Affiliation:
1. Department of Biology1and
2. Department of Chemistry,2Massachusetts Institute of Technology, Cambridge, Massachusetts 02139
Abstract
ABSTRACT
Polyhydroxyalkanoates (PHAs) are polyoxoesters that are produced by diverse bacteria and that accumulate as intracellular granules. Phasins are granule-associated proteins that accumulate to high levels in strains that are producing PHAs. The accumulation of phasins has been proposed to be dependent on PHA production, a model which is now rigorously tested for the phasin PhaP of
Ralstonia eutropha. R. eutropha phaC
PHA synthase and
phaP
phasin gene replacement strains were constructed. The strains were engineered to express heterologous and/or mutant PHA synthase alleles and a
phaP
-
gfp
translational fusion in place of the wild-type alleles of
phaC
and
phaP
. The strains were analyzed with respect to production of polyhydroxybutyrate (PHB), accumulation of PhaP, and expression of the
phaP
-
gfp
fusion. The results suggest that accumulation of PhaP is strictly dependent on the genetic capacity of strains to produce PHB, that PhaP accumulation is regulated at the level of both PhaP synthesis and PhaP degradation, and that, within mixed populations of cells, PhaP accumulation within cells of a given strain is not influenced by PHB production in cells of other strains. Interestingly, either the synthesis of PHB or the presence of relatively large amounts of PHB in cells (>50% of cell dry weight) is sufficient to enable PhaP synthesis. The results suggest that
R. eutropha
has evolved a regulatory mechanism that can detect the synthesis and presence of PHB in cells and that PhaP expression can be used as a marker for the production of PHB in individual cells.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
104 articles.
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