生物
甲基营养素
大肠杆菌
甲醇脱氢酶
生物化学
甲醇
代谢组
遗传学
计算生物学
基因
代谢物
化学
有机化学
作者
Frederic Y.-H. Chen,Hsin-Wei Jung,Chao-Yin Tsuei,James C. Liao
出处
期刊:Cell
[Elsevier]
日期:2020-08-01
卷期号:182 (4): 933-946.e14
被引量:193
标识
DOI:10.1016/j.cell.2020.07.010
摘要
Methanol, being electron rich and derivable from methane or CO2, is a potentially renewable one-carbon (C1) feedstock for microorganisms. Although the ribulose monophosphate (RuMP) cycle used by methylotrophs to assimilate methanol differs from the typical sugar metabolism by only three enzymes, turning a non-methylotrophic organism to a synthetic methylotroph that grows to a high cell density has been challenging. Here we reprogrammed E. coli using metabolic robustness criteria followed by laboratory evolution to establish a strain that can efficiently utilize methanol as the sole carbon source. This synthetic methylotroph alleviated a so far uncharacterized hurdle, DNA-protein crosslinking (DPC), by insertion sequence (IS)-mediated copy number variations (CNVs) and balanced the metabolic flux by mutations. Being capable of growing at a rate comparable with natural methylotrophs in a wide range of methanol concentrations, this synthetic methylotrophic strain illustrates genome editing and evolution for microbial tropism changes and expands the scope of biological C1 conversion.
科研通智能强力驱动
Strongly Powered by AbleSci AI