[金黄色葡萄球菌蛋白A的改进展示方法(作者译)]。

W Schaeg, J Brückler, H Blobel
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引用次数: 0

摘要

用浓甲酸处理金黄色葡萄球菌可完全提取蛋白A (PA)。这导致了通过血凝法半定量测定PA的发展(图1)。甲酸处理比常用的煮沸提取法更有效地产生PA(表1)。它可以直接在血琼脂中获得的葡萄球菌环上进行。它不需要在液体培养基中进行额外的培养。最适合进行血凝的是rh阳性的人红细胞(O型血)的商业制备,其中装载了来自人的rh抗体。这种相对稳定的制剂在载玻片试验中对PA的敏感性也较高,可以更好地检测PA阳性葡萄球菌(表2)。
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[Improved method for the demonstration of protein A of Staphylococcus aureus (author's transl)].

Protein A (PA) could be extracted completely from Staphylococcus aureus by treatment with concentrated formic acid. This led to the development of a semi-quantitative determination of PA by hemagglutination (fig. 1). The treatment with formic acid yielded PA more effectively than the commonly used extraction by boiling (table 1). It could be conducted directly on a loopfull of staphylococci obtained from blood agar. It required no additional cultivation in a fluid medium. Most suitable for the hemagglutination was a commercial preparation of Rh-positive human erythrocytes, blood group O, loaded with Rh-antibodies from humans. This relatively stable preparation had also a higher susceptibility for PA in the slide-test and served for a better detection of PA-positive staphylococci (table 2).

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