固碳
代谢途径
酶
化学
体外
合成生物学
代谢工程
生物量(生态学)
微生物
固定(群体遗传学)
二氧化碳
生物
生物化学
计算生物学
光合作用
细菌
生态学
基因
遗传学
作者
Thomas Schwander,Lennart Schada von Borzyskowski,Simon Burgener,Niña Socorro Cortina,Tobias J. Erb
出处
期刊:Science
[American Association for the Advancement of Science (AAAS)]
日期:2016-11-17
卷期号:354 (6314): 900-904
被引量:555
标识
DOI:10.1126/science.aah5237
摘要
Optimizing designer metabolisms in vitro Biological carbon fixation requires several enzymes to turn CO 2 into biomass. Although this pathway evolved in plants, algae, and microorganisms over billions of years, many reactions and enzymes could aid in the production of desired chemical products instead of biomass. Schwander et al. constructed an optimized synthetic carbon fixation pathway in vitro by using 17 enzymes—including three engineered enzymes—from nine different organisms across all three domains of life (see the Perspective by Gong and Li). The pathway is up to five times more efficient than the in vivo rates of the most common natural carbon fixation pathway. Further optimization of this and other metabolic pathways by using similar approaches may lead to a host of biotechnological applications. Science , this issue p. 900 ; see also p. 830
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