酿酒酵母
代谢工程
生物
代谢组学
代谢途径
蛋白质组学
计算生物学
胞浆
生物化学
新陈代谢
酵母
细胞生物学
酶
基因
生物信息学
作者
Rui Hou,Mengying Shan,Xinxin Liu,Mingdong Yao,Kaiguang Yang,Ying Wang,Zhigang Sui,Zhen Liang,Yukui Zhang,Lihua Zhang
标识
DOI:10.1002/biot.202300710
摘要
Abstract Reconstruction and optimization of biosynthetic pathways can help to overproduce target chemicals in microbial cell factories based on genetic engineering. However, the perturbation of biosynthetic pathways on cellular metabolism is not well investigated and profiling the engineered microbes remains challenging. The rapid development of omics tools has the potential to characterize the engineered microbial cell factory. Here, we performed label‐free quantitative proteomic analysis and metabolomic analysis of engineered sabinene overproducing Saccharomyces cerevisiae strains. Combined metabolic analysis andproteomic analysis of targeted mevalonate (MVA) pathway showed that co‐ordination of cytosolic and mitochondrial pathways had balanced metabolism, and genome integration of biosynthetic genes had higher sabinene production with less MVA enzymes. Furthermore, comparative proteomic analysis showed that compartmentalized mitochondria pathway had perturbation on central cellular metabolism. This study provided an omics analysis example for characterizing engineered cell factory, which can guide future regulation of the cellular metabolism and maintaining optimal protein expression levels for the synthesis of target products.
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