Nonproductive adsorption of cellulase is widely considered
as the
major roadblock to enzymatically hydrolyzing lignocellulosic biomass.
Cationic additives present a promising avenue for mitigating the issue
by effectively obstructing cellulase adsorption onto the lignin surface
through enhanced electrostatic interactions with the negatively charged
lignin, in contrast to nonionic additives. However, excessive positive
charges carried by ionic additives can potentially hamper enzyme activity.
To reconcile the dilemma, we synthesized a copolymer featuring modulatable
cationic content via control over the ratio of nonionic and cationic
units within the polymer backbone. Upon addition of 1.0 g/L of the
resultant cationic copolymer, a notable enhancement in glucose release
from 39 to 88% was observed, even at a low cellulase dosage of 5 FPU/g
glucan. Remarkably, these cationic copolymers exhibit versatile applicability
across diverse enzyme preparations, acid-treated lignocellulosic substrates,
and highly solid saccharification systems. Furthermore, an enzyme
saving of up to 80% was achieved. Mechanistic studies illuminated
that this copolymer can not only attenuate the occurrence of irreversible
binding between lignin and cellulase but also exert a favorable influence
on enzyme activity. The adaptability of the copolymer’s cationic
content endows it with the status of a promising and effective lignin-blocking
additive, holding considerable potential for advancing the economic
feasibility of biofuel production.