Matsushima P, Baltz R H
J Bacteriol. 1985 Jul;163(1):180-5. doi: 10.1128/jb.163.1.180-185.1985.
A procedure for efficient transformation of Streptomyces ambofaciens and Streptomyces fradiae protoplasts with plasmid DNA was developed. Transformation frequencies with S. fradiae protoplasts were strongly influenced by the temperatures for cell growth, protoplast formation, and protoplast regeneration. Transformation frequencies for both species were also influenced by the culture age before protoplast formation, the source and concentration of polyethylene glycol, the transformation-inducing agent, the concentration of protoplasts used in the transformation procedure, and the number of protoplasts added to regeneration plates. Transformation frequencies were substantially higher for both species when calf thymus DNA and protamine sulfate were added to the transformation mix. With S. fradiae, transformation frequencies were much lower with plasmid DNA prepared from other species than with the same plasmids prepared from S. fradiae, suggesting that S. fradiae expresses restriction and modification. With the modified transformation procedures using DNA prepared from homologous hosts, S. ambofaciens and S. fradiae are now transformed routinely at frequencies of 10(6) to 10(7) transformants per micrograms of plasmid DNA.
开发了一种用质粒DNA高效转化浅青紫链霉菌和弗氏链霉菌原生质体的方法。弗氏链霉菌原生质体的转化频率受细胞生长、原生质体形成和原生质体再生温度的强烈影响。这两个物种的转化频率还受原生质体形成前的培养龄、聚乙二醇的来源和浓度、转化诱导剂、转化过程中使用的原生质体浓度以及添加到再生平板上的原生质体数量的影响。当向转化混合物中添加小牛胸腺DNA和硫酸鱼精蛋白时,这两个物种的转化频率都显著更高。对于弗氏链霉菌,用从其他物种制备的质粒DNA的转化频率比用从弗氏链霉菌制备的相同质粒的转化频率低得多,这表明弗氏链霉菌表达限制和修饰作用。使用从同源宿主制备的DNA的改良转化程序,浅青紫链霉菌和弗氏链霉菌现在通常以每微克质粒DNA 10⁶至10⁷个转化体的频率进行转化。