A pH-stable, detergent and chelator resistant type I pullulanase from Bacillus pseudofirmus 703 with high catalytic efficiency

Int J Biol Macromol. 2018 Apr 1:109:1302-1310. doi: 10.1016/j.ijbiomac.2017.11.139. Epub 2017 Nov 22.

Abstract

Pullulanase with high catalytic efficiency has attracted great attention from both the academic and industrial communities for its wide application in cold starch hydrolysis. A novel pullulanase gene pul703 was cloned from a mesophilic bacteria Bacillus pseudofirmus 703. Pul703 was characterized to be a type I pullulanase with maximal activity at 45°C and good low-temperature stability, more than 70% of activity was detected after incubation at 25-35°C for 72h. Pul703 obtained the maximal activity around pH 7.0-8.0, and was highly active and stable over a wide pH range of 5.5-9.5, more than 80% of activity was retained after 12h incubation in these pHs. Pul703 was EDTA-resistant and detergent-tolerant, with a relative activity of 100, 99, and 114.8% at the presence of 10mM EDTA, 10% of Triton X-100 and Tween 20, respectively. Pul703 can efficiently hydrolyze pullulan with a specific activity of 270U/mg, which was higher than all reported type I pullulanases. In addition, Pul703 can act synergistically with α-amylase BLA to efficiently hydrolyze amylopectin. These results suggested that Pul703 was a good candidate for cold starch hydrolysis.

Keywords: Enzymatic characterization; Specific activity; Starch; Type I pullulanase.

MeSH terms

  • Bacillus / enzymology*
  • Bacillus / genetics
  • Catalysis
  • Chelating Agents / chemistry
  • Chelating Agents / pharmacology
  • Chromatography, High Pressure Liquid
  • Cloning, Molecular
  • Conserved Sequence
  • Detergents / chemistry
  • Detergents / pharmacology
  • Enzyme Activation
  • Gene Expression
  • Glycoside Hydrolases / chemistry*
  • Glycoside Hydrolases / genetics
  • Glycoside Hydrolases / isolation & purification
  • Glycoside Hydrolases / metabolism*
  • Hydrogen-Ion Concentration*
  • Hydrolysis
  • Kinetics
  • Mutation
  • Recombinant Proteins
  • Sequence Analysis, DNA
  • Substrate Specificity
  • Temperature

Substances

  • Chelating Agents
  • Detergents
  • Recombinant Proteins
  • Glycoside Hydrolases
  • pullulanase