Download Life in the Extreme Activity, Including Cards
Total Page:16
File Type:pdf, Size:1020Kb
Load more
Recommended publications
-
Where Less May Be More: How the Rare Biosphere Pulls Ecosystems Strings
The 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, -
Experimental and Statistical Analysis of Nutritional Requirements for the Growth of the Extremophile Deinococcus Geothermalis DSM 11300
Experimental 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. -
Microbial Interactions with Arsenite, Hydrogen and Sulfide In
MICROBIAL INTERACTIONS WITH ARSENITE, HYDROGEN AND SULFIDE IN AN ACID-SULFATE-CHLORIDE GEOTHERMAL SPRING by Seth D’Imperio A dissertation submitted in partial fulfillment of the requirements for the degree of Doctor of Philosophy in Ecology and Environmental Sciences MONTANA STATE UNIVERSITY Bozeman, Montana April, 2008 ©COPYRIGHT by Seth D’Imperio 2008 All Rights Reserved ii APPROVAL of a dissertation submitted by Seth D’Imperio This dissertation has been read by each member of the dissertation committee and has been found to be satisfactory regarding content, English usage, format, citation, bibliographic style, and consistency, and is ready for submission to the Division of Graduate Education. Dr. Timothy R. McDermott Approved for the Department Land Resources and Environmental Science Dr. Jon M. Wraith Approved for the Division of Graduate Education Dr. Carl A. Fox iii STATEMENT OF PERMISSION TO USE In presenting this dissertation in partial fulfillment of the requirements for a doctoral degree at Montana State University, I agree that the Library shall make it available to borrowers under rules of the Library. I further agree that copying of this dissertation is allowable only for scholarly purposes, consistent with “fair use” as prescribed in the U.S. Copyright Law. Requests for extensive copying or reproduction of this dissertation should be referred to ProQuest Information and Learning, 300 North Zeeb Road, Ann Arbor, Michigan 48106, to whom I have granted “the exclusive right to reproduce and distribute my dissertation in and from microform along with the non- exclusive right to reproduce and distribute my abstract in any format in whole or in part.” Seth D’Imperio April 2008 iv ACKNOWLEDGEMENTS Firstly, I would like to thank Dr. -
Life at Acidic Ph Imposes an Increased Energetic Cost for a Eukaryotic Acidophile Mark A
CORE 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. -
Role of Chemolithoautotrophic Microorganisms Involved in Nitrogen and Sulfur Cycling in Coastal Marine Sediments
Role of chemolithoautotrophic microorganisms involved in nitrogen and sulfur cycling in coastal marine sediments Yvonne Antonia Lipsewers THIS RESEARCH WAS FINANCIALLY SUPPORTED BY DARWIN CENTER FOR BIOGEOSCIENCES NIOZ – ROYAL NETHERLANDS INSTITUTE FOR SEA RESEARCH ISBN: 978-90-6266-492-4 Cover photos: S. Rampen, L. Villanueva, M. van der Meer Printed by Ipskamp Printing, The Netherlands Role of chemolithoautotrophic microorganisms involved in nitrogen and sulfur cycling in coastal marine sediments De rol van chemolithoautotrofe micro-organismen die deelnemen in de stikstof- en zwavelcyclus in mariene kustsedimenten (met een samenvatting in het Nederlands) Proefschrift ter verkrijging van de graad van doctor aan de Universiteit Utrecht op gezag van de rector magnificus, prof.dr. G.J. van der Zwaan, ingevolge het besluit van het college voor promoties in het openbaar te verdedigen op dinsdag 5 december 2017 des ochtends te 10.30 uur door Yvonne Antonia Lipsewers geboren op 18 juli 1977 te Salzkotten, Duitsland Promotor: Prof. dr. ir. J.S. Sinninghe Damsté Copromotor: Dr. L. Villanueva „Hinterher ist man immer schlauer…“ Für meine Familie Table of contents Chapter 1 – Introduction .....................................................................................................1 Chapter 2 – Seasonality and depth distribution of the abundance and activity of am- monia oxidizing microorganisms in marine coastal sediments (North Sea) ..........23 Chapter 3 – Lack of 13C-label incorporation suggests low turnover rates of thaumar- chaeal intact -
Science and Innovation: the Under-Fueled Engine of Prosperity
Science and Innovation: The Under-Fueled Engine of Prosperity JULY 14, 2021 AUTHOR Benjamin F. Jones* ABSTRACT Science and innovation are central to human progress and national economic success. Currently, the United States invests 2.8% of GDP in research and development, which is supported by a range of public policies. This paper asks whether the United States invests enough. To answer that question, the conceptual case for government intervention and skepticism about that case are reviewed. The paper then turns to systematic evidence, including the very latest evidence, regarding the operation of the science and innovation system and its social returns. This evidence suggests a clear answer: We massively underinvest in science and innovation, with implications for our standards of living, health, national competitiveness, and capacity to respond to crisis. * Kellogg School of Management and National Bureau of Economic Research. Email: [email protected]. 