Are There Benefits from Thermal Bacteria for Health?
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I. General Introduction
SECTION 3 ACIDITHIOBACILLUS I. General Introduction This document presents information that is accepted in the literature about the known characteristics of bacteria in the genus Acidithiobacillus. Regulatory officials may find the technical information useful in evaluating properties of micro-organisms that have been derived for various environmental applications. Consequently, this document provides a wide range of information without prescribing when the information would or would not be relevant to a specific risk assessment. The document represents a snapshot of current information (end-2002) that may be potentially relevant to such assessments. In considering information that should be presented on this taxonomic grouping, the Task Group on Micro-organisms has discussed the list of topics presented in the “Blue Book” (i.e. Recombinant DNA Safety Considerations (OECD, 1986)) and attempted to pare down that list to eliminate duplications as well as those topics whose meaning is unclear, and to rearrange the presentation of the topics covered to be more easily understood (the Task Group met in Vienna, 15-16 June, 2000). This document is a first draft of a proposed Consensus Document for environmental applications involving organisms from the genus Acidithiobacillus. II. General Considerations 1. Subject of Document: Species Included and Taxonomic Considerations The four species of Acidithiobacillus covered in this document were formerly placed in the genus Thiobacillus Beijerinck. In recent years several members of Thiobacillus were transferred to other genera while the remainder became part of three newly created genera, Acidithiobacillus, Halothiobacillus, Thermithiobacillus, and to the revised genus Thiobacillus sensu stricto (Kelly and Harrison, 1989; Kelly and Wood, 2000). -
Microbial Ecology of Biofiltration Units Used for the Desulfurization of Biogas
chemengineering Review Microbial Ecology of Biofiltration Units Used for the Desulfurization of Biogas Sylvie Le Borgne 1,* and Guillermo Baquerizo 2,3 1 Departamento de Procesos y Tecnología, Universidad Autónoma Metropolitana- Unidad Cuajimalpa, 05348 Ciudad de México, Mexico 2 Irstea, UR REVERSAAL, F-69626 Villeurbanne CEDEX, France 3 Departamento de Ingeniería Química, Alimentos y Ambiental, Universidad de las Américas Puebla, 72810 San Andrés Cholula, Puebla, Mexico * Correspondence: [email protected]; Tel.: +52–555–146–500 (ext. 3877) Received: 1 May 2019; Accepted: 28 June 2019; Published: 7 August 2019 Abstract: Bacterial communities’ composition, activity and robustness determines the effectiveness of biofiltration units for the desulfurization of biogas. It is therefore important to get a better understanding of the bacterial communities that coexist in biofiltration units under different operational conditions for the removal of H2S, the main reduced sulfur compound to eliminate in biogas. This review presents the main characteristics of sulfur-oxidizing chemotrophic bacteria that are the base of the biological transformation of H2S to innocuous products in biofilters. A survey of the existing biofiltration technologies in relation to H2S elimination is then presented followed by a review of the microbial ecology studies performed to date on biotrickling filter units for the treatment of H2S in biogas under aerobic and anoxic conditions. Keywords: biogas; desulfurization; hydrogen sulfide; sulfur-oxidizing bacteria; biofiltration; biotrickling filters; anoxic biofiltration; autotrophic denitrification; microbial ecology; molecular techniques 1. Introduction Biogas is a promising renewable energy source that could contribute to regional economic growth due to its indigenous local-based production together with reduced greenhouse gas emissions [1]. -
