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质粒 DNA 的分离和可视化:从临床样本中分离和表征质粒。

Plasmid DNA Isolation and Visualization: Isolation and Characterization of Plasmids from Clinical Samples.

机构信息

Centre for Infectious Diseases and Microbiology, The Westmead Institute for Medical Research, The University of Sydney, Westmead, NSW, Australia.

Centre for Infectious Diseases and Microbiology Laboratory Services, NSW Health Pathology, Westmead Hospital, Westmead, NSW, Australia.

出版信息

Methods Mol Biol. 2020;2075:3-20. doi: 10.1007/978-1-4939-9877-7_1.

Abstract

Plasmids are important in carrying antibiotic resistance and other genes between bacterial cells, and a number of methods can be employed to characterize plasmids from clinical isolates. Single colonies typically obtained as part of hospital workflow can undergo S1 nuclease treatment to linearize plasmids followed by pulsed-field gel electrophoresis to enable determination of the number and sizes of plasmids present. Hybridization of S1/PFGE gels can be used to associate replicon types and passenger genes, such as those conferring antibiotic resistance, with a particular plasmid band. Individual plasmids, obtained by conjugation or transformation, can be compared by gel electrophoresis following restriction digestion of plasmid DNA prepared by alkaline lysis methods, including using specialized kits.

摘要

质粒在细菌细胞之间携带抗生素耐药性和其他基因方面很重要,有许多方法可以用于表征临床分离株中的质粒。作为医院工作流程一部分获得的单个菌落可以进行 S1 核酸酶处理以线性化质粒,然后进行脉冲场凝胶电泳以确定存在的质粒数量和大小。S1/PFGE 凝胶的杂交可用于将复制子类型和携带基因(如赋予抗生素耐药性的基因)与特定的质粒带相关联。通过接合或转化获得的单个质粒,可以通过质粒 DNA 的碱性裂解方法(包括使用专用试剂盒)制备后进行限制性消化,通过凝胶电泳进行比较。

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