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J. Bacteriol., 01 1998, 400-402, Vol 180, No. 2
M Bruckmann, R Blasco, KN Timmis and DH Pieper
Protoanemonin is a toxic metabolite which may be formed during the
degradation of some chloroaromatic compounds, such as polychlorinated
biphenyls, by natural microbial consortia. We show here that protoanemonin
can be transformed by dienelactone hydrolase of Pseudomonas sp. strain B13
to cis-acetylacrylate. Although similar Km values were observed for
cis-dienelactone and protoanemonin, the turnover rate of protoanemonin was
only 1% that of cis-dienelactone. This indicates that at least this
percentage of the enzyme is in the active state, even in the absence of
activation. The trans-dienelactone hydrolase of Pseudomonas sp. strain RW10
did not detectably transform protoanemonin. Obviously, Pseudomonas sp.
strain B13 possesses at least two mechanisms to avoid protoanemonin
toxicity, namely a highly active chloromuconate cycloisomerase, which
routes most of the 3-chloro- cis,cis-muconate to the cis-dienelactone,
thereby largely preventing protoanemonin formation, and dienelactone
hydrolase, which detoxifies any small amount of protoanemonin that might
nevertheless be formed.
Copyright © 1998, American Society for Microbiology
Detoxification of protoanemonin by dienelactone hydrolase [In Process Citation]
Department of Microbiology, National Research Centre for Biotechnology, Braunschweig, Germany.
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