Thermithiobacillus Tepidarius DSM 3134T, a Moderately Thermophilic, Obligately Chemolithoautotrophic Member of the Acidithiobacillia
Boden et al. Standards in Genomic Sciences (2016) 11:74 DOI 10.1186/s40793-016-0188-0 SHORT GENOME REPORT Open Access Permanent draft genome of Thermithiobacillus tepidarius DSM 3134T, a moderately thermophilic, obligately chemolithoautotrophic member of the Acidithiobacillia Rich Boden1,2* , Lee P. Hutt1,2, Marcel Huntemann3, Alicia Clum3, Manoj Pillay3, Krishnaveni Palaniappan3, Neha Varghese3, Natalia Mikhailova3, Dimitrios Stamatis3, Tatiparthi Reddy3, Chew Yee Ngan3, Chris Daum3, Nicole Shapiro3, Victor Markowitz3, Natalia Ivanova3, Tanja Woyke3 and Nikos Kyrpides3 Abstract Thermithiobacillus tepidarius DSM 3134T was originally isolated (1983) from the waters of a sulfidic spring entering the Roman Baths (Temple of Sulis-Minerva) at Bath, United Kingdom and is an obligate chemolithoautotroph growing at the expense of reduced sulfur species. This strain has a genome size of 2,958,498 bp. Here we report the genome sequence, annotation and characteristics. The genome comprises 2,902 protein coding and 66 RNA coding genes. Genes responsible for the transaldolase variant of the Calvin-Benson-Bassham cycle were identified along with a biosynthetic horseshoe in lieu of Krebs’ cycle sensu stricto. Terminal oxidases were identified, viz. cytochrome c oxidase (cbb3, EC 1.9.3.1) and ubiquinol oxidase (bd, EC 1.10.3.10). Metalloresistance genes involved in pathways of arsenic and cadmium resistance were found. Evidence of horizontal gene transfer accounting for 5.9 % of the protein-coding genes was found, including transfer from Thiobacillus spp. and Methylococcus capsulatus Bath, isolated from the same spring. A sox gene cluster was found, similar in structure to those from other Acidithiobacillia – by comparison with Thiobacillus thioparus and Paracoccus denitrificans, an additional gene between soxA and soxB was found, annotated as a DUF302-family protein of unknown function. -
1 Two Pathways for Thiosulfate Oxidation in The
bioRxiv preprint doi: https://doi.org/10.1101/683490; this version posted June 27, 2019. The copyright holder for this preprint (which was not certified by peer review) is the author/funder. All rights reserved. No reuse allowed without permission. Two pathways for thiosulfate oxidation in the alphaproteobacterial chemolithotroph Paracoccus thiocyanatus SST Moidu Jameela Rameez1, Prosenjit Pyne1,$, Subhrangshu Mandal1, Sumit Chatterjee1, Masrure 5 Alam1,#, Sabyasachi Bhattacharya1, Nibendu Mondal1, Jagannath Sarkar1 and Wriddhiman Ghosh1* Addresses: Department of Microbiology, Bose Institute, P-1/12 CIT Scheme VIIM, Kolkata 700054, India. 10 Present address: $National Institute of Cholera and Enteric Diseases, P-33, C. I. T Road, Scheme XM, Beliaghata, Kolkata 700 010, India. #Department of Biological Sciences, Aliah University, IIA/27, New Town, Kolkata-700160, India. *Correspondence: [email protected] 15 Running title: Thiosulfate oxidation via tetrathionate in an alphaproteobacterium Keywords: sulfur-chemolithotrophy, Sox multienzyme system, Alphaproteobacteria, thiosulfate oxidation via tetrathionate-intermediate, thiosulfate 20 dehydrogenase, tetrathionate oxidation Abstract Chemolithotrophic bacteria oxidize various sulfur species for energy and electrons, thereby 25 operationalizing biogeochemical sulfur cycles in nature. The best-studied pathway of bacterial sulfur-chemolithotrophy, involving direct oxidation of thiosulfate to sulfate (without any free intermediate) by the SoxXAYZBCD multienzyme system, is apparently the exclusive -
