Unraveling the Stratification of an Iron-Oxidizing Microbial Mat by Metatranscriptomics
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Response of Heterotrophic Stream Biofilm Communities to a Gradient of Resources
The following supplement accompanies the article Response of heterotrophic stream biofilm communities to a gradient of resources D. J. Van Horn1,*, R. L. Sinsabaugh1, C. D. Takacs-Vesbach1, K. R. Mitchell1,2, C. N. Dahm1 1Department of Biology, University of New Mexico, Albuquerque, New Mexico 87131, USA 2Present address: Department of Microbiology & Immunology, University of British Columbia Life Sciences Centre, Vancouver BC V6T 1Z3, Canada *Email: [email protected] Aquatic Microbial Ecology 64:149–161 (2011) Table S1. Representative sequences for each OTU, associated GenBank accession numbers, and taxonomic classifications with bootstrap values (in parentheses), generated in mothur using 14956 reference sequences from the SILVA data base Treatment Accession Sequence name SILVA taxonomy classification number Control JF695047 BF8FCONT18Fa04.b1 Bacteria(100);Proteobacteria(100);Gammaproteobacteria(100);Pseudomonadales(100);Pseudomonadaceae(100);Cellvibrio(100);unclassified; Control JF695049 BF8FCONT18Fa12.b1 Bacteria(100);Proteobacteria(100);Alphaproteobacteria(100);Rhizobiales(100);Methylocystaceae(100);uncultured(100);unclassified; Control JF695054 BF8FCONT18Fc01.b1 Bacteria(100);Planctomycetes(100);Planctomycetacia(100);Planctomycetales(100);Planctomycetaceae(100);Isosphaera(50);unclassified; Control JF695056 BF8FCONT18Fc04.b1 Bacteria(100);Proteobacteria(100);Gammaproteobacteria(100);Xanthomonadales(100);Xanthomonadaceae(100);uncultured(64);unclassified; Control JF695057 BF8FCONT18Fc06.b1 Bacteria(100);Proteobacteria(100);Betaproteobacteria(100);Burkholderiales(100);Comamonadaceae(100);Ideonella(54);unclassified; -
Sites in the Virginia-Washington, D.C.-Maryland Metro Area to Observe Or Collect Bacteria That Precipitate Iron and Manganese Oxides1
SITES IN THE VIRGINIA-WASHINGTON, D.C.-MARYLAND METRO AREA TO OBSERVE OR COLLECT BACTERIA THAT PRECIPITATE IRON AND MANGANESE OXIDES1 by Eleanora I. Robbins U.S. Geological Survey Open-File Report 98-202 April 24, 1998 1 This report is preliminary and has not been reviewed for conformity with U.S. Geological Survey editorial standards. This publication is intended to be used along with U.S. Geological Survey EarthFax (1-800- USA-MAPS) What's the Red in the Water? What's the Black on the Rocks? What's the Oil on the Surface? and < http: //pubs.usgs. gov/publications/text/Norriemicrobes. html > SITES IN THE VIRGINIA-WASHINGTON, D.C.-MARYLAND METRO AREA TO OBSERVE OR COLLECT BACTERIA THAT PRECIPITATE IRON AND MANGANESE OXIDES VIRGINIA VA Site 1A. Fairfax County, Huntley Meadows Park: From the Beltway (495), go south on US 1. Turn right onto Lockheed Blvd.; travel to end of Lockheed Blvd., and then turn CAREFULLY into the Park at the sign. Park in parking lot, walk along the wetland path to the beginning of the boardwalk. Look to the right (north) and see red patches in the water where ground water is discharging. This ground water is anoxic and carries reduced iron. The iron bacteria here (predominantly Leptothrix ochracea^ oxidize the iron and turn it into a red flocculate. If you move the flocculate aside, you can see the underlying black color formed where the reducing bacteria reduce the iron to its black state in the zone of reduction in the mud. As you walk along the boardwalk, you will see much evidence of the iron bacterium, Leptothrix discophora] that forms glassy-looking patches that appear, at first glance, to be an nil-film VA Site IB. -
Microbial Communities Responses in Fluvial Biofilms Under Metal Stressed Scenarios
