Draft Genome Sequence of Strain R RK 3, an Iron-Depositing Isolate
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Phototrophic Oxidation of Ferrous Iron by a Rhodomicrobium Vannielii Strain
Phototrophic oxidation of ferrous iron by a Rhodomicrobium vannielii strain Silke Heising and Bernhard Schink Author for correspondence: Bernhard Schink. Tel: 49 7531 882140. Fax: 49 7531 882966. e-mail: Bernhard.Schink!uni-konstanz.de Fakulta$ tfu$r Biologie, Oxidation of ferrous iron was studied with the anaerobic phototrophic Universita$ t Konstanz, bacterial strain BS-1. Based on morphology, substrate utilization patterns, Postfach 5560, D-78434 Konstanz, Germany arrangement of intracytoplasmic membranes and the in vivo absorption spectrum, this strain was assigned to the known species Rhodomicrobium vannielii. Also, the type strain of this species oxidized ferrous iron in the light. Phototrophic growth of strain BS-1 with ferrous iron as electron donor was stimulated by the presence of acetate or succinate as cosubstrates. The ferric iron hydroxides produced precipitated on the cell surfaces as solid crusts which impeded further iron oxidation after two to three generations. The complexing agent nitrilotriacetate stimulated iron oxidation but the yield of cell mass did not increase stoichiometrically under these conditions. Other complexing agents inhibited cell growth. Ferric iron was not reduced in the dark, and manganese salts were neither oxidized nor reduced. It is concluded that ferrous iron oxidation by strain BS-1 is only a side activity of this bacterium that cannot support growth exclusively with this electron source over prolonged periods of time. Keywords: iron metabolism, phototrophic bacteria, Rhodomicrobium vannielii, iron complexation, nitrilotriacetate (NTA) INTRODUCTION anoxygenic purple bacteria, including a Rhodo- microbium vannielii-like isolate (Widdel et al., 1993). Iron is the fourth most important element in the Earth’s Other strains of purple phototrophs able to oxidize crust, making up about 5% of the total crust mass ferrous iron are strain L7, a non-motile rod with gas (Ehrlich, 1990). -
A Study on the Phototrophic Microbial Mat Communities of Sulphur Mountain Thermal Springs and Their Association with the Endangered, Endemic Snail Physella Johnsoni
A Study on the Phototrophic Microbial Mat Communities of Sulphur Mountain Thermal Springs and their Association with the Endangered, Endemic Snail Physella johnsoni By Michael Bilyj A thesis submitted to the Faculty of Graduate Studies in partial fulfillment of the requirements for the degree of Master of Science Department of Microbiology Faculty of Science University of Manitoba Winnipeg, Manitoba October 2011 © Copyright 2011, Michael A. Bilyj 1 Abstract The seasonal population fluctuation of anoxygenic phototrophs and the diversity of cyanobacteria at the Sulphur Mountain thermal springs of Banff, Canada were investigated and compared to the drastic population changes of the endangered snail Physella johnsoni. A new species and two strains of Rhodomicrobium were taxonomically characterized in addition to new species of Rhodobacter and Erythromicrobium. Major mat-forming organisms included Thiothrix-like species, oxygenic phototrophs of genera Spirulina, Oscillatoria, and Phormidium and purple nonsulfur bacteria Rhodobacter, Rhodopseudomonas and Rhodomicrobium. Aerobic anoxygenic phototrophs comprised upwards of 9.6 x 104 CFU/cm2 of mat or 18.9% of total aerobic heterotrophic bacterial isolates at certain sites, while maximal purple nonsulfur and purple sulfur bacteria were quantified at 3.2 x 105 and 2.0 x 106 CFU/cm2 of mat, respectively. Photosynthetic activity measurements revealed incredibly productive carbon fixation rates averaging 40.5 mg C/cm2/24 h. A temporal mismatch was observed for mat area and prokaryote-based organics to P. johnsoni population flux in a ―tracking inertia‖ manner. 2 Acknowledgements It is difficult to express sufficient gratitude to my supervisor Dr. Vladimir Yurkov for his unfaltering patience, generosity and motivation throughout this entire degree. -