Characterization of Sulfur Oxidizing Bacteria Related to Biogenic Sulfuric Acid Corrosion in Sludge Digesters Bettina Huber, Bastian Herzog, Jörg E
Huber et al. BMC Microbiology (2016) 16:153 DOI 10.1186/s12866-016-0767-7 RESEARCH ARTICLE Open Access Characterization of sulfur oxidizing bacteria related to biogenic sulfuric acid corrosion in sludge digesters Bettina Huber, Bastian Herzog, Jörg E. Drewes*, Konrad Koch and Elisabeth Müller Abstract Background: Biogenic sulfuric acid (BSA) corrosion damages sewerage and wastewater treatment facilities but is not well investigated in sludge digesters. Sulfur/sulfide oxidizing bacteria (SOB) oxidize sulfur compounds to sulfuric acid, inducing BSA corrosion. To obtain more information on BSA corrosion in sludge digesters, microbial communities from six different, BSA-damaged, digesters were analyzed using culture dependent methods and subsequent polymerase chain reaction denaturing gradient gel electrophoresis (PCR-DGGE). BSA production was determined in laboratory scale systems with mixed and pure cultures, and in-situ with concrete specimens from the digester headspace and sludge zones. Results: The SOB Acidithiobacillus thiooxidans, Thiomonas intermedia,andThiomonas perometabolis were cultivated and compared to PCR-DGGE results, revealing the presence of additional acidophilic and neutrophilic SOB. Sulfate concentrations of 10–87 mmol/L after 6–21 days of incubation (final pH 1.0–2.0)inmixedcultures,andupto 433 mmol/L after 42 days (final pH <1.0) in pure A. thiooxidans cultures showed huge sulfuric acid production potentials. Additionally, elevated sulfate concentrations in the corroded concrete of the digester headspace in contrast to the concrete of the sludge zone indicated biological sulfur/sulfide oxidation. Conclusions: The presence of SOB and confirmation of their sulfuric acid production under laboratory conditions reveal that these organisms might contribute to BSA corrosion within sludge digesters. -
Sulfur-Fueled Chemolithoautotrophs Replenish Organic Carbon Inventory
bioRxiv preprint doi: https://doi.org/10.1101/2021.01.26.428071; this version posted January 26, 2021. 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 4.0 International license. 1 Sulfur-fueled chemolithoautotrophs 2 replenish organic carbon inventory in 3 groundwater 4 Martin Taubert1,+, Beatrix M. Heinze1, Will A. Overholt1, Georgette Azemtsop2, Rola Houhou2, Nico 5 Jehmlich3, Martin von Bergen3,4, Petra Rösch2, Jürgen Popp2,5, Kirsten Küsel1,6 6 1Aquatic Geomicrobiology, Institute of Biodiversity, Friedrich Schiller University Jena, Dornburger Str. 7 159, 07743 Jena, Germany 8 2Institute of Physical Chemistry and Abbe Center of Photonics, Friedrich Schiller University Jena, 9 Helmholtzweg 4, 07743 Jena, Germany 10 3Department of Molecular Systems Biology, Helmholtz Centre for Environmental Research – UFZ, 11 Permoserstrasse 15, 04318 Leipzig, Germany 12 4Institute of Biochemistry, Faculty of Biosciences, Pharmacy and Psychology, University of Leipzig, 13 Brüderstraße 32, 04103 Leipzig, Germany 14 5Leibniz-Institute of Photonic Technology, Albert-Einstein-Straße 9, 07745 Jena, Germany 15 6German Centre for Integrative Biodiversity Research (iDiv) Halle-Jena-Leipzig, Deutscher Platz 5E, 16 04103 Leipzig, Germany 17 +Corresponding author: Martin Taubert; Tel.: +49 3641 949459; Fax: +49 3641 949402; E-mail: 18 [email protected] 13 19 Keywords: Chemolithoautotrophy, groundwater, CO2 stable isotope probing, genome-resolved 20 metaproteomics, metagenomics, Raman microspectroscopy 21 Short title: Chemolithoautotrophy in shallow groundwater 1 bioRxiv preprint doi: https://doi.org/10.1101/2021.01.26.428071; this version posted January 26, 2021. -
