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首页> 外文期刊>Plasmid: An International Journal Devoted to Extrachromosomal Gene Systems >Construction and analysis of a modified Tn4001 conferring chloramphenicol resistance in Mycoplasma pneumoniae.
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Construction and analysis of a modified Tn4001 conferring chloramphenicol resistance in Mycoplasma pneumoniae.

机译:赋予肺炎支原体抗氯霉素的改良Tn4001的构建和分析。

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摘要

The Staphylococcus aureus transposon Tn4001 and derivatives thereof have been transformed successfully in several mycoplasma species. In order to expand the versatility of Tn4001 for other genetic manipulations and for use in mycoplasma species resistant to gentamicin (Gm), chloramphenicol acetyltransferase (Cat) from S. aureus was evaluated as a selectable marker. The cat gene was cloned in both orientations into a modified Tn4001 and transformed into Mycoplasma pneumoniae, conferring resistance to Cm and Gm. Replacement of the gene for GmR in Tn4001 with cat likewise conferred CmR when transformed into M. pneumoniae. The minimum inhibitory concentration to Cm in transformants with cat derivatives of Tn4001 was 300-500 microg/ml, and Cat enzyme activity was demonstrated by using a fluorescent substrate. Copyright 1999 Academic Press.
机译:金黄色葡萄球菌转座子Tn4001及其衍生物已成功地转化到几种支原体中。为了扩大Tn4001在其他遗传操作中的多功能性,并用于对庆大霉素(Gm)有抗性的支原体物种中,金黄色葡萄球菌的氯霉素乙酰转移酶(Cat)被评估为选择标记。将cat基因在两个方向上克隆到修饰的Tn4001中,并转化成肺炎支原体,赋予对Cm和Gm的抗性。当转化为肺炎支原体时,用猫替换Tn4001中GmR的基因同样赋予了CmR。在含有Tn4001的cat衍生物的转化子中,对Cm的最低抑制浓度为300-500 microg / ml,并通过使用荧光底物证明了Cat酶的活性。版权所有1999 Academic Press。

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