首页> 外国专利> METHOD FOR DIFFERENTIATION OF VIBRIO CHOLERAE O139 STRAINS SERO GROUPS ON ALKYL SULPHATIC ACTIVITY

METHOD FOR DIFFERENTIATION OF VIBRIO CHOLERAE O139 STRAINS SERO GROUPS ON ALKYL SULPHATIC ACTIVITY

机译:区分霍乱弧菌O139菌株血清亚群的烷基硫活性

摘要

The method of differentiation of strains of Vibrio cholerae O139 serogroup by alkyl sulfatase activity, including the use of sodium dodecyl sulfate as a substrate in a nutrient medium, characterized in that they create a synthetic medium for the preparation of which per 100 ml is necessary: 0.5 g of sodium chloride, 2 g of agar, 0.002 g of bromothymol blue indicator, then the components are dissolved in 0.01 M Tris HCl buffer, having a pH of 7.8 and subjected to boiling for 30 minutes, obtaining a molten mass into which 0.1 g of sodium dodecyl sulfate substrate is introduced, then about The agar cultures under study are inoculated onto the obtained synthetic medium, followed by incubation at 37 ° C for 24-48 hours, after which they are differentiated by the alkyl sulfatase activity of the serogroup O139 cholera vibrios, which hydrolyze the sodium dodecyl sulfate substrate; therefore, agar sectors around the seed are clearly visible turbid - white zones 2-10 mm in size, which confirms the toxigenicity of the strain and its epidemiological significance, and if there are no such zones, they conclude that the strain is non-toxic and its epidemic insignificance.
机译:通过烷基硫酸酯酶活性区分霍乱弧菌O139血清群菌株的方法,包括在营养培养基中使用十二烷基硫酸钠作为底物,其特征在于它们创建了用于制备的合成培养基,每100毫升是必需的:将0.5 g氯化钠,2 g琼脂,0.002 g溴百里香酚蓝指示剂溶解,然后将组分溶解在pH值为7.8的0.01 M Tris HCl缓冲液中,并煮沸30分钟,得到0.1引入g的十二烷基硫酸钠底物,然后将约80%的琼脂培养物接种到获得的合成培养基上,然后在37°C下孵育24-48小时,之后通过血清烷基硫酸酯酶活性进行区分。 O139霍乱弧菌,水解十二烷基硫酸钠底物;因此,种子周围的琼脂区段清晰可见,呈浑浊-2-10毫米大小的白色区域,这证实了该菌株的产毒性及其流行病学意义,如果没有这样的区域,他们得出的结论是该菌株无毒。及其流行病的意义。

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