A thermostable pyrimidine nucleoside phosphorylase from Brevibacillus borstelensis LK01 for synthesizing halogenated nucleosides

Biotechnol Lett. 2017 Dec;39(12):1903-1910. doi: 10.1007/s10529-017-2423-1. Epub 2017 Sep 4.

Abstract

Objective: To isolate a thermostable pyrimidine nucleoside phosphorylase (PyNP) from mesophilic bacteria by gene mining.

Results: BbPyNP from Brevibacillus borstelensis LK01 was isolated by gene mining. BbPyNP had a highest 60% identity with that of reported PyNPs. BbPyNP could catalyze the phosphorolysis of thymidine, 2'-deoxyuridine, uridine and 5-methyuridine. BbPyNP had good thermostability and retained 73% of its original activity after 2 h incubation at 50 °C. BbPyNP had the highest activity at an optimum alkaline pH of 8.5. BbPyNP was stable from pH 7 to 9.8. Under preliminary optimized conditions, the biosynthesis of various 5-halogenated pyrimidine nucleosides by BbPyNP reached the yield of 61-84%.

Conclusion: An efficient approach was estimated in isolating thermostable PyNP from mesophilic bacteria.

Keywords: Gene mining; Halogenated nucleoside; Pyrimidine nucleoside phosphorylase.

MeSH terms

  • Brevibacillus / enzymology
  • Brevibacillus / genetics*
  • Enzyme Stability
  • Escherichia coli / genetics
  • Floxuridine / analysis
  • Floxuridine / metabolism*
  • Hot Temperature
  • Hydrogen-Ion Concentration
  • Metabolic Engineering / methods*
  • Nucleosides / chemistry
  • Nucleosides / metabolism*
  • Pyrimidine Phosphorylases / chemistry
  • Pyrimidine Phosphorylases / genetics
  • Pyrimidine Phosphorylases / metabolism*
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Substrate Specificity

Substances

  • Nucleosides
  • Recombinant Proteins
  • Floxuridine
  • Pyrimidine Phosphorylases