Methylamine As a Nitrogen Source for Microorganisms from a Coastal Marine Environment
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Methylamine As a Nitrogen Source for Microorganisms from a Coastal Marine
Methylamine as a Nitrogen Source for Microorganisms from a Coastal Marine Environment Martin Tauberta,b, Carolina Grobb, Alexandra M. Howatb, Oliver J. Burnsc, Jennifer Pratscherb, Nico Jehmlichd, Martin von Bergend,e,f, Hans H. Richnowg, Yin Chenh,1, J. Colin Murrellb,1 aAquatic Geomicrobiology, Institute of Ecology, Friedrich Schiller University Jena, Dornburger Str. 159, 07743 Jena, Germany bSchool of Environmental Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK cSchool of Biological Sciences, University of East Anglia, Norwich Research Park, Norwich, NR4 7TJ, UK dDepartment of Molecular Systems Biology, Helmholtz Centre for Environmental Research – UFZ, Leipzig, Germany eInstitute of Biochemistry, Faculty of Biosciences, Pharmacy and Psychology, University of Leipzig, Brüderstraße 32, 04103 Leipzig, Germany fDepartment of Chemistry and Bioscience, University of Aalborg, Fredrik Bajers Vej 7H, 9220 Aalborg East, Denmark. gDepartment of Isotope Biogeochemistry, Helmholtz-Centre for Environmental Research – UFZ, Permoserstrasse 15, 04318 Leipzig, Germany hSchool of Life Sciences, University of Warwick, Coventry, CV4 7AL, UK 1To whom correspondence should be addressed. J. Colin Murrell, Phone: +44 (0)1603 59 2959, Email: [email protected], and Yin Chen, Phone: +44 (0)24 76528976, Email: [email protected] Keywords: marine methylotrophs, 15N stable isotope probing, methylamine, metagenomics, metaproteomics Classification: BIOLOGICAL SCIENCES/Microbiology Short title: Methylamine as a Nitrogen Source for Marine Microbes This article has been accepted for publication and undergone full peer review but has not been through the copyediting, typesetting, pagination and proofreading process which may lead to differences between this version and the Version of Record. Please cite this article as an ‘Accepted Article’, doi: 10.1111/1462-2920.13709 This article is protected by copyright. -
Which Organisms Are Used for Anti-Biofouling Studies
Table S1. Semi-systematic review raw data answering: Which organisms are used for anti-biofouling studies? Antifoulant Method Organism(s) Model Bacteria Type of Biofilm Source (Y if mentioned) Detection Method composite membranes E. coli ATCC25922 Y LIVE/DEAD baclight [1] stain S. aureus ATCC255923 composite membranes E. coli ATCC25922 Y colony counting [2] S. aureus RSKK 1009 graphene oxide Saccharomycetes colony counting [3] methyl p-hydroxybenzoate L. monocytogenes [4] potassium sorbate P. putida Y. enterocolitica A. hydrophila composite membranes E. coli Y FESEM [5] (unspecified/unique sample type) S. aureus (unspecified/unique sample type) K. pneumonia ATCC13883 P. aeruginosa BAA-1744 composite membranes E. coli Y SEM [6] (unspecified/unique sample type) S. aureus (unspecified/unique sample type) graphene oxide E. coli ATCC25922 Y colony counting [7] S. aureus ATCC9144 P. aeruginosa ATCCPAO1 composite membranes E. coli Y measuring flux [8] (unspecified/unique sample type) graphene oxide E. coli Y colony counting [9] (unspecified/unique SEM sample type) LIVE/DEAD baclight S. aureus stain (unspecified/unique sample type) modified membrane P. aeruginosa P60 Y DAPI [10] Bacillus sp. G-84 LIVE/DEAD baclight stain bacteriophages E. coli (K12) Y measuring flux [11] ATCC11303-B4 quorum quenching P. aeruginosa KCTC LIVE/DEAD baclight [12] 2513 stain modified membrane E. coli colony counting [13] (unspecified/unique colony counting sample type) measuring flux S. aureus (unspecified/unique sample type) modified membrane E. coli BW26437 Y measuring flux [14] graphene oxide Klebsiella colony counting [15] (unspecified/unique sample type) P. aeruginosa (unspecified/unique sample type) graphene oxide P. aeruginosa measuring flux [16] (unspecified/unique sample type) composite membranes E. -
