Coevolutionary analysis reveals a distal amino acid residue pair affecting the catalytic activity of GH5 processive endoglucanase from Bacillus subtilis BS‐5. Issue 8 (5th May 2022)

• Record Type: Journal Article
• Authors: Wu, Mujunqi; Lv, Kemin; Li, Jiahuang; Wu, Bin; He, Bingfang
• Is Part Of: Biotechnology and bioengineering. Volume 119:Issue 8(2022)
• Page Start: 2105
• Page End: 2114
• Publication Date: 2022-05-05
• Subjects: coevolving residues -- distal residue -- family 5 processive endoglucanase -- iterative‐saturation mutagenesis; Biotechnology -- Periodicals; Bioengineering -- Periodicals; 660.6
• DOI: 10.1002/bit.28113
• Languages: English
• ISSNs: 0006-3592

Abstract

Abstract: EG5C‐1, processive endoglucanase from Bacillus subtilis, is a typical bifunctional cellulase with endoglucanase and exoglucanase activities. The engineering of processive endoglucanase focuses on the catalytic pocket or carbohydrate‐binding module tailoring based on sequence/structure information. Herein, a computational strategy was applied to identify the desired mutants in the enzyme molecule by evolutionary‐coupling analysis; subsequently, four residue pairs were selected as evolutionary mutational hotspots. Based on iterative‐saturation mutagenesis and subsequent enzymatic activity analysis, a superior mutant K51T/L93T has been identified away from the active center. This variant had increased specific activity from 4170 U/µmol of wild‐type (WT) to 5678 U/µmol towards carboxymethyl cellulose‐Na and an increase towards the substrate Avicel from 320 U/µmol in WT to 521 U/µmol. In addition, kinetic measurements suggested that superior mutant K51T/L93T had a high substrate affinity ( K m ) and a remarkable improvement in catalytic efficiency ( k cat / K m ). Furthermore, molecular dynamics simulations revealed that the K51T/L93T mutation altered the spatial conformation at the active site cleft, enhancing the interaction frequency between active site residues and substrate, and improving catalytic efficiency and substrate affinity. The current studies provided some perspectives on the effects of distal residue substitution, which might assist in the engineering of processive endoglucanase or other glycoside hydrolases. Abstract : A computational strategy was implemented to investigate the evolutionary and dynamic coupling of residue pairs in processive endoglucanase EG5C‐1 for enhancing its catalytic performance. Four distal residue pairs with strong evolutionary constraints were identified. Iterative‐saturation mutagenesis was conducted to construct mutant libraries and the best variant K51T/L93T was identified. The current studies provided some perspectives on the effects of distal residue substitution, which might assist in the engineering of processive endoglucanase or other glycoside hydrolases.