Beltrametti Fabrizio, Barucco Daniele, Rossi Roberta, Selva Enrico, Marinelli Flavia
Vicuron Pharmaceuticals S.r.l., Gerenzano, Italy.
J Antibiot (Tokyo). 2007 Jul;60(7):447-54. doi: 10.1038/ja.2007.57.
An efficient method for protoplast generation for the uncommon actinomycete Planobispora rosea, the producer of the thiazolylpeptide antibiotic GE2270, was developed using a combination of hen egg white lysozyme and Streptomyces globisporus mutanolysin. This method converted more than 70% of vegetative mycelium to protoplasts, which were then regenerated with 50% efficiency in an optimized medium. When P. rosea protoplasts were efficiently fused, recombination between different antibiotic (streptomycin and gentamicin) resistance markers originated sensitive strains (str(s)gen(s)) at frequencies as high as 18% and double resistant fusants (str(r)gen(r)) at frequencies as high as 29%. Double resistant fusants showed GE2270 productivity intermediate between the productivity of the parental strains. Protoplast generation and fusion in P. rosea makes whole genome shuffling feasible as an approach to be used alternately with classical random mutagenesis in industrial strain improvement programs.
利用蛋清溶菌酶和球形链霉菌变溶菌素相结合的方法,开发出了一种高效的原生质体制备方法,用于生产噻唑基肽抗生素GE2270的罕见放线菌玫瑰色扁平双孢菌。该方法可将70%以上的营养菌丝体转化为原生质体,然后在优化培养基中以50%的效率再生。当玫瑰色扁平双孢菌原生质体高效融合时,不同抗生素(链霉素和庆大霉素)抗性标记之间的重组产生敏感菌株(str(s)gen(s))的频率高达18%,双抗性融合子(str(r)gen(r))的频率高达29%。双抗性融合子的GE2270生产力介于亲本菌株生产力之间。玫瑰色扁平双孢菌原生质体的产生和融合使得全基因组重排作为一种方法在工业菌株改良计划中与经典随机诱变交替使用成为可行。