生物制造
代谢工程
生化工程
生物转化
合成生物学
无细胞蛋白质合成
商品化学品
代谢途径
蛋白质工程
生物技术
工业生物技术
定向进化
生物化学
酶
化学
计算生物学
生物
蛋白质生物合成
工程类
催化作用
发酵
基因
突变体
作者
Quentin M. Dudley,Ashty S. Karim,Michael C. Jewett
标识
DOI:10.1002/biot.201400330
摘要
Abstract Industrial biotechnology and microbial metabolic engineering are poised to help meet the growing demand for sustainable, low‐cost commodity chemicals and natural products, yet the fraction of biochemicals amenable to commercial production remains limited. Common problems afflicting the current state‐of‐the‐art include low volumetric productivities, build‐up of toxic intermediates or products, and byproduct losses via competing pathways. To overcome these limitations, cell‐free metabolic engineering (CFME) is expanding the scope of the traditional bioengineering model by using in vitro ensembles of catalytic proteins prepared from purified enzymes or crude lysates of cells for the production of target products. In recent years, the unprecedented level of control and freedom of design, relative to in vivo systems, has inspired the development of engineering foundations for cell‐free systems. These efforts have led to activation of long enzymatic pathways (>8 enzymes), near theoretical conversion yields, productivities greater than 100 mg L –1 h –1 , reaction scales of >100 L, and new directions in protein purification, spatial organization, and enzyme stability. In the coming years, CFME will offer exciting opportunities to: (i) debug and optimize biosynthetic pathways; (ii) carry out design‐build‐test iterations without re‐engineering organisms; and (iii) perform molecular transformations when bioconversion yields, productivities, or cellular toxicity limit commercial feasibility.
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