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PMID: 7954108 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Identification and mapping of the gene translation products involved in the first steps of the Comamonas testosteroni B-356 biphenyl/chlorobiphenyl biodegradation pathway.

Canadian journal of microbiology ·Vol. 40 ·No. 9 ·1994-09-00 ·Pages 743-53

Bergeron J, Ahmad D, Barriault D, Larose A, Sylvestre M, Powlowski J

Abstract

In this study, we have mapped Comamonas testosteroni B-356 genes encoding enzymes for the conversion of biphenyl and 4-chlorobiphenyl into the corresponding meta-cleavage compounds onto a 6.3-kb DNA fragment, and we have determined the subunit composition of the enzymes involved in this pathway. The various proteins encoded by this 6.3-kb DNA fragment and by subclones derived from it were overexpressed and selectively labelled using the T7 polymerase promoter system in Escherichia coli. They were then analyzed using SDS-PAGE, which allowed the encoding locus of each polypeptide to be mapped. Despite apparent dissimilarity in the congener selectivity patterns of the initial oxygenase of strain B-356 with those of Pseudomonas sp. strain LB400, the number and sizes of the polypeptides involved in the enzymatic conversion of biphenyl or 4-chlorobiphenyl into the meta-cleavage product appear to be similar in the two strains. In both strains, the bph operon encodes the following: the large (51-kDa polypeptide encoded by bphA) and the small (22-kDa polypeptide encoded by bphE) subunits of the iron sulphur protein, which is thought to interact directly with the substrate to introduce the oxygen molecule; the ferredoxin (12-kDa polypeptide encoded by bphF) involved in electron transfer from the reduced ferredoxin reductase to the oxidized iron sulphur protein; the 29-kDa polypeptide of the 2,3-dihydro-2,3-dihydroxybiphenyl dehydrogenase encoded by bphB; and the 32-kDa polypeptide of the 2,3-dihydroxybiphenyl-1,2-dioxygenase encoded by bphC, which catalyzes meta-1,2 fission of the aromatic ring. A major difference between strain B-356 and strain LB400 is that the bphG gene encoding biphenyl dioxygenase ferredoxin reductase is located outside the bph gene cluster in strain B-356. Several lines of evidence indicate that bphG is absent in clones carrying the bph operon from strain B-356.

MeSH Terms
Base Sequence Biodegradation, Environmental Biphenyl Compounds/metabolism Chromosome Mapping Ferrous Compounds/metabolism Gram-Negative Aerobic Bacteria/enzymology,genetics,metabolism Iron-Sulfur Proteins Molecular Sequence Data Multienzyme Complexes/genetics,isolation & purification,metabolism NAD/metabolism NADP/metabolism Operon/genetics Oxygenases/genetics,metabolism Pseudomonadaceae Pseudomonas/enzymology,genetics,metabolism
Chemicals
Biphenyl Compounds Ferrous Compounds Iron-Sulfur Proteins Multienzyme Complexes NAD ferrous sulfate NADP Oxygenases biphenyl-2,3-dioxygenase 4-chlorobiphenyl
Authors & Affiliations
6 authors, click to expand affiliations / ORCID
Bergeron J
Institut national de la recherche scientifique-santé, Université du Québec, Pointe-Claire, Canada.
Ahmad D
Barriault D
Larose A
Sylvestre M
Powlowski J
Article Info
Journal
Canadian journal of microbiology
Abbr.
Can J Microbiol
ISSN
0008-4166
Published
1994-09-00
Pages
743-53
Language
English
Region
Canada
NLM ID
0372707
Subset
IM
Corrections
ErratumIn
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