PMID- 10092655 OWN - NLM STAT- MEDLINE DCOM- 19990427 LR - 20210209 IS - 0021-9258 (Print) IS - 0021-9258 (Linking) VI - 274 IP - 14 DP - 1999 Apr 2 TI - Effect of cold shock on lipid A biosynthesis in Escherichia coli. Induction At 12 degrees C of an acyltransferase specific for palmitoleoyl-acyl carrier protein. PG - 9677-85 AB - Palmitoleate is not present in lipid A isolated from Escherichia coli grown at 30 degrees C or higher, but it comprises approximately 11% of the fatty acyl chains of lipid A in cells grown at 12 degrees C. The appearance of palmitoleate at 12 degrees C is accompanied by a decline in laurate from approximately 18% to approximately 5.5%. We now report that wild-type E. coli shifted from 30 degrees C to 12 degrees C acquire a novel palmitoleoyl-acyl carrier protein (ACP)-dependent acyltransferase that acts on the key lipid A precursor Kdo2-lipid IVA. The palmitoleoyl transferase is induced more than 30-fold upon cold shock, as judged by assaying extracts of cells shifted to 12 degrees C. The induced activity is maximal after 2 h of cold shock, and then gradually declines but does not disappear. Strains harboring an insertion mutation in the lpxL(htrB) gene, which encodes the enzyme that normally transfers laurate from lauroyl-ACP to Kdo2-lipid IVA (Clementz, T., Bednarski, J. J., and Raetz, C. R. H. (1996) J. Biol. Chem. 271, 12095-12102) are not defective in the cold-induced palmitoleoyl transferase. Recently, a gene displaying 54% identity and 73% similarity at the protein level to lpxL was found in the genome of E. coli. This lpxL homologue, designated lpxP, encodes the cold shock-induced palmitoleoyl transferase. Extracts of cells containing lpxP on the multicopy plasmid pSK57 exhibit a 10-fold increase in the specific activity of the cold-induced palmitoleoyl transferase compared with cells lacking the plasmid. The elevated specific activity of the palmitoleoyl transferase under conditions of cold shock is attributed to greatly increased levels of lpxP mRNA. The replacement of laurate with palmitoleate in lipid A may reflect the desirability of maintaining the optimal outer membrane fluidity at 12 degrees C. FAU - Carty, S M AU - Carty SM AD - Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710, USA. FAU - Sreekumar, K R AU - Sreekumar KR FAU - Raetz, C R AU - Raetz CR LA - eng SI - GENBANK/U49787 GR - GM-34123/GM/NIGMS NIH HHS/United States GR - GM-51310/GM/NIGMS NIH HHS/United States GR - GM08558/GM/NIGMS NIH HHS/United States GR - etc. PT - Journal Article PT - Research Support, U.S. Gov't, P.H.S. PL - United States TA - J Biol Chem JT - The Journal of biological chemistry JID - 2985121R RN - 0 (Acyl Carrier Protein) RN - 0 (Bacterial Proteins) RN - 0 (Escherichia coli Proteins) RN - 0 (Fatty Acids, Monounsaturated) RN - 0 (Lipid A) RN - 0 (RNA, Messenger) RN - 143600-83-3 (3-deoxy-2-octulosonic acid(2)-lipid IV(A)) RN - 209B6YPZ4I (palmitoleic acid) RN - EC 2.3.- (Acyltransferases) RN - EC 2.3.- (LpxL protein, E coli) RN - EC 2.3.- (LpxL protein, bacteria) RN - EC 2.3.1.- (lpxP protein, E coli) SB - IM MH - Acyl Carrier Protein/*metabolism MH - Acylation MH - Acyltransferases/*biosynthesis/chemistry/genetics MH - Amino Acid Sequence MH - *Bacterial Proteins MH - Carbohydrate Sequence MH - *Cold Temperature MH - Enzyme Induction MH - Escherichia coli/*metabolism MH - *Escherichia coli Proteins MH - Fatty Acids, Monounsaturated/metabolism MH - Lipid A/analogs & derivatives/*biosynthesis/metabolism MH - Models, Chemical MH - Molecular Sequence Data MH - RNA, Messenger/metabolism MH - Salmonella typhimurium EDAT- 1999/03/27 00:00 MHDA- 1999/03/27 00:01 CRDT- 1999/03/27 00:00 PHST- 1999/03/27 00:00 [pubmed] PHST- 1999/03/27 00:01 [medline] PHST- 1999/03/27 00:00 [entrez] AID - S0021-9258(19)87304-0 [pii] AID - 10.1074/jbc.274.14.9677 [doi] PST - ppublish SO - J Biol Chem. 1999 Apr 2;274(14):9677-85. doi: 10.1074/jbc.274.14.9677.