脱羧
代谢工程
生物过程
生化工程
生物催化
合成生物学
化学
碳纤维
生物化学
计算生物学
生物
催化作用
计算机科学
酶
工程类
反应机理
复合数
算法
古生物学
作者
Calvin A. Henard,Emily F. Freed,Michael T. Guarnieri
标识
DOI:10.1016/j.copbio.2015.08.018
摘要
Recent advances in metabolic engineering have facilitated the development of microbial biocatalysts capable of producing an array of bio-products, ranging from fuels to drug molecules. These bio-products are commonly generated through an acetyl-CoA intermediate, which serves as a key precursor in the biological conversion of carbon substrates. Conventional biocatalytic upgrading strategies proceeding through this route are limited by low carbon efficiencies, in large part due to carbon losses associated with pyruvate decarboxylation to acetyl-CoA. Bypass of pyruvate decarboxylation offers a means to dramatically enhance carbon yields and, in turn, bioprocess economics. Herein, we discuss recent advances and prospects for employing the phosphoketolase pathway for direct biosynthesis of acetyl-CoA from carbon substrates, and phosphoketolase-based metabolic engineering strategies for carbon efficient biocatalysis.
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