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Applied and Environmental Microbiology, March 1999, p. 1180-1185, Vol. 65, No. 3
Department of Chemical Engineering,
University of Wisconsin
Received 21 September 1998/Accepted 5 January 1999
1,2-Propanediol (1,2-PD) is a major commodity chemical that is
currently derived from propylene, a nonrenewable resource. A goal of our research is to develop fermentation routes to 1,2-PD from
renewable resources. Here we report the production of
enantiomerically pure R-1,2-PD from glucose in
Escherichia coli expressing NADH-linked glycerol
dehydrogenase genes (E. coli gldA or Klebsiella
pneumoniae dhaD). We also show that E. coli
overexpressing the E. coli methylglyoxal synthase gene
(mgs) produced 1,2-PD. The expression of
either glycerol dehydrogenase or methylglyoxal synthase resulted in
the anaerobic production of approximately 0.25 g of 1,2-PD per
liter. R-1,2-PD production was further improved to 0.7 g of 1,2-PD per liter when methylglyoxal synthase
and glycerol dehydrogenase (gldA) were coexpressed. In
vitro studies indicated that the route to R-1,2-PD involved
the reduction of methylglyoxal to R-lactaldehyde by the
recombinant glycerol dehydrogenase and the reduction of R-lactaldehyde to R-1,2-PD by a native
E. coli activity. We expect that R-1,2-PD
production can be significantly improved through further metabolic
and bioprocess engineering.
0099-2240/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Metabolic Engineering of a 1,2-Propanediol
Pathway in Escherichia coli
Madison, Madison, Wisconsin 53706-1691
*
Corresponding author. Present address: Cargill Central
Research, P.O. Box 5702, Minneapolis, MN 55440-5702. Phone: (612)
742-3001. Fax: (612) 742-3010. E-mail:
doug_cameron{at}cargill.com.
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