Characterization of CprK1, a CRP/FNR-type transcriptional regulator of halorespiration from Desulfitobacterium hafniense
The recently identified CprK branch of the CRP (cyclic AMP receptor protein)-FNR (fumarate and nitrate reduction regulator) family of transcriptional regulators includes proteins that activate the transcription of genes encoding proteins involved in reductive dehalogenation of chlorinated aromatic compounds. Here we report the characterization of the CprK1 protein from Desulfitobacterium hafniense, an anaerobic low-G+C gram-positive bacterium that is capable of reductive dechlorination of 3-chloro-4-hydroxyphenylacetic acid (Cl-OHPA). The gene encoding CprK1 was cloned and functionally overexpressed in Escherichia coli, and the protein was subsequently purified to homogeneity. To investigate the interaction of CprK1 with three of its predicted binding sequences (dehaloboxes), we performed in vitro DNA-binding assays (electrophoretic mobility shift assays) as well as in vivo promoter probe assays. Our results show that CprK1 binds its target dehaloboxes with high affinity (dissociation constant, 90 nM) in the presence of Cl-OHPA and that transcriptional initiation by CprK1 is influenced by deviations in the dehaloboxes from the consensus TTAAT----ATTAA sequence. A mutant CprK1 protein was created by a ValGlu substitution at a conserved position in the recognition -helix that gained FNR-type DNA-binding specificity, recognizing the TTGAT----ATCAA sequence (FNR box) instead of the dehaloboxes. CprK1 was subject to oxidative inactivation in vitro, most likely caused by the formation of an intermolecular disulfide bridge between Cys11 and Cys200. The possibility of redox regulation of CprK1 by a thiol-disulfide exchange reaction was investigated by using two CysSer mutants. Our results indicate that a Cys11-Cys200 disulfide bridge does not appear to play a physiological role in the regulation of CprK1
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Format: | Article/Letter to editor biblioteca |
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Subjects: | activator protein cap, dependent promoters, disulfide bond, dna complex, escherichia-coli, gene-expression, receptor protein, reductive dehalogenase, rna-polymerase, structural basis, |
Online Access: | https://research.wur.nl/en/publications/characterization-of-cprk1-a-crpfnr-type-transcriptional-regulator |
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dig-wur-nl-wurpubs-3461062024-12-04 Gabor, K. Verissimo, C.S. Cyran, B.C. Ter Horst, P. Meijer, N.P. Smidt, H. de Vos, W.M. van der Oost, J. Article/Letter to editor Journal of Bacteriology 188 (2006) 7 ISSN: 0021-9193 Characterization of CprK1, a CRP/FNR-type transcriptional regulator of halorespiration from Desulfitobacterium hafniense 2006 The recently identified CprK branch of the CRP (cyclic AMP receptor protein)-FNR (fumarate and nitrate reduction regulator) family of transcriptional regulators includes proteins that activate the transcription of genes encoding proteins involved in reductive dehalogenation of chlorinated aromatic compounds. Here we report the characterization of the CprK1 protein from Desulfitobacterium hafniense, an anaerobic low-G+C gram-positive bacterium that is capable of reductive dechlorination of 3-chloro-4-hydroxyphenylacetic acid (Cl-OHPA). The gene encoding CprK1 was cloned and functionally overexpressed in Escherichia coli, and the protein was subsequently purified to homogeneity. To investigate the interaction of CprK1 with three of its predicted binding sequences (dehaloboxes), we performed in vitro DNA-binding assays (electrophoretic mobility shift assays) as well as in vivo promoter probe assays. Our results show that CprK1 binds its target dehaloboxes with high affinity (dissociation constant, 90 nM) in the presence of Cl-OHPA and that transcriptional initiation by CprK1 is influenced by deviations in the dehaloboxes from the consensus TTAAT----ATTAA sequence. A mutant CprK1 protein was created by a ValGlu substitution at a conserved position in the recognition -helix that gained FNR-type DNA-binding specificity, recognizing the TTGAT----ATCAA sequence (FNR box) instead of the dehaloboxes. CprK1 was subject to oxidative inactivation in vitro, most likely caused by the formation of an intermolecular disulfide bridge between Cys11 and Cys200. The possibility of redox regulation of CprK1 by a thiol-disulfide exchange reaction was investigated by using two CysSer mutants. Our results indicate that a Cys11-Cys200 disulfide bridge does not appear to play a physiological role in the regulation of CprK1 en application/pdf https://research.wur.nl/en/publications/characterization-of-cprk1-a-crpfnr-type-transcriptional-regulator 10.1128/JB.188.7.2604-2613.2006 https://edepot.wur.nl/45752 activator protein cap dependent promoters disulfide bond dna complex escherichia-coli gene-expression receptor protein reductive dehalogenase rna-polymerase structural basis Wageningen University & Research |
