XacR - a novel transcriptional regulator of D-xylose and L-arabinose catabolism in the haloarchaeon Haloferax volcanii

Summary The haloarchaeon Haloferax volcanii degrades D‐xylose and L‐arabinose via oxidative pathways to α‐ketoglutarate. The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene clus...

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Veröffentlicht in:Environmental microbiology 2015-05, Vol.17 (5), p.1663-1676
Hauptverfasser: Johnsen, Ulrike, Sutter, Jan-Moritz, Schulz, Anne-Christine, Tästensen, Julia-Beate, Schönheit, Peter
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container_issue 5
container_start_page 1663
container_title Environmental microbiology
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creator Johnsen, Ulrike
Sutter, Jan-Moritz
Schulz, Anne-Christine
Tästensen, Julia-Beate
Schönheit, Peter
description Summary The haloarchaeon Haloferax volcanii degrades D‐xylose and L‐arabinose via oxidative pathways to α‐ketoglutarate. The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene cluster, a putative IclR‐like transcriptional regulator, HVO_B0040, was identified. It is shown that HVO_B0040, designated xacR, encodes an activator of both D‐xylose and L‐arabinose catabolism: in ΔxacR cells, transcripts of genes involved in pentose catabolism could not be detected; transcript formation could be recovered by complementation, indicating XacR dependent transcriptional activation. Upstream activation promoter regions and nucleotide sequences that were essential for XacR‐mediated activation of pentose‐specific genes were identified by in vivo deletion and scanning mutagenesis. Besides its activator function XacR acted as repressor of its own synthesis: xacR deletion resulted in an increase of xacR promoter activity. A palindromic sequence was identified at the operator site of xacR promoter, and mutation of this sequence also resulted in an increase and thus derepression of xacR promoter activity. It is concluded that the palindromic sequence represents the binding site of XacR as repressor. This is the first report of a transcriptional regulator of pentose catabolism in the domain of archaea.
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The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene cluster, a putative IclR‐like transcriptional regulator, HVO_B0040, was identified. It is shown that HVO_B0040, designated xacR, encodes an activator of both D‐xylose and L‐arabinose catabolism: in ΔxacR cells, transcripts of genes involved in pentose catabolism could not be detected; transcript formation could be recovered by complementation, indicating XacR dependent transcriptional activation. Upstream activation promoter regions and nucleotide sequences that were essential for XacR‐mediated activation of pentose‐specific genes were identified by in vivo deletion and scanning mutagenesis. Besides its activator function XacR acted as repressor of its own synthesis: xacR deletion resulted in an increase of xacR promoter activity. A palindromic sequence was identified at the operator site of xacR promoter, and mutation of this sequence also resulted in an increase and thus derepression of xacR promoter activity. It is concluded that the palindromic sequence represents the binding site of XacR as repressor. 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A palindromic sequence was identified at the operator site of xacR promoter, and mutation of this sequence also resulted in an increase and thus derepression of xacR promoter activity. It is concluded that the palindromic sequence represents the binding site of XacR as repressor. 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The genes involved in these pathways are clustered and were transcriptionally upregulated by both D‐xylose and L‐arabinose suggesting a common regulator. Adjacent to the gene cluster, a putative IclR‐like transcriptional regulator, HVO_B0040, was identified. It is shown that HVO_B0040, designated xacR, encodes an activator of both D‐xylose and L‐arabinose catabolism: in ΔxacR cells, transcripts of genes involved in pentose catabolism could not be detected; transcript formation could be recovered by complementation, indicating XacR dependent transcriptional activation. Upstream activation promoter regions and nucleotide sequences that were essential for XacR‐mediated activation of pentose‐specific genes were identified by in vivo deletion and scanning mutagenesis. Besides its activator function XacR acted as repressor of its own synthesis: xacR deletion resulted in an increase of xacR promoter activity. A palindromic sequence was identified at the operator site of xacR promoter, and mutation of this sequence also resulted in an increase and thus derepression of xacR promoter activity. It is concluded that the palindromic sequence represents the binding site of XacR as repressor. This is the first report of a transcriptional regulator of pentose catabolism in the domain of archaea.</abstract><cop>England</cop><pub>Blackwell Publishing Ltd</pub><pmid>25141768</pmid><doi>10.1111/1462-2920.12603</doi><tpages>14</tpages></addata></record>
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subjects Amino Acid Sequence
Arabinose - metabolism
Bacteriology
Base Sequence
Binding Sites - genetics
Carbohydrate Metabolism - genetics
DNA, Archaeal - analysis
DNA, Archaeal - genetics
Gene Expression Regulation, Archaeal
Genes
Haloferax volcanii - genetics
Haloferax volcanii - metabolism
Inverted Repeat Sequences - genetics
Ketoglutaric Acids - metabolism
Molecular Sequence Data
Oxidation-Reduction
Promoter Regions, Genetic - genetics
Sequence Alignment
Sequence Analysis, DNA
Sequence Deletion - genetics
Transcription, Genetic - genetics
Transcriptional Activation - genetics
Xylose - metabolism
title XacR - a novel transcriptional regulator of D-xylose and L-arabinose catabolism in the haloarchaeon Haloferax volcanii
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