Deoxyribonucleic Acid Base Sequence Homologies of Some Budding and Prosthecate Bacterla RICHARD L
JOURNAL OF BACTERIOLOGY, Apr. 1972, p. 256-261 Vol. 110, No. 1 Copyright © 1972 American Society for Microbiology Printed in U.S.A. Deoxyribonucleic Acid Base Sequence Homologies of Some Budding and Prosthecate Bacterla RICHARD L. MOORE' AND PETER HIRSCH2 Department of Microbiology and Public Health, Michigan State University, East Lansing, Michigan 48823 Received for publication 21 December 1971 The genetic relatedness of a number of budding and prosthecate bacteria was determined by deoxyribonucleic acid (DNA) homology experiments of the di- rect binding type. Strains of Hyphomicrobium sp. isolated from aquatic habi- tats were found to have relatedness values ranging from 9 to 70% with strain "EA-617," a subculture of the Hyphomicrobium isolated by Mevius from river water. Strains obtained from soil enrichments had lower values with EA-617, ranging from 3 to 5%. Very little or no homology was detected between the amino acid-utilizing strain Hyphomicrobium neptunium and other Hyphomi- crobium strains, although significant homology was observed with the two Hyphomonas strains examined. No homology could be detected between pros- thecate bacteria of the genera Rhodomicrobium, Prosthecomicrobium, Ancal- omicrobium, or Caulobacter, and Hyphomicrobium strain EA-617 or H. nep- tunium LE-670. The grouping of Hyphomicrobium strains by their relatedness values agrees well with a grouping according to the base composition of their DNA species. It is concluded that bacteria possessing cellular extensions repre- sent a widely diverse group of organisms. Two genera of bacteria, Hyphomicrobium drum, P. pneumaticum, Ancalomicrobium adetum, and Rhodomicrobium, are listed under the and Caulobacter crescentus were obtained from J. T. family of Hyphomicrobiaceae in the seventh Staley (Seattle); Rhodomicrobium vannielii was re- edition of Bergey's Manual of Determinative ceived from H. -
Research Collection
Research Collection Doctoral Thesis Development and application of molecular tools to investigate microbial alkaline phosphatase genes in soil Author(s): Ragot, Sabine A. Publication Date: 2016 Permanent Link: https://doi.org/10.3929/ethz-a-010630685 Rights / License: In Copyright - Non-Commercial Use Permitted This page was generated automatically upon download from the ETH Zurich Research Collection. For more information please consult the Terms of use. ETH Library DISS. ETH NO.23284 DEVELOPMENT AND APPLICATION OF MOLECULAR TOOLS TO INVESTIGATE MICROBIAL ALKALINE PHOSPHATASE GENES IN SOIL A thesis submitted to attain the degree of DOCTOR OF SCIENCES of ETH ZURICH (Dr. sc. ETH Zurich) presented by SABINE ANNE RAGOT Master of Science UZH in Biology born on 25.02.1987 citizen of Fribourg, FR accepted on the recommendation of Prof. Dr. Emmanuel Frossard, examiner PD Dr. Else Katrin Bünemann-König, co-examiner Prof. Dr. Michael Kertesz, co-examiner Dr. Claude Plassard, co-examiner 2016 Sabine Anne Ragot: Development and application of molecular tools to investigate microbial alkaline phosphatase genes in soil, c 2016 ⃝ ABSTRACT Phosphatase enzymes play an important role in soil phosphorus cycling by hydrolyzing organic phosphorus to orthophosphate, which can be taken up by plants and microorgan- isms. PhoD and PhoX alkaline phosphatases and AcpA acid phosphatase are produced by microorganisms in response to phosphorus limitation in the environment. In this thesis, the current knowledge of the prevalence of phoD and phoX in the environment and of their taxonomic distribution was assessed, and new molecular tools were developed to target the phoD and phoX alkaline phosphatase genes in soil microorganisms. -
