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J. Bacteriol., 10 1996, 5793-5796, Vol 178, No. 19
M Seyfried, R Daniel and G Gottschalk
The genes encoding coenzyme B12-dependent glycerol dehydratase of
Citrobacter freundii were cloned and overexpressed in Escherichia coli. The
B12-free enzyme was purified to homogeneity. It consists of three types of
subunits whose N-terminal sequences are in accordance with those deduced
from the open reading frames dhaB, dhaC, and dhaE, coding for subunits of
60,433 (alpha), 21,487 (beta), and 16,121 (gamma) Da, respectively. The
enzyme complex has the composition alpha2beta2gamma2. Amino acid alignments
with the subunits of the recently sequenced diol dehydratase of Klebsiella
oxytoca (T. Tobimatsu, T. Hara, M. Sakaguchi, Y. Kishimoto, Y. Wada, M.
Isoda, T. Sakai, and T. Toraya, J. Biol. Chem. 270:7142-7148, 1995)
revealed identities between 51.8 and 70.9%.
Copyright © 1996, American Society for Microbiology
Cloning, sequencing, and overexpression of the genes encoding coenzyme B12-dependent glycerol dehydratase of Citrobacter freundii
Institut fur Mikrobiologie der Georg-August-Universitat, Gottingen, Germany.
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