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J Biol Chem, Vol. 273, Issue 14, 8033-8039, April 3, 1998
From the Neurobiotechnology Center and Departments of Biochemistry
and Medical Biochemistry, The Ohio State University,
Columbus, Ohio 43210
An open reading frame, ORF3, first
identified adjacent to the mycocerosic acid synthase gene in
Mycobacterium bovis BCG encodes a protein with acyl-CoA
synthase (ACoAS) activity. Genes homologous to acoas are
found adjacent to other multifunctional polyketide synthase genes in
the mycobacterial genome. To test whether these gene products are
necessary to esterify the fatty acids generated by the adjacent
polyketide synthase gene products, the acoas gene was
disrupted in M. bovis BCG using a suicide vector containing the acoas gene with an internal deletion and the
hygromycin-resistant gene as selection marker. Allelic exchange at the
acoas locus was confirmed by Southern hybridization and
polymerase chain reaction amplification of both flanking regions
expected from homologous recombination. Immunoblot analysis indicated
that the 65-kDa ACoAS protein product was absent in the mutant.
Chromatographic analysis of lipids derived from
[1-14C]propionate showed that the mutant did not produce
mycocerosyl lipids, although it produced normal levels of mycocerosic
acid synthase. These results suggest that ACoAS is involved in the synthesis of mycocerosyl lipids of the mycobacterial cell wall.
An Acyl-CoA Synthase (acoas) Gene Adjacent to the
Mycocerosic Acid Synthase (mas) Locus Is Necessary for
Mycocerosyl Lipid Synthesis in Mycobacterium tuberculosis
var. bovis BCG
Copyright © 1998 by The American Society for Biochemistry and Molecular Biology, Inc.
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