Hmelo Thesis.Pdf (3.770Mb)
MICROBIAL INTERACTIONS ASSOCIATED WITH BIOFILMS ATTACHED TO TRICHODESMIUM SPP. AND DETRITAL PARTICLES IN THE OCEAN By Laura Robin Hmelo B.A., Carleton College, 2002 Submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy at the MASSACHUSETTS INSTITUTE OF TECHNOLOGY and the WOODS HOLE OCEANOGRAPHIC INSTITUTION June 2010 © 2010 Laura R. Hmelo. All rights reserved. The author hereby grants to MIT and WHOI permission to reproduce and distribute publicly paper and electronic copies of this thesis document in whole or in part in any medium now known or hereafter created. Author ________________________________________________________________________ Joint Program in Oceanography/Applied Ocean Science and Engineering Massachusetts Institute of Technology And Woods Hole Oceanographic Institution May 11, 2010 Certified by ________________________________________________________________________ Dr. Benjamin A.S. Van Mooy Associate Scientist of Marine Chemistry and Geochemistry, WHOI Thesis Supervisor Accepted by ________________________________________________________________________ Prof. Roger E. Summons Professor of Earth, Atmospheric, and Planetary Sciences, MIT Chair, Joint Committee for Chemical Oceanography Woods Hole Oceanographic Institution 2 MICROBIAL INTERACTIONS ASSOCIATED WITH BIOFILMS ATTACHED TO TRICHODESMIUM SPP. AND DETRITAL PARTICLES IN THE OCEAN By Laura R. Hmelo Submitted to the MIT/WHOI Joint Program in Oceanography in partial fulfillment of the requirements for the degree of Doctor of Philosophy in the field of Chemical Oceanography THESIS ABSTRACT Quorum sensing (QS) via acylated homoserine lactones (AHLs) was discovered in the ocean, yet little is known about its role in the ocean beyond its involvement in certain symbiotic interactions. The objectives of this thesis were to constrain the chemical stability of AHLs in seawater, explore the production of AHLs in marine particulate environments, and probe selected behaviors which might be controlled by AHL-QS. -
Stable-Isotope Probing Implicates Methylophaga Spp and Novel Gammaproteobacteria in Marine Methanol and Methylamine Metabolism
The ISME Journal (2007) 1, 480–491 & 2007 International Society for Microbial Ecology All rights reserved 1751-7362/07 $30.00 www.nature.com/ismej ORIGINAL ARTICLE Stable-isotope probing implicates Methylophaga spp and novel Gammaproteobacteria in marine methanol and methylamine metabolism Josh D Neufeld1, Hendrik Scha¨fer, Michael J Cox2, Rich Boden, Ian R McDonald3 and J Colin Murrell Department of Biological Sciences, University of Warwick, Coventry, UK The metabolism of one-carbon (C1) compounds in the marine environment affects global warming, seawater ecology and atmospheric chemistry. Despite their global significance, marine micro- organisms that consume C1 compounds in situ remain poorly characterized. Stable-isotope probing (SIP) is an ideal tool for linking the function and phylogeny of methylotrophic organisms by the metabolism and incorporation of stable-isotope-labelled substrates into nucleic acids. By combining DNA-SIP and time-series sampling, we characterized the organisms involved in the assimilation of methanol and methylamine in coastal sea water (Plymouth, UK). Labelled nucleic acids were analysed by denaturing gradient gel electrophoresis (DGGE) and clone libraries of 16S rRNA genes. In addition, we characterized the functional gene complement of labelled nucleic acids with an improved primer set targeting methanol dehydrogenase (mxaF) and newly designed primers for methylamine dehydrogenase (mauA). Predominant DGGE phylotypes, 16S rRNA, methanol and methylamine dehydrogenase gene sequences, and cultured isolates all implicated Methylophaga spp, moderately halophilic marine methylotrophs, in the consumption of both methanol and methylamine. Additionally, an mxaF sequence obtained from DNA extracted from sea water clustered with those detected in 13C-DNA, suggesting a predominance of Methylophaga spp among marine methylotrophs. -
