Protein engineering for bioenergy and biomass-based chemicals

被引:14
作者
Clarke, Neil D. [1 ]
机构
[1] Genome Inst Singapore, Singapore 138672, Singapore
关键词
SITE-DIRECTED MUTAGENESIS; CIRCULAR PERMUTATION; LIPASE-B; BIOSYNTHESIS; EXPLORATION; METABOLISM; EVOLUTION; BIOLOGY; FUELS;
D O I
10.1016/j.sbi.2010.06.001
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The conversion of biomass to fuels and chemicals faces substantial challenges if it is to be done on a large scale, in a sustainable manner, and at reasonable cost. Some of these challenges can be addressed through protein engineering technologies, for example by improving biomass-processing enzymes or by manipulating the activities and substrate specificity of enzymes in metabolic pathways. Recent highlights include structure-guided chimera design to improve the properties of cellulases, the engineering of synthetic scaffold proteins to enhance metabolic flux, and the broadening of substrate specificity to co-opt metabolic pathways to the production of long-chain branched alcohols.
引用
收藏
页码:527 / 532
页数:6
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