Literature DB >> 16349092

Disaggregation of Methanosarcina spp. and Growth as Single Cells at Elevated Osmolarity.

K R Sowers1, J E Boone, R P Gunsalus.   

Abstract

The effect of medium osmolarity on the morphology and growth of Methanosarcina barkeri, Methanosarcina thermophila, Methanosarcina mazei, Methanosarcina vacuolata, and Methanosarcina acetivorans was examined. Each strain was adapted for growth in NaCl concentrations ranging from 0.05 to 1.0 M. Methanosarcina spp. isolated from both marine and nonmarine sources exhibited similar growth characteristics at all NaCl concentrations tested, demonstrating that these species are capable of adapting to a similar range of medium osmolarities. Concomitant with the adaptation in 0.4 to 1.0 M NaCl, all strains disaggregated and grew as single cells rather than in the characteristic multicellular aggregates. Aggregated cells had a methanochondroitin outer layer, while disaggregated single cells lacked the outer layer but retained the protein S-layer adjacent to the cell membrane. Synthesis of glucuronic acid, a major component of methanochondroitin, was reduced 20-fold in the single-cell form of M. barkeri when compared with synthesis in aggregated cells. Strains with the methanochondroitin outer cell layer exhibited enhanced stability at low (<0.2 M NaCl) osmolarity and grew at higher temperatures. Disaggregated cells could be converted back to aggregated cells by gradually readapting cultures to lower NaCl (<0.2 M) and Mg (<0.005 M) concentrations. Disaggregated Methanosarcina spp. could also be colonized and replica plated with greater than 95% recovery rates on solidified agar basal medium that contained 0.4 to 0.6 M NaCl and either trimethylamine, methanol, or acetate as the substrate. The ability to disaggregate and grow Methanosarcina spp. as viable, detergent-sensitive, single cells on agar medium makes these species amenable to mutant selection and screening for genetic studies and enables cells to be gently lysed for the isolation of intact genetic material.

Entities:  

Year:  1993        PMID: 16349092      PMCID: PMC182538          DOI: 10.1128/aem.59.11.3832-3839.1993

Source DB:  PubMed          Journal:  Appl Environ Microbiol        ISSN: 0099-2240            Impact factor:   4.792


  19 in total

1.  FORMATION OF METHANE BY BACTERIAL EXTRACTS.

Authors:  E A WOLIN; M J WOLIN; R S WOLFE
Journal:  J Biol Chem       Date:  1963-08       Impact factor: 5.157

2.  Isolation and Characterization of a Methylotrophic Marine Methanogen, Methanococcoides methylutens gen. nov., sp. nov.

Authors:  K R Sowers; J G Ferry
Journal:  Appl Environ Microbiol       Date:  1983-02       Impact factor: 4.792

3.  Control of the Life Cycle of Methanosarcina mazei S-6 by Manipulation of Growth Conditions.

Authors:  L Xun; D R Boone; R A Mah
Journal:  Appl Environ Microbiol       Date:  1988-08       Impact factor: 4.792

4.  Spontaneous Disaggregation of Methanosarcina mazei S-6 and Its Use in the Development of Genetic Techniques for Methanosarcina spp.

Authors:  J E Harris
Journal:  Appl Environ Microbiol       Date:  1987-10       Impact factor: 4.792

5.  Methanosarcina mazei LYC, a New Methanogenic Isolate Which Produces a Disaggregating Enzyme.

Authors:  Y Liu; D R Boone; R Sleat; R A Mah
Journal:  Appl Environ Microbiol       Date:  1985-03       Impact factor: 4.792

6.  Lack of peptidoglycan in the cell walls of Methanosarcina barkeri.

Authors:  O Kandler; H Hippe
Journal:  Arch Microbiol       Date:  1977-05-13       Impact factor: 2.552

Review 7.  Methanogens and the diversity of archaebacteria.

Authors:  W J Jones; D P Nagle; W B Whitman
Journal:  Microbiol Rev       Date:  1987-03

8.  Adaptation for growth at various saline concentrations by the archaebacterium Methanosarcina thermophila.

Authors:  K R Sowers; R P Gunsalus
Journal:  J Bacteriol       Date:  1988-02       Impact factor: 3.490

Review 9.  Methanogens: reevaluation of a unique biological group.

