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质粒DNA介导的F群链球菌转化

Transformation of group F streptococci by plasmid DNA.

作者信息

Leblanc D J, Cohen L, Jensen L

出版信息

J Gen Microbiol. 1978 May;106(1):49-54. doi: 10.1099/00221287-106-1-49.

Abstract

When the Challis strain of Streptococcus sanguis was transformed by the 17 megadalton beta plasmid from Streptococcus faecalis strain DS5, the plasmid underwent a 1.5 megadalton deletion (LeBlanc & Hassell, 1976). Furthermore, the covalently closed circular (CCC) plasmid DNA isolated from Challis transformants was rapidly converted to a linear form which did not possess any detectable transforming activity. To obtain stable CCC plasmid DNA a competent culture of a Lancefield group F streptococcus, strain DL8 (ATCC 12393), was used as a recipient of beta plasmid DNA. The plasmid DNA isolated from group F transformants exhibited the same configuration and size characteristics as the DS5 beta plasmid, and the CCC configuration was stable upon storage. CCC plasmid DNA from a group F transformant was biologically active and, when added to competent cultures of strain DL8, transformed them at frequencies about 100-fold greater than did beta plasmid DNA from DS5. This suggests the existence of a restriction--modification system in strain DL8.

摘要

当血链球菌的查利斯菌株被来自粪链球菌DS5菌株的17兆道尔顿β质粒转化时,该质粒发生了1.5兆道尔顿的缺失(勒布朗和哈塞尔,1976年)。此外,从查利斯转化子中分离出的共价闭合环状(CCC)质粒DNA迅速转变为线性形式,且不具备任何可检测到的转化活性。为了获得稳定的CCC质粒DNA,将兰斯菲尔德F组链球菌DL8菌株(ATCC 12393)的感受态培养物用作β质粒DNA的受体。从F组转化子中分离出的质粒DNA表现出与DS5 β质粒相同的构型和大小特征,并且CCC构型在储存时是稳定的。来自F组转化子的CCC质粒DNA具有生物活性,当添加到DL8菌株的感受态培养物中时,其转化频率比来自DS5的β质粒DNA高约100倍。这表明DL8菌株中存在一种限制修饰系统。

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