Literature DB >> 7765916

The glucose dehydrogenase-mediated energization of Acinetobacter calcoaceticus as a tool for evaluating its susceptibility to, and defence against, hazardous chemicals.

N Loffhagen1, C Härtig, W Babel.   

Abstract

Cells of Acinetobacter calcoaceticus 69-V could be energized by glucose oxidation after the growth on acetate, ethanol, hexanol and benzoate. The velocities of glucose oxidation-driven ATP syntheses were relatively constant in the range from pH 5.4 to 7.5. With decreasing pH values (7.0, 6.0, 5.4) ATP synthesis was inhibited more strongly by the action of 2,4-dinitrophenol and at the same pH value glucose oxidation was nearly unimpaired or inhibited more weakly. This finding is expressed by a decrease of the P/O ratios, indicating the uncoupling of the electron-transport phosphorylation by 2,4-dinitrophenol. The sensitivity towards this uncoupling effect was higher in ethanol-grown cells of Acinetobacter calcoaceticus 69-V than in hexanol- or acetate-grown cells. This increase in sensitivity was accompanied by a decrease of the ratio of saturated (mainly C16:0) to unsaturated (C16:1, C18:1) fatty acids in ethanol-grown cells compared with hexanol-grown ones. The knowledge of such differences in the susceptibility and its molecular background, e.g. possible substrate-induced changes of the fatty acid composition of the cytoplasmic membranes, should help elucidate mechanisms of poisoning by membrane-active hazardous chemicals and develop defence strategies.

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Year:  1995        PMID: 7765916     DOI: 10.1007/BF00171955

Source DB:  PubMed          Journal:  Appl Microbiol Biotechnol        ISSN: 0175-7598            Impact factor:   4.813


  23 in total

1.  Cytochrome b-562 from Acinetobacter calcoaceticus L.M.D. 79.41. Its characteristics and role as electron acceptor for quinoprotein glucose dehydrogenase.

Authors:  P Dokter; J E van Wielink; M A van Kleef; J A Duine
Journal:  Biochem J       Date:  1988-08-15       Impact factor: 3.857

2.  Method of determining oxygen concentrations in biological media, suitable for calibration of the oxygen electrode.

Authors:  J Robinson; J M Cooper
Journal:  Anal Biochem       Date:  1970-02       Impact factor: 3.365

3.  A study of the Moraxella group. II. Oxidative-negative species (genus Acinetobacter).

Authors:  P Baumann; M Doudoroff; R Y Stanier
Journal:  J Bacteriol       Date:  1968-05       Impact factor: 3.490

Review 4.  Transport of protons across membranes by weak acids.

Authors:  S G McLaughlin; J P Dilger
Journal:  Physiol Rev       Date:  1980-07       Impact factor: 37.312

5.  Conversion of cis unsaturated fatty acids to trans, a possible mechanism for the protection of phenol-degrading Pseudomonas putida P8 from substrate toxicity.

Authors:  H J Heipieper; R Diefenbach; H Keweloh
Journal:  Appl Environ Microbiol       Date:  1992-06       Impact factor: 4.792

6.  Alteration of the fatty acid composition of Escherichia coli by growth in the presence of normal alcohols.

Authors:  K H Sullivan; G D Hegeman; E H Cordes
Journal:  J Bacteriol       Date:  1979-04       Impact factor: 3.490

7.  Energy transduction by electron transfer via a pyrrolo-quinoline quinone-dependent glucose dehydrogenase in Escherichia coli, Pseudomonas aeruginosa, and Acinetobacter calcoaceticus (var. lwoffi).

Authors:  B J van Schie; K J Hellingwerf; J P van Dijken; M G Elferink; J M van Dijl; J G Kuenen; W N Konings
Journal:  J Bacteriol       Date:  1985-08       Impact factor: 3.490

8.  The molecular mechanism of action of the proton ionophore FCCP (carbonylcyanide p-trifluoromethoxyphenylhydrazone).

Authors:  R Benz; S McLaughlin
Journal:  Biophys J       Date:  1983-03       Impact factor: 4.033

9.  Topological analysis of quinoprotein glucose dehydrogenase in Escherichia coli and its ubiquinone-binding site.

Authors:  M Yamada; K Sumi; K Matsushita; O Adachi; Y Yamada
Journal:  J Biol Chem       Date:  1993-06-15       Impact factor: 5.157

10.  Extracellular oxidation of D-glucose by some members of the Enterobacteriaceae.

Authors:  O M Bouvet; P A Grimont
Journal:  Ann Inst Pasteur Microbiol       Date:  1988 Jan-Feb
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