Extremophiles
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												  Diversity of Bacteria and Archaea in the Deep-Sea Low-Temperature Hydrothermal Sulfide Chimney of the Northeastern Pacific OceanAfrican Journal of Biotechnology Vol. 11(2), pp. 337-345, 5 January, 2012 Available online at http://www.academicjournals.org/AJB DOI: 10.5897/AJB11.2692 ISSN 1684–5315 © 2012 Academic Journals Full Length Research Paper Diversity of bacteria and archaea in the deep-sea low-temperature hydrothermal sulfide chimney of the Northeastern Pacific Ocean Xia Ding1*, Xiao-Jue Peng1#, Xiao-Tong Peng2 and Huai-Yang Zhou3 1College of Life Sciences and Key Laboratory of Poyang Lake Environment and Resource Utilization, Ministry of Education, Nanchang University, Nanchang 330031, China. 2Guangzhou Institute of Geochemistry, Chinese Academy of Sciences, Guangzhou 510640, China. 3National Key Laboratory of Marine Geology, Tongji University, Shanghai 200092, China. Accepted 4 November, 2011 Our knowledge of the diversity and role of hydrothermal vents microorganisms has considerably expanded over the past decade, while little is known about the diversity of microorganisms in low-temperature hydrothermal sulfide chimney. In this study, denaturing gradient gel electrophoresis (DGGE) and 16S rDNA sequencing were used to examine the abundance and diversity of microorganisms from the exterior to the interior of the deep sea low-temperature hydrothermal sulfide chimney of the Northeastern Pacific Ocean. DGGE profiles revealed that both bacteria and archaea could be examined in all three zones of the chimney wall and the compositions of microbial communities within different zones were vastly different. Overall, for archaea, cell abundance was greatest in the outermost zone of the chimney wall. For bacteria, there was no significant difference in cell abundance among three zones. In addition, phylogenetic analysis revealed that Verrucomicrobia and Deltaproteobacteria were the predominant bacterial members in exterior zone, beta Proteobacteria were the dominant members in middle zone, and Bacillus were the abundant microorganisms in interior zone.
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												  Extremozymes of the Hot and Salty Halothermothrix OreniiExtremozymes of the Hot and Salty Halothermothrix orenii Author Kori, Lokesh D Published 2012 Thesis Type Thesis (PhD Doctorate) School School of Biomolecular and Physical Sciences DOI https://doi.org/10.25904/1912/2191 Copyright Statement The author owns the copyright in this thesis, unless stated otherwise. Downloaded from http://hdl.handle.net/10072/366220 Griffith Research Online https://research-repository.griffith.edu.au Extremozymes of the hot and salty Halothermothrix orenii LOKESH D. KORI (M.Sc. Biotechnology) School of Biomolecular and Physical Sciences Science, Environment, Engineering and Technology Griffith University, Australia Submitted in fulfillment of the requirements of the degree of Doctor of Philosophy December 2011 STATEMENT OF ORIGINALITY STATEMENT OF ORIGINALITY This work has not previously been submitted for a degree or diploma in any university. To the best of my knowledge and belief, the thesis contains no material previously published or written by another person except where due reference is made in the thesis itself. LOKESH DULICHAND KORI II ACKNOWLEDGEMENTS ACKNOWLEDGEMENTS I owe my deepest gratitude to my supervisor Prof. Bharat Patel, for offering me an opportunity for being his postgraduate. His boundless knowledge motivates me for keep going and enjoy the essence of science. Without his guidance, great patience and advice, I could not finish my PhD program successfully. I take this opportunity to give my heartiest thanks to Assoc. Prof. Andreas Hofmann, (Structural Chemistry, Eskitis Institute for Cell & Molecular Therapies, Griffith University) for his support and encouragement for crystallographic work. I am grateful to him for teaching me about the protein structures, in silico analysis and their hidden chemistry.