MICROBIAL COMMUNITIES RESPONSES IN FLUVIAL BIOFILMS UNDER METAL STRESSED SCENARIOS María Argudo Fernández Per citar o enllaçar aquest document: Para citar o enlazar este documento: Use this url to cite or link to this publication: http://hdl.handle.net/10803/671673 http://creativecommons.org/licenses/by-nc-sa/4.0/deed.ca Aquesta obra està subjecta a una llicència Creative Commons Reconeixement- NoComercial-CompartirIgual Esta obra está bajo una licencia Creative Commons Reconocimiento-NoComercial- CompartirIgual This work is licensed under a Creative Commons Attribution-NonCommercial- ShareAlike licence DOCTORAL THESIS Microbial communities responses in fluvial biofilms under metal stressed scenarios María Argudo Fernández 2020 Doctoral Programme in Water Science and Technology Supervised by: Frederic Gich Batlle Helena Guasch Padró Tutor: Anna M. Romaní Cornet Doctor candidate: María Argudo Fernández Thesis submitted in fulfilment of the requirements for the doctoral degree at the University of Girona Dr. Frederic Gich Batlle of the Biology Department of the University of Girona and Dra Helena Guasch Padró of Continental Ecology Department of CEAB-CSIC, DECLARE: That the thesis entitled “Microbial communities responses in fluvial biofilms under metal stressed scenarios” presented by MARÍA ARGUDO FERNÁNDEZ to obtain a doctoral degree, has been conducted under our supervision. For all intents and purposes, we hereby sign this document. Dr Frederic Gich Batlle Dra Helena Guasch Padró Girona, December 2020 A mi padre “The essence of the ocean cannot be seen in a drop of seawater” Kurt Tucholsky, 1925 ACKNOWLEDGEMENTS Sinceramente no sé cómo empezar porque creí que nunca llegaría el momento de rellenar este folio, los que me conocen lo saben (nunca se acaba recordadlo, sigo repasando)….Entonces empezaré por el principio. -
Characterization of Bacterial Community Structure in a Drinking
APPLIED AND ENVIRONMENTAL MICROBIOLOGY, Nov. 2010, p. 7171–7180 Vol. 76, No. 21 0099-2240/10/$12.00 doi:10.1128/AEM.00832-10 Copyright © 2010, American Society for Microbiology. All Rights Reserved. Characterization of Bacterial Community Structure in a Drinking ᰔ Water Distribution System during an Occurrence of Red Water Downloaded from Dong Li,1 Zheng Li,1 Jianwei Yu,1 Nan Cao,2 Ruyin Liu,1 and Min Yang1* State Key Laboratory of Environmental Aquatic Chemistry, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China,1 and Water Quality Monitoring Center, Beijing Waterworks Group, Beijing 100085, China2 Received 6 April 2010/Accepted 1 September 2010 The role of bacteria in the occasional emergence of red water, which has been documented worldwide, has http://aem.asm.org/ yet to be determined. To better understand the mechanisms that drive occurrences of red water, the bacterial community composition and the relative abundance of several functional bacterial groups in a water distri- bution system of Beijing during a large-scale red water event were determined using several molecular methods. Individual clone libraries of the 16S rRNA gene were constructed for three red water samples and one sample of normal water. Beta-, Alpha-, and Gammaproteobacteria comprised the major bacterial communities in both red water and normal water samples, in agreement with previous reports. A high percentage of red water clones (25.2 to 57.1%) were affiliated with or closely related to a diverse array of iron-oxidizing bacteria, including the neutrophilic microaerobic genera Gallionella and Sideroxydans, the acidophilic species Acidothio- bacillus ferrooxidans, and the anaerobic denitrifying Thermomonas bacteria. -
The Interplay of Microbially Mediated and Abiotic Reactions in the Biogeochemical Fe Cycle
