标题:Recombineering for Genetic Engineering of Natural Product Biosynthetic Pathways
作者:Abbasi M.N.; Fu J.; Bian X.; Wang H.; Zhang Y.; Li A.
作者机构:[Abbasi, M.N] Helmholtz International Lab for Anti-Infectives, Shandong University–Helmholtz Institute of Biotechnology, State Key Laboratory of Micr 更多
通讯作者:Abbasi, MN(nazeerabbasi@sdu.edu.cn)
通讯作者地址:[Abbasi, M.N] Helmholtz International Lab for Anti-Infectives, Shandong University–Helmholtz Institute of Biotechnology, State Key Laboratory of Micr 更多
来源:Trends in Biotechnology
出版年:2020
DOI:10.1016/j.tibtech.2019.12.018
关键词:biosynthetic gene cluster; direct cloning; homologous recombination; natural product; Recombineering
摘要:Microbial genomes encode many cryptic and uncharacterized biosynthetic gene clusters (BGCs). Exploiting this unexplored genetic wealth to discover microbial novel natural products (NPs) remains a challenging issue. We review homologous recombination (HR)-based recombineering, mediated by the recombinases RecE/RecT from Rac prophage and Redα/Redβ from lambda phage, which has developed into a highly inclusive tool for direct cloning of large DNA up to 100 kb, seamless mutation, multifragment assembly, and heterologous expression of microbial NP BGCs. Its utilization in the refactoring, engineering, and functional expression of long BGCs for NP biosynthesis makes it easy to elucidate NP-producing potential in microbes. This review also highlights various applications of recombineering in NP-derived drug discovery. © 2019 Elsevier Ltd
收录类别:SCOPUS
资源类型:期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85077975521&doi=10.1016%2fj.tibtech.2019.12.018&partnerID=40&md5=699a036af0c4257560039945b93ff6e0
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