TY - JOUR
T1 - FabQ, a dual-function dehydratase/isomerase, circumvents the last step of the classical fatty acid synthesis cycle
AU - Bi, Hongkai
AU - Wang, Haihong
AU - Cronan, John E.
N1 - Funding Information:
This work was supported by National Institutes of Health grant AI15650 from the National Institute of Allergy and Infectious Diseases. We thank Dr. Peter Yau and Dr. Alexander Ulanov of the Roy J. Carver Biotechnology Center and Dr. Furong Sun and Elizabeth Eves of the Mass Spectrometry Laboratory at the University of Illinois at Urbana-Champaign for help with protein identification and gas chromatography-mass spectrometry analysis.
PY - 2013/9/19
Y1 - 2013/9/19
N2 - Summary In the classical anaerobic pathway of unsaturated fatty acid biosynthesis, that of Escherichia coli, the double bond is introduced into the growing acyl chain by the FabA dehydratase/isomerase. Another dehydratase, FabZ, functions in the chain elongation cycle. In contrast, Aerococcus viridans has only a single FabA/FabZ homolog we designate FabQ. FabQ can not only replace the function of E. coli FabZ in vivo, but it also catalyzes the isomerization required for unsaturated fatty acid biosynthesis. Most strikingly, FabQ in combination with E. coli FabB imparts the surprising ability to bypass reduction of the trans-2-acyl-ACP intermediates of classical fatty acid synthesis. FabQ allows elongation by progressive isomerization reactions to form the polyunsaturated fatty acid, 3-hydroxy-cis-5, 7-hexadecadienoic acid, both in vitro and in vivo. FabQ therefore provides a potential pathway for bacterial synthesis of polyunsaturated fatty acids.
AB - Summary In the classical anaerobic pathway of unsaturated fatty acid biosynthesis, that of Escherichia coli, the double bond is introduced into the growing acyl chain by the FabA dehydratase/isomerase. Another dehydratase, FabZ, functions in the chain elongation cycle. In contrast, Aerococcus viridans has only a single FabA/FabZ homolog we designate FabQ. FabQ can not only replace the function of E. coli FabZ in vivo, but it also catalyzes the isomerization required for unsaturated fatty acid biosynthesis. Most strikingly, FabQ in combination with E. coli FabB imparts the surprising ability to bypass reduction of the trans-2-acyl-ACP intermediates of classical fatty acid synthesis. FabQ allows elongation by progressive isomerization reactions to form the polyunsaturated fatty acid, 3-hydroxy-cis-5, 7-hexadecadienoic acid, both in vitro and in vivo. FabQ therefore provides a potential pathway for bacterial synthesis of polyunsaturated fatty acids.
UR - http://www.scopus.com/inward/record.url?scp=84884533441&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84884533441&partnerID=8YFLogxK
U2 - 10.1016/j.chembiol.2013.07.007
DO - 10.1016/j.chembiol.2013.07.007
M3 - Article
C2 - 23972938
AN - SCOPUS:84884533441
SN - 2451-9448
VL - 20
SP - 1157
EP - 1167
JO - Cell Chemical Biology
JF - Cell Chemical Biology
IS - 9
ER -