Literature DB >> 16345475

Capture of arginine at low concentrations by a marine psychrophilic bacterium.

G G Geesey1, R Y Morita.   

Abstract

The cells of the marine bacterium Ant-300 were found to take up arginine when this substrate was at low concentrations. The cells possessed an uptake system(s) that specifically transported l-arginine. The kinetic parameters for uptake appeared to differ when the cells were exposed to nanomolar and micromolar concentrations of the amino acid. Uptake over this concentration range functioned in the absence of an exogenous energy source, even after the cells had been preincubated in unsupplemented artificial seawater. Respiratory activity appeared to be a more important driving force for arginine uptake than adenosine 5'-triphosphate hydrolysis. The cells also exhibited chemotaxis toward l-arginine. The minimum arginine concentration needed to elicit a chemotactic response was between 10 and 10 M. It is proposed that the capture of arginine by cells of Ant-300 in nutrient-depleted waters, which are typical of the open ocean, proceeds via high-affinity active transport, whereas in substrate-enriched seawater, capture involves chemotaxis and an active transport mechanism with reduced affinity for the substrate.

Entities:  

Year:  1979        PMID: 16345475      PMCID: PMC291251          DOI: 10.1128/aem.38.6.1092-1097.1979

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


  19 in total

1.  Some physiological effects of near-maximum growth temperatures on an obligately psychrophilic marine bacterium.

Authors:  G G Geesey; R Y Morita
Journal:  Can J Microbiol       Date:  1975-06       Impact factor: 2.419

2.  Protein measurement with the Folin phenol reagent.

Authors:  O H LOWRY; N J ROSEBROUGH; A L FARR; R J RANDALL
Journal:  J Biol Chem       Date:  1951-11       Impact factor: 5.157

3.  Na + -dependent amino acid transport in isolated membrane vesicles of a marine pseudomonad energized by electron donors.

Authors:  G D Sprott; R A MacLeod
Journal:  Biochem Biophys Res Commun       Date:  1972-05-26       Impact factor: 3.575

4.  Energization of active transport by Escherichia coli.

Authors:  W L Klein; P D Boyer
Journal:  J Biol Chem       Date:  1972-11-25       Impact factor: 5.157

5.  A method for measuring chemotaxis and use of the method to determine optimum conditions for chemotaxis by Escherichia coli.

Authors:  J Adler
Journal:  J Gen Microbiol       Date:  1973-01

6.  Role of the galactose binding protein in chemotaxis of Escherichia coli toward galactose.

Authors:  G L Hazelbauer; J Adler
Journal:  Nat New Biol       Date:  1971-03-24

7.  Negative cooperativity in regulatory enzymes.

Authors:  A Levitzki; D E Koshland
Journal:  Proc Natl Acad Sci U S A       Date:  1969-04       Impact factor: 11.205

8.  The galactose binding protein and its relationship to the beta-methylgalactoside permease from Escherichia coli.

Authors:  W Boos
Journal:  Eur J Biochem       Date:  1969-08

9.  Energy coupling for methionine transport in Escherichia coli.

Authors:  R J Kadner; H H Winkler
Journal:  J Bacteriol       Date:  1975-09       Impact factor: 3.490

10.  Changes in active transport, intracellular adenosine 5'-triphosphate levels, macromolecular syntheses, and glycolysis in an energy-uncoupled mutant of Escherichia coli.

Authors:  M A Lieberman; J S Hong
Journal:  J Bacteriol       Date:  1976-03       Impact factor: 3.490

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  24 in total

1.  Protein Patterns of Growing and Starved Cells of a Marine Vibrio sp.

Authors:  P S Amy; R Y Morita
Journal:  Appl Environ Microbiol       Date:  1983-06       Impact factor: 4.792

2.  Isolation of Typical Marine Bacteria by Dilution Culture: Growth, Maintenance, and Characteristics of Isolates under Laboratory Conditions.

Authors:  F Schut; E J de Vries; J C Gottschal; B R Robertson; W Harder; R A Prins; D K Button
Journal:  Appl Environ Microbiol       Date:  1993-07       Impact factor: 4.792

3.  Chemotactic Responses of Marine Vibrio sp. Strain S14 (CCUG 15956) to Low-Molecular-Weight Substances under Starvation and Recovery Conditions.

Authors:  K Malmcrona-Friberg; A Goodman; S Kjelleberg
Journal:  Appl Environ Microbiol       Date:  1990-12       Impact factor: 4.792

4.  Effect of growth rate and starvation-survival on cellular DNA, RNA, and protein of a psychrophilic marine bacterium.

Authors:  C L Moyer; R Y Morita
Journal:  Appl Environ Microbiol       Date:  1989-10       Impact factor: 4.792

5.  Exoprotease Activity of Two Marine Bacteria during Starvation.

Authors:  N H Albertson; T Nyström; S Kjelleberg
Journal:  Appl Environ Microbiol       Date:  1990-01       Impact factor: 4.792

6.  The physical base of marine bacterial ecology.

Authors:  D K Button
Journal:  Microb Ecol       Date:  1994-09       Impact factor: 4.552

7.  Maintenance of Different Mannitol Uptake Systems during Starvation in Oxidative and Fermentative Marine Bacteria.

Authors:  C L Davis; F T Robb
Journal:  Appl Environ Microbiol       Date:  1985-10       Impact factor: 4.792

8.  Utilization of low concentrations of starch by a flavobacterium species isolated from tap water.

Authors:  D van der Kooij; W A Hijnen
Journal:  Appl Environ Microbiol       Date:  1981-01       Impact factor: 4.792

9.  Relationship of cell envelope stability to substrate capture in a marine psychrophilic bacterium.

Authors:  G G Geesey; R Y Morita
Journal:  Appl Environ Microbiol       Date:  1981-09       Impact factor: 4.792

10.  Starvation-survival processes of a marine Vibrio.

Authors:  P S Amy; C Pauling; R Y Morita
Journal:  Appl Environ Microbiol       Date:  1983-03       Impact factor: 4.792

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