SIP Metagenomics Identifies Uncultivated Methylophilaceae As Dimethylsulphide Degrading Bacteria in Soil and Lake Sediment
The ISME Journal (2015) 9, 2336–2348 © 2015 International Society for Microbial Ecology All rights reserved 1751-7362/15 OPEN www.nature.com/ismej ORIGINAL ARTICLE SIP metagenomics identifies uncultivated Methylophilaceae as dimethylsulphide degrading bacteria in soil and lake sediment Özge Eyice1, Motonobu Namura2, Yin Chen1, Andrew Mead1,3, Siva Samavedam1 and Hendrik Schäfer1 1School of Life Sciences, University of Warwick, Coventry, UK and 2MOAC Doctoral Training Centre, University of Warwick, Coventry, UK Dimethylsulphide (DMS) has an important role in the global sulphur cycle and atmospheric chemistry. Microorganisms using DMS as sole carbon, sulphur or energy source, contribute to the cycling of DMS in a wide variety of ecosystems. The diversity of microbial populations degrading DMS in terrestrial environments is poorly understood. Based on cultivation studies, a wide range of bacteria isolated from terrestrial ecosystems were shown to be able to degrade DMS, yet it remains unknown whether any of these have important roles in situ. In this study, we identified bacteria using DMS as a carbon and energy source in terrestrial environments, an agricultural soil and a lake sediment, by DNA stable isotope probing (SIP). Microbial communities involved in DMS degradation were analysed by denaturing gradient gel electrophoresis, high-throughput sequencing of SIP gradient fractions and metagenomic sequencing of phi29-amplified community DNA. Labelling patterns of time course SIP experiments identified members of the Methylophilaceae family, not previously implicated in DMS degradation, as dominant DMS-degrading populations in soil and lake sediment. Thiobacillus spp. were also detected in 13C-DNA from SIP incubations. Metagenomic sequencing also suggested involvement of Methylophilaceae in DMS degradation and further indicated shifts in the functional profile of the DMS-assimilating communities in line with methylotrophy and oxidation of inorganic sulphur compounds. -
Experimental Horizontal Gene Transfer of Methylamine
Experimental Horizontal Gene Transfer of Methylamine Dehydrogenase Mimics Prevalent Exchange in Nature and Overcomes the Methylamine Growth Constraints Posed by the Sub- Optimal N-Methylglutamate Pathway The Harvard community has made this article openly available. Please share how this access benefits you. Your story matters Citation Nayak, Dipti D., and Christopher J. Marx. 2015. “Experimental Horizontal Gene Transfer of Methylamine Dehydrogenase Mimics Prevalent Exchange in Nature and Overcomes the Methylamine Growth Constraints Posed by the Sub-Optimal N-Methylglutamate Pathway.” Microorganisms 3 (1): 60-79. doi:10.3390/microorganisms3010060. http://dx.doi.org/10.3390/ microorganisms3010060. Published Version doi:10.3390/microorganisms3010060 Citable link http://nrs.harvard.edu/urn-3:HUL.InstRepos:29407840 Terms of Use This article was downloaded from Harvard University’s DASH repository, and is made available under the terms and conditions applicable to Other Posted Material, as set forth at http:// nrs.harvard.edu/urn-3:HUL.InstRepos:dash.current.terms-of- use#LAA Microorganisms 2015, 3, 60-79; doi:10.3390/microorganisms3010060 OPEN ACCESS microorganisms ISSN 2076-2607 www.mdpi.com/journal/microorganisms Article Experimental Horizontal Gene Transfer of Methylamine Dehydrogenase Mimics Prevalent Exchange in Nature and Overcomes the Methylamine Growth Constraints Posed by the Sub-Optimal N-Methylglutamate Pathway Dipti D. Nayak 1,2,† and Christopher J. Marx 1,2,3,4,* 1 Organismic and Evolutionary Biology, Harvard University, Cambridge, MA 02138, USA; E-Mail: [email protected] 2 Biological Sciences, University of Idaho, Moscow, ID 83844, USA 3 Faculty of Arts and Sciences Center for Systems Biology, Harvard University, Cambridge, MA 02138, USA 4 Institute for Bioinformatics and Evolutionary Studies, University of Idaho, Moscow, ID 83844, USA † Present Address: Institute for Genomic Biology, University of Illinois, Urbana, IL 61801, USA. -
