 1 bioRxiv preprint doi: https://doi.org/10.1101/563387; this version posted February 28, 2019. 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. 18 Abstract: 19 Linking the genomic content of uncultivated microbes to their metabolic functions remains a 20 critical challenge in microbial ecology. Resolving this challenge has implications for improving 21 our management of key microbial interactions in biotechnologies such as anaerobic digestion, 22 which relies on slow-growing syntrophic and methanogenic communities to produce renewable 23 methane from organic waste. -
Community Analysis of Plant Biomass-Degrading Microorganisms from Obsidian Pool, Yellowstone National Park
Microb Ecol DOI 10.1007/s00248-014-0500-8 ENVIRONMENTAL MICROBIOLOGY Community Analysis of Plant Biomass-Degrading Microorganisms from Obsidian Pool, Yellowstone National Park Tatiana A. Vishnivetskaya & Scott D. Hamilton-Brehm & Mircea Podar & Jennifer J. Mosher & Anthony V. Palumbo & Tommy J. Phelps & Martin Keller & James G. Elkins Received: 12 May 2014 /Accepted: 16 September 2014 # Springer Science+Business Media New York (outside the USA) 2014 Abstract The conversion of lignocellulosic biomass into (OBP), was examined for potential biomass-active microorgan- biofuels can potentially be improved by employing robust mi- isms using cultivation-independent and enrichment techniques. croorganisms and enzymes that efficiently deconstruct plant Analysis of 33,684 archaeal and 43,784 bacterial quality-filtered polysaccharides at elevated temperatures. Many of the geother- 16S rRNA gene pyrosequences revealed that archaeal diversity mal features of Yellowstone National Park (YNP) are surrounded in the main pool was higher than bacterial; however, in the by vegetation providing a source of allochthonic material to vegetated area, overall bacterial diversity was significantly support heterotrophic microbial communities adapted to utilize higher. Of notable interest was a flooded depression adjacent to plant biomass as a primary carbon and energy source. In this OBP supporting a stand of Juncus tweedyi, a heat-tolerant rush study, a well-known hot spring environment, Obsidian Pool commonly found growing near geothermal features in YNP. The microbial community from heated sediments surrounding the The submitted manuscript has been authored by a contractor of the U.S. plants was enriched in members of the Firmicutes including Government under contract DE-AC05-00OR22725. Accordingly, the potentially (hemi)cellulolytic bacteria from the genera U.S. -
Ecophysiology of Sulfate-Reducing Bacteria and Syntrophic Communities in Marine Anoxic Sediments” Derya Özüölmez Wageningen, 12 September 2017
Propositions 1. Prolonged incubation is a key strategy toward the enrichment of marine syntrophs. (this thesis) 2. Hydrogen-consuming methanogens can effectively compete with hydrogen- consuming sulfate reducers even at high sulfate concentration. (this thesis) 3. The plastic-eating wax worm, Galleria mellonella, can help cleaning up existing plastic mass (Bombelli et al. 2017, Current Biology 27(8): 292-293), but the real solution to environmental pollution still relies on shifting from disposable plastics to reusable and biodegradable materials. 4. With the discovery of abundant molecular hydrogen in Enceladus’ salty ocean (Waite et al. (2017) Science 356:6334, 155-159) extraterrestrial life in our solar system has become highly probable, and should shift our life-hunting focus from distant stars to our nearby neighbors. 5. With the "Help me to do it myself" motto, the Montessori education leads children to grow into mature, creative and self-confident adults. 6. Nothing is impossible as long as the dream is held close to the heart and patience and persistence are applied for the accomplishment. Propositions belonging to the PhD thesis entitled: “Ecophysiology of sulfate-reducing bacteria and syntrophic communities in marine anoxic sediments” Derya Özüölmez Wageningen, 12 September 2017 Ecophysiology of sulfate-reducing bacteria and syntrophic communities in marine anoxic sediments Derya Özüölmez Thesis committee Promotor Prof. Dr Alfons J.M. Stams Personal chair at the Laboratory of Microbiology Wageningen University & Research Co-promotor Dr Caroline M. Plugge Associate professor, Laboratory of Microbiology Wageningen University & Research Other members Prof. Dr Tinka Murk, Wageningen University & Research Prof. Dr Gerard Muyzer, University of Amsterdam, The Netherlands Prof. -