1 Anoxygenic Phototrophic Chloroflexota Member Uses a Type
Anoxygenic phototrophic Chloroflexota member uses a Type I reaction center Supplementary Materials J. M. Tsuji, N. A. Shaw, S. Nagashima, J. J. Venkiteswaran, S. L. Schiff, S. Hanada, M. Tank, J. D. Neufeld Correspondence to: [email protected]; [email protected]; [email protected] This PDF file includes: Materials and Methods Supplementary Text, Sections S1 to S4 Figs. S1 to S9 Tables S1 to S3 1 Materials and Methods Enrichment cultivation of ‘Ca. Chx. allophototropha’ To culture novel anoxygenic phototrophs, we sampled Lake 227, a seasonally anoxic and ferruginous Boreal Shield lake at the International Institute for Sustainable Development Experimental Lakes Area (IISD-ELA; near Kenora, Canada). Lake 227 develops up to ~100 μM concentrations of dissolved ferrous iron in its anoxic water column (31), and anoxia is more pronounced than expected naturally due to the long-term experimental eutrophication of the lake (32). The lake’s physico-chemistry has been described in detail previously (31). We collected water from the illuminated portion of the upper anoxic zone of Lake 227 in September 2017, at 3.875 and 5 m depth, and transported this water anoxically and chilled in 120 mL glass serum bottles, sealed with black rubber stoppers (Geo-Microbial Technology Company; Ochelata, Oklahoma, USA), to the laboratory. Water was supplemented with 2% v/v of a freshwater medium containing 8 mM ferrous chloride (33) and was distributed anoxically into 120 mL glass serum bottles, also sealed with black rubber stoppers (Geo-Microbial Technology Company), that had a headspace of dinitrogen gas at 1.5 atm final pressure. -
Rhodopseudomonas Acidophila, Sp. N., a New Species
JOURNAL OP BACrERiOLOGY, Aug. 1969, p. 597-602 Vol. 99, No. 2 Copyright @ 1969 American Society for Microbiology Printed In U.S.A. Rhodopseudomonas acidophila, sp. n., a New Species of the Budding Purple Nonsulfur Bacteria NORBERT PFENNIG Department of Microbiology, University of Illinois, Urbana, Illinois, and Institutfur Mikrobiologie der Universitdt Gottingen, Gottingen, Germany Received for publication 24 May 1969 A succinate-mineral salts medium ofpH 5.2 provided selective enrichment condi- tions for Rhodomicrobium vannielii and for a new species belonging to the Athiorho- daceae, described herein as Rhodopseudomonas acidophila. Sev'en strains of the new species have been isolated from different soUirces in the United States and Ger- many. The cells are rod-shaped or ovoid, 1.0 to 1.3 lum wide and 2 to 5 ,um long, and motile by means of polar flagella. Multiplication occurs by budding. The photopigments consist of bacteriochlorophyll a and carotenoids of the spirilloxan- thin series, together with new carotenoids. All strains can grow either under anaero- bic conditions in the light or under microaerophilic to aerobic conditions in the dark. No growth factors are required. The range of simple organic substrates photo- assimilated resembles that characteristic of Rhodomicrobium. Good photolitho- trophic growth is possible at the expense of molecular hydrogen; thiosulfate and sulfide are not utilized. In his monograph on the purple nonsulfur bac- the following natural sources: strain 7150, Lake teria, van Niel (4) showed that the use of different Monroe near Bloomington, Ind.; strain 7250, cypress substrates provides a convenient means for the swamp, Okeefenokee State Park, Ga.; strain 77550, selective enrichment of different members of the mud vulcano (pH: 4.5), Yellowstone National Park, Wyo.; strain 7750, farm pond near Athens, Ga.; Athiorhodaceae. -
Evolution of Methanotrophy in the Beijerinckiaceae&Mdash
