Journal
MOLECULAR MICROBIOLOGY
Volume 71, Issue 2, Pages 332-349Publisher
WILEY
DOI: 10.1111/j.1365-2958.2008.06525.x
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Funding
- National Science Foundation [MCB-9631093]
- National Institutes of Health [GM042025]
- Department of Energy [FG05-95ER20175]
- Deutsche Forschungsgemeinschaft
- NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [R01GM042025] Funding Source: NIH RePORTER
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This work describes the identification and characterization of SurR, Pyrococcus furiosus sulphur (S-0) response regulator. SurR was captured from cell extract using promoter DNA of a hydrogenase operon that is downregulated in the primary response of P. furiosus to S-0, as revealed by DNA microarray experiments. SurR was validated as a sequence-specific DNA binding protein, and characterization of the SurR DNA binding motif GTTn(3)AAC led to the identification of several target genes that contain an extended motif in their promoters. A number of these were validated to contain upstream SurR binding sites. These SurR targets strongly correspond with open reading frames and operons both up- and downregulated in the primary response to S-0. In vitro transcription revealed that SurR is an activator for its own gene as well as for two hydrogenase operons whose expression is downregulated during the primary S-0 response; it is also a repressor for two genes upregulated during the primary S-0 response, one of which encodes the primary S-0-reducing enzyme NAD(P)H sulphur reductase. Herein we give evidence for the role of SurR in both mediating the primary response to S-0 and controlling hydrogen production in P. furiosus.
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