Pelospora Glutarica Gen. Nov., Sp. Nov., a Glutarate-Fermenting, Strictly Anaerobic, Spore-Forming Bacterium
Pelospora glutarica gen. nov., sp. nov., a glutarate-fermenting, strictly anaerobic, spore-forming bacterium Carola Matthies,1 Nina Springer,2 Wolfgang Ludwig2 and Bernhard Schink3 Author for correspondence: Bernhard Schink. Tel: j49 7531 882140. Fax: j49 7531 882966. e-mail: bernhard.schink!uni-konstanz.de 1 Lehrstuhl fu$ rO$ kologische The strictly anaerobic, Gram-negative, spore-forming bacterium strain WoGl3T $ Mikrobiologie, BITOK, had been enriched and isolated in mineral medium with glutarate as the sole Universita$ t Bayreuth, 95440 Bayreuth, Germany source of energy and organic carbon. Glutarate was fermented to a mixture of butyrate, isobutyrate, CO and small amounts of acetate. Strain WoGl3T grew 2 Lehrstuhl fu$ r 2 Mikrobiologie, Technische only with the dicarboxylates glutarate, methylsuccinate and succinate. 16S Universita$ tMu$ nchen, rDNA sequence analysis revealed an affiliation of strain WoGl3T to the family Arcisstr. 16, 80290 Syntrophomonadaceae. This monophyletic group is comprised of strain WoGl3T Mu$ nchen, Germany and the genera Syntrophomonas, Syntrophospora and Thermosyntropha, 3 Lehrstuhl fu$ r Mikrobielle within the phylum of Gram-positive bacteria with a low DNA GMC content. O$ kologie, Fakulta$ tfu$ r Biologie, Universita$ t Overall intra-group 16S rRNA sequence similarities of 892–939% document a Konstanz, Fach M 654, separate phylogenetic status for strain WoGl3T. Strain WoGl3T (l DSM 6652T)is 78457 Konstanz, Germany described as the type strain of a new species within a new genus, Pelospora glutarica gen. nov., sp. nov. Keywords: Pelospora glutarica sp. nov., anaerobic degradation, dicarboxylic acids, glutarate INTRODUCTION and nitrate-reducing pseudomonads (Anders et al., 1995). In a study on the degradation of higher Fermentative degradation of short-chain dicarboxylic dicarboxylic acids, we isolated a strictly anaerobic acids such as oxalate, malonate and succinate has been bacterium, strain WoGl3T, that grew only with gluta- documented. -
Clostridium Manihotivorum Sp. Nov., a Novel Mesophilic Anaerobic Bacterium That Produces Cassava Pulp-Degrading Enzymes
Clostridium manihotivorum sp. nov., a novel mesophilic anaerobic bacterium that produces cassava pulp-degrading enzymes Pattsarun Cheawchanlertfa1, Sawannee Sutheeworapong2, Piroon Jenjaroenpun3,4, Thidathip Wongsurawat3,4, Intawat Nookaew4,5, Supapon Cheevadhanarak1,2, Akihiko Kosugi6, Patthra Pason1,2, Rattiya Waeonukul1,2, Khanok Ratanakhanokchai1 and Chakrit Tachaapaikoon1,2 1 School of Bioresources and Technology, King Mongkut's University of Technology Thonburi, Bangkok, Thailand 2 Pilot Plant Development and Training Institute, King Mongkut's University of Technology Thonburi, Bangkok, Thailand 3 Division of Bioinformatics and Data Management for Research, Department of Research and Development, Faculty of Medicine, Siriraj Hospital, Mahidol University, Bangkok, Thailand 4 Department of Biomedical Informatics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, USA 5 Department of Physiology and Biophysics, College of Medicine, University of Arkansas for Medical Sciences, Little Rock, AR, USA 6 Biological Resources and Post-harvest Division, Japan International Research Center for Agricultural Sciences, Ibaraki, Japan ABSTRACT Background. Cassava pulp is a promising starch-based biomasses, which consists of residual starch granules entrapped in plant cell wall containing non-starch polysaccha- rides, cellulose and hemicellulose. Strain CT4T, a novel mesophilic anaerobic bacterium isolated from soil collected from a cassava pulp landfill, has a strong ability to degrade polysaccharides in cassava pulp. -