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												  Where Less May Be More: How the Rare Biosphere Pulls Ecosystems StringsThe ISME Journal (2017) 11, 853–862 OPEN © 2017 International Society for Microbial Ecology All rights reserved 1751-7362/17 www.nature.com/ismej MINI REVIEW Where less may be more: how the rare biosphere pulls ecosystems strings Alexandre Jousset1, Christina Bienhold2,3, Antonis Chatzinotas4,5, Laure Gallien6,7, Angélique Gobet8, Viola Kurm9, Kirsten Küsel10,5, Matthias C Rillig11,12, Damian W Rivett13, Joana F Salles14, Marcel GA van der Heijden15,16,17, Noha H Youssef18, Xiaowei Zhang19, Zhong Wei20 and WH Gera Hol9 1Utrecht University, Department of Biology, Institute of Environmental Biology, Ecology and Biodiversity Group, Utrecht, The Netherlands; 2Alfred Wegener Institute Helmholtz Centre for Polar and Marine Research, Bremerhaven, Germany; 3Max Planck Institute for Marine Microbiology, Bremen, Germany; 4Helmholtz Centre for Environmental Research – UFZ, Leipzig, Germany; 5German Centre for Integrative Biodiversity Research (iDiv), Halle-Jena-Leipzig, Leipzig, Germany; 6Swiss Federal Institute for Forest, Snow and Landscape Research WSL, Birmensdorf, Switzerland; 7Center for Invasion Biology, Department of Botany & Zoology, Stellenbosch University, Matieland, South Africa; 8Sorbonne Universités, UPMC Université Paris 06, CNRS, UMR 8227, Integrative Biology of Marine Models, Station Biologique de Roscoff, F-29688, Roscoff Cedex, France; 9Netherlands Institute of Ecology, Department of Terrestrial Ecology, Wageningen, The Netherlands; 10Friedrich Schiller University Jena, Institute of Ecology, Jena, Germany; 11Freie Universtät Berlin,
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												  Experimental and Statistical Analysis of Nutritional Requirements for the Growth of the Extremophile Deinococcus Geothermalis DSM 11300Experimental and statistical analysis of nutritional requirements for the growth of the extremophile Deinococcus geothermalis DSM 11300 Julie Bornot, Cesar Arturo Aceves-Lara, Carole Molina-Jouve, Jean-Louis Uribelarrea, Nathalie Gorret To cite this version: Julie Bornot, Cesar Arturo Aceves-Lara, Carole Molina-Jouve, Jean-Louis Uribelarrea, Nathalie Gor- ret. Experimental and statistical analysis of nutritional requirements for the growth of the ex- tremophile Deinococcus geothermalis DSM 11300. Extremophiles, Springer Verlag, 2014, 18 (6), pp.1009-1021. 10.1007/s00792-014-0671-8. hal-01268947 HAL Id: hal-01268947 https://hal.archives-ouvertes.fr/hal-01268947 Submitted on 11 Mar 2019 HAL is a multi-disciplinary open access L’archive ouverte pluridisciplinaire HAL, est archive for the deposit and dissemination of sci- destinée au dépôt et à la diffusion de documents entific research documents, whether they are pub- scientifiques de niveau recherche, publiés ou non, lished or not. The documents may come from émanant des établissements d’enseignement et de teaching and research institutions in France or recherche français ou étrangers, des laboratoires abroad, or from public or private research centers. publics ou privés. OATAO is an open access repository that collects the work of Toulouse researchers and makes it freely available over the web where possible This is an author’s version published in: http://oatao.univ-toulouse.fr/22999 Official URL: https://doi.org/10.1007/s00792-014-0671-8 To cite this version: Bornot, Julie and Aceves-Lara, César-Arturo and Molina-Jouve, Carole and Uribelarrea, Jean-Louis and Gorret, Nathalie Experimental and statistical analysis of nutritional requirements for the growth of the extremophile Deinococcus geothermalis DSM 11300.
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												  A Virus That Infects a Hyperthermophile Encapsidates A-FormRESEARCH | REPORTS we observe sets of regulatory sites that exhibit Illumina, Inc. One or more embodiments of one or more patents SUPPLEMENTARY MATERIALS patterns of coordinated regulation (e.g., LYN, and patent applications filed by Illumina may encompass the www.sciencemag.org/content/348/6237/910/suppl/DC1 encoding a tyrosine kinase involved in B cell methods, reagents, and data disclosed in this manuscript. All Materials and Methods methods for making the transposase complexes are described in signaling) (Fig. 4B), although reproducibility of Figs. S1 to S22 (18); however, Illumina will provide transposase complexes in Tables S1 and S2 these patterns across biological replicates was response to reasonable requests from the scientific community References (24–39) modest (fig. S22). Given the sparsity of the data, subject to a material transfer agreement. Some work in this study identifying pairs of coaccessible DNA elements is related to technology described in patent applications 19 March 2015; accepted 24 April 2015 WO2014142850, 2014/0194324, 2010/0120098, 2011/0287435, Published online 7 May 2015; within individual loci is statistically challenging 2013/0196860, and 2012/0208705. 10.1126/science.aab1601 and merits further development. We report chromatin accessibility maps for >15,000 single cells. Our combinatorial cellular indexing scheme could feasibly be scaled to col- VIROLOGY lect data from ~17,280 cells per experiment by using 384-by-384 barcoding and sorting 100 nu- clei per well (assuming similar cell recovery and A virus that infects a collision rates) (fig. S1) (19). Particularly as large- scale efforts to build a human cell atlas are con- templated (23), it is worth noting that because hyperthermophile encapsidates DNA is at uniform copy number, single-cell chro- matin accessibility mapping may require far fewer A-form DNA reads per single cell to define cell types, relative to single-cell RNA-seq.
