Molecular origins of reduced activity and binding commitment of processive cellulases and associated carbohydrate-binding proteins to cellulose III

• Published in: The Journal of biological chemistry Vol. 296; no. C; p. 100431
• Main Authors: Chundawat, Shishir P.S., Nemmaru, Bhargava, Hackl, Markus, Brady, Sonia K., Hilton, Mark A., Johnson, Madeline M., Chang, Sungrok, Lang, Matthew J., Huh, Hyun, Lee, Sang-Hyuk, Yarbrough, John M., López, Cesar A., Gnanakaran, Sandrasegaram
• Format: Journal Article
• Language: English
• Published: United States Elsevier Inc 01.01.2021; Elsevier; American Society for Biochemistry and Molecular Biology
• Subjects: BASIC BIOLOGICAL SCIENCES; carbohydrate-active enzymes; carbohydrate-binding proteins; cellulases; cellulose; lignocellulosic biofuels; molecular dynamics; optical tweezers force spectroscopy; carbohydrate-binding proteins; CD; lignocellulosic biofuels; AFM; PMF; carbohydrate-active enzymes; XRD; molecular dynamics; CBM; optical tweezers force spectroscopy; cellulases; cellulose; MD; FRAP; EA; Molecular Dynamics; Cellulases; Cellulose; Optical Tweezers Force Spectroscopy; Lignocellulosic Biofuels; Carbohydrate-Active Enzymes; Carbohydrate-Binding Proteins
• ISSN: 0021-9258; 1083-351X
• DOI: 10.1016/j.jbc.2021.100431

Efficient enzymatic saccharification of cellulosic biomass into fermentable sugars can enable production of bioproducts like ethanol. Native crystalline cellulose, or cellulose I, is inefficiently processed via enzymatic hydrolysis but can be converted into the structurally distinct cellulose III allomorph that is processed via cellulase cocktails derived from Trichoderma reesei up to 20-fold faster. However, characterization of individual cellulases from T. reesei, like the processive exocellulase Cel7A, shows reduced binding and activity at low enzyme loadings toward cellulose III. To clarify this discrepancy, we monitored the single-molecule initial binding commitment and subsequent processive motility of Cel7A enzymes and associated carbohydrate-binding modules (CBMs) on cellulose using optical tweezers force spectroscopy. We confirmed a 48% lower initial binding commitment and 32% slower processive motility of Cel7A on cellulose III, which we hypothesized derives from reduced binding affinity of the Cel7A binding domain CBM1. Classical CBM–cellulose pull-down assays, depending on the adsorption model fitted, predicted between 1.2- and 7-fold reduction in CBM1 binding affinity for cellulose III. Force spectroscopy measurements of CBM1–cellulose interactions, along with molecular dynamics simulations, indicated that previous interpretations of classical binding assay results using multisite adsorption models may have complicated analysis, and instead suggest simpler single-site models should be used. These findings were corroborated by binding analysis of other type-A CBMs (CBM2a, CBM3a, CBM5, CBM10, and CBM64) on both cellulose allomorphs. Finally, we discuss how complementary analytical tools are critical to gain insight into the complex mechanisms of insoluble polysaccharides hydrolysis by cellulolytic enzymes and associated carbohydrate-binding proteins.