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分选酶的尴尬——底物丰富?

An embarrassment of sortases - a richness of substrates?

作者信息

Pallen M J, Lam A C, Antonio M, Dunbar K

机构信息

Department of Microbiology and Immunobiology, Queen's University Belfast, Belfast, UK BT12 6BN.

出版信息

Trends Microbiol. 2001 Mar;9(3):97-102. doi: 10.1016/s0966-842x(01)01956-4.

Abstract

A range of surface proteins is anchored to the cell walls of Gram-positive pathogens such as Staphylococcus aureus by the transpeptidase sortase. Until now, sortase-like proteins and their substrates appeared to be limited mainly to such pathogens. However, by searching for sortase homologues among complete and incomplete genome sequences, we have found them to be present in almost all Gram-positives, a single Gram-negative bacterium and an archaean. There is usually more than one sortase-like protein encoded in each Gram-positive genome, and the genes encoding the sortase-like proteins are often clustered with genes encoding their likely substrates.

摘要

一系列表面蛋白通过转肽酶分选酶锚定在革兰氏阳性病原体(如金黄色葡萄球菌)的细胞壁上。到目前为止,分选酶样蛋白及其底物似乎主要局限于此类病原体。然而,通过在完整和不完整的基因组序列中搜索分选酶同源物,我们发现它们几乎存在于所有革兰氏阳性菌、一种革兰氏阴性菌和一种古生菌中。每个革兰氏阳性菌基因组中通常编码不止一种分选酶样蛋白,并且编码分选酶样蛋白的基因常常与编码其可能底物的基因成簇排列。

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