Department of Chemistry, Princeton University, Princeton, NJ, United States.
Department of Chemistry, Princeton University, Princeton, NJ, United States; Department of Molecular Biology, Princeton University, Princeton, NJ, United States.
Curr Opin Microbiol. 2018 Oct;45:156-163. doi: 10.1016/j.mib.2018.05.001. Epub 2018 Jun 5.
The explosion of microbial genome sequences has shown that bacteria harbor an immense, largely untapped potential for the biosynthesis of diverse natural products, which have traditionally served as an important source of pharmaceutical compounds. Most of the biosynthetic genes that can be detected bioinformatically are not, or only weakly, expressed under standard laboratory growth conditions. Herein we review three recent approaches that have been developed for inducing these so-called silent biosynthetic gene cluster: insertion of constitutively active promoters using CRISPR-Cas9, high-throughput elicitor screening for identification of small molecule inducers, and reporter-guided mutant selection for creation of overproducing strains. Together with strategies implemented previously, these approaches promise to unleash the products of silent gene clusters in years to come.
微生物基因组序列的爆炸式增长表明,细菌蕴藏着巨大的、尚未充分开发的潜力,可以用于合成多样化的天然产物,而这些天然产物一直是药物化合物的重要来源。在生物信息学上能够检测到的大多数生物合成基因,在标准实验室生长条件下并不表达,或者表达很弱。本文综述了三种最近开发的方法,用于诱导这些所谓的沉默生物合成基因簇:使用 CRISPR-Cas9 插入组成型激活的启动子,高通量筛选鉴定小分子诱导剂,以及报告基因指导的突变体选择以创建高产菌株。结合以前实施的策略,这些方法有望在未来几年内释放沉默基因簇的产物。