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												  Life at Acidic Ph Imposes an Increased Energetic Cost for a Eukaryotic Acidophile Mark ACORE Metadata, citation and similar papers at core.ac.uk Provided by e-Prints Soton The Journal of Experimental Biology 208, 2569-2579 2569 Published by The Company of Biologists 2005 doi:10.1242/jeb.01660 Life at acidic pH imposes an increased energetic cost for a eukaryotic acidophile Mark A. Messerli1,2,*, Linda A. Amaral-Zettler1, Erik Zettler3,4, Sung-Kwon Jung2, Peter J. S. Smith2 and Mitchell L. Sogin1 1The Josephine Bay Paul Center for Comparative Molecular Biology and Evolution, Marine Biological Laboratory, Woods Hole, MA 02543, USA, 2BioCurrents Research Center, Program in Molecular Physiology, Marine Biological Laboratory, Woods Hole, MA 02543, USA, 3Sea Education Association, PO Box 6, Woods Hole, MA 02543, USA and 4Centro de Biología Molecular, Universidad Autónoma de Madrid, Cantoblanco, Madrid 28049, Spain *Author for correspondence (e-mail: [email protected]) Accepted 25 April 2005 Summary Organisms growing in acidic environments, pH·<3, potential difference of Chlamydomonas sp., measured would be expected to possess fundamentally different using intracellular electrodes at both pH·2 and 7, is close molecular structures and physiological controls in to 0·mV, a rare value for plants, animals and protists. The comparison with similar species restricted to neutral pH. 40·000-fold difference in [H+] could be the result of either We begin to investigate this premise by determining the active or passive mechanisms. Evidence for active magnitude of the transmembrane electrochemical H+ maintenance was detected by monitoring the rate of ATP gradient in an acidophilic Chlamydomonas sp. (ATCC® consumption. At the peak, cells consume about 7% more PRA-125) isolated from the Rio Tinto, a heavy metal ATP per second in medium at pH·2 than at pH·7.
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												  FORMATION of HABITABLE WORLDS and FATE of HABITABLE ENVIRONMENTS 6:00 P.M45th Lunar and Planetary Science Conference (2014) sess726.pdf Thursday, March 20, 2014 [R726] POSTER SESSION: FORMATION OF HABITABLE WORLDS AND FATE OF HABITABLE ENVIRONMENTS 6:00 p.m. Town Center Exhibit Area Johnson T. A. Park A. Hand K. P. POSTER LOCATION #473 The Workman-Reynolds Effect: An Investigation of the Ice-Water Interface of Dilute Salt Solutions [#1672] We report on experiments on the voltage potential that results from rapidly freezing dilute aqueous solutions. These results have application to icy satellites. Taylor A. R. Olsen A. A. Hausrath E. M. POSTER LOCATION #474 Serpentinite Dissolution: An Analog to Mantle-Ocean Interaction on Europa [#1903] Laboratory-based dissolution experiments between serpentinite rock and a variety of acids represent mantle-ocean interaction on the jovian moon, Europa. Hausrath E. M. Adcock C. T. Elwood Madden M. E. Gainey S. R. Olsen A. A. et al. POSTER LOCATION #475 Using Geochemical Kinetics to Interpret Potential Habitability [#2376] Geochemical kinetics can help shed light on factors affecting habitability, including water, release of nutrients, redox, pH, temperature, and ionic strength. Som S. M. Fristad K. E. Hoehler T. M. POSTER LOCATION #476 An Integrative Approach to Assessing Habitability of H2 Metabolisms in Hydrothermal Springs [#2828] We present an ongoing project that surveys H2 from springs sourced in rocks of varying silica content and in parallel investigate habitability numerically. Djordjevic S. Mickol R. L. Kral T. A. POSTER LOCATION #477 Simulating Martian Conditions: Methanogen Survivability During Freeze-Thaw Cycles [#2539] Methanogens are obligate anaerobes that tolerate a wide range of conditions. It is proposed that these Archaea are able to persist in a martian environment.
