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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 Ho
Published 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.
Keyphrases
  • anaerobic digestion
  • wastewater treatment
  • crispr cas
  • molecular docking
  • amino acid
  • lactic acid