Linking Activity and Function to Ecosystem Dynamics in a Coastal Bacterioplankton Community
Linking activity and function to ecosystem dynamics in a coastal bacterioplankton community The MIT Faculty has made this article openly available. Please share how this access benefits you. Your story matters. Citation Gifford, Scott M., Shalabh Sharma, and Mary Ann Moran. “Linking Activity and Function to Ecosystem Dynamics in a Coastal Bacterioplankton Community.” Frontiers in Microbiology 5 (April 24, 2014). As Published http://dx.doi.org/10.3389/fmicb.2014.00185 Publisher Frontiers Research Foundation Version Final published version Citable link http://hdl.handle.net/1721.1/88031 Terms of Use Article is made available in accordance with the publisher's policy and may be subject to US copyright law. Please refer to the publisher's site for terms of use. ORIGINAL RESEARCH ARTICLE published: 24 April 2014 doi: 10.3389/fmicb.2014.00185 Linking activity and function to ecosystem dynamics in a coastal bacterioplankton community Scott M. Gifford †, Shalabh Sharma and Mary Ann Moran* Department of Marine Sciences, University of Georgia, Athens, GA, USA Edited by: For bacterial communities containing hundreds to thousands of distinct populations, Anton F.Post, Marine Biological connecting functional processes and environmental dynamics at high taxonomic Laboratory, USA resolution has remained challenging. Here we use the expression of ribosomal proteins Reviewed by: (%RP) as a proxy for in situ activity of 200 taxa within 20 metatranscriptomic samples in Gerhard Josef Herndl, University of Vienna, Austria a coastal ocean time series encompassing both seasonal variability and diel dynamics. Frank Stewart, Georgia Institute of %RP patterns grouped the taxa into seven activity clusters with distinct profiles in Technology, USA functional gene expression and correlations with environmental gradients. -
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Manuscript version: Author’s Accepted Manuscript The version presented in WRAP is the author’s accepted manuscript and may differ from the published version or, Version of Record. Persistent WRAP URL: http://wrap.warwick.ac.uk/117505 How to cite: Please refer to published version for the most recent bibliographic citation information. If a published version is known of, the repository item page linked to above, will contain details on accessing it. Copyright and reuse: The Warwick Research Archive Portal (WRAP) makes this work of researchers of the University of Warwick available open access under the following conditions. This article is made available under the Creative Commons Attribution 4.0 International license (CC BY 4.0) and may be reused according to the conditions of the license. For more details see: http://creativecommons.org/licenses/by/4.0/. Publisher’s statement: Please refer to the repository item page, publisher’s statement section, for further information. For more information, please contact the WRAP Team at: [email protected]. warwick.ac.uk/lib-publications 1 Identification of proteins and genes expressed by Methylophaga thiooxydans during 2 growth on dimethylsulfide and their presence in other members of the genus 3 4 5 6 Eileen Kröber1,2, Hendrik Schäfer1* 7 8 9 10 1 School of Life Sciences, Gibbet Hill Campus, University of Warwick, Coventry, CV4 7AL, 11 United Kingdom 12 2 Current address: Microbial Biogeochemistry, RA Landscape Functioning, ZALF Leibniz 13 Centre for Agricultural Landscape Research, Müncheberg, Germany 14 15 16 17 *Correspondence to 18 H Schäfer, School of Life Sciences, Gibbet Hill Campus, University of Warwick, Coventry, 19 CV4 7AL, United Kingdom 1 20 Abstract 21 Dimethylsulfide is a volatile organic sulfur compound that provides the largest input of biogenic 22 sulfur from the oceans to the atmosphere, and thence back to land, constituting an important 23 link in the global sulfur cycle. -