REVIEWS The interplay of microbially mediated and abiotic reactions in the biogeochemical Fe cycle Emily D. Melton, Elizabeth D. Swanner, Sebastian Behrens, Caroline Schmidt and Andreas Kappler Abstract | Many iron (Fe) redox processes that were previously assumed to be purely abiotic, such as photochemical Fe reactions, are now known to also be microbially mediated. Owing to this overlap, discerning whether biotic or abiotic processes control Fe redox chemistry is a major challenge for geomicrobiologists and biogeochemists alike. Therefore, to understand the network of reactions within the biogeochemical Fe cycle, it is necessary to determine which abiotic or microbially mediated reactions are dominant under various environmental conditions. In this Review, we discuss the major microbially mediated and abiotic reactions in the biogeochemical Fe cycle and provide an integrated overview of biotic and chemically mediated redox transformations. Fe speciation The environmental abundance of iron (Fe) and its pos‑ and temporal distribution of Fe redox species in some Refers to the redox state of session of electrons in d orbitals with π‑character, which environments, such as heterogeneous sediments, plant iron (Fe) and the identity of its can form complexes with carbon (C), oxygen (O), nitro‑ rhizospheres and microbial mats6, and abiotic Fe trans‑ ligands. The two most common gen (N) and sulphur (S) species, make it an essential ele‑ formations with biologically produced intermediates environmental Fe redox ment for nearly all living organisms. Fe occurs in two must be taken into account7,8. species are Fe(II) and Fe(III). main redox states in the environment: oxidized ferric Fe Despite our growing knowledge of the wide‑ (Fe(iii)), which is poorly soluble at circumneutral pH; spread environmental occurrence and the importance and reduced ferrous Fe (Fe(ii)), which is easily soluble of microbial Fe redox cycling for the degradation and and therefore more bioavailable. -
Understanding the Molecular Mechanism of Manganese
UNDERSTANDING THE MOLECULAR MECHANISM OF MANGANESE OXIDATION IN LEPTOTHRIX DISCOPHORA SS-1 A Dissertation Presented to the Faculty of the Graduate School of Cornell University In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy by Daniela Bocioaga August, 2013 © Daniela Bocioaga Understanding the molecular mechanism of Mn oxidation in Leptothrix discophora SS-1 Daniela Bocioaga, Ph.D. Cornell University 2013 The purpose of this research is to understand the molecular mechanism of manganese oxidation in Leptothrix discophora SS1 which until now has been hampered by the lack of a genetic system. Leptothrix discophora SS1 is an important model organism that has been used to study the mechanism and consequences of biological manganese oxidation. In this study we report on the development of a genetic system for L. discophora. First, the antibiotic sensitivity of L. discophora was characterized and a procedure for transformation with exogenous DNA via conjugation was developed and optimized, resulting in a maximum transfer frequency of 5.2*10-1 (transconjugant/donor). Genetic manipulation of Leptothrix was demonstrated by disrupting pyrF via chromosomal integration of a plasmid with an R6Kɣ ori through homologous recombination. This resulted in resistance to fluoroorotidine which was abolished by complementation with an ectopically expressed copy of pyrF cloned into pBBR1MCS-5. This genetic system was further used to disrupt five genes in Leptothrix discophora SS1, which were considered to be the best candidates for the enzyme encoding the manganese oxidizing activity in this bacterium. All of the disrupted mutants continued to oxidize manganese, suggesting that these genes may not play a role in manganese oxidation, as hypothesized. -
Discovery of Sheath-Forming, Iron-Oxidizing Zetaproteobacteria at Loihi Seamount, Hawaii, USA Emily J