Degradation of Biological Macromolecules Supports Uncultured Microbial Populations in Guaymas Basin Hydrothermal Sediments
The ISME Journal https://doi.org/10.1038/s41396-021-01026-5 ARTICLE Degradation of biological macromolecules supports uncultured microbial populations in Guaymas Basin hydrothermal sediments 1 2 1,5 3,6 Sherlynette Pérez Castro ● Mikayla A. Borton ● Kathleen Regan ● Isabella Hrabe de Angelis ● 2 4 3 1 Kelly C. Wrighton ● Andreas P. Teske ● Marc Strous ● S. Emil Ruff Received: 8 December 2020 / Revised: 26 May 2021 / Accepted: 27 May 2021 © The Author(s) 2021. This article is published with open access Abstract Hydrothermal sediments contain large numbers of uncultured heterotrophic microbial lineages. Here, we amended Guaymas Basin sediments with proteins, polysaccharides, nucleic acids or lipids under different redox conditions and cultivated heterotrophic thermophiles with the genomic potential for macromolecule degradation. We reconstructed 20 metagenome- assembled genomes (MAGs) of uncultured lineages affiliating with known archaeal and bacterial phyla, including endospore- forming Bacilli and candidate phylum Marinisomatota.OneMarinisomatota MAG had 35 different glycoside hydrolases often in multiple copies, seven extracellular CAZymes, six polysaccharide lyases, and multiple sugar transporters. This population has 1234567890();,: 1234567890();,: the potential to degrade a broad spectrum of polysaccharides including chitin, cellulose, pectin, alginate, chondroitin, and carrageenan. We also describe thermophiles affiliating with the genera Thermosyntropha, Thermovirga,andKosmotoga with the capability to make a living on nucleic acids, lipids, or multiple macromolecule classes, respectively. Several populations seemed to lack extracellular enzyme machinery and thus likely scavenged oligo- or monomers (e.g., MAGs affiliating with Archaeoglobus) or metabolic products like hydrogen (e.g., MAGs affiliating with Thermodesulfobacterium or Desulforudaceae). The growth of methanogens or the production of methane was not observed in any condition, indicating that the tested macromolecules are not degraded into substrates for methanogenesis in hydrothermal sediments. -
DNA-SIP Based Genome-Centric Metagenomics Identifies Key Long-Chain Fatty Acid-Degrading Populations in Anaerobic Digesters with Different Feeding Frequencies
OPEN The ISME Journal (2018) 12, 112–123 www.nature.com/ismej ORIGINAL ARTICLE DNA-SIP based genome-centric metagenomics identifies key long-chain fatty acid-degrading populations in anaerobic digesters with different feeding frequencies Ryan M Ziels1,2, Diana Z Sousa3, H David Stensel2 and David AC Beck4,5 1Department of Civil Engineering, University of British Columbia, Vancouver, British Columbia, Canada; 2Department of Civil and Environmental Engineering, University of Washington, Seattle, WA, USA; 3Laboratory of Microbiology, Wageningen University, Wageningen, The Netherlands; 4eScience Institute, University of Washington, Seattle, WA, USA and 5Department of Chemical Engineering, University of Washington, Seattle, WA, USA Fats, oils and greases (FOG) are energy-dense wastes that can be added to anaerobic digesters to substantially increase biomethane recovery via their conversion through long-chain fatty acids (LCFAs). However, a better understanding of the ecophysiology of syntrophic LCFA-degrading microbial communities in anaerobic digesters is needed to develop operating strategies that mitigate inhibitory LCFA accumulation from FOG. In this research, DNA stable isotope probing (SIP) was coupled