Literature DB >> 9882674

Polyhydroxyalkanoate inclusion body-associated proteins and coding region in Bacillus megaterium.

G J McCool1, M C Cannon.   

Abstract

Polyhydroxyalkanoic acids (PHA) are carbon and energy storage polymers that accumulate in inclusion bodies in many bacteria and archaea in response to environmental conditions. This work presents the results of a study of PHA inclusion body-associated proteins and an analysis of their coding region in Bacillus megaterium 11561. A 7, 917-bp fragment of DNA was cloned and shown to carry a 4,104-bp cluster of 5 pha genes, phaP, -Q, -R, -B, and -C. The phaP and -Q genes were shown to be transcribed in one orientation, each from a separate promoter, while immediately upstream, phaR, -B, and -C were divergently transcribed as a tricistronic operon. Transfer of this gene cluster to Escherichia coli and to a PhaC- mutant of Pseudomonas putida gave a Pha+ phenotype in both strains. Translational fusions to the green fluorescent protein localized PhaP and PhaC to the PHA inclusion bodies in living cells. The data presented are consistent with the hypothesis that the extremely hydrophilic protein PhaP is a storage protein and suggests that PHA inclusion bodies are not only a source of carbon, energy, and reducing equivalents but are also a source of amino acids.

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Year:  1999        PMID: 9882674      PMCID: PMC93414     

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


  35 in total

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Authors:  S Y Lee
Journal:  Biotechnol Bioeng       Date:  1996-01-05       Impact factor: 4.530

8.  Purification and characterization of a 14-kilodalton protein that is bound to the surface of polyhydroxyalkanoic acid granules in Rhodococcus ruber.

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Journal:  J Bacteriol       Date:  1994-07       Impact factor: 3.490

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Journal:  J Biol Chem       Date:  1991-02-05       Impact factor: 5.157

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  32 in total

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Journal:  J Bacteriol       Date:  2009-03-06       Impact factor: 3.490

3.  Tolerance of the Ralstonia eutropha class I polyhydroxyalkanoate synthase for translational fusions to its C terminus reveals a new mode of functional display.

Authors:  Anika C Jahns; Bernd H A Rehm
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4.  Identification and characterization of a novel intracellular poly(3-hydroxybutyrate) depolymerase from Bacillus megaterium.

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5.  Comparative proteome analysis reveals four novel polyhydroxybutyrate (PHB) granule-associated proteins in Ralstonia eutropha H16.

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7.  Identification and characterization of the Bacillus thuringiensis phaZ gene, encoding new intracellular poly-3-hydroxybutyrate depolymerase.

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8.  PhaC and PhaR are required for polyhydroxyalkanoic acid synthase activity in Bacillus megaterium.

Authors:  G J McCool; M C Cannon
Journal:  J Bacteriol       Date:  2001-07       Impact factor: 3.490

9.  Polyhydroxyalkanoate (PHA) accumulation in sulfate-reducing bacteria and identification of a class III PHA synthase (PhaEC) in Desulfococcus multivorans.

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10.  Bacillus subtilis as potential producer for polyhydroxyalkanoates.

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