Literature DB >> 96104

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

J C Williams, E Weiss.   

Abstract

The obligate intracellular bacterium Rickettsia typhi was examined for its ability to generate and maintain an adenylate energy charge in an extracellular environment. Freshly purified organisms were incubated, at 34 degrees C and pH 7.4, with or without glutamate and various other metabolites, and the levels of ATP, ADP, and AMP were determined. Of the metabolites tested, glutamate and glutamine were the most effective for the generation of ATP. In the presence of glutamate, there was a rapid increase in the level of ATP, followed by a moderate decrease during 150 min of incubation. The energy charge increased from a level of 0.2 to 0.5 to about 0.7 to 0.75, and then slowly declined to about 0.45 to 0.6. In the absence of glutamate, after an occasional initial surge in ATP level as the temperature was changed from 4 to 34 degrees C, there was a sharp decline in both ATP and energy charge (to 0.1 and sometimes to 0.01). The rickettsiae maintained their ability to regenerate their energy charge upon the addition of glutamate for about 30 min, but this ability declined with further incubation. In contrast to Escherichia coli, the decline in ATP in R. typhi was accompanied by a sharp increase in the level of AMP and the total adenylate pool. No adenine or adenosine was recovered from rickettsiae incubated with labeled AMP, ADP, or ATP. From these experiments and the demonstration reported elsewhere that rickettsiae transport the adenine nucleotides, it can be concluded that the adenylate energy charge in R. typhi is governed by the salvage of the adenine nucleotides rather than their unphosphorylated precursors. Thus, R. typhi undergoes greater shifts in energy charge than other bacteria, a phenomenon which may account for their instability in an extracellular environment. Under optimal conditions the adenylate energy charge of R. typhi approaches levels that border on those generally regarded as adequate for growth.

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Year:  1978        PMID: 96104      PMCID: PMC222335          DOI: 10.1128/jb.134.3.884-892.1978

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


  21 in total

1.  Assay of picomole amounts of ATP, ADP, and AMP using the luciferase enzyme system.

Authors:  G A Kimmich; J Randles; J S Brand
Journal:  Anal Biochem       Date:  1975-11       Impact factor: 3.365

2.  The incorporation of glycine-1-C14 by typhus rickettsiae.

Authors:  M R BOVARNICK; L SCHNEIDER
Journal:  J Biol Chem       Date:  1960-06       Impact factor: 5.157

3.  Reversible inactivation of the toxicity and hemolytic activity of typhus rickettsiae by starvation.

Authors:  M R BOVARNICK; E G ALLEN
Journal:  J Bacteriol       Date:  1957-11       Impact factor: 3.490

4.  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

5.  Metabolic studies of rickettsiae. II. Studies on the pathway of glutamate oxidation by purified suspensions of Rickettsia mooseri.

Authors:  C L WISSEMAN; F E HAHN; E B JACKSON; M F BOZEMAN; J E SMADEL
Journal:  J Immunol       Date:  1952-03       Impact factor: 5.422

6.  Purine and pyrimidine ribonucleotide contents of rat liver and hepatoma 3924A and the effect of ischemia.

Authors:  R C Jackson; T J Boritzki; H P Morris; G Weber
Journal:  Life Sci       Date:  1976-11-15       Impact factor: 5.037

7.  Physiological characteristics of chemostatically grown Citrobacter freundii as a function of the specific growth rate and type of nutrient limitation.

Authors:  J Dolezal; F Kaprálek
Journal:  Folia Microbiol (Praha)       Date:  1976       Impact factor: 2.099

8.  Rickettsial permeability. An ADP-ATP transport system.

Authors:  H H Winkler
Journal:  J Biol Chem       Date:  1976-01-25       Impact factor: 5.157

9.  Relation of growth and protein synthesis to the adenylate energy charge in an adenine-requiring mutant of Escherichia coli.

Authors:  J S Swedes; R J Sedo; D E Atkinson
Journal:  J Biol Chem       Date:  1975-09-10       Impact factor: 5.157

10.  Biological properties of Rickettsia prowazekii strains isolated from flying squirrels.

Authors:  D R Woodman; E Weiss; G A Dasch; F M Bozeman
Journal:  Infect Immun       Date:  1977-06       Impact factor: 3.441

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  22 in total

1.  Preservation of ATP in hypersaline environments.

Authors:  B J Tuovila; F C Dobbs; P A Larock; B Z Siegel
Journal:  Appl Environ Microbiol       Date:  1987-12       Impact factor: 4.792

2.  Acquisition of glucose by Rickettsia prowazekii through the nucleotide intermediate uridine 5'-diphosphoglucose.

Authors:  H H Winkler; R M Daugherty
Journal:  J Bacteriol       Date:  1986-09       Impact factor: 3.490

3.  Rickettsia prowazekii requires host cell serine and glycine for growth.

Authors:  F E Austin; J Turco; H H Winkler
Journal:  Infect Immun       Date:  1987-01       Impact factor: 3.441

Review 4.  Comparative biology of intracellular parasitism.

Authors:  J W Moulder
Journal:  Microbiol Rev       Date:  1985-09

5.  Modulation of adenylate energy charge during the swarmer cycle of Hyphomicrobium neptunium.

Authors:  M A Emala; R M Weiner
Journal:  J Bacteriol       Date:  1983-03       Impact factor: 3.490

6.  Adenine nucleotide degradation by the obligate intracellular bacterium Rickettsia typhi.

Authors:  J C Williams
Journal:  Infect Immun       Date:  1980-04       Impact factor: 3.441

7.  Biochemical stratagem for obligate parasitism of eukaryotic cells by Coxiella burnetii.

Authors:  T Hackstadt; J C Williams
Journal:  Proc Natl Acad Sci U S A       Date:  1981-05       Impact factor: 11.205

8.  Stability of the adenosine 5'-triphosphate pool in Coxiella burnetii: influence of pH and substrate.

Authors:  T Hackstadt; J C Williams
Journal:  J Bacteriol       Date:  1981-11       Impact factor: 3.490

9.  Regulatory role of phosphate and other anions in transport of ADP and ATP by Rickettsia prowazekii.

Authors:  H H Winkler; R M Daugherty
Journal:  J Bacteriol       Date:  1984-10       Impact factor: 3.490

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

Authors:  W C Barrette; D M Hannum; W D Wheeler; J K Hurst
Journal:  J Bacteriol       Date:  1988-08       Impact factor: 3.490

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