with metagenomic sequencing for a genome-centric comparison of oleate (C18:1)-degrading populations in two anaerobic codigesters operated with either a pulse feeding or continuous-feeding strategy. The pulse-fed codigester microcosms converted oleate into methane at over 20% higher rates than the continuous-fed codigester microcosms. Differential coverage binning was demon- strated for the first time to recover population genome bins (GBs) from DNA-SIP metagenomes. About 70% of the 13C-enriched GBs were taxonomically assigned to the Syntrophomonas genus, thus substantiating the importance of Syntrophomonas species to LCFA degradation in anaerobic digesters. -
Title Domain-Centric Dissection and Classification of Prokaryotic Poly(3
bioRxiv preprint doi: https://doi.org/10.1101/693432; this version posted July 5, 2019. 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. 1 Title 2 3 Domain-centric dissection and classification of prokaryotic poly(3-hydroxyalkanoate) 4 synthases 5 6 Running Title 7 8 Domain organizations and interactions in prokaryotic PHA synthases 9 10 Authorship 11 12 Zhanzhong Liu1#, Zuobin Zhu2#, Jianye Yang3, Sheng Wu3, Qinghua Liu4,5, Mengmeng 13 Wang4,5, Huiling Cheng3, Jiawei Yan1, Liang Wang3,4* 14 15 Affiliation 16 17 1Xuzhou Infectious Diseases Hospital, Xuzhou Jiangsu, 221000, China 18 2Department of Genetics, School of Biological Sciences and Technology, Xuzhou Medical 19 University, Xuzhou Jiangsu, 221000, China 20 3Department of Bioinformatics, School of Medical Informatics, Xuzhou Medical University, 21 Xuzhou Jiangsu, 221000, China 22 4Jiangsu Key Laboratory of New Drug Research and Clinical Pharmacy, School of Pharmacy, 23 Xuzhou Medical University, Xuzhou Jiangsu, 221000, China 24 5Department of Pharmaceutical Analysis, School of Pharmacy, Xuzhou Medical University, 25 Xuzhou Jiangsu, 221000, China 26 27 #These authors contribute equally to the study. 28 29 *Correspondence author: for all correspondence, please refer to Dr. Liang Wang 30 [email protected] 31 32 33 34 bioRxiv preprint doi: https://doi.org/10.1101/693432; this version posted July 5, 2019. 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. -
This Is a Pre-Copyedited, Author-Produced Version of an Article Accepted for Publication, Following Peer Review
This is a pre-copyedited, author-produced version of an article accepted for publication, following peer review. Spang, A.; Stairs, C.W.; Dombrowski, N.; Eme, E.; Lombard, J.; Caceres, E.F.; Greening, C.; Baker, B.J. & Ettema, T.J.G. (2019). Proposal of the reverse flow model for the origin of the eukaryotic cell based on comparative analyses of Asgard archaeal metabolism. Nature Microbiology, 4, 1138–1148 Published version: https://dx.doi.org/10.1038/s41564-019-0406-9 Link NIOZ Repository: http://www.vliz.be/nl/imis?module=ref&refid=310089 [Article begins on next page] The NIOZ Repository gives free access to the digital collection of the work of the Royal Netherlands Institute for Sea Research. This archive is managed according to the principles of the Open Access Movement, and the Open Archive Initiative. Each publication should be cited to its original source - please use the reference as presented. When using parts of, or whole publications in your own work, permission from the author(s) or copyright holder(s) is always needed. 1 Article to Nature Microbiology 2 3 Proposal of the reverse flow model for the origin of the eukaryotic cell based on 4 comparative analysis of Asgard archaeal metabolism 5 6 Anja Spang1,2,*, Courtney W. Stairs1, Nina Dombrowski2,3, Laura Eme1, Jonathan Lombard1, Eva Fernández 7 Cáceres1, Chris Greening4, Brett J. Baker3 and Thijs J.G. Ettema1,5* 8 9 1 Department of Cell- and Molecular Biology, Science for Life Laboratory, Uppsala University, SE-75123, 10 Uppsala, Sweden 11 2 NIOZ, Royal Netherlands Institute for Sea Research, Department of Marine Microbiology and 12 Biogeochemistry, and Utrecht University, P.O.