Affiliation:
1. Institute of Biology, Carleton University, Ottawa, Ontario, Canada K1S 5B6
2. Department of Biology, The University of Konstanz, D-78457 Konstanz, Germany
Abstract
ABSTRACT
In
Comamonas testosteroni
strain BR6020, metabolism of isovanillate (iVan; 3-hydroxy-4-methoxybenzoate), vanillate (Van; 4-hydroxy-3-methoxybenzoate), and veratrate (Ver; 3,4-dimethoxybenzoate) proceeds via protocatechuate (Pca; 3,4-dihydroxybenzoate). A 13.4-kb locus coding for the catabolic enzymes that channel the three substrates to Pca was cloned. O demethylation is mediated by the phthalate family oxygenases IvaA (converts iVan to Pca and Ver to Van) and VanA (converts Van to Pca and Ver to iVan). Reducing equivalents from NAD(P)H are transferred to the oxygenases by the class IA oxidoreductase IvaB. Studies using whole cells, cell extracts, and reverse transcriptase PCR showed that degradative activity and expression of
vanA
,
ivaA
, and
ivaB
are inducible. In succinate- and Pca-grown cells, there is negligible degradative activity towards Van, Ver, and iVan and little to no expression of
vanA
,
ivaA
, and
ivaB
. Growth on Van or Ver results in production of oxygenases with activity towards Van, Ver, and iVan and expression of
vanA
,
ivaA
, and
ivaB
. With iVan-grown cultures,
ivaA
and
ivaB
are expressed, and in assays with whole cells, production of the iVan oxygenase is observed, but there is little activity towards Van or Ver. In cell extracts, though, Ver metabolism is observed, which suggests that the system mediating iVan uptake in whole cells does not mediate Ver uptake.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
28 articles.
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