Dueber John E, Wu Gabriel C, Malmirchegini G Reza, Moon Tae Seok, Petzold Christopher J, Ullal Adeeti V, Prather Kristala L J, Keasling Jay D
California Institute of Quantitative Biomedical Research (QB3), University of California, Berkeley, California, USA.
Nat Biotechnol. 2009 Aug;27(8):753-9. doi: 10.1038/nbt.1557. Epub 2009 Aug 2.
Engineered metabolic pathways constructed from enzymes heterologous to the production host often suffer from flux imbalances, as they typically lack the regulatory mechanisms characteristic of natural metabolism. In an attempt to increase the effective concentration of each component of a pathway of interest, we built synthetic protein scaffolds that spatially recruit metabolic enzymes in a designable manner. Scaffolds bearing interaction domains from metazoan signaling proteins specifically accrue pathway enzymes tagged with their cognate peptide ligands. The natural modularity of these domains enabled us to optimize the stoichiometry of three mevalonate biosynthetic enzymes recruited to a synthetic complex and thereby achieve 77-fold improvement in product titer with low enzyme expression and reduced metabolic load. One of the same scaffolds was used to triple the yield of glucaric acid, despite high titers (0.5 g/l) without the synthetic complex. These strategies should prove generalizeable to other metabolic pathways and programmable for fine-tuning pathway flux.
由生产宿主异源的酶构建的工程代谢途径常常受到通量失衡的影响,因为它们通常缺乏天然代谢所特有的调节机制。为了提高目标途径各组分的有效浓度,我们构建了合成蛋白质支架,以可设计的方式在空间上招募代谢酶。带有后生动物信号蛋白相互作用结构域的支架特异性地积累与其同源肽配体标记的途径酶。这些结构域的天然模块化使我们能够优化招募到合成复合物中的三种甲羟戊酸生物合成酶的化学计量,从而在低酶表达和降低代谢负荷的情况下使产物滴度提高77倍。尽管在没有合成复合物的情况下滴度很高(0.5 g/l),但使用相同的一种支架使葡萄糖二酸的产量提高了两倍。这些策略应可推广到其他代谢途径,并可进行编程以微调途径通量。