Literature DB >> 320953

Alterations of alkaline phosphatase activity during adaptation of Escherichia coli to phosphite and hypophosphite.

A M Lauwers, W Heinen.   

Abstract

When Escherichia coli cells were grown in media containing either phosphite or hypophosphite as the sole source of phosphorus, the responded to this situation primarily in the same way as phosphate-limited cultures: The activity of alkaline phosphatase increased drastically, which under natural conditions would enable the cells to compensate for the shortage of phosphate. Subsequent transfers, however, resulted in a quite different response: While the phosphatase activity of phosphate-limited cells stays at a high derepressed level, its increase was followed by a gradual decline in organisms grown on phosphite of hypophosphite. After eight to ten transfers on these P-compounds, phosphatase activity was back to its initial, repressed, low level, indicating that the cells were fully adapted to these substrates. Adaptation to either PO3-3 or PO3-2 was completely abolished if the cells were again grown with PO3-3 as P-source, whereafter the entire process of adaptation had to be repeated. The observed adaptation pattern, reflected by the alterations of phosphatase activity, was qualitatively equal with PO3-3 and PO3-2, but quantitatively different, because the response to hypophosphite gave much higher values than the increase obtained with phosphite. Phosphite-adapted cells are not simultaneously adapted to hypophosphite, but their response to the latter was less intense than observed after direct transfers from PO3-4 to PO3-2. Adaptation to hypophosphite, however, led simultaneously to phosphite adaptation, so that these cells can utilize both P-compounds as a substitute for phosphate.

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Year:  1977        PMID: 320953     DOI: 10.1007/bf00446661

Source DB:  PubMed          Journal:  Arch Microbiol        ISSN: 0302-8933            Impact factor:   2.552


  5 in total

1.  Influence of inorganic phosphate in the formation of phosphatases by Escherichia coli.

Authors:  A TORRIANI
Journal:  Biochim Biophys Acta       Date:  1960-03-11

2.  Microbial oxidation and utilization of orthophosphite during growth.

Authors:  L E CASIDA
Journal:  J Bacteriol       Date:  1960-08       Impact factor: 3.490

3.  Excretion of alkaline phosphatase of Bacillus subtilis.

Authors:  M Cashel; E Freese
Journal:  Biochem Biophys Res Commun       Date:  1964-08-11       Impact factor: 3.575

4.  Bacterial oxidation of orthophosphate.

Authors:  G Malacinski; W A Konetzka
Journal:  J Bacteriol       Date:  1966-02       Impact factor: 3.490

5.  Orthophosphite-nicotinamide adenine dinucleotide oxidoreductase from Pseudomonas fluorescens.

Authors:  G M Malacinski; W A Konetzka
Journal:  J Bacteriol       Date:  1967-06       Impact factor: 3.490

  5 in total
  2 in total

1.  Molecular genetic analysis of phosphite and hypophosphite oxidation by Pseudomonas stutzeri WM88.

Authors:  W W Metcalf; R S Wolfe
Journal:  J Bacteriol       Date:  1998-11       Impact factor: 3.490

2.  The htx and ptx operons of Pseudomonas stutzeri WM88 are new members of the pho regulon.

Authors:  Andrea K White; William W Metcalf
Journal:  J Bacteriol       Date:  2004-09       Impact factor: 3.490

  2 in total

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