Hauschild Tomasz, Lüthje Petra, Schwarz Stefan
University of Bialystok, Institute of Biology, Department of Microbiology, 15-950 Bialystok, Swierkowa 20 B, Poland.
Vet Microbiol. 2006 Jun 15;115(1-3):258-63. doi: 10.1016/j.vetmic.2006.01.007. Epub 2006 Feb 17.
An erm(C)-carrying plasmid of unusual size and restriction map, designated pSES22, was identified in a Staphylococcus saprophyticus strain and sequenced completely. Constitutive expression of the erm(C) gene from pSES22 is based on a novel 22-bp tandem duplication in the erm(C) translational attenuator. Comparative analysis of the deduced Erm(C) amino acid sequence revealed that Erm(C) from pSES22 - together with an Erm(C) methylase from S. hyicus - represented a separate branch in the homology tree of Erm(C) methylases. Structural comparisons showed that plasmid pSES22 differed distinctly from all other completely sequenced erm(C)-carrying resistance plasmids. However, pSES22 was similar to several members of a diverse group of small plasmids, all of which carried closely related plasmid backbones consisting of the genes repU and pre/mob, but differed in their resistance genes.
在一株腐生葡萄球菌中鉴定出一个携带erm(C)的大小和限制酶切图谱异常的质粒,命名为pSES22,并对其进行了全序列测定。pSES22中erm(C)基因的组成型表达基于erm(C)翻译弱化子中一个新的22 bp串联重复序列。对推导的Erm(C)氨基酸序列的比较分析表明,pSES22中的Erm(C)与来自猪葡萄球菌的一种Erm(C)甲基化酶在Erm(C)甲基化酶同源树中代表一个独立的分支。结构比较表明,质粒pSES22与所有其他已完全测序的携带erm(C)的抗性质粒明显不同。然而,pSES22与一组不同的小质粒中的几个成员相似,所有这些小质粒都携带由repU和pre/mob基因组成的密切相关的质粒骨架,但抗性基因不同。