Physiology and Genetics of Acidithiobacillus Species: Applications for Biomining
Physiology and Genetics of Acidithiobacillus species: Applications for Biomining by Olena I. Rzhepishevska ISBN 978-91-7264-509-7 Umeå University Umeå 2008 1 2 TABLE OF CONTENTS ABSTRACT 5 ABBREVIATIONS AND CHEMICAL COMPOUNDS 6 PAPERS IN THIS THESIS 7 1. INTRODUCTION 9 1.1 General characteristics of the Acidithiobacillus genus 9 1.1.1 Classification 9 1.1.2 Natural habitats and growth requirements 9 1.1.3 Iron and RISCs in natural and mining environments 10 1.1.4 The sulphur cycle and acidithiobacilli 11 1.1.5 Genetic manipulations in Acidithiobacillus spp. 13 1.1.6 Importance in industry and other applications 14 1.2 Acidithiobacillus spp. RISC and iron oxidation 15 1.2.1 RISC oxidation by Acidithiobacillus spp. 15 1.2.2 A. ferrooxidans iron oxidation and regulation 23 1.3 Mineral sulphide oxidation 26 1.4 Acid mine and rock drainage 30 1.5 Biomining 36 1.5.1 Biomining as an industrial process 36 1.5.2 Acidophilic microorganisms in industrial bioleaching 38 2. AIMS OF THE STUDY 41 3. RESULTS AND DISCUSSION 43 4. CONCLUSIONS 51 5. ACKNOWLEDGMENTS 53 6. REFERENCES 55 7. PAPERS 75 3 4 ABSTRACT Bacteria from the genus Acidithiobacillus are often associated with biomining and acid mine drainage. Biomining utilises acidophilic, sulphur and iron oxidising microorganisms for recovery of metals from sulphidic low grade ores and concentrates. Acid mine drainage results in acidification and contamination with metals of soil and water emanating from the dissolution of metal sulphides from deposits and mine waste storage. Acidophilic microorganisms play a central role in these processes by catalysing aerobic oxidation of sulphides. -
Investigation of Biofilms Formed on Steelmaking Slags in Marine
International Journal of Molecular Sciences Article Investigation of Biofilms Formed on Steelmaking Slags in Marine Environments for Water Depuration Akiko Ogawa 1,* , Reiji Tanaka 2, Nobumitsu Hirai 1, Tatsuki Ochiai 1, Ruu Ohashi 1, Karin Fujimoto 1, Yuka Akatsuka 1 and Masanori Suzuki 3 1 National Institute of Technology (KOSEN), Suzuka College, Shiroko-cho, Suzuka, Mie 510-0294, Japan; [email protected] (N.H.); [email protected] (T.O.); [email protected] (R.O.); [email protected] (K.F.); [email protected] (Y.A.) 2 Graduate School of Bioresources, Mie University, 1577 Kurimamachiya-cho, Tsu, Mie 514-8507, Japan; [email protected] 3 Graduate School of Engineering, Osaka University, 1-1 Yamadaoka, Suita, Osaka 565-0871, Japan; [email protected] * Correspondence: [email protected]; Tel.: +81-(0)59-368-1768 Received: 21 July 2020; Accepted: 18 September 2020; Published: 22 September 2020 Abstract: Steelmaking slags are a promising resource as artificial seaweed beds for the reconstitution of marine environments. To grow seaweed well, the formation of biofilms is an essential process in biofouling. This study focused on the formation of initial biofilms on steelmaking slag samples and analyzed the resulting bacterial communities using the next-generation sequencing technique. Three types of steelmaking slag were submerged in an area of Ise Bay in Mie Prefecture, Japan, for 3 and 7 days in the summer and winter seasons to allow the formation of biofilms. The bacterial communities of these biofilms were richer in sulfur-oxidizing bacteria compared to the biofilms formed on polyurethane sponges. -
Structure, Function, and Evolution of the Thiomonas Spp. Genome