Production of Indigo and Indirubin Using Recombinant Escherichia Coli Harboring a Novel Flavin-Containing Monooxygenase Gene
August 2012 Ph.D. Dissertation Production of indigo and indirubin using recombinant Escherichia coli harboring a novel flavin-containing monooxygenase gene Graduate School of Chosun University Department of Environmental Engineering Gui Hwan Han Production of indigo and indirubin using recombinant Escherichia coli harboring a novel flavin-containing monooxygenase gene Methylophaga aminisulfidivorans MPT 유래 flavin-containing monooxygenase 유전자를 내포시킨 재조합 대장균을 이용한 인디고 및 인디루빈의 생산 August 24 2012 Graduate School of Chosun University Department of Environmental Engineering Gui Hwan Han Production of indigo and indirubin using recombinant Escherichia coli harboring a novel flavin-containing monooxygenase gene Supervisor : Prof. Si Wouk Kim A dissertation submitted to the Department of Environmental Engineering and the Graduate School of Chosun University in fulfillment of the requirements for the degree of Doctor of Philosophy April 2012 Graduate School of Chosun University Department of Environmental Engineering Gui Hwan Han This certifies that the degree of Doctor of Philosophy of Gui Hwan Han is approved by Heon Man Lim Chair of committee Il Soo Bang Committee member Hyung Joon Cha Committee member Jintae Lee Committee member Si Wouk Kim Committee member June 2012 Graduate School of Chosun University Contents Contents ······································································································································ i List of tables ···························································································································· -
Bacterial Diversity Associated with the Coccolithophorid Algae Emiliania Huxleyi and Coccolithus Pelagicus F
Hindawi Publishing Corporation BioMed Research International Volume 2015, Article ID 194540, 15 pages http://dx.doi.org/10.1155/2015/194540 Research Article Bacterial Diversity Associated with the Coccolithophorid Algae Emiliania huxleyi and Coccolithus pelagicus f. braarudii David H. Green,1 Virginia Echavarri-Bravo,1,2 Debra Brennan,1 and Mark C. Hart1 1 Microbial & Molecular Biology, Scottish Association for Marine Science, Oban, Argyll PA37 1QA, UK 2School of Life Science, Heriot-Watt University, Edinburgh EH14 4AS, UK Correspondence should be addressed to David H. Green; [email protected] Received 28 August 2014; Accepted 30 January 2015 Academic Editor: Ameur Cherif Copyright © 2015 David H. Green et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Coccolithophores are unicellular calcifying marine phytoplankton that can form large and conspicuous blooms in the oceans and make significant contributions to oceanic carbon cycling and atmospheric CO2 regulation. Despite their importance, the bacterial diversity associated with these algae has not been explored for ecological or biotechnological reasons. Bacterial membership of Emiliania huxleyi and Coccolithus pelagicus f. braarudii cultures was assessed using cultivation and cultivation-independent methods. The communities were species rich compared to other phytoplankton cultures. Community analysis identified specific taxa which cooccur in all cultures (Marinobacter and Marivita). Hydrocarbon-degrading bacteria were found in all cultures. The presence of Acidobacteria, Acidimicrobidae, Schlegelella,andThermomonas was unprecedented but were potentially explained by calcification associated with coccolith production. One strain of Acidobacteria was cultivated and is closely related toa marine Acidobacteria isolated from a sponge. -
