Gorman J A, Dove W F, Shaibe E
Mol Gen Genet. 1977 Mar 16;151(3):253-9. doi: 10.1007/BF00268788.
The haploid myxamoebae of Physarum polycephalum reversibly differentiate to form dormant microcysts under conditions of starvation. The thin-walled cysts can be selective recovered from a cell suspension which has been treated with the surfactant Triton X-100 to lyse amoeboid forms. Excystment, which is initiated by suspension in liquid medium, is inhibited by antibiotics which block protein synthesis. Cysts of drug resistant mutants excyst rapidly in media containing sufficient antibiotic to maintain drug sensitive strains in the encysted state. The selective survival of non-excysted cells following Triton X-100 treatment has been employed to enrich for drug sensitive mutants. Several anisomycin sensitive mutants have been isolated, one of which has been analysed genetically. The possible applications of this mutant enrichment technique are discussed.
多头绒泡菌的单倍体变形虫在饥饿条件下可逆地分化形成休眠微囊肿。薄壁囊肿可从已用表面活性剂 Triton X-100 处理以裂解变形虫形态的细胞悬液中选择性回收。由悬浮于液体培养基引发的脱囊作用受到阻断蛋白质合成的抗生素的抑制。耐药突变体的囊肿在含有足够抗生素的培养基中迅速脱囊,而这些抗生素足以使药物敏感菌株维持在包囊状态。Triton X-100 处理后未脱囊细胞的选择性存活已被用于富集药物敏感突变体。已分离出几个茴香霉素敏感突变体,其中一个已进行遗传分析。讨论了这种突变体富集技术的可能应用。