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by HAL AMU Structure, function, and evolution of the Thiomonas spp. genome. Florence Ars`ene-Ploetze, Sandrine Koechler, Marie Marchal, Jean-Yves Copp´ee,Michael Chandler, Violaine Bonnefoy, C´elineBrochier-Armanet, Mohamed Barakat, Val´erieBarbe, Fabienne Battaglia-Brunet, et al. To cite this version: Florence Ars`ene-Ploetze, Sandrine Koechler, Marie Marchal, Jean-Yves Copp´ee,Michael Chan- dler, et al.. Structure, function, and evolution of the Thiomonas spp. genome.. PLoS Genetics, Public Library of Science, 2010, 6 (2), pp.e1000859. <10.1371/journal.pgen.1000859>. <hal- 00463879> HAL Id: hal-00463879 https://hal.archives-ouvertes.fr/hal-00463879 Submitted on 29 Jun 2010 HAL is a multi-disciplinary open access L'archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destin´eeau d´ep^otet `ala diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publi´esou non, lished or not. The documents may come from ´emanant des ´etablissements d'enseignement et de teaching and research institutions in France or recherche fran¸caisou ´etrangers,des laboratoires abroad, or from public or private research centers. publics ou priv´es. Structure, Function, and Evolution of the Thiomonas spp. Genome Florence Arse`ne-Ploetze1, Sandrine Koechler1, Marie Marchal1, Jean-Yves Coppe´e2, Michael Chandler3, Violaine Bonnefoy4,Ce´line Brochier-Armanet4, Mohamed Barakat5, Vale´rie Barbe6, Fabienne Battaglia- Brunet7, Odile Bruneel8, Christopher G. Bryan1¤a, Jessica Cleiss-Arnold1, Ste´phane Cruveiller6,9, Mathieu Erhardt10, Audrey Heinrich-Salmeron1, Florence Hommais11, Catherine Joulian7, Evelyne Krin12, Aure´lie Lieutaud4, Didier Lie`vremont1, Caroline Michel7, Daniel Muller1¤b, Philippe Ortet5, Caroline Proux2, Patricia Siguier3, David Roche6,9, Zoe´ Rouy6, Gre´gory Salvignol9, Djamila Slyemi4, Emmanuel Talla4, Ste´phanie Weiss1, Jean Weissenbach6,9, Claudine Me´digue6,9, Philippe N. -
Thiobacillus Prosperus’ Huber and Stetter 1989 As Acidihalobacter Prosperus Gen
International Journal of Systematic and Evolutionary Microbiology (2015), 65, 3641–3644 DOI 10.1099/ijsem.0.000468 Reclassification of ‘Thiobacillus prosperus’ Huber and Stetter 1989 as Acidihalobacter prosperus gen. nov., sp. nov., a member of the family Ectothiorhodospiraceae Juan Pablo Ca´rdenas,1,2,3 Rodrigo Ortiz,1,3 Paul R. Norris,4 Elizabeth Watkin5 and David S. Holmes1,2 Correspondence 1Departamento de Ciencias Biologicas, Facultad de Ciencias Biologicas, Universidad Andres Bello, David S. Holmes Santiago, Chile [email protected] 2Center for Bioinformatics and Genome Biology, Fundacion Ciencia & Vida, Santiago, Chile 3Laboratorio de Ecofisiologı´a Microbiana, Fundacion Ciencia & Vida, Santiago, Chile 4Environment and Sustainability Institute, University of Exeter, UK 5School of Biomedical Sciences, Curtin University, Perth, Australia Analysis of phylogenomic metrics of a recently released draft genome sequence of the halotolerant, acidophile ‘Thiobacillus prosperus’ DSM 5130 indicates that it is not a member of the genus Thiobacillus within the class Betaproteobacteria as originally proposed. Based on data from 16S rRNA gene phylogeny, and analyses of multiprotein phylogeny and average nucleotide identity (ANI), we show that it belongs to a new genus within the family Ectothiorhodospiraceae, for which we propose the name Acidihalobacter gen. nov. In accordance, it is proposed that ‘Thiobacillus prosperus’ DSM 5130 be named Acidihalobacter prosperus gen. nov., sp. nov. DSM 5130T (5JCM 30709T) and that it becomes the type strain of the type species of this genus. ‘Thiobacillus prosperus’ DSM 5130, is a halotolerant 2000) and the genus Acidithiobacillus was moved out of (growth with up to 0.6 M NaCl) acidophile (,pH 3) the class Gammaproteobacteria into the class Acidithiobacil- that was isolated from a geothermally heated seafloor at lia (Williams & Kelly, 2013). -
