Impact of pnpR, a LysR-type regulator-encoding gene, on the cellular processes of Pseudomonas putida DLL-E4

FEMS Microbiol Lett. 2016 Jun;363(12):fnw110. doi: 10.1093/femsle/fnw110. Epub 2016 Apr 25.

Abstract

LysR-type transcriptional regulators (LTTRs) regulate various cellular processes in bacteria. pnpR is an LTTR-encoding gene involved in the regulation of hydroquinone (HQ) degradation, and its effects on the cellular processes of Pseudomonas putida DLL-E4 were investigated at the physiological, biochemical and molecular levels. Reverse transcription polymerase chain reaction revealed that pnpR positively regulated its own expression and that of the pnpC1C2DECX1X2 operon; additionally, pnpR partially regulated the expression of pnpA when P. putida was grown on para-nitrophenol (PNP) or HQ. Strains DLL-E4 and DLL-ΔpnpR exhibited similar cellular morphologies and growth rates. Transcriptome analysis revealed that pnpR regulated the expression of genes in addition to those involved in PNP degradation. A total of 20 genes were upregulated and 19 genes were downregulated by at least 2-fold in strain DLL-ΔpnpR relative to strain DLL-E4. Bioinformatic analysis revealed putative PnpR-binding sites located in the upstream regions of genes involved in PNP degradation, carbon catabolite repression and other cellular processes. The utilization of L-aspartic acid, L-histidine, L-pyroglutamic acid, L-serine, γ-aminobutyric acid, D,L-lactic acid, D-saccharic acid, succinic acid and L-alaninamide was increased at least 1.3-fold in strain DLL-ΔpnpR as shown by BIOLOG assays, indicating that pnpR plays a potential negative regulation role in the utilization of carbon sources.

Keywords: PNP degradation; Pseudomonas putida DLL-E4; carbon source utilization; cellular process; gene regulation; pnpR deletion.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aspartic Acid / metabolism
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Catabolite Repression
  • Computational Biology
  • Gene Expression Profiling
  • Gene Expression Regulation, Bacterial*
  • Genes, Regulator*
  • Histidine / metabolism
  • Lactic Acid / metabolism
  • Nitrophenols / metabolism
  • Operon
  • Pseudomonas putida / genetics*
  • Pseudomonas putida / growth & development
  • Pseudomonas putida / physiology*
  • Serine / metabolism
  • Transcriptional Activation

Substances

  • Bacterial Proteins
  • Nitrophenols
  • Aspartic Acid
  • Lactic Acid
  • Serine
  • Histidine