Literature DB >> 3136145

Viability and metabolic capability are maintained by Escherichia coli, Pseudomonas aeruginosa, and Streptococcus lactis at very low adenylate energy charge.

W C Barrette1, D M Hannum, W D Wheeler, J K Hurst.   

Abstract

Metabolic regulation by nucleotides has been examined in several bacteria within the context of the adenylate energy charge (EC) concept. The ECs of bacteria capable of only fermentative metabolism (Streptococcus lactis and the ATPase-less mutant Escherichia coli AN718) fell to less than 0.2 under carbon-limiting conditions, but the bacteria were able to step up the EC to greater than 0.8 upon exposure to nutrient sugars. Similarly, nongrowing E. coli 25922, whose EC had been artificially lowered to less than 0.1 by the addition of the protonophore carbonyl cyanide m-chlorophenylhydrazone (CCCP), was able to immediately step up the EC to 0.8 to 0.9 upon the addition of glucose but was unable to respond to respiratory substrates. The EC of respiring bacteria (E. coli 25922 and Pseudomonas aeruginosa 27853) fell to 0.3 to 0.4 under certain limiting growth conditions, but the bacteria also responded immediately when challenged with succinate to give EC values greater than 0.8. These bacteria could not step up the EC with respiratory substrates in the presence of CCCP. For all bacteria, the loss of the ability to step up the EC was attributable to the loss of nutrient transport function. Mixtures of viable and HOCl-killed E. coli 25922 were able to step up the EC in proportion to the fraction of surviving cells. The data indicate that nucleotide phosphorylation levels are not regulatory in nongrowing bacteria but that the EC step-up achievable upon nutrient addition may be an accurate index of viability.

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Year:  1988        PMID: 3136145      PMCID: PMC211341          DOI: 10.1128/jb.170.8.3655-3659.1988

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


  15 in total

Review 1.  Adenine nucleotide concentrations and turnover rates. Their correlation with biological activity in bacteria and yeast.

Authors:  A G Chapman; D E Atkinson
Journal:  Adv Microb Physiol       Date:  1977       Impact factor: 3.517

2.  Hypochlorous acid-promoted loss of metabolic energy in Escherichia coli.

Authors:  W C Barrette; J M Albrich; J K Hurst
Journal:  Infect Immun       Date:  1987-10       Impact factor: 3.441

3.  Energy metabolism of Rickettsia typhi: pools of adenine nucleotides and energy charge in the presence and absence of glutamate.

Authors:  J C Williams; E Weiss
Journal:  J Bacteriol       Date:  1978-06       Impact factor: 3.490

4.  Transport of succinate in Escherichia coli. I. Biochemical and genetic studies of transport in whole cells.

Authors:  T C Lo; M K Rayman; B D Sanwal
Journal:  J Biol Chem       Date:  1972-10-10       Impact factor: 5.157

5.  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

6.  The energy charge of the adenylate pool as a regulatory parameter. Interaction with feedback modifiers.

Authors:  D E Atkinson
Journal:  Biochemistry       Date:  1968-11       Impact factor: 3.162

7.  Adenylate energy charge in Saccharomyces cerevisiae during starvation.

Authors:  W J Ball; D E Atkinson
Journal:  J Bacteriol       Date:  1975-03       Impact factor: 3.490

8.  Adenylate degradation in Escherichia coli. The role of AMP nucleosidase and properties of the purified enzyme.

Authors:  H B Leung; V L Schramm
Journal:  J Biol Chem       Date:  1980-11-25       Impact factor: 5.157

9.  The importance of inorganic phosphate in regulation of energy metabolism of Streptococcus lactis.

Authors:  P W Mason; D P Carbone; R A Cushman; A S Waggoner
Journal:  J Biol Chem       Date:  1981-02-25       Impact factor: 5.157

10.  Adenylate energy charge in Escherichia coli during growth and starvation.

Authors:  A G Chapman; L Fall; D E Atkinson
Journal:  J Bacteriol       Date:  1971-12       Impact factor: 3.490

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  9 in total

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Review 2.  What really happens in the neutrophil phagosome?

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Authors:  G J Leyer; E A Johnson
Journal:  Appl Environ Microbiol       Date:  1997-02       Impact factor: 4.792

5.  Specificity and regulation of interaction between the PII and AmtB1 proteins in Rhodospirillum rubrum.

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Journal:  J Bacteriol       Date:  2007-07-20       Impact factor: 3.490

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Journal:  Environ Microbiol Rep       Date:  2011-02       Impact factor: 3.541

7.  Comparisons of resistance of CF and non-CF pathogens to hydrogen peroxide and hypochlorous acid oxidants in vitro.

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Journal:  BMC Microbiol       Date:  2011-05-20       Impact factor: 3.605

8.  Intracellular Metabolite Pool Changes in Response to Nutrient Depletion Induced Metabolic Switching in Streptomyces coelicolor.

Authors:  Alexander Wentzel; Havard Sletta; Trond E Ellingsen; Per Bruheim
Journal:  Metabolites       Date:  2012-02-17

9.  On the dynamics of the adenylate energy system: homeorhesis vs homeostasis.

Authors:  Ildefonso M De la Fuente; Jesús M Cortés; Edelmira Valero; Mathieu Desroches; Serafim Rodrigues; Iker Malaina; Luis Martínez
Journal:  PLoS One       Date:  2014-10-10       Impact factor: 3.240

  9 in total

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