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通过转化导入枯草芽孢杆菌的金黄色葡萄球菌质粒的特性分析。

Characterization of Staphylococcus aureus plasmids introduced by transformation into Bacillus subtilis.

作者信息

Gryczan T J, Contente S, Dubnau D

出版信息

J Bacteriol. 1978 Apr;134(1):318-29. doi: 10.1128/jb.134.1.318-329.1978.

Abstract

Covalently closed circular DNA from five Staphylococcus aureus plasmids has been introduced into Bacillus subtilis. Four of these plasmids (pUB110, pCM194, pSA2100, and pSA0501) have been selected for further study. These plasmids replicate as multicopy autonomous replicons in both Rec+ and Rec- B. subtilis strains. They may be transduced between B. subtilis strains or transformed at a frequency of 10(4) to 10(5) transformants per microgram of DNA. The molecular weights of these plasmids were estimated, and restriction endonuclease cleavage site maps are presented. Evidence is given that pSA2100, an in vivo recombinant of pSA0501 and pCM194 (S. Iordănescu, J. Bacteriol. 124:597-601, 1975), arose by a fusion of the latter plasmids, possibly by insertion of one element into another as a translocatable element. Genetic information from three other S. aureus plasmids (pK545, pSH2, and pUB101) has also been introduced into B. subtilis, although no covalently closed circular plasmid DNA was recovered.

摘要

来自五种金黄色葡萄球菌质粒的共价闭合环状DNA已被导入枯草芽孢杆菌。已选择其中四种质粒(pUB110、pCM194、pSA2100和pSA0501)进行进一步研究。这些质粒在Rec⁺和Rec⁻枯草芽孢杆菌菌株中均作为多拷贝自主复制子进行复制。它们可以在枯草芽孢杆菌菌株之间进行转导,或以每微克DNA 10⁴至10⁵个转化子的频率进行转化。估计了这些质粒的分子量,并给出了限制性内切酶切割位点图谱。有证据表明,pSA2100是pSA0501和pCM194的体内重组体(S. Iordănescu,《细菌学杂志》124:597 - 601,1975),它是由后两种质粒融合产生的,可能是作为一种可转位元件将一个元件插入另一个元件中。来自其他三种金黄色葡萄球菌质粒(pK545、pSH2和pUB101)的遗传信息也已被导入枯草芽孢杆菌,尽管未回收共价闭合环状质粒DNA。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2471/222249/b72189848a9d/jbacter00293-0333-a.jpg

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