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activator protein cap dependent promoters disulfide bond dna complex escherichia-coli gene-expression receptor protein reductive dehalogenase rna-polymerase structural basis activator protein cap dependent promoters disulfide bond dna complex escherichia-coli gene-expression receptor protein reductive dehalogenase rna-polymerase structural basis |
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activator protein cap dependent promoters disulfide bond dna complex escherichia-coli gene-expression receptor protein reductive dehalogenase rna-polymerase structural basis activator protein cap dependent promoters disulfide bond dna complex escherichia-coli gene-expression receptor protein reductive dehalogenase rna-polymerase structural basis Gabor, K. Verissimo, C.S. Cyran, B.C. Ter Horst, P. Meijer, N.P. Smidt, H. de Vos, W.M. van der Oost, J. Characterization of CprK1, a CRP/FNR-type transcriptional regulator of halorespiration from Desulfitobacterium hafniense |
description |
The recently identified CprK branch of the CRP (cyclic AMP receptor protein)-FNR (fumarate and nitrate reduction regulator) family of transcriptional regulators includes proteins that activate the transcription of genes encoding proteins involved in reductive dehalogenation of chlorinated aromatic compounds. Here we report the characterization of the CprK1 protein from Desulfitobacterium hafniense, an anaerobic low-G+C gram-positive bacterium that is capable of reductive dechlorination of 3-chloro-4-hydroxyphenylacetic acid (Cl-OHPA). The gene encoding CprK1 was cloned and functionally overexpressed in Escherichia coli, and the protein was subsequently purified to homogeneity. To investigate the interaction of CprK1 with three of its predicted binding sequences (dehaloboxes), we performed in vitro DNA-binding assays (electrophoretic mobility shift assays) as well as in vivo promoter probe assays. Our results show that CprK1 binds its target dehaloboxes with high affinity (dissociation constant, 90 nM) in the presence of Cl-OHPA and that transcriptional initiation by CprK1 is influenced by deviations in the dehaloboxes from the consensus TTAAT----ATTAA sequence. A mutant CprK1 protein was created by a ValGlu substitution at a conserved position in the recognition -helix that gained FNR-type DNA-binding specificity, recognizing the TTGAT----ATCAA sequence (FNR box) instead of the dehaloboxes. CprK1 was subject to oxidative inactivation in vitro, most likely caused by the formation of an intermolecular disulfide bridge between Cys11 and Cys200. The possibility of redox regulation of CprK1 by a thiol-disulfide exchange reaction was investigated by using two CysSer mutants. Our results indicate that a Cys11-Cys200 disulfide bridge does not appear to play a physiological role in the regulation of CprK1 |
format |
Article/Letter to editor |
topic_facet |
activator protein cap dependent promoters disulfide bond dna complex escherichia-coli gene-expression receptor protein reductive dehalogenase rna-polymerase structural basis |
author |
Gabor, K. Verissimo, C.S. Cyran, B.C. Ter Horst, P. Meijer, N.P. Smidt, H. de Vos, W.M. van der Oost, J. |
author_facet |
Gabor, K. Verissimo, C.S. Cyran, B.C. Ter Horst, P. Meijer, N.P. Smidt, H. de Vos, W.M. van der Oost, J. |
author_sort |
Gabor, K. |
title |
Characterization of CprK1, a CRP/FNR-type transcriptional regulator of halorespiration from Desulfitobacterium hafniense |
title_short |
Characterization of CprK1, a CRP/FNR-type transcriptional regulator of halorespiration from Desulfitobacterium hafniense |
title_full |
Characterization of CprK1, a CRP/FNR-type transcriptional regulator of halorespiration from Desulfitobacterium hafniense |
title_fullStr |
Characterization of CprK1, a CRP/FNR-type transcriptional regulator of halorespiration from Desulfitobacterium hafniense |
title_full_unstemmed |
Characterization of CprK1, a CRP/FNR-type transcriptional regulator of halorespiration from Desulfitobacterium hafniense |
title_sort |
characterization of cprk1, a crp/fnr-type transcriptional regulator of halorespiration from desulfitobacterium hafniense |
url |
https://research.wur.nl/en/publications/characterization-of-cprk1-a-crpfnr-type-transcriptional-regulator |
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