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												  Analysis of a Multicomponent Thermostable DNA Polymerase III Replicase from an Extreme Thermophile*THE JOURNAL OF BIOLOGICAL CHEMISTRY Vol. 277, No. 19, Issue of May 10, pp. 17334–17348, 2002 © 2002 by The American Society for Biochemistry and Molecular Biology, Inc. Printed in U.S.A. Analysis of a Multicomponent Thermostable DNA Polymerase III Replicase from an Extreme Thermophile* Received for publication, October 23, 2001, and in revised form, February 18, 2002 Published, JBC Papers in Press, February 21, 2002, DOI 10.1074/jbc.M110198200 Irina Bruck‡, Alexander Yuzhakov§¶, Olga Yurieva§, David Jeruzalmi§, Maija Skangalis‡§, John Kuriyan‡§, and Mike O’Donnell‡§ʈ From §The Rockefeller University and ‡Howard Hughes Medical Institute, New York, New York 10021 This report takes a proteomic/genomic approach to polymerase III (pol III) structure and function has been ob- characterize the DNA polymerase III replication appa- tained from studies of the Escherichia coli replicase, DNA ratus of the extreme thermophile, Aquifex aeolicus. polymerase III holoenzyme (reviewed in Ref. 6). Therefore, a Genes (dnaX, holA, and holB) encoding the subunits re- brief overview of its structure and function is instructive for the  ␦ ␦ quired for clamp loading activity ( , , and ) were iden- comparisons to be made in this report. In E. coli, the catalytic Downloaded from tified. The dnaX gene produces only the full-length subunit of DNA polymerase III is the ␣ subunit (129.9 kDa)  product, , and therefore differs from Escherichia coli encoded by dnaE; it lacks a proofreading exonuclease (7). The dnaX that produces two proteins (␥ and ). Nonetheless, Ј Ј ⑀ ␦␦ proofreading 3 –5 -exonuclease activity is contained in the the A. aeolicus proteins form a complex. The dnaN ␣ ,␦␦ (27.5 kDa) subunit (dnaQ) that forms a 1:1 complex with (8  gene encoding the clamp was identified, and the ␣Ϫ⑀  9).
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												  Dynamic Consolidated Bioprocessing for Innovative Lab-Scale Production of Bacterial Alkaline Phosphatase from Bacillus Paralichewww.nature.com/scientificreports OPEN Dynamic consolidated bioprocessing for innovative lab‑scale production of bacterial alkaline phosphatase from Bacillus paralicheniformis strain APSO Soad A. Abdelgalil1,2*, Nadia A. Soliman1, Gaber A. Abo‑Zaid1 & Yasser R. Abdel‑Fattah1 To meet the present and forecasted market demand, bacterial alkaline phosphatase (ALP) production must be increased through innovative and efcient production strategies. Using sugarcane molasses and biogenic apatite as low‑cost and easily available raw materials, this work demonstrates the scalability of ALP production from a newfound Bacillus paralicheniformis strain APSO isolated from a black liquor sample. Mathematical experimental designs including sequential Plackett– Burman followed by rotatable central composite designs were employed to select and optimize the concentrations of the statistically signifcant media components, which were determined to be molasses, (NH4)2NO3, and KCl. Batch cultivation in a 7‑L stirred‑tank bioreactor under uncontrolled pH conditions using the optimized medium resulted in a signifcant increase in both the volumetric and specifc productivities of ALP; the alkaline phosphatase throughput 6650.9 U L−1, and µ = 0.0943 h−1; respectively, were obtained after 8 h that, ameliorated more than 20.96, 70.12 and 94 folds compared to basal media, PBD, and RCCD; respectively. However, neither the increased cell growth nor enhanced productivity of ALP was present under the pH‑controlled batch cultivation. Overall, this work presents novel strategies for the statistical optimization and scaling up of bacterial ALP production using biogenic apatite. Te bioeconomy represents the value chain of sustainable manufacturing using renewable, low-cost biological resources to sustainably produce food, energy, and industrial products1.
