Acceptor Subsite Mutants of Limosilactobacillus fermentum NCC 2970 GtfB 4,3-α-Glucanotransferase Regulate the Ratio of (α1 → 3)/(α1 → 6) Linkages in Biosynthesized α-Glucans

J Agric Food Chem. 2024 Sep 11;72(36):19994-20004. doi: 10.1021/acs.jafc.4c06121. Epub 2024 Aug 28.

Abstract

Limosilactobacillus fermentum NCC 2970 GtfB (Lf2970 GtfB) is the only characterized 4,3-α-glucanotransferase (4,3-α-GTase) in the glycoside hydrolase (GH) 70 family belonging to the GtfB subfamily. However, the mechanism for its (α1 → 3) linkage formation remains unclear, and the structural determinants of its linkage specificity remain to be explored. Here, sequence alignment and structural comparison were conducted to identify key amino acids that may be critical for linkage specificity. Five residues of Lf2970 GtfB (D991, G1028, A1398, T1400, and E1405), located at donor and acceptor subsites, were selected for mutation. Product structure analysis revealed that D991 and G1028, located near the acceptor binding subsites, played crucial roles in linkage formation. Besides native (α1 → 4) and (α1 → 3) linkages, mutants G1028R and D991N showed 8 and 10% (α1 → 6) linkage increases compared to 1% for wild-type in products. Additionally, molecular docking studies demonstrated that the orientation of acceptor binding in G1028R and D991N mutants was favorable for (α1 → 6) linkage synthesis. However, the mutation at positions A1398, T1400, and E1405 indicated that the donor subsites contribute less to the linkage specificity. These results shed light on the structural determinants of linkage specificity of 4,3-α-GTase Lf2970 GtfB and provided insights into the structure-function relationship of family GH70.

Keywords: acceptor subsites; amylose; linkage specificity; mutation; α-glucan; α-glucanotransferase.

MeSH terms

  • Amino Acid Sequence
  • Bacterial Proteins* / chemistry
  • Bacterial Proteins* / genetics
  • Bacterial Proteins* / metabolism
  • Glucans* / chemistry
  • Glucans* / metabolism
  • Glycogen Debranching Enzyme System / chemistry
  • Glycogen Debranching Enzyme System / genetics
  • Glycogen Debranching Enzyme System / metabolism
  • Limosilactobacillus fermentum* / chemistry
  • Limosilactobacillus fermentum* / enzymology
  • Limosilactobacillus fermentum* / genetics
  • Limosilactobacillus fermentum* / metabolism
  • Mutation
  • Sequence Alignment
  • Substrate Specificity

Substances

  • Bacterial Proteins
  • Glucans
  • Glycogen Debranching Enzyme System
  • 4 alpha-glucanotransferase