RESEARCH ARTICLE Hidden in plain sight: discovery of sheath-forming, iron-oxidizing Zetaproteobacteria at Loihi Seamount, Hawaii, USA Emily J. Fleming1, Richard E. Davis2, Sean M. McAllister3,, Clara S. Chan4, Craig L. Moyer3, Bradley M. Tebo2 & David Emerson1 1Bigelow Laboratory for Ocean Sciences, East Boothbay, ME, USA; 2Department of Environmental and Biomolecular Systems, Oregon Health and Science University, Portland, OR, USA; 3Department of Biology, Western Washington University, Bellingham, WA, USA and 4Department of Geological Sciences, University of Delaware, Newark, DE, USA Correspondence: David Emerson, Bigelow Abstract Laboratory for Ocean Sciences, PO Box 380, East Boothbay, ME 04544, USA. Tel.: +1 207 Lithotrophic iron-oxidizing bacteria (FeOB) form microbial mats at focused 315 2567; fax: +1 207 315 2329; flow or diffuse flow vents in deep-sea hydrothermal systems where Fe(II) is a e-mail: [email protected] dominant electron donor. These mats composed of biogenically formed Fe(III)-oxyhydroxides include twisted stalks and tubular sheaths, with sheaths Present address: Sean M. McAllister, typically composing a minor component of bulk mats. The micron diameter Department of Geological Sciences, Fe(III)-oxyhydroxide-containing tubular sheaths bear a strong resemblance to University of Delaware, Newark, DE, USA sheaths formed by the freshwater FeOB, Leptothrix ochracea. We discovered that Received 20 December 2012; revised 28 veil-like surface layers present in iron-mats at the Loihi Seamount were domi- – February 2013; accepted 28 February 2013. nated by sheaths (40 60% of total morphotypes present) compared with deeper Final version published online 15 April 2013. (> 1 cm) mat samples (0–16% sheath). By light microscopy, these sheaths appeared nearly identical to those of L. -
Comparative Genomic Insights Into Ecophysiology of Neutrophilic, Microaerophilic Iron Oxidizing Bacteria
Lawrence Berkeley National Laboratory Recent Work Title Comparative Genomic Insights into Ecophysiology of Neutrophilic, Microaerophilic Iron Oxidizing Bacteria. Permalink https://escholarship.org/uc/item/89m829jp Journal Frontiers in microbiology, 6(NOV) ISSN 1664-302X Authors Kato, Shingo Ohkuma, Moriya Powell, Deborah H et al. Publication Date 2015 DOI 10.3389/fmicb.2015.01265 Peer reviewed eScholarship.org Powered by the California Digital Library University of California ORIGINAL RESEARCH published: 13 November 2015 doi: 10.3389/fmicb.2015.01265 Comparative Genomic Insights into Ecophysiology of Neutrophilic, Microaerophilic Iron Oxidizing Bacteria Shingo Kato1,2* †, Moriya Ohkuma2, Deborah H. Powell3, Sean T. Krepski1, Kenshiro Oshima4, Masahira Hattori4,NicoleShapiro5,TanjaWoyke5 and Clara S. Chan1* 1 Department of Geological Sciences, University of Delaware, Newark, DE, USA, 2 Japan Collection of Microorganisms, Edited by: RIKEN BioResource Center, Tsukuba, Japan, 3 Delaware Biotechnology Institute, University of Delaware, Newark, DE, USA, Beth Orcutt, 4 Center for Omics and Bioinformatics, Graduate School of Frontier Sciences, University of Tokyo, Kashiwa, Japan, Bigelow Laboratory for Ocean 5 Department of Energy Joint Genome Institute, Walnut Creek, CA, USA Sciences, USA Reviewed by: Neutrophilic microaerophilic iron-oxidizing bacteria (FeOB) are thought to play a James Hemp, California Institute of Technology, USA significant role in cycling of carbon, iron and associated elements in both freshwater Roman Barco, and marine iron-rich environments. However, the roles of the neutrophilic microaerophilic University of Southern California, USA FeOB are still poorly understood due largely to the difficulty of cultivation and lack of *Correspondence: functional gene markers. Here, we analyze the genomes of two freshwater neutrophilic Shingo Kato [email protected]; microaerophilic stalk-forming FeOB, Ferriphaselus amnicola OYT1 and Ferriphaselus Clara S. -
