National Chemical Laboratory, NCIM Resource Center, Pune, 411 008 Maharashtra India.
Indian J Microbiol. 2010 Mar;50(1):97-100. doi: 10.1007/s12088-010-0008-y. Epub 2010 Mar 5.
Method for production and regeneration of Lactobacillus delbrueckii protoplasts are described. The protoplasts were obtained by treatment with a mixture of lysozyme and mutanolysin in protoplast buffer at pH 6.5 with different osmotic stabilizers. The protoplasts were regenerated on deMan, Rogosa and Sharpe (MRS) with various osmotic stabilizers. Maximum protoplast formation was obtained in protoplast buffer with sucrose as an osmotic stabilizer using a combination of lysozyme (1 mg/ml) and mutanolysin (10 μg/ml). Maximum protoplast regeneration was obtained on MRS medium with sucrose (0.5 M) as an osmotic stabilizer. The regeneration medium was also applicable to other species of lactobacilli as well. This is, to our knowledge, the first report on protoplast formation and efficient regeneration in case of L. delbrueckii.
描述了德氏乳杆菌原生质体制备和再生的方法。采用溶菌酶和黏菌素混合物在 pH 值为 6.5 的原生质体缓冲液中处理,使用不同的渗透压稳定剂获得原生质体。在含有不同渗透压稳定剂的德氏乳杆菌-马丁氏培养基(MRS)上再生原生质体。使用溶菌酶(1 mg/ml)和黏菌素(10 μg/ml)的组合,在含有蔗糖作为渗透压稳定剂的原生质体缓冲液中获得最大的原生质体形成。在含有蔗糖(0.5 M)作为渗透压稳定剂的 MRS 培养基上获得最大的原生质体再生。再生培养基也适用于其他乳杆菌属的物种。据我们所知,这是首次报道德氏乳杆菌原生质体的形成和有效再生。