Affiliation:
1. Department of Biochemistry, Sri Krishnadevraya University, Anantapur-515 003, India
2. Department of Molecular Microbiology, John Innes Centre, Norwich NR4 7UH, United Kingdom
Abstract
ABSTRACT
Several bacterial strains that can use organophosphate pesticides as a source of carbon have been isolated from soil samples collected from diverse geographical regions. All these organisms synthesize an enzyme called parathion hydrolase, and in each case the enzyme is encoded by a gene (
opd
) located on a large indigenous plasmid. These plasmids show considerable genetic diversity, but the region containing the
opd
gene is highly conserved. Two
opd
plasmids, pPDL2 from
Flavobacterium
sp. and pCMS1 from
Pseudomonas diminuta
, are well characterized, and in each of them a region of about 5.1 kb containing the
opd
gene shows an identical restriction pattern. We now report the complete sequence of the conserved region of plasmid pPDL2. The
opd
gene is flanked upstream by an insertion sequence, ISFlsp
1
, that is a member of the IS
21
family, and downstream by a Tn
3
-like element encoding a transposase and a resolvase. Adjacent to
opd
but transcribed in the opposite direction is an open reading frame (
orf243
) with the potential to encode an aromatic hydrolase somewhat similar to
Pseudomonas putida
TodF. We have shown that
orf243
encodes a polypeptide of 27 kDa, which plays a role in the degradation of
p
-nitrophenol and is likely to act in concert with
opd
in the degradation of parathion. The linkage of
opd
and
orf243
, the organization of the genes flanking
opd
, and the wide geographical distribution of these genes suggest that this DNA sequence may constitute a complex catabolic transposon.
Publisher
American Society for Microbiology
Subject
Ecology,Applied Microbiology and Biotechnology,Food Science,Biotechnology
Cited by
72 articles.
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