Previous Article | Next Article ![]()
Appl. Environ. Microbiol., 08 1997, 3003-3009, Vol 63, No. 8
RG Kranz, KK Gabbert, TA Locke and MT Madigan
Like many other prokaryotes, the photosynthetic bacterium Rhodobacter
capsulatus produces high levels of polyhydroxyalkanoates (PHAs) when a
suitable carbon source is available. The three genes that are traditionally
considered to be necessary in the PHA biosynthetic pathway, phaA
(beta-ketothiolase), phaB (acetoacetylcoenzyme A reductase), and phaC (PHA
synthase), were cloned from Rhodobacter capsulatus. In R. capsulatus, the
phaAB genes are not linked to the phaC gene. Translational
beta-galactosidase fusions to phaA and phaC were constructed and recombined
into the chromosome. Both phaC and phaA were constitutively expressed
regardless of whether PHA production was induced, suggesting that control
is posttranslational at the enzymatic level. Consistent with this
conclusion, it was shown that the R. capsulatus transcriptional
nitrogen-sensing circuits were not involved in PHA synthesis. The doubling
times of R. capsulatus transcriptional nitrogen-sensing circuits were not
involved in PHA synthesis. The doubling times of R. capsulatus grown on
numerous carbon sources were determined, indicating that this bacterium
grows on C2 to C12 fatty acids. Grown on acetone, caproate, or heptanoate,
wild-type R. capsulatus produced high levels of PHAs. Although a phaC
deletion strain was unable to synthesize PHAs on any carbon source, phaA
and phaAB deletion strains were able to produce PHAs, indicating that
alternative routes for the synthesis of substrates for the synthase are
present. The nutritional versatility and bioenergetic versatility of R.
capsulatus, coupled with its ability to produce large amounts of PHAs and
its genetic tractability, make it an attractive model for the study of PHA
production.
Copyright © 1997, American Society for Microbiology
Polyhydroxyalkanoate production in Rhodobacter capsulatus: genes, mutants, expression, and physiology
Department of Biology, Washington University, St. Louis, Missouri 63130, USA. kranz@wustlb.wustlb.edu
This article has been cited by other articles:
| J. Bacteriol. | Microbiol. Mol. Biol. Rev. | Eukaryot. Cell | All ASM Journals |
|---|