Standards in Genomic Sciences
View metadata, citation and similar papers at core.ac.uk brought to you by CORE provided by Plymouth Electronic Archive and Research Library Standards in Genomic Sciences Permanent draft genome of Thiobacillus thioparus DSM 505T, an obligately chemolithoautotrophic member of the Betaproteobacteria --Manuscript Draft-- Manuscript Number: SIGS-D-16-00109R3 Full Title: Permanent draft genome of Thiobacillus thioparus DSM 505T, an obligately chemolithoautotrophic member of the Betaproteobacteria Article Type: Short genome report Funding Information: U.S. Department of Energy Dr Nikos C Kyrpides (DE-AC02-05CH11231) Royal Society Dr Rich Boden (RG120444) Abstract: Thiobacillus thioparus DSM 505T is one of first two isolated strains of inorganic sulfur- oxidising Bacteria. The original strain of T. thioparus was lost almost 100 years ago and the working type strain is Culture CT (=DSM 505T = ATCC 8158T) isolated by Starkey in 1934 from agricultural soil at Rutgers University, New Jersey, USA. It is an obligate chemolithoautotroph that conserves energy from the oxidation of reduced inorganic sulfur compounds using the Kelly-Trudinger pathway and uses it to fix carbon dioxide It is not capable of heterotrophic or mixotrophic growth. The strain has a genome size of 3,201,518 bp. Here we report the genome sequence, annotation and characteristics. The genome contains 3,135 protein coding and 62 RNA coding genes. Genes encoding the transaldolase variant of the Calvin-Benson-Bassham cycle were also identified and an operon encoding carboxysomes, along with Smith's biosynthetic horseshoe in lieu of Krebs' cycle sensu stricto. Terminal oxidases were identified, viz. cytochrome c oxidase (cbb3, EC 1.9.3.1) and ubiquinol oxidase (bd, EC 1.10.3.10). -
Genomic Analyses of Novel Iron-Oxidizing Thiomonas
GENOMIC ANALYSES OF NOVEL IRON-OXIDIZING THIOMONAS ISOLATES FROM ACID MINE DRAINAGE by Michelle Hallenbeck A thesis submitted to the Faculty of the University of Delaware in partial fulfillment of the requirements for the degree of Honors Bachelor of Science in Biological Sciences with a concentration in Cell & Molecular Biology and Genetics with Distinction Spring 2019 © 2019 Hallenbeck All Rights Reserved i GENOMIC ANALYSES OF NOVEL IRON-OXIDIZING THIOMONAS ISOLATES FROM ACID MINE DRAINAGE by Michelle Hallenbeck Approved: __________________________________________________________ Clara Chan, Ph.D. Professor in charge of thesis on behalf of the Advisory Committee Approved: __________________________________________________________ Fidelma Boyd, Ph.D. Committee member from the Department of Biological Sciences Approved: __________________________________________________________ Christopher Kloxin, Ph.D. Committee member from the Board of Senior Thesis Readers Approved: __________________________________________________________ Earl Lee II, Ph.D. Deputy Faculty Director, University Honors Program ii ACKNOWLEDGMENTS "A scientist lives with all of reality. There is nothing better. To know reality is to accept it and eventually to love it." -Sir Charles Scott Sherrington This thesis would not have been possible without the aid and assistance of so many people. First, I want to thank my advisor, Dr. Clara Chan, for supporting my growth as a scientist and providing valuable mentorship and guidance. I would like to thank our collaborators, Dr. Denise Akob and Dr. Kirsten Küsel, for providing us with the FB strains and their genomes. I would also like to thank the other members of my committee, Dr. Fidelma Boyd and Dr. Christopher Kloxin, for taking the time to read my thesis and to support my undergraduate research career.