The ISME Journal (2014) 8, 369–382 & 2014 International Society for Microbial Ecology All rights reserved 1751-7362/14 www.nature.com/ismej ORIGINAL ARTICLE The (d)evolution of methanotrophy in the Beijerinckiaceae—a comparative genomics analysis Ivica Tamas1, Angela V Smirnova1, Zhiguo He1,2 and Peter F Dunfield1 1Department of Biological Sciences, University of Calgary, Calgary, Alberta, Canada and 2Department of Bioengineering, School of Minerals Processing and Bioengineering, Central South University, Changsha, Hunan, China The alphaproteobacterial family Beijerinckiaceae contains generalists that grow on a wide range of substrates, and specialists that grow only on methane and methanol. We investigated the evolution of this family by comparing the genomes of the generalist organotroph Beijerinckia indica, the facultative methanotroph Methylocella silvestris and the obligate methanotroph Methylocapsa acidiphila. Highly resolved phylogenetic construction based on universally conserved genes demonstrated that the Beijerinckiaceae forms a monophyletic cluster with the Methylocystaceae, the only other family of alphaproteobacterial methanotrophs. Phylogenetic analyses also demonstrated a vertical inheritance pattern of methanotrophy and methylotrophy genes within these families. Conversely, many lateral gene transfer (LGT) events were detected for genes encoding carbohydrate transport and metabolism, energy production and conversion, and transcriptional regulation in the genome of B. indica, suggesting that it has recently acquired these genes. A key difference between the generalist B. indica and its specialist methanotrophic relatives was an abundance of transporter elements, particularly periplasmic-binding proteins and major facilitator transporters. The most parsimonious scenario for the evolution of methanotrophy in the Alphaproteobacteria is that it occurred only once, when a methylotroph acquired methane monooxygenases (MMOs) via LGT. -
Chapter 3 Transposon Mutagenesis of Rhodobacter Sphaeroides
Chapter 3 Transposon Mutagenesis of Rhodobacter sphaeroides Timothy D. Paustian and Robin S. Kurtz Department of Bacteriology University of Wisconsin–Madison Madison, Wisconsin 53706 (608) 263-4921, [email protected] Robin and Tim are associate faculty and coordinate the instructional labs for the Department of Bacteriology. Tim earned his B.S. in Biochemistry from the University of Wisconsin–Madison and Ph.D. from the Department of Bacteriology at UW–Madison. His interests include curriculum development, computer-aided instruction, and development of computer programs. Robin earned her B.S. and Ph.D. in Bacteriology from UW-Madison. Her interests include instructional lab development, curriculum improvement, and immunology. Robin and Tim have co-authored three lab manuals that are used in the introductory and advanced microbiology laboratories at UW–Madison. Reprinted from: Paustian, T. D., and R. S. Kurtz. 1994. Transposon mutagenesis of rhodobacter sphaeroides. Pages 45-61, in Tested studies for laboratory teaching, Volume 15 (C. A. Goldman, Editor). Proceedings of the 15th Workshop/Conference of the Association for Biology Laboratory Education (ABLE), 390 pages. - Copyright policy: http://www.zoo.utoronto.ca/able/volumes/copyright.htm Although the laboratory exercises in ABLE proceedings volumes have been tested and due consideration has been given to safety, individuals performing these exercises must assume all responsibility for risk. The Association for Biology Laboratory Education (ABLE) disclaims any liability with regards -
Structural and Functional Insights from the Metagenome of an Acidic Hot Spring Microbial Planktonic Community in the Colombian Andes
