Genome engineering and direct cloning of antibiotic gene clusters via phage ϕBT1 integrase-mediated site-specific recombination in Streptomyces

Scientific Reports
Deyao DuGuoqing Niu

Abstract

Several strategies have been used to clone large DNA fragments directly from bacterial genome. Most of these approaches are based on different site-specific recombination systems consisting of a specialized recombinase and its target sites. In this study, a novel strategy based on phage ϕBT1 integrase-mediated site-specific recombination was developed, and used for simultaneous Streptomyces genome engineering and cloning of antibiotic gene clusters. This method has been proved successful for the cloning of actinorhodin gene cluster from Streptomyces coelicolor M145, napsamycin gene cluster and daptomycin gene cluster from Streptomyces roseosporus NRRL 15998 at a frequency higher than 80%. Furthermore, the system could be used to increase the titer of antibiotics as we demonstrated with actinorhodin and daptomycin, and it will be broadly applicable in many Streptomyces.

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Citations

Sep 14, 2015·Journal of Industrial Microbiology & Biotechnology·Richard H Baltz
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Jul 31, 2021·Frontiers in Bioengineering and Biotechnology·Wenfang WangYinhua Lu
Sep 6, 2019·ACS Synthetic Biology·Weixin TaoYuhui Sun

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Methods Mentioned

BETA
two hybrid
PCR
genetic modifications

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