Characterization and Application of BiLA, a Psychrophilic α-Amylase from Bifidobacterium longum

J Agric Food Chem. 2016 Apr 6;64(13):2709-18. doi: 10.1021/acs.jafc.5b05904. Epub 2016 Mar 24.

Abstract

In this study, a novel α-amylase was cloned from Bifidobacterium longum and named BiLA. The enzyme exhibited optimal activity at 20 °C and a pH value of 5.0. Kinetic analysis using various carbohydrate substrates revealed that BiLA had the highest k(cat/)K(m) value for amylose. Interestingly, analysis of the enzymatic reaction products demonstrated that BiLA specifically catalyzed the hydrolysis of oligosaccharides and starches up to G5 from the nonreducing ends. To determine whether BiLA can be used to generate slowly digestible starch (SDS), starch was treated with BiLA, and the kinetic parameters were analyzed using porcine pancreatic α-amylase (PPA) and amyloglucosidase (AMG). Compared to normal starch, BiLA-treated starch showed lower k(cat)/K(m) values with PPA and AMG, suggesting that BiLA is a potential candidate for the production of SDS.

Keywords: Bifidobacterium longum; resistant starch; slowly digestible starch; α-amylase.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amylose / analysis
  • Amylose / metabolism
  • Animals
  • Bifidobacterium / enzymology*
  • Electrophoresis, Polyacrylamide Gel
  • Glucan 1,4-alpha-Glucosidase / metabolism
  • Hydrolysis
  • Kinetics
  • Pancreatic alpha-Amylases / metabolism
  • Starch / chemistry
  • Swine
  • alpha-Amylases / genetics
  • alpha-Amylases / metabolism*

Substances

  • Starch
  • Amylose
  • Pancreatic alpha-Amylases
  • alpha-Amylases
  • Glucan 1,4-alpha-Glucosidase