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Microbiol. Mol. Biol. Rev., Dec 1997, 429-441, Vol 61, No. 4
DW Grogan and JE Cronan Jr
It has been known for several decades that cyclopropane fatty acids (CFAs)
occur in the phospholipids of many species of bacteria. CFAs are formed by
the addition of a methylene group, derived from the methyl group of
S-adenosylmethionine, across the carbon-carbon double bond of unsaturated
fatty acids (UFAs). The C1 transfer does not involve free fatty acids or
intermediates of phospholipid biosynthesis but, rather, mature phospholipid
molecules already incorporated into membrane bilayers. Furthermore, CFAs
are typically produced at the onset of the stationary phase in bacterial
cultures. CFA formation can thus be considered a conditional, postsynthetic
modification of bacterial membrane lipid bilayers. This modification is
noteworthy in several respects. It is catalyzed by a soluble enzyme,
although one of the substrates, the UFA double bond, is normally
sequestered deep within the hydrophobic interior of the phospholipid
bilayer. The enzyme, CFA synthase, discriminates between phospholipid
vesicles containing only saturated fatty acids and those containing UFAs;
it exhibits no affinity for vesicles of the former composition. These and
other properties imply that topologically novel protein-lipid interactions
occur in the biosynthesis of CFAs. The timing and extent of the UFA-to- CFA
conversion in batch cultures and the widespread distribution of CFA
synthesis among bacteria would seem to suggest an important physiological
role for this phenomenon, yet its rationale remains unclear despite
experimental tests of a variety of hypotheses. Manipulation of the CFA
synthase of Escherichia coli by genetic methods has nevertheless provided
valuable insight into the physiology of CFA formation. It has identified
the CFA synthase gene as one of several rpoS-regulated genes of E. coli and
has provided for the construction of strains in which proposed cellular
functions of CFAs can be properly evaluated. Cloning and manipulation of
the CFA synthase structural gene have also enabled this novel but extremely
unstable enzyme to be purified and analyzed in molecular terms and have led
to the identification of mechanistically related enzymes in clinically
important bacterial pathogens.
Copyright © 1997, American Society for Microbiology
Cyclopropane ring formation in membrane lipids of bacteria [In Process Citation]
Department of Biological Sciences, University of Cincinnati, Ohio 45221- 0006, USA.
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