Literature DB >> 7961934

Generation of a proton motive force by the excretion of metal-phosphate in the polyphosphate-accumulating Acinetobacter johnsonii strain 210A.

H W van Veen1, T Abee, G J Kortstee, H Pereira, W N Konings, A J Zehnder.   

Abstract

The strictly aerobic, polyphosphate-accumulating Acinetobacter johnsonii strain 210A degrades its polyphosphate when oxidative phosphorylation is impaired. The endproducts of this degradation, divalent metal ions and inorganic phosphate, are excreted as a neutral metal-phosphate (MeHPO4) chelate via the electrogenic MeHPO4/H+ symport system of the organism. The coupled excretion of MeHPO4 and H+ in A. johnsonii 210A can generate a proton motive force. In membrane vesicles and deenergized cells, a membrane potential of about -70 mV and transmembrane pH gradient of about -8 mV were formed in response to an imposed outwardly directed MeHPO4 concentration gradient of 120 mV (initial value). The MeHPO4 efflux-induced proton motive force could drive energy-requiring processes, such as the accumulation of L-proline and L-lysine and the synthesis of ATP via the membrane-bound F0F1 H(+)-ATPase. In vivo 31P NMR studies of polyphosphate degradation in anaerobic cell suspensions revealed the presence of a considerable outwardly directed phosphate gradient across the cytoplasmic membrane corresponding to a MgHPO4 concentration gradient of at least 100 mV. This MgHPO4 concentration gradient was maintained for several hours. Thus, energy recycling by MeHPO4/H+ efflux will contribute significantly to the overall production of metabolic energy from the degradation of polyphosphate in A. johnsonii 210A.

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Year:  1994        PMID: 7961934

Source DB:  PubMed          Journal:  J Biol Chem        ISSN: 0021-9258            Impact factor:   5.157


  16 in total

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Authors:  S J Van Dien; S Keyhani; C Yang; J D Keasling
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Authors:  J D Keasling; G A Hupf
Journal:  Appl Environ Microbiol       Date:  1996-02       Impact factor: 4.792

Review 8.  Solute transport and energy transduction in bacteria.

Authors:  W N Konings; B Poolman; H W van Veen
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Authors:  R M Harris; D C Webb; S M Howitt; G B Cox
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10.  In situ 31P nuclear magnetic resonance for observation of polyphosphate and catabolite responses of chemostat-cultivated Saccharomyces cerevisiae after alkalinization.

Authors:  C D Castro; A J Meehan; A P Koretsky; M M Domach
Journal:  Appl Environ Microbiol       Date:  1995-12       Impact factor: 4.792

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