Structural and Functional Insights from the Metagenome of an Acidic Hot Spring Microbial Planktonic Community in the Colombian Andes Diego Javier Jime´nez1,5*, Fernando Dini Andreote3, Diego Chaves1, Jose´ Salvador Montan˜ a1,2, Cesar Osorio-Forero1,4, Howard Junca1,4, Marı´a Mercedes Zambrano1,4, Sandra Baena1,2 1 Colombian Center for Genomic and Bioinformatics from Extreme Environments (GeBiX), Bogota´, Colombia, 2 Departamento de Biologı´a, Unidad de Saneamiento y Biotecnologı´a Ambiental, Pontificia Universidad Javeriana, Bogota´, Colombia, 3 Department of Soil Science, ‘‘Luiz de Queiroz’’ College of Agriculture, University of Sao Paulo, Piracicaba, Brazil, 4 Molecular Genetics and Microbial Ecology Research Groups, Corporacio´n CorpoGen, Bogota´, Colombia, 5 Department of Microbial Ecology, Center for Ecological and Evolutionary Studies (CEES), University of Groningen, Groningen, The Netherlands Abstract A taxonomic and annotated functional description of microbial life was deduced from 53 Mb of metagenomic sequence retrieved from a planktonic fraction of the Neotropical high Andean (3,973 meters above sea level) acidic hot spring El Coquito (EC). A classification of unassembled metagenomic reads using different databases showed a high proportion of Gammaproteobacteria and Alphaproteobacteria (in total read affiliation), and through taxonomic affiliation of 16S rRNA gene fragments we observed the presence of Proteobacteria, micro-algae chloroplast and Firmicutes. Reads mapped against the genomes Acidiphilium cryptum JF-5, Legionella pneumophila str. Corby and Acidithiobacillus caldus revealed the presence of transposase-like sequences, potentially involved in horizontal gene transfer. Functional annotation and hierarchical comparison with different datasets obtained by pyrosequencing in different ecosystems showed that the microbial community also contained extensive DNA repair systems, possibly to cope with ultraviolet radiation at such high altitudes. -
Energy-Dispersive X-Ray Spectroscopy Procedure for Analysing Cellular Elemental Affinity of Pigmented Phototrophs
IOSR Journal of Pharmacy and Biological Sciences (IOSR-JPBS) e-ISSN: 2278-3008, p-ISSN:2319-7676. Volume 10, Issue 1 Ver. II (Jan -Feb. 2015), PP 15-21 www.iosrjournals.org Energy-Dispersive X-Ray Spectroscopy Procedure for Analysing Cellular Elemental Affinity of Pigmented Phototrophs 1,2,*Dr. Olawale Faith-Anthony Akinnuoye 1Academic Research and Administration, MFM Group Sdn Bhd, Kuala Lumpur, Malaysia 2Formerly in School of Biosciences and Biotechnology, Faculty of Science, National University of Malaysia, 43600 Bangi, Selangor DE, Malaysia *[email protected] _________________________________________________________________________________________ Abstract: Four phototrophic bacterial species Blastochloris sulfoviridis, Rhodocista pekingensis, Rhodopseudomonas palustris and Rhodomicrobium vannielii, isolated from hot springs were analysed for cellular elemental affinity between them and to determine possible relationship between physiological features and the constituent elements. A novel methodology using Energy-dispersive X-ray spectroscopy (EDS/EDX) of pigments produced by the bacteria was adopted and applied. Results did show close affinity of cellular elements with little or no difference in weighted and atomic percentages of the constituent elements. There was also little or no inference in the effects of these elements on the pigments and other features of the bacteria such as colour and morphological differences could not be fully attributed to the elemental inclusions. It was concluded that systemic factors that were responsible for extraneous features such as pigmentation, pigment density etc, could be a combination of elemental inclusion variations, genetics and other factors in-between rather than one. Required energy sources and metabolic factors were assumed to play key roles in contents and types of cellular elements in relation to pigmentation. -
Microbial Hitchhikers on Intercontinental Dust: Catching a Lift in Chad
