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错配碱基对在肺炎链球菌转化中对供体DNA命运的影响。

Effect of mismatched base pairs on the fate of donor DNA in transformation of Streptococcus pneumoniae.

作者信息

Méjean V, Claverys J P

出版信息

Mol Gen Genet. 1984;197(3):467-71. doi: 10.1007/BF00329944.

Abstract

Investigation of the mechanism that discriminates against mismatched base pairs in transformation of Streptococcus pneumoniae of genotype hex+ was based on the use of a radioactively labeled cloned fragment of pneumococcal DNA as donor in transformation. The fate of the donor label was followed by lysis of the transformed cells and separation by agarose gel electrophoresis of DNA fragments generated by restriction endonucleases. As a result of Hex action, most of the donor DNA fragment, which was a few kilobases in length, was lost when a mismatched base pair occurred between donor and recipient DNA. This was not observed in hex- recipient cells. Kinetic studies of mismatch-induced donor DNA loss showed that the process is faster in strain 800, an R6 derivative, than in DP1601, a strain of different origin. In the latter strain, the amount of donor label that becomes double stranded rises substantially, indicating extensive formation of donor-recipient heteroduplex structures, before falling to the expected level. At 30 degrees C the process is essentially completed 15 min after entry.

摘要

对基因型hex+的肺炎链球菌转化过程中区分错配碱基对机制的研究,是基于使用放射性标记的肺炎球菌DNA克隆片段作为转化供体。通过裂解转化细胞并对限制性内切酶产生的DNA片段进行琼脂糖凝胶电泳分离,来追踪供体标记的去向。由于Hex的作用,当供体与受体DNA之间出现错配碱基对时,大多数长度为几千碱基的供体DNA片段会丢失。在hex-受体细胞中未观察到这种情况。错配诱导的供体DNA丢失的动力学研究表明,在R6衍生物800菌株中,该过程比不同来源的DP1601菌株更快。在后者菌株中,变为双链的供体标记量大幅上升,表明在降至预期水平之前,供体-受体异源双链结构大量形成。在30摄氏度时,该过程在进入后15分钟基本完成。

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