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Enhancing The Sporulation Of Streptomyces Kasugaensis By Culture Optimization

机译:通过培养优化提高春日链霉菌的形成

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摘要

To be an effective microbial biocide, Streptomyces kasugaensis should be converted into spore during cultivation process for successful long-term storage. By statistical design methods, culture conditions including medium components and operating parameters were optimized and more than 100 times increase in spore yield was achieved. Addition of spent culture fluid (100ppm), EDTA (30 ppm), mycophenolic acid (32 ppm) with combination of pH up-shock (5.5 to 8.5) increased total viable cell and spore conversion rate, resulting in 1.6× 10~7 (spore/mL) in 5 days of culture in a fermenter. This result provides a practical method for obtaining high spore number for commercial production of Streptomyces kasugaensis as a microbial pesticide.
机译:为了成为有效的微生物杀菌剂,春日链霉菌应在培养过程中转化为孢子以成功长期保存。通过统计设计方法,优化了包括培养基成分和操作参数在内的培养条件,孢子产量提高了100倍以上。添加废培养液(100ppm),EDTA(30 ppm),麦考酚酸(32 ppm)以及pH值升高(5.5至8.5)的组合可增加总活细胞和孢子转化率,从而获得1.6×10〜7(孢子/ mL)在发酵罐中培养5天。该结果提供了一种获得高孢子数的实用方法,用于商业生产春日链霉菌作为微生物农药。

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