Authors:  W E Balch; G E Fox; L J Magrum; C R Woese; R S Wolfe
Journal:  Microbiol Rev       Date:  1979-06

10.  New method for the isolation and identification of methanogenic bacteria.

Authors:  T Edwards; B C McBride
Journal:  Appl Microbiol       Date:  1975-04
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  83 in total

1.  The genome of M. acetivorans reveals extensive metabolic and physiological diversity.

Authors:  James E Galagan; Chad Nusbaum; Alice Roy; Matthew G Endrizzi; Pendexter Macdonald; Will FitzHugh; Sarah Calvo; Reinhard Engels; Serge Smirnov; Deven Atnoor; Adam Brown; Nicole Allen; Jerome Naylor; Nicole Stange-Thomann; Kurt DeArellano; Robin Johnson; Lauren Linton; Paul McEwan; Kevin McKernan; Jessica Talamas; Andrea Tirrell; Wenjuan Ye; Andrew Zimmer; Robert D Barber; Isaac Cann; David E Graham; David A Grahame; Adam M Guss; Reiner Hedderich; Cheryl Ingram-Smith; H Craig Kuettner; Joseph A Krzycki; John A Leigh; Weixi Li; Jinfeng Liu; Biswarup Mukhopadhyay; John N Reeve; Kerry Smith; Timothy A Springer; Lowell A Umayam; Owen White; Robert H White; Everly Conway de Macario; James G Ferry; Ken F Jarrell; Hua Jing; Alberto J L Macario; Ian Paulsen; Matthew Pritchett; Kevin R Sowers; Ronald V Swanson; Steven H Zinder; Eric Lander; William W Metcalf; Bruce Birren
Journal:  Genome Res       Date:  2002-04       Impact factor: 9.043

2.  Structure of the surface layer of the methanogenic archaean Methanosarcina acetivorans.

Authors:  Mark A Arbing; Sum Chan; Annie Shin; Tung Phan; Christine J Ahn; Lars Rohlin; Robert P Gunsalus
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-02       Impact factor: 11.205

3.  Development of a plasmid-mediated reporter system for in vivo monitoring of gene expression in the archaeon Methanosarcina acetivorans.

Authors:  Ethel E Apolinario; Karin M Jackson; Kevin R Sowers
Journal:  Appl Environ Microbiol       Date:  2005-08       Impact factor: 4.792

4.  Biochemical Characterization of the Methylmercaptopropionate:Cob(I)alamin Methyltransferase from Methanosarcina acetivorans.

Authors:  He Fu; Michelle N Goettge; William W Metcalf
Journal:  J Bacteriol       Date:  2019-05-22       Impact factor: 3.490

5.  New methods for tightly regulated gene expression and highly efficient chromosomal integration of cloned genes for Methanosarcina species.

Authors:  Adam M Guss; Michael Rother; Jun Kai Zhang; Gargi Kulkarni; William W Metcalf
Journal:  Archaea       Date:  2008-12       Impact factor: 3.273

6.  Methanol-dependent gene expression demonstrates that methyl-coenzyme M reductase is essential in Methanosarcina acetivorans C2A and allows isolation of mutants with defects in regulation of the methanol utilization pathway.

Authors:  Michael Rother; Paolo Boccazzi; Arpita Bose; Matthew A Pritchett; W W Metcalf
Journal:  J Bacteriol       Date:  2005-08       Impact factor: 3.490

7.  Synthesis of catalytically active form III ribulose 1,5-bisphosphate carboxylase/oxygenase in archaea.

Authors:  Michael W Finn; F Robert Tabita
Journal:  J Bacteriol       Date:  2003-05       Impact factor: 3.490

8.  Functional analysis of the three TATA binding protein homologs in Methanosarcina acetivorans.

Authors:  Matthew J Reichlen; Katsuhiko S Murakami; James G Ferry
Journal:  J Bacteriol       Date:  2010-01-15       Impact factor: 3.490

9.  The appearance of pyrrolysine in tRNAHis guanylyltransferase by neutral evolution.

Authors:  Ilka U Heinemann; Patrick O'Donoghue; Catherine Madinger; Jack Benner; Lennart Randau; Christopher J Noren; Dieter Söll
Journal:  Proc Natl Acad Sci U S A       Date:  2009-11-24       Impact factor: 11.205

10.  Differences in hydrogenase gene expression between Methanosarcina acetivorans and Methanosarcina barkeri.

Authors:  Adam M Guss; Gargi Kulkarni; William W Metcalf
Journal:  J Bacteriol       Date:  2009-02-06       Impact factor: 3.490

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