Olivier Bochet Préparée À L’Unité De Recherche UMR6118 GR Géosciences Rennes UFR Sciences Et Propriété De La Matière
ANNÉE 2017 THÈSE / UNIVERSITÉ DE RENNES 1 sous le sceau de l’Université Bretagne Loire pour le grade de DOCTEUR DE L’UNIVERSITÉ DE RENNES 1 Mention : Sciences de la Terre Ecole doctorale EGAAL Olivier Bochet Préparée à l’unité de recherche UMR6118 GR Géosciences Rennes UFR Sciences et Propriété de la Matière Thèse soutenue à Rennes Caractérisation des hot le 8 décembre 2017 spots de réactivité devant le jury composé de : Hélène PAUWELS biogéochimique dans Directrice de la Recherche au BRGM (Orléans) / rapporteur les eaux souterraines Richard MARTEL Professeur à l'INRS (Québec, Canada) / rapporteur Florence ARSENE-PLOETZE Maître de conférences à l'université de Strasbourg / examinateur Khalil Hanna Professeur à ENSC Rennes / examinateur Tom Battin Professeur à l'EPFL (Lausanne, Suisse) / examinateur Massimo Rolle Professeur associé, DTU Environment (Kongens Lyngby, Danemark) / examinateur Tanguy LE BORGNE Physicien, Université de Rennes 1 / directeur de thèse Luc AQUILINA Professeur, Université de Rennes 1 / directeur de thèse Table des matières Introduction Générale..................................................................................................................4 Hot spots et hot moments Observations sur le terrain Etude expérimentale de la réactivité biogéochimique Principes des essais de traçage réactifs Les traçages réactifs en mode « push-pull » "Smart-tracer", des traceurs innovants en hydrologie et hydrogéologie Questions abordées dans la thèse Chapitre 1: Analyse et modélisation d’un hot spot d'activité microbienne -
Diversity of Aerobic Anoxygenic Phototrophs and Rhodopsin-Containing Bacteria in the Surface Microlayer, Water Column and Epilithic Biofilms of Lake Baikal
microorganisms Article Diversity of Aerobic Anoxygenic Phototrophs and Rhodopsin-Containing Bacteria in the Surface Microlayer, Water Column and Epilithic Biofilms of Lake Baikal Agnia Dmitrievna Galachyants 1,*, Andrey Yurjevich Krasnopeev 1 , Galina Vladimirovna Podlesnaya 1 , Sergey Anatoljevich Potapov 1 , Elena Viktorovna Sukhanova 1 , Irina Vasiljevna Tikhonova 1 , Ekaterina Andreevna Zimens 1, Marsel Rasimovich Kabilov 2 , Natalia Albertovna Zhuchenko 1, Anna Sergeevna Gorshkova 1, Maria Yurjevna Suslova 1 and Olga Ivanovna Belykh 1,* 1 Limnological Institute Siberian Branch of the Russian Academy of Sciences, Ulan-Batorskaya 3, 664033 Irkutsk, Russia; [email protected] (A.Y.K.); [email protected] (G.V.P.); [email protected] (S.A.P.); [email protected] (E.V.S.); [email protected] (I.V.T.); [email protected] (E.A.Z.); [email protected] (N.A.Z.); [email protected] (A.S.G.); [email protected] (M.Y.S.) 2 Chemical Biology and Fundamental Medicine Siberian Branch of the Russian Academy of Sciences, Lavrentiev Avenue 8, 630090 Novosibirsk, Russia; [email protected] * Correspondence: [email protected] (A.D.G.); [email protected] (O.I.B.); Citation: Galachyants, A.D.; Tel.: +73-952-425-415 (A.D.G. & O.I.B.) Krasnopeev, A.Y.; Podlesnaya, G.V.; Potapov, S.A.; Sukhanova, E.V.; Abstract: The diversity of aerobic anoxygenic phototrophs (AAPs) and rhodopsin-containing bac- Tikhonova, I.V.; Zimens, E.A.; teria in the surface microlayer, water column, and epilithic biofilms of Lake Baikal was studied for Kabilov, M.R.; Zhuchenko, N.A.; the first time, employing pufM and rhodopsin genes, and compared to 16S rRNA diversity. -
Occurrence of Manganese-Oxidizing Microorganisms and Manganese Deposition During Bio¢Lm Formation on Stainless Steel in a Brackish Surface Water
