生产过剩
代谢物
代谢工程
刚度(电磁)
焊剂(冶金)
代谢途径
代谢网络
生物化学
细胞代谢
化学
产量(工程)
生物系统
新陈代谢
计算生物学
生物
生化工程
酶
计算机科学
工程类
物理
有机化学
结构工程
热力学
作者
Gregory Stephanopoulos,Joseph J. Vallino
出处
期刊:Science
[American Association for the Advancement of Science]
日期:1991-06-21
卷期号:252 (5013): 1675-1681
被引量:575
标识
DOI:10.1126/science.1904627
摘要
In order to enhance the yield and productivity of metabolite production, researchers have focused almost exclusively on enzyme amplification or other modifications of the product pathway. However, overproduction of many metabolites requires significant redirection of flux distributions in the primary metabolism, which may not readily occur following product deregulation because metabolic pathways have evolved to exhibit control architectures that resist flux alterations at branch points. This problem can be addressed through the use of some general concepts of metabolic rigidity, which include a means for identifying and removing rigid branch points within an experimental framework.
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