Pollock M E, Bonner S V
J Bacteriol. 1969 Feb;97(2):522-5. doi: 10.1128/jb.97.2.522-525.1969.
In examining the medium used in cultivation of Mycoplasma for deoxyribonucleic acid isolation, it was found that an aggregate was present which sedimented with the organisms and which was ethyl alcohol-precipitated during deoxyribonucleic acid purification. To eliminate the contaminating material, a method was devised to obtain only the dialyzable constituents of the medium. This report describes the preparation of a dialysate of soy peptone-yeast extract. The medium, obtained by immersion of the encased dehydrated ingredients in sodium chloride solution for 5.5 hr at approximately 80 C, has been employed as the basal medium for cultivation of a number of Mycoplasma species. Comparative growth curves of two saprophytic strains and two parasitic species indicated that multiplication in dialysate, with suitable supplement, followed the pattern typical of the common eubacteria. Thus, by elimination of the sediment which occurred in nondialyzed medium, Mycoplasma could be concentrated without concomitant accumulation of contaminating macromolecules.
在检查用于培养支原体以分离脱氧核糖核酸的培养基时,发现存在一种聚集体,它与生物体一起沉淀,并且在脱氧核糖核酸纯化过程中可被乙醇沉淀。为了去除污染物质,设计了一种方法来仅获得培养基的可透析成分。本报告描述了大豆蛋白胨 - 酵母提取物透析液的制备。通过将封装的脱水成分在约80℃的氯化钠溶液中浸泡5.5小时获得的培养基,已被用作多种支原体物种培养的基础培养基。两种腐生菌株和两种寄生菌的比较生长曲线表明,在添加合适补充物的透析液中繁殖遵循常见真细菌的典型模式。因此,通过去除未透析培养基中出现的沉淀物,可以浓缩支原体而不会伴随污染大分子的积累。