Chaetomella raphigera β-glucosidase D2-BGL has intriguing structural features and a high substrate affinity that renders it an efficient cellulase supplement for lignocellulosic biomass hydrolysis.
Mu-Rong KaoHsion-Wen KuoCheng-Chung LeeKuan-Ying HuangTing-Yen HuangChen-Wei LiC Will ChenAndrew H-J WangSu-May YuTuan-H Ua David HoPublished in: Biotechnology for biofuels (2019)
D2-BGL is an efficient supplement for lignocellulosic biomass saccharification, and we upscaled production of this enzyme using a 1-ton bioreactor. Enzyme production could be further improved using optimized fermentation, which could reduce biofuel production costs. Our structure analysis of D2-BGL offers new insights into GH3 β-glucosidases, which will be useful for strain improvements via a structure-based mutagenesis approach.