Baltz R H, Matsushima P
J Gen Microbiol. 1981 Nov;127(1):137-46. doi: 10.1099/00221287-127-1-137.
Protoplasts from four different species of Streptomyces regenerated cells efficiently in hypertonic soft agar medium overlaid on partially dehydrated regeneration medium. The efficiencies of regeneration were strongly dependent upon the incubation temperatures for cell growth and for protoplast regeneration. Cell growth temperatures (before protoplast formation) required for efficient protoplast regeneration varied from species to species, and did not necessarily correlate with the optimum temperatures for protoplast regeneration. Under the best conditions, protoplasts from all four species were able to regenerate viable cells at nearly 100% efficiency and also formed confluent lawns of mycelia when plated in high concentrations. The temperatures for cell growth and protoplast regeneration also affected the frequencies of genetic recombinants obtained by protoplast fusion in S. fradiae, and highest recombinant frequencies were obtained under conditions which favoured efficient protoplast regeneration. With the modified procedure described, maximum frequencies of genetic recombinants were obtained by treating parental protoplasts with 40 to 60% polyethylene glycol 1000.
来自四种不同链霉菌属物种的原生质体,在覆盖于部分脱水再生培养基上的高渗软琼脂培养基中能高效再生细胞。再生效率在很大程度上取决于细胞生长和原生质体再生的培养温度。高效原生质体再生所需的细胞生长温度(原生质体形成前)因物种而异,且不一定与原生质体再生的最适温度相关。在最佳条件下,所有四个物种的原生质体都能够以近100%的效率再生活细胞,并且当以高浓度接种时还能形成菌丝体的汇合菌苔。细胞生长和原生质体再生的温度也影响了弗氏链霉菌原生质体融合获得的遗传重组体的频率,并且在有利于高效原生质体再生的条件下获得了最高的重组频率。采用所述的改良方法,通过用40%至60%的聚乙二醇1000处理亲本原生质体,获得了最大频率的遗传重组体。