Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan; Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, CA 90095, USA.
Institute of Biological Chemistry, Academia Sinica, Taipei, Taiwan.
Cell. 2020 Aug 20;182(4):933-946.e14. doi: 10.1016/j.cell.2020.07.010. Epub 2020 Aug 10.
Methanol, being electron rich and derivable from methane or CO, 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.
甲醇富含电子,可由甲烷或 CO 衍生而来,是微生物潜在的可再生一碳(C1)原料。尽管甲醇营养菌用来同化甲醇的核酮糖单磷酸(RuMP)循环与典型的糖代谢仅相差三种酶,但将非甲醇营养菌转变为能够高密度生长的合成甲醇营养菌一直具有挑战性。在这里,我们使用代谢稳健性标准和实验室进化重新编程大肠杆菌,以建立一种能够有效利用甲醇作为唯一碳源的菌株。这种合成甲醇营养菌通过插入序列(IS)介导的拷贝数变异(CNVs)和突变来缓解迄今为止未被表征的障碍,即 DNA-蛋白质交联(DPC),并平衡代谢通量。该合成甲醇营养菌能够在广泛的甲醇浓度范围内以与天然甲醇营养菌相当的速度生长,这表明了基因组编辑和进化可用于微生物嗜性的改变,并扩展了生物 C1 转化的范围。