Affiliation:
1. Graduate Program in Microbiology, Immunology, and Cancer Biology
2. BioTechnology Institute
3. Department of Biochemistry, Molecular Biology and Biophysics
4. Department of Microbiology, University of Minnesota, St. Paul, Minnesota 55108
Abstract
ABSTRACT
Previous studies identified the
oleABCD
genes involved in head-to-head olefinic hydrocarbon biosynthesis. The present study more fully defined the OleABCD protein families within the thiolase, α/β-hydrolase, AMP-dependent ligase/synthase, and short-chain dehydrogenase superfamilies, respectively. Only 0.1 to 1% of each superfamily represents likely Ole proteins. Sequence analysis based on structural alignments and gene context was used to identify highly likely
ole
genes. Selected microorganisms from the phyla
Verucomicrobia
,
Planctomyces
,
Chloroflexi
,
Proteobacteria
, and
Actinobacteria
were tested experimentally and shown to produce long-chain olefinic hydrocarbons. However, different species from the same genera sometimes lack the
ole
genes and fail to produce olefinic hydrocarbons. Overall, only 1.9% of 3,558 genomes analyzed showed clear evidence for containing
ole
genes. The type of olefins produced by different bacteria differed greatly with respect to the number of carbon-carbon double bonds. The greatest number of organisms surveyed biosynthesized a single long-chain olefin, 3,6,9,12,15,19,22,25,28-hentriacontanonaene, that contains nine double bonds.
Xanthomonas campestris
produced the greatest number of distinct olefin products, 15 compounds ranging in length from C
28
to C
31
and containing one to three double bonds. The type of long-chain product formed was shown to be dependent on the
oleA
gene in experiments with
Shewanella oneidensis
MR-1
ole
gene deletion mutants containing native or heterologous
oleA
genes expressed in
trans
. A strain deleted in
oleABCD
and containing
oleA
in
trans
produced only ketones. Based on these observations, it was proposed that OleA catalyzes a nondecarboxylative thiolytic condensation of fatty acyl chains to generate a β-ketoacyl intermediate that can decarboxylate spontaneously to generate ketones.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
100 articles.
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