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Appl. Environ. Microbiol., 07 1997, 2695-2701, Vol 63, No. 7
L Stols and MI Donnelly
NAD(+)-dependent malic enzyme was cloned from the Escherichia coli genome
by PCR based on the published partial sequence of the gene. The enzyme was
overexpressed and purified to near homogeneity in two chromatographic steps
and was analyzed kinetically in the forward and reverse directions. The Km
values determined in the presence of saturating cofactor and manganese ion
were 0.26 mM for malate (physiological direction) and 16 mM for pyruvate
(reverse direction). When malic enzyme was induced under appropriate
culture conditions in a strain of E. coli that was unable to ferment
glucose and accumulated pyruvate, fermentative metabolism of glucose was
restored. Succinic acid was the major fermentation product formed. When
this fermentation was performed in the presence of hydrogen, the yield of
succinic acid increased. The constructed pathway represents an alternative
metabolic route for the fermentative production of dicarboxylic acids from
renewable feedstocks.
Production of succinic acid through overexpression of NAD(+)-dependent malic enzyme in an Escherichia coli mutant
Environmental Research Division, Argonne National Laboratory, Illinois 60439, USA.
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