Vohra R M
Institute of Microbial Technology, Chandigarh, India.
Appl Environ Microbiol. 1992 Jan;58(1):403-4. doi: 10.1128/aem.58.1.403-404.1992.
A simple method that allows easy identification of rifamycin B-producing strains is described. This method involves the use of an enzyme, rifamycin oxidase, which converts inactive rifamycin B to active rifamycin S. In this method, colonies to be tested are grown in pairs. The two colonies are then transferred to two plates seeded with a sensitive strain of Staphylococcus aureus, one plate of which contains the enzyme rifamycin oxidase. All paired colonies which show a larger inhibition zone diameter on the enzyme-containing plate are identified as rifamycin B producers.
描述了一种能够轻松鉴定产利福霉素B菌株的简单方法。该方法涉及使用一种酶,即利福霉素氧化酶,它可将无活性的利福霉素B转化为有活性的利福霉素S。在这种方法中,待测试的菌落成对培养。然后将这两个菌落转移到接种了金黄色葡萄球菌敏感菌株的两个平板上,其中一个平板含有利福霉素氧化酶。在含有该酶的平板上显示出更大抑菌圈直径的所有成对菌落被鉴定为产利福霉素B的菌株。