Microbiology
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
 QUICK SEARCH:   [advanced]


     


Published online ahead of print on 10 September 2009 as doi:10.1099/mic.0.032110-0
Microbiology (2009), DOI 10.1099/mic.0.032110-0
© 2009 Society for General Microbiology

This Article
Right arrow Full Text (Papers in Press[PDF])
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Right arrow reprints & permissions
Citing Articles
Right arrow Citing Articles via CrossRef
Google Scholar
Right arrow Articles by Kunze, M.
Right arrow Articles by Reineke, W.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Kunze, M.
Right arrow Articles by Reineke, W.
Agricola
Right arrow Articles by Kunze, M.
Right arrow Articles by Reineke, W.
Microbiology 0 (2009), mic.0.032110; DOI  10.1099/mic.0.032110-0
© 2009 Society for General Microbiology


Degradation of chloroaromatics by Pseudomonas putida GJ31: assembled route for chlorobenzene degradation encoded by clusters on plasmid pKW1 and the chromosome

Markus Kunze1, Kay F. Zerlin2, Alexander Retzlaff3, Jens O. Pohl3, Eberhard Schmidt3, Dick B. Janssen4, Ramiro Vilchez-Vargas5, Dietmar H. Pieper5 and Walter Reineke3,6

1 Sandoz; Basel, Switzerland;
2 Forschungszentrum Jülich GmbH, Geschäftsstelle BIO NRW, Düsseldorf;
3 Bergische Universität Wuppertal;
4 University of Groningen;
5 Helmholtz Centre for Infection Research, Braunschweig

Pseudomonas putida GJ31 has been reported to grow on chlorobenzene using a meta-cleavage pathway with chlorocatechol 2,3-dioxygenase (CbzE) as key enzyme. The CbzE encoding gene was now found to be localized on the 180-kbp plasmid pKW1 in a cbzTEXGS cluster which is flanked by transposases and encodes only a partial (chloro)catechol meta-cleavage pathway comprising ferredoxin reductase, chlorocatechol 2,3-dioxygenase, an unknown protein, 2-hydroxymuconic semialdehyde dehydrogenase and glutathione S-transferase. Downstream of cbzTEXGS, cbzJ, encoding a novel type of 2-hydroxypent-2,4-dienoate hydratase and a transposon region highly similar to Tn5501 are located. Upstream of cbzTEXGS, traNEOFG transfer genes were found. The search for gene clusters possibly completing the (chloro)catechol metabolic pathway of GJ31 revealed the presence of two additional catabolic gene clusters on pKW1. The mhpRBCDFETP cluster encodes enzymes for the dissimilation of 2,3-dihydroxyphenylpropionate in a novel arrangement characterized by the absence of a gene encoding 3-(3-hydroxyphenyl)propionate monooxygenase and the presence of a GntR-type regulator, whereas the nahINLOMKJ cluster encodes a part of the naphthalene metabolic pathway. Transcription studies supported their possible involvement in chlorobenzene degradation. The upper pathway cluster comprising genes encoding a chlorobenzene dioxygenase and a chlorobenzene dihydrodiol dehydrogenase was localized on the chromosome. High level of transcription in response to chlorobenzene revealed it to be crucial for chlorobenzene degradation. The chlorobenzene degradation pathway in strain GJ31 is thus a mosaic encoded by 4 gene clusters.

6 E-mail: reineke{at}uni-wuppertal.de







HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH
INT J SYST EVOL MICROBIOL MICROBIOLOGY J GEN VIROL
J MED MICROBIOL ALL SGM JOURNALS
Copyright © 2009 Society for General Microbiology.