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Genetic transformation system for Bacillus velezensis NSZ-YBGJ001 and curing of the endogenous plasmid pBV01

文献类型： 外文期刊

作者： Tian, Hui 1 ; Liu, Bo 1 ; Yang, Juan 1 ; Zhou, Chengfang 2 ; Xu, Xinxin 1 ; Zhang, Yuhong 1 ; Lu, Zhijun 2 ; Zhang, Wei 1 ;

作者机构： 1.Chinese Acad Agr Sci, Biotechnol Res Inst, 12 Zhongguancun South St, Beijing 100081, Peoples R China

2.Beijing Plant Protect Stn, 9 Beisanhuan Zhonglu, Beijing 100026, Peoples R China

关键词： Bacillus velezensis; Endogenous plasmid; Genetic transformation system; Plasmid curing

期刊名称：BIOTECHNOLOGY LETTERS （ 影响因子：1.977； 五年影响因子：1.982 ）

ISSN： 0141-5492

年卷期：

页码：

收录情况： SCI

摘要： Objectives To construct a genetic transformation system for Bacillus velezensis NSZ-YBGJ001 and identify the origin element in an endogenous plasmidpBV01 for curing pBV01 by plasmid incompatibility. Results A plasmid pUBC01 was constructed, and then an electrotransformation system for B. velezensis NSZ-YBGJ001 was developed, which reached similar to 1000 transformants per microgram of pUBC01 DNA. Additionally, a 7276-bp circular plasmid pBV01 with a G + C content of 37.5% was isolated from B. velezensis NSZ-YBGJ001 and analyzed via sequence analysis. To cure pBV01, an incompatible plasmid pBV02 harboring the replication element of pBV01 was developed and functionally replicated in both Bacillus subtilis WB600 and B. velezensis NSZ-YBGJ001. pBV01 was cured through introduction of pBV02 into B. velezensis NSZ-YBGJ001 after serial subculturing for approximately 40 generations. Finally, another plasmid, pBV03, was constructed based on pBV-ori, and exogenous genes in pBV03 could be efficiently expressed in B. subtilis. Conclusions The results of this study, including the genetic transformation system, plasmid-curing strategy, and exogenous gene expression, will support genetic manipulation of B. velezensis to promote its application in biocontrol and industry.

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