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叶酸类似物甲氨蝶呤对肺炎链球菌膜特性的改变。

Alteration of Streptococcus pneumoniae membrane properties by the folate analog methotrexate.

作者信息

Trombe M C

出版信息

J Bacteriol. 1984 Dec;160(3):849-53. doi: 10.1128/jb.160.3.849-853.1984.

Abstract

The antifolate compound methotrexate (MTX) is toxic to the gram-positive bacterium Streptococcus pneumoniae. Interaction of MTX with this bacterium resulted in an increase in the electric transmembrane potential (delta psi) and enhanced the delta psi-dependent uptake of isoleucine and MTX. In contrast, delta psi-independent uptake of glutamine was not changed. Folate, a nontoxic analog of MTX, did not exhibit these membrane effects, nor did it prevent the effect of MTX, suggesting that the NH2 in position 4 of the pteridine ring of the MTX molecule is involved in the MTX response. A strain bearing the nonsense mutation amiA9, selected for MTX resistance, did not exhibit increased membrane potential after MTX pretreatment. This suggests that MTX interacts with a specific membrane component in S. pneumoniae. A resulting change in ion permeability could lead to changes in the magnitude of the delta psi. The MTX-sensitive component is altered or absent in mutant amiA9.

摘要

抗叶酸化合物甲氨蝶呤(MTX)对革兰氏阳性菌肺炎链球菌有毒性。MTX与这种细菌相互作用导致跨膜电位(δψ)增加,并增强了δψ依赖性的异亮氨酸和MTX摄取。相比之下,δψ非依赖性的谷氨酰胺摄取没有变化。叶酸是MTX的无毒类似物,既不表现出这些膜效应,也不能阻止MTX的作用,这表明MTX分子蝶啶环4位的NH2参与了MTX反应。一株因对MTX耐药而选择的携带无义突变amiA9的菌株,在MTX预处理后没有表现出膜电位增加。这表明MTX与肺炎链球菌中的一种特定膜成分相互作用。离子通透性的变化可能导致δψ大小的改变。在突变体amiA9中,MTX敏感成分发生改变或缺失。

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