Literature DB >> 6259132

Adenylate energy charge in Escherichia coli CR341T28 and properties of heat-sensitive adenylate kinase.

C C Glembotski, A G Chapman, D E Atkinson.   

Abstract

Escherichia coli strain CR341T28 will not grow at temperatures above 34 degrees C in liquid medium, and the adenylate kinase of this strain is heat sensitive. When a culture was shifted from a permissive (30 degrees C) to a nonpermissive (36 degrees C) temperature, the adenylate energy charge fell from 0.9 to 0.2, with a concurrent decrease in the number of viable cells and in the specific activity of adenylate kinase. When cultures of the temperature-sensitive strain were grown at temperatures above 30 degrees C, the adenylate energy charge, the specific activity of adenylate kinase, and the growth rate were lower than the corresponding parameters for the parental strain. By isotopic labeling of the adenine nucleotides in vivo, it was determined that increasing growth temperatures between 30 and 34 degrees C for the heat-sensitive strain resulted in a decrease in the adenosine triphosphate-to-adenosine monophosphate and adenosine triphosphate-to-adenosine diphosphate ratios. Between 26 and 30 degrees C the adenosine triphosphate-to-adenosine diphosphate ratio was essentially normal in the temperature-sensitive strain, but the adenosine triphosphate-to-adenosine diphosphate ratio was decreased. The adenylate ratios in the parental strain did not change between 30 and 34 degrees C. The adenylate kinase mass action ratio for each strain was essentially constant under all growth conditions. When assayed at 30 degrees C, the affinities of the enzyme from the mutant strain were somewhat lower than those of the parent adenylate kinase. The mutant enzyme also did not exhibit the substrate inhibition that was observed at high adenosine monophosphate concentrations with the parental enzyme. An increase in the assay temperature from 30 degrees to 40 degrees C had little or no effect on the Km values determined for the parental adenylate kinase, but caused the Km values determined for the mutant adenylate kinase to increase by a factor of two or more.

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Year:  1981        PMID: 6259132      PMCID: PMC217142          DOI: 10.1128/jb.145.3.1374-1385.1981

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  21 in total

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Journal:  J Bacteriol       Date:  1971-12       Impact factor: 3.490

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  12 in total

1.  Evolution of a single gene highlights the complexity underlying molecular descriptions of fitness.

Authors:  Matthew I Peña; Elizabeth Van Itallie; Matthew R Bennett; Yousif Shamoo
Journal:  Chaos       Date:  2010-06       Impact factor: 3.642

2.  Initiation of RNA decay in Escherichia coli by 5' pyrophosphate removal.

Authors:  Helena Celesnik; Atilio Deana; Joel G Belasco
Journal:  Mol Cell       Date:  2007-07-06       Impact factor: 17.970

3.  Energy metabolism response to low-temperature and frozen conditions in Psychrobacter cryohalolentis.

Authors:  Pierre Amato; Brent C Christner
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Authors:  Rafael Couñago; Yousif Shamoo
Journal:  Extremophiles       Date:  2005-01-13       Impact factor: 2.395

7.  Adenosine thiamine triphosphate accumulates in Escherichia coli cells in response to specific conditions of metabolic stress.

Authors:  Tiziana Gigliobianco; Bernard Lakaye; Pierre Wins; Benaïssa El Moualij; Willy Zorzi; Lucien Bettendorff
Journal:  BMC Microbiol       Date:  2010-05-21       Impact factor: 3.605

8.  Isolation and characterization of adenylate kinase (adk) mutations in Salmonella typhimurium which block the ability of glycine betaine to function as an osmoprotectant.

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Journal:  J Bacteriol       Date:  1995-01       Impact factor: 3.490

9.  Adenine nucleotide levels in and nitrogen fixation by the cyanobacterium Anabaena sp. strain 7120.

Authors:  L S Privalle; R H Burris
Journal:  J Bacteriol       Date:  1983-04       Impact factor: 3.490

10.  An alternative role of FoF1-ATP synthase in Escherichia coli: synthesis of thiamine triphosphate.

Authors:  Tiziana Gigliobianco; Marjorie Gangolf; Bernard Lakaye; Bastien Pirson; Christoph von Ballmoos; Pierre Wins; Lucien Bettendorff
Journal:  Sci Rep       Date:  2013-01-15       Impact factor: 4.379

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