Affiliation:
1. Division of Microbiology, GBF - National Research Centre for Biotechnology, D-38124 Braunschweig, Germany
Abstract
ABSTRACT
The bacterium
Sphingomonas
sp. strain RW1 is able to use dibenzo-
p
-dioxin, dibenzofuran, and several hydroxylated derivatives as sole sources of carbon and energy. We have determined and analyzed the nucleic acid sequence of a 9,997-bp
Hin
dIII fragment downstream of cistrons
dxnA1A2
, which encode the dioxygenase component of the initial dioxygenase system of the corresponding catabolic pathways. This fragment contains 10 colinear open reading frames (ORFs), apparently organized in one compact operon. The enzymatic activities of some proteins encoded by these genes were analyzed in the strain RW1 and, after hyperexpression, in
Escherichia coli
. The first three ORFs of the locus, designated
dxnC
, ORF2, and
fdx3
, specify a protein with a low homology to bacterial siderophore receptors, a polypeptide representing no significant homology to known proteins, and a putative ferredoxin, respectively.
dxnD
encodes a 69-kDa phenol monooxygenase-like protein with activity for the turnover of 4-hydroxysalicylate, and
dxnE
codes for a 37-kDa protein whose sequence and activity are similar to those of known maleylacetate reductases. The following gene,
dxnF
, encodes a 33-kDa intradiol dioxygenase which efficiently cleaves hydroxyquinol, yielding maleylacetate, the ketoform of 3-hydroxy-
cis,cis
-muconate. The heteromeric protein encoded by
dxnGH
is a 3-oxoadipate succinyl coenzyme A (succinyl-CoA) transferase, whereas
dxnI
specifies a protein exhibiting marked homology to acetyl-CoA acetyltransferases (thiolases). The last ORF of the sequenced fragment codes for a putative transposase. DxnD, DxnF, DxnE, DxnGH, and DxnI (the activities of most of them have also been detected in strain RW1) thus form a complete 4-hydroxysalicylate/hydroxyquinol degradative pathway. A route for the mineralization of the growth substrates 3-hydroxydibenzofuran and 2-hydroxydibenzo-
p
-dioxin in
Sphingomonas
sp. strain RW1 thus suggests itself.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
77 articles.
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