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金黄色葡萄球菌从亚致死热损伤中修复所需的镁

Magnesium requirement of Staphylococcus aureus for repair from sublethal heat injury.

作者信息

Hughes A, Hurst A

出版信息

Can J Microbiol. 1976 Aug;22(8):1202-5. doi: 10.1139/m76-177.

Abstract

Heating in potassium phosphate buffer causes Staphylococcus aureus to lose its salt tolerance and 30-40% of its cellular Mg2+. Repair from injury (regain of salt tolerance) occurred when injured cells were incubated under optimal conditions in synthetic media containing penicillin to prevent growth. Cells died when phosphates or amin acids were omitted from the medium. Omission of vitamins, glucose, Na+, and K+ had no effect. Omission of Mg2+ diminished repair. In a minimal repair medium (MRM) which contained only 3 X 10(-6) M Mg (as an impurity), injured cells rapidly regained their original Mg content. About 20-50% of the cells also regained their salt tolerance provided that less than 10(9) cells/ml were used. With 10(10) cells/ml there was no repair and cellular Mg content was half that of the control. Addition of 10(-3) M ethylenediamine-tetraacetic acid (EDTA) to MRM also prevented repair. Addition of 10(-2) M Mg to MRM EDTA permitted complete repair.

摘要

在磷酸钾缓冲液中加热会导致金黄色葡萄球菌失去耐盐性并使其细胞内30 - 40%的镁离子流失。当受伤细胞在含有青霉素以防止生长的合成培养基中于最佳条件下培养时,会出现损伤修复(耐盐性恢复)。当培养基中省略磷酸盐或氨基酸时,细胞会死亡。省略维生素、葡萄糖、钠离子和钾离子没有影响。省略镁离子会减少修复。在仅含有3×10⁻⁶ M镁(作为杂质)的最低修复培养基(MRM)中,受伤细胞迅速恢复其原来的镁含量。只要使用的细胞浓度低于10⁹个细胞/毫升,约20 - 50%的细胞也会恢复其耐盐性。当细胞浓度为10¹⁰个细胞/毫升时,没有修复,细胞内镁含量是对照的一半。向MRM中添加10⁻³ M乙二胺四乙酸(EDTA)也会阻止修复。向MRM - EDTA中添加10⁻² M镁可实现完全修复。

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