The ISME Journal (2013) 7, 850–867 & 2013 International Society for Microbial Ecology All rights reserved 1751-7362/13 www.nature.com/ismej ORIGINAL ARTICLE Microbial hitchhikers on intercontinental dust: catching a lift in Chad Jocelyne Favet1, Ales Lapanje2, Adriana Giongo3, Suzanne Kennedy4, Yin-Yin Aung1, Arlette Cattaneo1, Austin G Davis-Richardson3, Christopher T Brown3, Renate Kort5, Hans-Ju¨ rgen Brumsack6, Bernhard Schnetger6, Adrian Chappell7, Jaap Kroijenga8, Andreas Beck9,10, Karin Schwibbert11, Ahmed H Mohamed12, Timothy Kirchner12, Patricia Dorr de Quadros3, Eric W Triplett3, William J Broughton1,11 and Anna A Gorbushina1,11,13 1Universite´ de Gene`ve, Sciences III, Gene`ve 4, Switzerland; 2Institute of Physical Biology, Ljubljana, Slovenia; 3Department of Microbiology and Cell Science, Institute of Food and Agricultural Sciences, University of Florida, Gainesville, FL, USA; 4MO BIO Laboratories Inc., Carlsbad, CA, USA; 5Elektronenmikroskopie, Carl von Ossietzky Universita¨t, Oldenburg, Germany; 6Microbiogeochemie, ICBM, Carl von Ossietzky Universita¨t, Oldenburg, Germany; 7CSIRO Land and Water, Black Mountain Laboratories, Black Mountain, ACT, Australia; 8Konvintsdyk 1, Friesland, The Netherlands; 9Botanische Staatssammlung Mu¨nchen, Department of Lichenology and Bryology, Mu¨nchen, Germany; 10GeoBio-Center, Ludwig-Maximilians Universita¨t Mu¨nchen, Mu¨nchen, Germany; 11Bundesanstalt fu¨r Materialforschung, und -pru¨fung, Abteilung Material und Umwelt, Berlin, Germany; 12Geomatics SFRC IFAS, University of Florida, Gainesville, FL, USA and 13Freie Universita¨t Berlin, Fachbereich Biologie, Chemie und Pharmazie & Geowissenschaften, Berlin, Germany Ancient mariners knew that dust whipped up from deserts by strong winds travelled long distances, including over oceans. Satellite remote sensing revealed major dust sources across the Sahara. Indeed, the Bode´le´ Depression in the Republic of Chad has been called the dustiest place on earth. -
Roseobacter Clade Bacteria Are Abundant in Coastal Sediments and Encode a Novel Combination of Sulfur Oxidation Genes
The ISME Journal (2012) 6, 2178–2187 & 2012 International Society for Microbial Ecology All rights reserved 1751-7362/12 www.nature.com/ismej ORIGINAL ARTICLE Roseobacter clade bacteria are abundant in coastal sediments and encode a novel combination of sulfur oxidation genes Sabine Lenk1, Cristina Moraru1, Sarah Hahnke2,4, Julia Arnds1, Michael Richter1, Michael Kube3,5, Richard Reinhardt3,6, Thorsten Brinkhoff2, Jens Harder1, Rudolf Amann1 and Marc Mumann1 1Molecular Ecology, Max Planck Institute for Marine Microbiology, Bremen, Germany; 2Institute for Chemistry and Biology of the Marine Environment, University of Oldenburg, Oldenburg, Germany and 3Max Planck Institute for Molecular Genetics, Berlin, Germany Roseobacter clade bacteria (RCB) are abundant in marine bacterioplankton worldwide and central to pelagic sulfur cycling. Very little is known about their abundance and function in marine sediments. We investigated the abundance, diversity and sulfur oxidation potential of RCB in surface sediments of two tidal flats. Here, RCB accounted for up to 9.6% of all cells and exceeded abundances commonly known for pelagic RCB by 1000-fold as revealed by fluorescence in situ hybridization (FISH). Phylogenetic analysis of 16S rRNA and sulfate thiohydrolase (SoxB) genes indicated diverse, possibly sulfur-oxidizing RCB related to sequences known from bacterioplankton and marine biofilms. To investigate the sulfur oxidation potential of RCB in sediments in more detail, we analyzed a metagenomic fragment from a RCB. This fragment encoded the reverse dissimilatory sulfite reductase (rDSR) pathway, which was not yet found in RCB, a novel type of sulfite dehydro- genase (SoeABC) and the Sox multi-enzyme complex including the SoxCD subunits. This was unexpected as soxCD and dsr genes were presumed to be mutually exclusive in sulfur-oxidizing prokaryotes.