FEMS Microbiology Ecology 39 (2002) 41^55 www.fems-microbiology.org Occurrence of manganese-oxidizing microorganisms and manganese deposition during bio¢lm formation on stainless steel in a brackish surface water Jan Kielemoes a, Isabelle Bultinck b, Hedwig Storms b, Nico Boon a, Willy Verstraete a;* Downloaded from https://academic.oup.com/femsec/article/39/1/41/535962 by guest on 29 September 2021 a Laboratory of Microbial Ecology and Technology (LabMET), Faculty of Agricultural and Applied Biological Sciences, Ghent University, Coupure Links 653, B-9000 Ghent, Belgium b OCAS N.V., John Kennedylaan 3, B-9060 Zelzate, Belgium Received 25 May 2001; received in revised form 8 October 2001; accepted 10 October 2001 First published online 5 December 2001 Abstract Biofilm formation on 316L stainless steel was investigated in a pilotscale flow-through system fed with brackish surface water using an alternating flow/stagnation/flow regime. Microbial community analysis by denaturing gradient gel electrophoresis and sequencing revealed the presence of complex microbial ecosystems consisting of, amongst others, Leptothrix-related manganese-oxidizing bacteria in the adjacent water, and sulfur-oxidizing, sulfate-reducing and slime-producing bacteria in the biofilm. Selective plating of the biofilm indicated the presence of high levels of manganese-oxidizing microorganisms, while microscopic and chemical analyses of the biofilm confirmed the presence of filamentous manganese-precipitating microorganisms, most probably Leptothrix species. Strong accumulation of iron and manganese occurred in the biofilm relative to the adjacent water. No evidence of selective colonization of the steel surface or biocorrosion was found over the experimental period. The overall results of this study highlight the potential formation of complex microbial biofilm communities in flow-through systems thriving on minor concentrations of manganese. -
Conference on Life Detection in Extraterrestrial Samples
Program and Abstract Volume LPI Contribution No. 1650 CONFERENCE ON LIFE DETECTION IN EXTRATERRESTRIAL SAMPLES February 13–15, 2012 • San Diego, California Sponsors NASA Mars Program Office NASA Planetary Protection Office Universities Space Research Association Lunar and Planetary Institute Conveners Dave Beaty Mary Voytek NASA Mars Program Office NASA Astrobiology Cassie Conley Jorge Vago NASA Planetary Protection ESA Mars Program Gerhard Kminek Michael Meyer ESA Planetary Protection NASA Mars Exploration Program Dave Des Marais Mars Exploration Program Analysis Group (MEPAG) Chair Scientific Organizing Committee Carl Allen Charles Cockell NASA Johnson Space Center University of Edinburgh Doug Bartlett John Parnell Scripps Institution of Oceanography University of Aberdeen Penny Boston Mike Spilde New Mexico Tech University of New Mexico Karen Buxbaum Andrew Steele NASA Mars Program Office Carnegie Institution for Science Frances Westall Centre de Biophysique Moléculaire Lunar and Planetary Institute 3600 Bay Area Boulevard Houston TX 77058-1113 LPI Contribution No. 1650 Compiled in 2011 by Meeting and Publication Services Lunar and Planetary Institute USRA Houston 3600 Bay Area Boulevard, Houston TX 77058-1113 The Lunar and Planetary Institute is operated by the Universities Space Research Association under a cooperative agreement with the Science Mission Directorate of the National Aeronautics and Space Administration. Any opinions, findings, and conclusions or recommendations expressed in this volume are those of the author(s) and do not necessarily reflect the views of the National Aeronautics and Space Administration. Material in this volume may be copied without restraint for library, abstract service, education, or personal research purposes; however, republication of any paper or portion thereof requires the written permission of the authors as well as the appropriate acknowledgment of this publication.