Literature DB >> 2082817

Formation and breakdown of glycine betaine and trimethylamine in hypersaline environments.

A Oren1.   

Abstract

Glycine betaine is accumulated as a compatible solute in many photosynthetic and non-photosynthetic bacteria--the last being unable to synthesize the compound--and thus large pools of betaine can be expected to be present in hypersaline environments. A variety of aerobic and anaerobic microorganisms degrade betaine to among other products trimethylamine and methylamine, in a number of different pathways. Curiously, very few of these betaine breakdown processes have yet been identified in hypersaline environments. Trimethylamine can also be formed by bacterial reduction of trimethylamine N-oxide (also by extremely halophilic archaeobacteria). Degradation of trimethylamine in hypersaline environments by halophilic methanogenic bacteria is relatively well documented, and leads to the formation of methane, carbon dioxide and ammonia.

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Year:  1990        PMID: 2082817     DOI: 10.1007/BF00399342

Source DB:  PubMed          Journal:  Antonie Van Leeuwenhoek        ISSN: 0003-6072            Impact factor:   2.271


  21 in total

1.  Pathway of betaine and choline synthesis in Beta vulgaris.

Authors:  C C DELWICHE; H M BREGOFF
Journal:  J Biol Chem       Date:  1958-08       Impact factor: 5.157

2.  Isolation and characterization of a halophilic methanogen from great salt lake.

Authors:  J R Paterek; P H Smith
Journal:  Appl Environ Microbiol       Date:  1985-10       Impact factor: 4.792

3.  Metabolism of trimethylamine, choline, and glycine betaine by sulfate-reducing and methanogenic bacteria in marine sediments.

Authors:  G M King
Journal:  Appl Environ Microbiol       Date:  1984-10       Impact factor: 4.792

4.  Betaine fermentation and oxidation by marine desulfuromonas strains.

Authors:  J H Heijthuijsen; T A Hansen
Journal:  Appl Environ Microbiol       Date:  1989-04       Impact factor: 4.792

5.  Formation of N,N-Dimethylglycine, Acetic Acid, and Butyric Acid from Betaine by Eubacterium limosum.

Authors:  E Müller; K Fahlbusch; R Walther; G Gottschalk
Journal:  Appl Environ Microbiol       Date:  1981-09       Impact factor: 4.792

6.  Utilization of trimethylamine and other N-methyl compounds for growth and methane formation by Methanosarcina barkeri.

Authors:  H Hippe; D Caspari; K Fiebig; G Gottschalk
Journal:  Proc Natl Acad Sci U S A       Date:  1979-01       Impact factor: 11.205

7.  Physiology of dark fermentative growth of Rhodopseudomonas capsulata.

Authors:  M T Madigan; J C Cox; H Gest
Journal:  J Bacteriol       Date:  1980-06       Impact factor: 3.490

8.  Detection of the osmoregulator betaine in methanogens.

Authors:  D E Robertson; D Noll; M F Roberts; J A Menaia; D R Boone
Journal:  Appl Environ Microbiol       Date:  1990-02       Impact factor: 4.792

9.  Trimethylamine oxide: a terminal electron acceptor in anaerobic respiration of bacteria.

Authors:  A R Strøm; J A Olafsen; H Larsen
Journal:  J Gen Microbiol       Date:  1979-06

10.  Studies on halotolerance in a moderately halophilic bacterium. Effect of betaine on salt resistance of the respiratory system.

Authors:  D Rafaeli-Eshkol; Y Avi-Dor
Journal:  Biochem J       Date:  1968-10       Impact factor: 3.857

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  29 in total

1.  Bacterial Diversity in Microbial Mats and Sediments from the Atacama Desert.

Authors:  Maria Cecilia Rasuk; Ana Beatriz Fernández; Daniel Kurth; Manuel Contreras; Fernando Novoa; Daniel Poiré; María Eugenia Farías
Journal:  Microb Ecol       Date:  2015-07-30       Impact factor: 4.552

2.  Bacterial flavin-containing monooxygenase is trimethylamine monooxygenase.

Authors:  Yin Chen; Nisha A Patel; Andrew Crombie; James H Scrivens; J Colin Murrell
Journal:  Proc Natl Acad Sci U S A       Date:  2011-10-17       Impact factor: 11.205

3.  Nutrient-Colimited Trichodesmium as a Nitrogen Source or Sink in a Future Ocean.

Authors:  Nathan G Walworth; Fei-Xue Fu; Michael D Lee; Xiaoni Cai; Mak A Saito; Eric A Webb; David A Hutchins
Journal:  Appl Environ Microbiol       Date:  2018-01-17       Impact factor: 4.792

4.  Differential Effects of Dimethylsulfoniopropionate, Dimethylsulfonioacetate, and Other S-Methylated Compounds on the Growth of Sinorhizobium meliloti at Low and High Osmolarities.

Authors:  V Pichereau; J A Pocard; J Hamelin; C Blanco; T Bernard
Journal:  Appl Environ Microbiol       Date:  1998-04       Impact factor: 4.792

5.  Dimethylglycine provides salt and temperature stress protection to Bacillus subtilis.

Authors:  Abdallah Bashir; Tamara Hoffmann; Sander H J Smits; Erhard Bremer
Journal:  Appl Environ Microbiol       Date:  2014-02-21       Impact factor: 4.792

6.  A nonpyrrolysine member of the widely distributed trimethylamine methyltransferase family is a glycine betaine methyltransferase.

Authors:  Tomislav Ticak; Duncan J Kountz; Kimberly E Girosky; Joseph A Krzycki; Donald J Ferguson
Journal:  Proc Natl Acad Sci U S A       Date:  2014-10-13       Impact factor: 11.205

Review 7.  Bioenergetic aspects of halophilism.

Authors:  A Oren
Journal:  Microbiol Mol Biol Rev       Date:  1999-06       Impact factor: 11.056

8.  Trimethylamine and Organic Matter Additions Reverse Substrate Limitation Effects on the δ13C Values of Methane Produced in Hypersaline Microbial Mats.

Authors:  Cheryl A Kelley; Brooke E Nicholson; Claire S Beaudoin; Angela M Detweiler; Brad M Bebout
Journal:  Appl Environ Microbiol       Date:  2014-09-19       Impact factor: 4.792

Review 9.  Anaerobic bacteria from hypersaline environments.

Authors:  B Ollivier; P Caumette; J L Garcia; R A Mah
Journal:  Microbiol Rev       Date:  1994-03

Review 10.  Homeostasis and catabolism of choline and glycine betaine: lessons from Pseudomonas aeruginosa.

Authors:  Matthew J Wargo
Journal:  Appl Environ Microbiol       Date:  2013-01-25       Impact factor: 4.792

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