Phosphate Solubilization and Gene Expression of Phosphate-Solubilizing Bacterium Burkholderia multivorans WS-FJ9 under Different Levels of Soluble Phosphate

J Microbiol Biotechnol. 2017 Apr 28;27(4):844-855. doi: 10.4014/jmb.1611.11057.

Abstract

Phosphate-solubilizing bacteria (PSB) have the ability to dissolve insoluble phosphate and enhance soil fertility. However, the growth and mineral phosphate solubilization of PSB could be affected by exogenous soluble phosphate and the mechanism has not been fully understood. In the present study, the growth and mineral phosphate-solubilizing characteristics of PSB strain Burkholderia multivorans WS-FJ9 were investigated at six levels of exogenous soluble phosphate (0, 0.5, 1, 5, 10, and 20 mM). The WS-FJ9 strain showed better growth at high levels of soluble phosphate. The phosphate-solubilizing activity of WS-FJ9 was reduced as the soluble phosphate concentration increased, as well as the production of pyruvic acid. Transcriptome profiling of WS-FJ9 at three levels of exogenous soluble phosphate (0, 5, and 20 mM) identified 446 differentially expressed genes, among which 44 genes were continuously up-regulated when soluble phosphate concentration was increased and 81 genes were continuously down-regulated. Some genes related to cell growth were continuously up-regulated, which would account for the better growth of WS-FJ9 at high levels of soluble phosphate. Genes involved in glucose metabolism, including glycerate kinase, 2-oxoglutarate dehydrogenase, and sugar ABC-type transporter, were continuously down-regulated, which indicates that metabolic channeling of glucose towards the phosphorylative pathway was negatively regulated by soluble phosphate. These findings represent an important first step in understanding the molecular mechanisms of soluble phosphate effects on the growth and mineral phosphate solubilization of PSB.

Keywords: Burkholderia multivorans; Transcriptome analysis; glucose phosphorylative pathway; mineral phosphate solubilization; soluble phosphate.

MeSH terms

  • Bacterial Proteins / biosynthesis
  • Bacterial Proteins / drug effects
  • Bacterial Proteins / genetics
  • Burkholderia / enzymology
  • Burkholderia / genetics*
  • Burkholderia / growth & development
  • Burkholderia / metabolism*
  • Culture Media / chemistry
  • DNA, Bacterial
  • Gene Expression Profiling / methods
  • Gene Expression Regulation, Bacterial / drug effects
  • Gene Expression Regulation, Bacterial / genetics*
  • Gene Ontology
  • Genes, Bacterial / genetics
  • Glucose / metabolism
  • Hydrogen-Ion Concentration
  • Ketoglutarate Dehydrogenase Complex / biosynthesis
  • Ketoglutarate Dehydrogenase Complex / drug effects
  • Ketoglutarate Dehydrogenase Complex / genetics
  • Metabolic Networks and Pathways / drug effects
  • Metabolic Networks and Pathways / genetics
  • Molecular Sequence Annotation
  • Phosphates / administration & dosage
  • Phosphates / chemistry*
  • Phosphates / metabolism*
  • Phosphotransferases (Alcohol Group Acceptor) / biosynthesis
  • Phosphotransferases (Alcohol Group Acceptor) / drug effects
  • Phosphotransferases (Alcohol Group Acceptor) / genetics
  • Pyruvic Acid / metabolism
  • RNA, Bacterial / isolation & purification
  • Real-Time Polymerase Chain Reaction / methods
  • Soil
  • Soil Microbiology*
  • Solubility
  • Transcriptome / genetics
  • Up-Regulation

Substances

  • Bacterial Proteins
  • Culture Media
  • DNA, Bacterial
  • Phosphates
  • RNA, Bacterial
  • Soil
  • Pyruvic Acid
  • Ketoglutarate Dehydrogenase Complex
  • Phosphotransferases (Alcohol Group Acceptor)
  • glycerate kinase
  • Glucose