1. Introduction Scientific and technological advances have long been recognized as engines of economic growth and rising prosperity. The fruits of these advances—instantaneous global communications, vaccines, airplanes, heart surgery, computers, skyscrapers, industrial robots, on-demand entertainment, to name a few—might seem almost magical to our ancestors from not-too-many generations ago. The power of this progress has been broadly evident since the Industrial Revolution and was recognized at the time, including by political leaders. As the British Prime Minister Benjamin Disraeli noted in 1873, “How much has happened in these fifty years … I am thinking of those revolutions of science which … have changed the position and prospects of mankind more than all the conquests and all the codes and all the legislators that ever lived.” Disraeli was talking of things like the steam engine, the telegraph, and textile manufacturing. -
Life at Low Water Activity
Published online 12 July 2004 Life at low water activity W. D. Grant Department of Infection, Immunity and Inflammation, University of Leicester, Maurice Shock Building, University Road, Leicester LE1 9HN, UK ([email protected]) Two major types of environment provide habitats for the most xerophilic organisms known: foods pre- served by some form of dehydration or enhanced sugar levels, and hypersaline sites where water availability is limited by a high concentration of salts (usually NaCl). These environments are essentially microbial habitats, with high-sugar foods being dominated by xerophilic (sometimes called osmophilic) filamentous fungi and yeasts, some of which are capable of growth at a water activity (aw) of 0.61, the lowest aw value for growth recorded to date. By contrast, high-salt environments are almost exclusively populated by prokaryotes, notably the haloarchaea, capable of growing in saturated NaCl (aw 0.75). Different strategies are employed for combating the osmotic stress imposed by high levels of solutes in the environment. Eukaryotes and most prokaryotes synthesize or accumulate organic so-called ‘compatible solutes’ (osmolytes) that have counterbalancing osmotic potential. A restricted range of bacteria and the haloar- chaea counterbalance osmotic stress imposed by NaCl by accumulating equivalent amounts of KCl. Haloarchaea become entrapped and survive for long periods inside halite (NaCl) crystals. They are also found in ancient subterranean halite (NaCl) deposits, leading to speculation about survival over geological time periods. Keywords: xerophiles; halophiles; haloarchaea; hypersaline lakes; osmoadaptation; microbial longevity 1. INTRODUCTION aw = P/P0 = n1/n1 ϩ n2, There are two major types of environment in which water where n is moles of solvent (water); n is moles of solute; availability can become limiting for an organism. -
Extreme Organisms on Earth Show Us Just How Weird Life Elsewhere Could Be. by Chris Impey Astrobiology
Astrobiology 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. -
Marine Extremophiles: a Source of Hydrolases for Biotechnological Applications
Mar. Drugs 2015, 13, 1925-1965; doi:10.3390/md13041925 OPEN ACCESS marine drugs ISSN 1660-3397 www.mdpi.com/journal/marinedrugs Article Marine Extremophiles: A Source of Hydrolases for Biotechnological Applications Gabriel Zamith Leal Dalmaso 1,2, Davis Ferreira 3 and Alane Beatriz Vermelho 1,* 1 BIOINOVAR—Biotechnology laboratories: Biocatalysis, Bioproducts and Bioenergy, Institute of Microbiology Paulo de Góes, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, 373, 21941-902 Rio de Janeiro, Brazil; E-Mail: [email protected] 2 Graduate Program in Plant Biotechnology, Health and Science Centre, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, 373, 21941-902 Rio de Janeiro, Brazil 3 BIOINOVAR—Biotechnology Laboratories: Virus-Cell Interaction, Institute of Microbiology Paulo de Góes, Federal University of Rio de Janeiro, Av. Carlos Chagas Filho, 373, 21941-902 Rio de Janeiro, Brazil; E-Mail: [email protected] * Author to whom correspondence should be addressed; E-Mail: [email protected]; Tel.: +55-(21)-3936-6743; Fax: +55-(21)-2560-8344. Academic Editor: Kirk Gustafson Received: 1 December 2014 / Accepted: 25 March 2015 / Published: 3 April 2015 Abstract: The marine environment covers almost three quarters of the planet and is where evolution took its first steps. Extremophile microorganisms are found in several extreme marine environments, such as hydrothermal vents, hot springs, salty lakes and deep-sea floors. The ability of these microorganisms to support extremes of temperature, salinity and pressure demonstrates their great potential for biotechnological processes. Hydrolases including amylases, cellulases, peptidases and lipases from hyperthermophiles, psychrophiles, halophiles and piezophiles have been investigated for these reasons. -
