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利用不稳定复制区域从苏云金芽孢杆菌YBT-020中消除质粒pBMB28

Curing of plasmid pBMB28 from Bacillus thuringiensis YBT-020 using an unstable replication region.

作者信息

Wang Pengxia, Zhu Qian, Shang Hui, Zhu Yiguang, Sun Ming

机构信息

State Key Laboratory of Agricultural Microbiology, College of Life Science and Technology, Huazhong Agricultural University, Wuhan, P. R. China.

出版信息

J Basic Microbiol. 2016 Feb;56(2):206-10. doi: 10.1002/jobm.201500256. Epub 2015 Sep 10.

Abstract

Bacillus thuringiensis serovar finitimus strain YBT-020 is the well-studied spore-crystal association (SCA) phenotypic strain, whose parasporal crystals adhere to spore after lysis of the mother cell. Its endogenous plasmids pBMB26 and pBMB28 were proved essential for this SCA phenotype. In our previous study, using conventional methods, pBMB26 cured derivative and both pBMB26 and pBMB28 cured derivative of YBT-020 were obtained. However, YBT-020 solely cured of pBMB28 could not be obtained. In this study, an unstable replication region of pBMB28 was identified and was used to construct an incompatible plasmid pRep28B. This incompatible plasmid was successfully used to cure plasmid pBMB28 and was easily eliminated through segregational instability under the optimum growth temperature of YBT-020. Therefore, an endogenous plasmid was cured from the B. thuringiensis strain utilizing plasmid incompatibility. Moreover, using an unstable replication region instead of a temperature sensitive (Ts) replication region is better to cure the incompatible plasmid because it can avoid culturing at higher temperature. This method provides an efficient method for plasmid curing in B. thuringiensis and other bacteria.

摘要

苏云金芽孢杆菌有限亚种YBT-020菌株是一种经过充分研究的芽孢-晶体联合体(SCA)表型菌株,其伴胞晶体在母细胞裂解后会附着在芽孢上。已证实其内源质粒pBMB26和pBMB28对这种SCA表型至关重要。在我们之前的研究中,使用传统方法获得了YBT-020的pBMB26消除衍生物以及pBMB26和pBMB28均消除的衍生物。然而,无法获得仅消除了pBMB28的YBT-020。在本研究中,鉴定出pBMB28的一个不稳定复制区域,并用于构建不相容质粒pRep28B。该不相容质粒成功用于消除质粒pBMB28,并在YBT-020的最适生长温度下通过分离不稳定性很容易被消除。因此,利用质粒不相容性从苏云金芽孢杆菌菌株中消除了一个内源质粒。此外,使用不稳定复制区域而非温度敏感(Ts)复制区域来消除不相容质粒更好,因为这样可以避免在较高温度下培养。该方法为苏云金芽孢杆菌及其他细菌中的质粒消除提供了一种有效方法。

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