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赖氨酰内肽酶(Lif)和表皮溶素(Epr)将位点特异性丝氨酸掺入葡萄球菌肽聚糖交联桥的第3和第5位。

Site-specific serine incorporation by Lif and Epr into positions 3 and 5 of the Staphylococcal peptidoglycan interpeptide bridge.

作者信息

Ehlert K, Tschierske M, Mori C, Schröder W, Berger-Bächi B

机构信息

Bayer AG, PH Research Antiinfectives I, D-42096 Wuppertal, Germany.

出版信息

J Bacteriol. 2000 May;182(9):2635-8. doi: 10.1128/JB.182.9.2635-2638.2000.

Abstract

The FemAB-like factors Lif and Epr confer resistance to glycylglycine endopeptidases lysostaphin and Ale-1, respectively, by incorporating serine residues into the staphylococcal peptidoglycan interpeptide bridges specifically at positions 3 and 5. This required the presence of FemA and/or FemB, in contrast to earlier postulations.

摘要

FemAB样因子Lif和Epr分别通过将丝氨酸残基特异性地掺入葡萄球菌肽聚糖肽间桥的第3位和第5位,赋予对甘氨酰甘氨酸内肽酶溶葡萄球菌素和Ale-1的抗性。与早期假设相反,这需要FemA和/或FemB的存在。

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本文引用的文献

3
Lif, the lysostaphin immunity factor, complements FemB in staphylococcal peptidoglycan interpeptide bridge formation.
FEMS Microbiol Lett. 1997 Aug 15;153(2):261-4. doi: 10.1016/s0378-1097(97)00234-6.
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Staphylococcal peptidoglycan interpeptide bridge biosynthesis: a novel antistaphylococcal target?
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