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												  Diversity of Halophilic Archaea in Fermented Foods and Human Intestines and Their Application Han-Seung Lee1,2*J. Microbiol. Biotechnol. (2013), 23(12), 1645–1653 http://dx.doi.org/10.4014/jmb.1308.08015 Research Article Minireview jmb Diversity of Halophilic Archaea in Fermented Foods and Human Intestines and Their Application Han-Seung Lee1,2* 1Department of Bio-Food Materials, College of Medical and Life Sciences, Silla University, Busan 617-736, Republic of Korea 2Research Center for Extremophiles, Silla University, Busan 617-736, Republic of Korea Received: August 8, 2013 Revised: September 6, 2013 Archaea are prokaryotic organisms distinct from bacteria in the structural and molecular Accepted: September 9, 2013 biological sense, and these microorganisms are known to thrive mostly at extreme environments. In particular, most studies on halophilic archaea have been focused on environmental and ecological researches. However, new species of halophilic archaea are First published online being isolated and identified from high salt-fermented foods consumed by humans, and it has September 10, 2013 been found that various types of halophilic archaea exist in food products by culture- *Corresponding author independent molecular biological methods. In addition, even if the numbers are not quite Phone: +82-51-999-6308; high, DNAs of various halophilic archaea are being detected in human intestines and much Fax: +82-51-999-5458; interest is given to their possible roles. This review aims to summarize the types and E-mail: [email protected] characteristics of halophilic archaea reported to be present in foods and human intestines and pISSN 1017-7825, eISSN 1738-8872 to discuss their application as well. Copyright© 2013 by The Korean Society for Microbiology Keywords: Halophilic archaea, fermented foods, microbiome, human intestine, Halorubrum and Biotechnology Introduction Depending on the optimal salt concentration needed for the growth of strains, halophilic microorganisms can be Archaea refer to prokaryotes that used to be categorized classified as halotolerant (~0.3 M), halophilic (0.2~2.0 M), as archaeabacteria, a type of bacteria, in the past.
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												  Extremely Thermophilic Microorganisms As Metabolic Engineering Platforms for Production of Fuels and Industrial ChemicalsREVIEW published: 05 November 2015 doi: 10.3389/fmicb.2015.01209 Extremely thermophilic microorganisms as metabolic engineering platforms for production of fuels and industrial chemicals Benjamin M. Zeldes 1, Matthew W. Keller 2, Andrew J. Loder 1, Christopher T. Straub 1, Michael W. W. Adams 2 and Robert M. Kelly 1* 1 Department of Chemical and Biomolecular Engineering, North Carolina State University, Raleigh, NC, USA, 2 Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA, USA Enzymes from extremely thermophilic microorganisms have been of technological interest for some time because of their ability to catalyze reactions of industrial significance at elevated temperatures. Thermophilic enzymes are now routinely produced in recombinant mesophilic hosts for use as discrete biocatalysts. Genome and metagenome sequence data for extreme thermophiles provide useful information for putative biocatalysts for a wide range of biotransformations, albeit involving at most a few enzymatic steps. However, in the past several years, unprecedented progress has been made in establishing molecular genetics tools for extreme thermophiles to the point Edited by: that the use of these microorganisms as metabolic engineering platforms has become Bettina Siebers, University of Duisburg-Essen, possible. While in its early days, complex metabolic pathways have been altered or Germany engineered into recombinant extreme thermophiles, such that the production of fuels and Reviewed by: chemicals at elevated temperatures has become possible. Not only does this expand the Haruyuki Atomi, thermal range for industrial biotechnology, it also potentially provides biodiverse options Kyoto University, Japan Phillip Craig Wright, for specific biotransformations unique to these microorganisms. The list of extreme University of Sheffield, UK thermophiles growing optimally between 70 and 100◦C with genetic toolkits currently *Correspondence: available includes archaea and bacteria, aerobes and anaerobes, coming from genera Robert M.
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												  Extreme Organisms on Earth Show Us Just How Weird Life Elsewhere Could Be. by Chris Impey AstrobiologyAstrobiology Extreme organisms on Earth show us just how weird life elsewhere could be. by Chris Impey How life could thrive on hostile worlds Humans have left their mark all over Earth. We’re proud of our role as nature’s generalists — perhaps not as swift as the gazelle or as strong as the gorilla, but still pretty good at most things. Alone among all species, technology has given us dominion over the planet. Humans are endlessly plucky and adaptable; it seems we can do anything. Strain 121 Yet in truth, we’re frail. From our safe living rooms, we may admire the people who conquer Everest or cross deserts. But without technology, we couldn’t live beyond Earth’s temperate zones. We cannot survive for long in temperatures below freezing or above 104° Fahrenheit (40° Celsius). We can stay underwater only as long as we can hold our breath. Without water to drink we’d die in 3 days. Microbes, on the other hand, are hardy. And within the microbial world lies a band of extremists, organisms that thrive in conditions that would cook, crush, smother, and dissolve most other forms of life. Collectively, they are known as extremophiles, which means, literally, “lovers of extremes.” Extremophiles are found at temperatures above the boiling point and below the freezing point of water, in high salinity, and in strongly acidic conditions. Some can live deep inside rock, and others can go into a freeze-dried “wait state” for tens of thousands of years. Some of these microbes harvest energy from meth- ane, sulfur, and even iron.