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Applied and Environmental Microbiology, October 2005, p. 6104-6114, Vol. 71, No. 10
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.10.6104-6114.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.

Role of the ssu and seu Genes of Corynebacterium glutamicum ATCC 13032 in Utilization of Sulfonates and Sulfonate Esters as Sulfur Sources{dagger}

D. J. Koch,1,2,{ddagger} C. Rückert,1,2,{ddagger} D. A. Rey,2 A. Mix,3 A. Pühler,4 and J. Kalinowski2*

International Graduate School in Bioinformatics & Genome Research, Center for Biotechnology, Universität Bielefeld, Universitätsstr. 25, D-33615 Bielefeld, Germany,1 Institut für Genomforschung, Universität Bielefeld, Universitätsstr. 25, D-33615 Bielefeld, Germany,2 Lehrstuhl für Anorganische Chemie III, Universität Bielefeld, Universitätsstr. 25, D-33615 Bielefeld, Germany,3 Lehrstuhl für Genetik, Universität Bielefeld, Universitätsstr. 25, D-33615 Bielefeld, Germany4

Received 6 May 2005/ Accepted 10 May 2005

Corynebacterium glutamicum ATCC 13032 was found to be able to utilize a broad range of sulfonates and sulfonate esters as sulfur sources. The two gene clusters potentially involved in sulfonate utilization, ssuD1CBA and ssuI-seuABC-ssuD2, were identified in the genome of C. glutamicum ATCC 13032 by similarity searches. While the ssu genes encode proteins resembling Ssu proteins from Escherichia coli or Bacillus subtilis, the seu gene products exhibited similarity to the dibenzothiophene-degrading Dsz monooxygenases of Rhodococcus strain IGTS8. Growth tests with the C. glutamicum wild-type and appropriate mutant strains showed that the clustered genes ssuC, ssuB, and ssuA, putatively encoding the components of an ABC-type transporter system, are required for the utilization of aliphatic sulfonates. In C. glutamicum sulfonates are apparently degraded by sulfonatases encoded by ssuD1 and ssuD2. It was also found that the seu genes seuA, seuB, and seuC can effectively replace ssuD1 and ssuD2 for the degradation of sulfonate esters. The utilization of all sulfonates and sulfonate esters tested is dependent on a novel putative reductase encoded by ssuI. Obviously, all monooxygenases encoded by the ssu and seu genes, including SsuD1, SsuD2, SeuA, SeuB, and SeuC, which are reduced flavin mononucleotide dependent according to sequence similarity, have SsuI as an essential component. Using real-time reverse transcription-PCR, the ssu and seu gene cluster was found to be expressed considerably more strongly during growth on sulfonates and sulfonate esters than during growth on sulfate.

* Corresponding author. Mailing address: Institut für Genomforschung, Universität Bielefeld, Universitätsstr. 25, D-33615 Bielefeld, Germany. Phone: (49) 521 106-4825. Fax: (49) 521 106-5626. E-mail: Joern.Kalinowski{at}CeBiTec.Uni-Bielefeld.de.

{dagger} Supplemental material for this article may be found at http://aem.asm.org/.

{ddagger} D.J.K. and C.R. contributed equally to this work.

Applied and Environmental Microbiology, October 2005, p. 6104-6114, Vol. 71, No. 10
0099-2240/05/$08.00+0     doi:10.1128/AEM.71.10.6104-6114.2005
Copyright © 2005, American Society for Microbiology. All Rights Reserved.



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