A DNA Ligase from the Psychrophile Pseudoalteromonas Haloplanktis Gives Insights Into the Adaptation of Proteins to Low Temperatures
Eur. J. Biochem. 267, 3502±3512 (2000) q FEBS 2000 A DNA ligase from the psychrophile Pseudoalteromonas haloplanktis gives insights into the adaptation of proteins to low temperatures D. Georlette1,Z.O.JoÂnsson2,3, F. Van Petegem4, J.-P. Chessa1, J. Van Beeumen4,U.HuÈ bscher2 and C. Gerday1 1Laboratory of Biochemistry, Institute of Chemistry, B6a Universite de LieÁge, Sart-Tilman, Belgium; 2Institute of Veterinary Biochemistry, UniversitaÈtZuÈrich-Irchel, ZuÈrich, Switzerland; 3Department of Pathology, Brigham & Women's Hospital, Boston, MA, USA; 4Laboratory for Protein Biochemistry and Protein Engineering, Department of Biochemistry Physiology and Microbiology, Gent, Belgium The cloning, overexpression and characterization of a cold-adapted DNA ligase from the Antarctic sea water bacterium Pseudoalteromonas haloplanktis are described. Protein sequence analysis revealed that the cold- adapted Ph DNA ligase shows a significant level of sequence similarity to other NAD1-dependent DNA ligases and contains several previously described sequence motifs. Also, a decreased level of arginine and proline residues in Ph DNA ligase could be involved in the cold-adaptation strategy. Moreover, 3D modelling of the N-terminal domain of Ph DNA ligase clearly indicates that this domain is destabilized compared with its thermophilic homologue. The recombinant Ph DNA ligase was overexpressed in Escherichia coli and purified to homogeneity. Mass spectroscopy experiments indicated that the purified enzyme is mainly in an adenylated form with a molecular mass of 74 593 Da. Ph DNA ligase shows similar overall catalytic properties to other NAD1-dependent DNA ligases but is a cold-adapted enzyme as its catalytic efficiency (kcat/Km) at low and moderate temperatures is higher than that of its mesophilic counterpart E. -
The First Recorded Incidence of Deinococcus Radiodurans R1 Biofilm
bioRxiv preprint doi: https://doi.org/10.1101/234781; this version posted December 15, 2017. 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. 1 The first recorded incidence of Deinococcus radiodurans R1 biofilm 2 formation and its implications in heavy metals bioremediation 3 4 Sudhir K. Shukla1,2, T. Subba Rao1,2,* 5 6 Running title : Deinococcus radiodurans R1 biofilm formation 7 8 1Biofouling & Thermal Ecology Section, Water & Steam Chemistry Division, 9 BARC Facilities, Kalpakkam, 603 102 India 10 11 2Homi Bhabha National Institute, Mumbai 400094, India 12 13 *Corresponding Author: T. Subba Rao 14 Address: Biofouling & Thermal Ecology Section, Water & Steam Chemistry Division, 15 BARC Facilities, Kalpakkam, 603 102 India 16 E-mail: [email protected] 17 Phone: +91 44 2748 0203, Fax: +91 44 2748 0097 18 1 bioRxiv preprint doi: https://doi.org/10.1101/234781; this version posted December 15, 2017. 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. 19 Significance and Impact of this Study 20 This is the first ever recorded study on the Deinococcus radiodurans R1 biofilm. This 21 organism, being the most radioresistant micro-organism ever known, has always been 22 speculated as a potential bacterium to develop a bioremediation process for radioactive heavy 23 metal contaminants. However, the lack of biofilm forming capability proved to be a bottleneck 24 in developing such technology. This study records the first incidence of biofilm formation in a 25 recombinant D. -
Functionalized Membrane Domains: an Ancestral Feature of Archaea? Maxime Tourte, Philippe Schaeffer, Vincent Grossi, Phil Oger
Functionalized Membrane Domains: An Ancestral Feature of Archaea? Maxime Tourte, Philippe Schaeffer, Vincent Grossi, Phil Oger To cite this version: Maxime Tourte, Philippe Schaeffer, Vincent Grossi, Phil Oger. Functionalized Membrane Domains: An Ancestral Feature of Archaea?. Frontiers in Microbiology, Frontiers Media, 2020, 11, pp.526. 10.3389/fmicb.2020.00526. hal-02553764 HAL Id: hal-02553764 https://hal.archives-ouvertes.fr/hal-02553764 Submitted on 20 May 2020 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. fmicb-11-00526 March 30, 2020 Time: 21:44 # 1 ORIGINAL RESEARCH published: 31 March 2020 doi: 10.3389/fmicb.2020.00526 Functionalized Membrane Domains: An Ancestral Feature of Archaea? Maxime Tourte1†, Philippe Schaeffer2†, Vincent Grossi3† and Phil M. Oger1*† 1 Université de Lyon, INSA Lyon, CNRS, MAP UMR 5240, Villeurbanne, France, 2 Université de Strasbourg-CNRS, UMR 7177, Laboratoire de Biogéochimie Moléculaire, Strasbourg, France, 3 Université de Lyon, ENS Lyon, CNRS, Laboratoire de Géologie de Lyon, UMR 5276, Villeurbanne, France Bacteria and Eukarya organize their plasma membrane spatially into domains of distinct functions. Due to the uniqueness of their lipids, membrane functionalization in Archaea remains a debated area.