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Applied and Environmental Microbiology, March 2000, p. 904-908, Vol. 66, No. 3
Institute of Biotechnology, University of
Cambridge, Cambridge CB2 1QT, United Kingdom
Received 6 August 1999/Accepted 1 December 1999
A strain of Rhodococcus designated MB1, which was
capable of utilizing cocaine as a sole source of carbon and nitrogen
for growth, was isolated from rhizosphere soil of the tropane
alkaloid-producing plant Erythroxylum coca. A cocaine
esterase was found to initiate degradation of cocaine, which was
hydrolyzed to ecgonine methyl ester and benzoate; both of these
esterolytic products were further metabolized by
Rhodococcus sp. strain MB1. The structural gene encoding a
cocaine esterase, designated cocE, was cloned from Rhodococcus sp. strain MB1 genomic libraries by screening
recombinant strains of Rhodococcus erythropolis CW25 for
growth on cocaine. The nucleotide sequence of cocE
corresponded to an open reading frame of 1,724 bp that codes for a
protein of 574 amino acids. The amino acid sequence of cocaine esterase
has a region of similarity with the active serine consensus of X-prolyl
dipeptidyl aminopeptidases, suggesting that the cocaine esterase is a
serine esterase. The cocE coding sequence was subcloned
into the pCFX1 expression plasmid and expressed in Escherichia
coli. The recombinant cocaine esterase was purified to apparent
homogeneity and was found to be monomeric, with an
Mr of approximately 65,000. The apparent
Km of the enzyme (mean ± standard
deviation) for cocaine was measured as 1.33 ± 0.085 mM. These
findings are of potential use in the development of a linked assay for
the detection of illicit cocaine.
0099-2240/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Gene Cloning and Nucleotide Sequencing and
Properties of a Cocaine Esterase from Rhodococcus sp.
Strain MB1
*
Corresponding author. Mailing address: Institute of
Biotechnology, University of Cambridge, Tennis Court Rd., Cambridge CB2 1QT, United Kingdom. Phone: 44 (0) 1223 334168. Fax: 44 (0) 1223 334162. E-mail: n.bruce{at}biotech.cam.ac.uk.
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