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从金黄色葡萄球菌中分离出的接合质粒上的4',4''腺苷酸转移酶活性由pUB110的整合拷贝编码。

4',4'' adenyltransferase activity on conjugative plasmids isolated from Staphylococcus aureus is encoded on an integrated copy of pUB110.

作者信息

Byrne M E, Gillespie M T, Skurray R A

机构信息

Department of Microbiology, Monash University, Clayton, Victoria, Australia.

出版信息

Plasmid. 1991 Jan;25(1):70-5. doi: 10.1016/0147-619x(91)90008-k.

Abstract

In staphylococci, linked resistance to the aminoglycosides kanamycin, neomycin, paromomycin, and tobramycin (KmNmPmTmr) is generally mediated by an aadD determinant which encodes production of an adenyltransferase aminoglycoside modifying enzyme, AAD(4',4''). The aadD resistance determinant is located on small multicopy plasmids such as pUB110, and has also been found on large multiresistance plasmids and on the chromosome in some strains. Examination of two conjugative plasmids from strains of Staphylococcus aureus isolated in North America indicated that the aadD determinant on these plasmids is located on an integrated copy of pUB110. The integrated pUB110 is flanked by direct repeats of the staphylococcal insertion sequence IS257. Analysis of the conjugative plasmid pSK41 showed an 8-bp duplication of the pUB110 sequence immediately adjacent to flanking IS257 elements, suggesting that integration of pUB110 was mediated by IS257.

摘要

在葡萄球菌中,对氨基糖苷类抗生素卡那霉素、新霉素、巴龙霉素和妥布霉素(KmNmPmTmr)的连锁抗性通常由aadD决定簇介导,该决定簇编码一种腺苷转移酶氨基糖苷修饰酶AAD(4',4'')的产生。aadD抗性决定簇位于小多拷贝质粒如pUB110上,在一些菌株的大多抗性质粒和染色体上也有发现。对从北美分离的金黄色葡萄球菌菌株的两个接合质粒进行检测表明,这些质粒上的aadD决定簇位于pUB110的一个整合拷贝上。整合的pUB110两侧是葡萄球菌插入序列IS257的同向重复序列。对接合质粒pSK41的分析显示,紧邻侧翼IS257元件的pUB110序列有一个8个碱基对的重复,这表明pUB110的整合是由IS257介导的。

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