Uitendaal M P, DeBruyn C H, Hatanaka M, Hösli P
In Vitro. 1979 Feb;15(2):103-8. doi: 10.1007/BF02618104.
A sensitive ultramicrochemical enzyme test for mycoplasmal contamination of cultured cells, based on the determination of the activity of adenosine phosphorylase, is described. The test was performed by assaying the enzymatic conversion of [8-14C]adenine and ribose-1-phosphate to [8-14C]adenosine by incubating a plastic leaflet carrying a counted number of cells (1 to 10). These leaflets were isolated from the bottom of the same plastic film dish in which the cells were cultured for experimental or diagnostic purposes, e.g. prenatal diagnosis or inborn errors of metabolism. The present test should be several 1000-fold more sensitive than the originally reported enzymatic method because (a) the adenosine-phosphorylase reaction is measured in the nucleoside forming direction which is by far the most active; and (b) the assay is performed with the cells and not with the culture medium. The latter is of special importance for the detection of those low-grade contamination in which most of the mycoplasma particles are attached to cell membranes.
本文描述了一种基于腺苷磷酸化酶活性测定的、用于检测培养细胞支原体污染的灵敏超微化学酶检测方法。该检测方法通过将载有计数细胞(1至10个)的塑料薄片与[8-¹⁴C]腺嘌呤和核糖-1-磷酸一起孵育,测定其酶促转化为[8-¹⁴C]腺苷的过程来进行。这些薄片是从用于实验或诊断目的(例如产前诊断或先天性代谢缺陷)培养细胞的同一塑料薄膜培养皿底部分离得到的。本检测方法的灵敏度应比最初报道的酶法高数千倍,原因如下:(a) 腺苷磷酸化酶反应是在核苷形成方向上进行测定的,该方向活性最强;(b) 检测是针对细胞而非培养基进行的。对于检测大多数支原体颗粒附着于细胞膜的低水平污染而言,后者尤为重要。