诱饵
生产过剩
质粒
番茄红素
抄写(语言学)
诱导剂
化学
抑制因子
转录因子
转染
核酸
生物
生物化学
重组DNA
DNA
阿维菌素
细胞生物学
发起人
代谢工程
同源重组
分子生物学
遗传学
拉伤
基因
分子工程
寡核苷酸
作者
Ruili Huang,Mengyao Yang,Yifan Zhao,Xinyu Wu,Ying Wen
标识
DOI:10.1021/acs.jafc.5c09050
摘要
Here, we applied a transcription factor (TF) decoy strategy to enhance avermectin (AVE) production and activate the cryptic lycopene biosynthetic gene cluster (BGC) in industrial species Streptomyces avermitilis. Two decoy systems based on multicopy plasmid pKC1139 for repressors AfsR and AveI significantly increased AVE titers by 526.1% and 417.6%, respectively, compared to the wild-type (WT) strain. We further constructed a series of integrative decoy plasmids harboring varying numbers of AfsR decoys to demonstrate the dose-dependent effect, followed by a pKC1139-based AfsR decoy library to screen for optimal AVE-producing sequences. Three top-performing sequences were identified, increasing AVE titers by up to 1040.2% in the WT strain and 36.1% in an industrial strain. Finally, we successfully activated lycopene production (45.5 μg/mL) by using the crtY–crtE intergenic region as a decoy. These findings demonstrate that the simple, easy-to-implement TF decoy strategy can be applied to Streptomyces metabolic engineering for the overproduction of secondary metabolites.
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