1 Bacterial SBP56 Identified As a Cu-Dependent Methanethiol Oxidase Widely Distributed in the Biosphere Özge Eyicea,B1, Natalii
Bacterial SBP56 identified as a Cu-dependent methanethiol oxidase widely distributed in the biosphere Özge Eyicea,b1, Nataliia Myronovaa,1, Arjan Polc, Ornella Carriónd, Jonathan Toddd, Tom J. Smithe, Stephen J. Gurmanf, Adam Cuthbertsona, Sophie Mazarda,2, Monique A.S.H. 5 Mennink-Kerstenc, Timothy D.H. Buggg, K. Kristoffer Anderssonh, Andrew W.B. Johnstond, Huub J.M. Op den Campc,3 , Hendrik Schäfera,3 Author contributions: HS, HOdC, NM, AP, KKA, TJS, SJG, JT, TDHB, AWBJ designed research; OE, NM, OC, JT, TJS, SJG, MMK, AP, HS, KKA, AC, SM performed research; HS, JT, TJS, KKA, AWBJ, AP, HOdC wrote the paper with editorial help of co-authors. 10 a School of Life Sciences, University of Warwick, Coventry, CV4 7AL, United Kingdom b School of Biological and Chemical Sciences, Queen Mary University of London, London, E1 4NS, United Kingdom c Department of Microbiology, Institute for Water and Wetland Research, Faculty of 15 Science, Radboud University, Heyendaalseweg 135, 6525 AJ Nijmegen, The Netherlands d School of Biological Sciences, University of East Anglia, Norwich, NR4 7TJ, United Kingdom e Department of Biosciences and Chemistry, Sheffield Hallam University, Howard Street, Sheffield, S1 1WB, United Kingdom 20 f Department of Physics and Astronomy, University of Leicester, Leicester, LE1 7RH, United Kingdom g Department of Chemistry, University of Warwick, Coventry, CV4 7AL, United Kingdom h Department of Bioscience, University of Oslo, PO Box 1066 Blindern, Blindernveien 31, 0371 Oslo, Norway 25 1 These authors contributed equally to the work 2 present address: Department of Chemistry and Biomolecular Sciences, Macquarie University, Sydney, NSW, Australia 2109 3 Corresponding authors: 30 Hendrik Schäfer, Email: [email protected]; Phone: +44 2476 575052 Huub J.M. -
Novel Magnetite-Producing Magnetotactic Bacteria Belonging to the Gammaproteobacteria
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by DigitalCommons@CalPoly Novel magnetite-producing magnetotactic bacteria belonging to the Gammaproteobacteria Christopher T Lefe`vre , Nathan Viloria , Marian L Schmidt , Miha´ly Po´sfai , Richard B Frankel and Dennis A Bazylinski Two novel magnetotactic bacteria (MTB) were isolated from sediment and water collected from the Badwater Basin, Death Valley National Park and southeastern shore of the Salton Sea, respectively, and were designated as strains BW-2 and SS-5, respectively. Both organisms are rod-shaped, biomineralize magnetite, and are motile by means of flagella. The strains grow chemolithoauto- trophically oxidizing thiosulfate and sulfide microaerobically as electron donors, with thiosulfate oxidized stoichiometrically to sulfate. They appear to utilize the Calvin–Benson–Bassham cycle for autotrophy based on ribulose-1,5-bisphosphate carboxylase/oxygenase (RubisCO) activity and the presence of partial sequences of RubisCO genes. Strains BW-2 and SS-5 biomineralize chains of octahedral magnetite crystals, although the crystals of SS-5 are elongated. Based on 16S rRNA gene sequences, both strains are phylogenetically affiliated with the Gammaproteobacteria class. Strain SS-5 belongs to the order Chromatiales; the cultured bacterium with the highest 16S rRNA gene sequence identity to SS-5 is Thiohalocapsa marina (93.0%). Strain BW-2 clearly belongs to the Thiotrichales; interestingly, the organism with the highest 16S rRNA gene sequence identity to this strain is Thiohalospira alkaliphila (90.2%), which belongs to the Chromatiales. Each strain represents a new genus. This is the first report of magnetite-producing MTB phylogenetically associated with the Gammaproteobacteria.