XacR – a novel transcriptional regulator of D‐xylose and L‐arabinose catabolism in the haloarchaeon Haloferax volcanii. (7th October 2014)

• Record Type: Journal Article
• Authors: Johnsen, Ulrike; Sutter, Jan‐Moritz; Schulz, Anne‐Christine; Tästensen, Julia‐Beate; Schönheit, Peter
• Is Part Of: Environmental microbiology. Volume 17:Number 5(2015:May)
• Page Start: 1663
• Page End: 1676
• Publication Date: 2014-10-07
• Subjects: Microbial ecology -- Periodicals; Environmental Microbiology -- Periodicals; 579.17
• DOI: 10.1111/1462-2920.12603
• Languages: English
• ISSNs: 1462-2912

Abstract

Summary: The haloarchaeon H aloferax 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 Δ xacR 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.