Effects of mutations at threonine-654 on the insoluble glucan synthesized by Leuconostoc mesenteroides NRRL B-1118 glucansucrase

Appl Microbiol Biotechnol. 2014 Aug;98(15):6651-8. doi: 10.1007/s00253-014-5622-x. Epub 2014 Feb 28.

Abstract

Twelve different amino acids were each substituted for threonine-654 in a cloned glucansucrase from Leuconostoc mesenteroides NRRL B-1118. Both the native and the cloned enzyme with threonine at position 654 produced a water-insoluble glucan containing approximately 44 mol% 1,3-disubstituted α-D-glucopyranosyl units and 29 mol% 1,6-disubstituted α-D-glucopyranosyl units. Several substitutions yielded an enzyme that produced an increased percentage of 1,3-disubstituted α-D-glucopyranosyl units, with corresponding decreases in 1,6-disubstituted α-D-glucopyranosyl units. Only one substitution, tyrosine, resulted in a significant increase in the percentage of 1,6-disubstituted α-D-glucopyranosyl units, with a concomitant increase in glucan yield. The mutated enzymes that produced the highest levels of 1,3-disubstituted α-D-glucopyranosyl units were also significantly activated by the addition of dextran, but glucan yields were also lower in these mutants.

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics*
  • Bacterial Proteins / metabolism
  • Glucans / biosynthesis*
  • Glucans / chemistry
  • Glycosyltransferases / chemistry*
  • Glycosyltransferases / genetics*
  • Glycosyltransferases / metabolism
  • Leuconostoc / chemistry
  • Leuconostoc / enzymology*
  • Leuconostoc / genetics
  • Molecular Sequence Data
  • Mutation*
  • Sequence Alignment
  • Solubility
  • Threonine / genetics*
  • Threonine / metabolism

Substances

  • Bacterial Proteins
  • Glucans
  • Threonine
  • Glycosyltransferases
  • alternansucrase