Guojun Yang, Yuping He, Yan Jiang, Kaichun Lin, Haiyang Xia
Hubei Nature's Favor Biotechnology, Hanchuan, Hubei, People's Republic of China.
College of Plant Science and Technology, Huazhong Agricultural University, Wuhan, Hubei, People's Republic of China.
Jundishapur J Microbiol. 2016 May 30;9(6):e16765. doi: 10.5812/jjm.16765. eCollection 2016 Jun.
Spinosad (a mixture of spinosyns A and D) is a unique natural pesticide produced by Saccharopolyspora spinosa. With regard to attempts to improve S. spinosa by classical mutagenesis, we propose that the bottleneck of screening out high-spinosad-production strains is probably caused by the fermentation media.
The current study aimed to identify a new medium to extensively investigate the potential of S. spinosa strains to produce spinosad.
Statistical and regressive modeling methods were used to investigate the effects of the carbon source and to optimize the production media.
The spinosad production of S. spinosa Co121 increased 77.13%, from 310.44 ± 21.84 μg/mL in the initial fermentation medium (with glucose as the main carbon source) to 549.89 ± 38.59 μg/mL in a new optimized fermentation medium (98.0 g of mannitol, 43.0 g of cottonseed flour, 12.9 g of corn steep liquor, 0.5 g of KH2PO4, and 3.0 g of CaCO3 in 1 L of H2O; pH was adjusted to 7.0 before autoclaving). After screening 4,000 strains, an overall 3.33-fold increase was observed in spinosad titers, starting from the parental strain Co121 in the original fermentation medium and ending with the mutant strain J78 (1035 ± 34 μg/mL) in the optimized medium.
The optimized fermentation medium developed in this study can probably be used to improve spinosad production in screening industrial strains of S. spinosa.
多杀菌素(多杀菌素A和D的混合物)是由刺糖多孢菌产生的一种独特的天然杀虫剂。关于通过经典诱变改进刺糖多孢菌的尝试,我们认为筛选高多杀菌素生产菌株的瓶颈可能是由发酵培养基造成的。
本研究旨在确定一种新的培养基,以广泛研究刺糖多孢菌菌株产生多杀菌素的潜力。
采用统计和回归建模方法研究碳源的影响并优化生产培养基。
刺糖多孢菌Co121的多杀菌素产量提高了77.13%,从初始发酵培养基(以葡萄糖为主要碳源)中的310.44±21.84μg/mL增加到新优化发酵培养基(1L水中含有98.0g甘露醇、43.0g棉籽粉、12.9g玉米浆、0.5g KH2PO4和3.0g CaCO3;高压灭菌前将pH调至7.0)中的549.89±38.59μg/mL。筛选4000株菌株后,从原始发酵培养基中的亲本菌株Co121开始,到优化培养基中的突变菌株J78(1035±34μg/mL),多杀菌素效价总体提高了3.33倍。
本研究开发的优化发酵培养基可能可用于提高刺糖多孢菌工业筛选菌株的多杀菌素产量。