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The Unmodified (Apo) Form of Escherichia coliAcyl Carrier Protein Is a Potent Inhibitor of Cell Growth (∗)
- Source :
- Journal of Biological Chemistry; September 1995, Vol. 270 Issue: 38 p22229-22235, 7p
- Publication Year :
- 1995
-
Abstract
- Acyl carrier protein (ACP) is the carrier of fatty acids during their synthesis and utilization. ACPs (or ACP-like protein domains) have been found throughout biology and share significant amino acid sequence similarities. All ACPs undergo a post-translational modification in which 4′-phosphopantetheine is transferred from CoA to a specific serine of apo-ACP. This modification is essential for activity because fatty acids are bound in thioester linkage to the sulfhydryl of the prosthetic group. Overproduction of Escherichia coliACP from multicopy plasmids strongly inhibits growth of E. coli. We report that upon overexpression of ACP in E. colipost-translational modification is inefficient and the apo protein accumulates and blocks cell growth by inhibition of lipid metabolism. Moreover, a mutant form of ACP that is unable to undergo post-translational modification is a potent inhibitor of growth. Finally, we observed that an increase in the efficiency of modification of overexpressed ACP results in decreased toxicity. The accumulated apo-ACP acts as a potent in vitroinhibitor of the sn-glycerol-3-phosphate acyltransferase resulting in an inability to transfer the completed fatty acid to sn-glycerol 3-phosphate. The degree of inhibition depended upon the species of donor acyl chain. Utilization of cis-vaccenoyl-ACP by the sn-glycerol-3-phosphate acyltransferase was inhibited to a much greater extent by apo-ACP than was utilization of palmitoyl-ACP. 1-Acyl glycerol-3-phosphate acyltransferase was also inhibited in vitroby apo-ACP, although not at physiologically relevant concentrations. These in vitrodata are supported by in vivolabeling data, which showed a large decrease in cis-vaccenate incorporation into phospholipid during overproduction of ACP, but no decrease in the rate of synthesis of long chain acyl-ACPs. These data indicate that acylation of sn-glycerol 3-phosphate is the major site of inhibition by apo-ACP.
Details
- Language :
- English
- ISSN :
- 00219258 and 1083351X
- Volume :
- 270
- Issue :
- 38
- Database :
- Supplemental Index
- Journal :
- Journal of Biological Chemistry
- Publication Type :
- Periodical
- Accession number :
- ejs55939260
- Full Text :
- https://doi.org/10.1074/jbc.270.38.22229