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地衣芽孢杆菌WIO发酵产生抗茵蛋白的研究
引用本文:纪兆林,宋浩,徐敬友,张清霞,陈夕军,童蕴慧.地衣芽孢杆菌WIO发酵产生抗茵蛋白的研究[J].中国生物防治,2013(4):579-585.
作者姓名:纪兆林  宋浩  徐敬友  张清霞  陈夕军  童蕴慧
作者单位:[1]扬州大学园艺与植物保护学院,扬州225009 [2]沭阳县农业科学研究所,沭阳223600
基金项目:现代农业产业技术体系建设专项(CARS.31-2.02);扬州大学高层次人才科研启动基金(0274983014811)
摘    要:地衣芽孢杆菌BacilluslicheniformisW10是1株生防细菌,其能产生抗菌蛋白,对多种植物病原菌有较好的抑制效果。本试验研究了菌株W10产生抗菌蛋白的发酵条件,为工厂化生产工艺提供技术支持。试验结果表明,接种菌龄12h,2%接种量,发酵液pH7.0,发酵培养60h是菌株W10产生抗菌蛋白的适宜发酵条件。控制发酵温度有利于抗菌蛋白积累,第一段温度为30℃培养20h,第二段温度为28℃至发酵结束。最佳溶氧量为20%。2次补料发酵效果要高于分批发酵,补料为500mL含10g.L-1葡萄糖和5g·L-1蛋白胨的培养基;选用200mg·L-1聚氧丙烯聚氧乙烯甘油醚(GPE消泡剂,泡敌)为消泡剂。利用优化的控制条件发酵培养菌株W10,与优化前相比,对目标病菌的抑菌率增加了34.6%。

关 键 词:地衣芽孢杆菌  发酵条件  抗菌蛋白  生物防治

Fermentation Process of Antifungal Protein Produced by Bacillus licheniformis W10
JI Zhaolin,SONG Hao,',XU Jingyou,ZHANG Qingxia,CHEN Xijun,TONG Yunhui.Fermentation Process of Antifungal Protein Produced by Bacillus licheniformis W10[J].Chinese Journal of Biological Control,2013(4):579-585.
Authors:JI Zhaolin  SONG Hao    XU Jingyou  ZHANG Qingxia  CHEN Xijun  TONG Yunhui
Institution:1. (1. College of Horticulture and Plant Protection, Yangzhou University, Yangzhou 225009; 2. Agricultural Scientific Research Institute of Shuyang, Shuyang 223600, China)
Abstract:Bacillus licheniformis W10 is an antagonistic bacterium, which can produce antifungal protein inhibiting growth to a variety of plant pathogenic fungi. The technical conditions of fermentation W 10 to produce antifungal protein were studied. The results indicated that yield of antifungal protein was promising under the conditions of inoculation bacteria for 12 h, 2% inoculum volume, fermentation for 60 h and pH 7.0. During the fermentation, changing culture temperature was favorable to the antifungal protein accumulation and increased its inhibitory effect against plant pathogen Botrytis cinerea, with fermentation temperature of first stage was 30 ~C for 20 h, and then was adjusted to 28 ~C until the end of fermentation. The suitable dissolved oxygen value was 20%. The better fermentation method was two fed-batch culture with 10 g.L-1 glucose and 5 g.L-1 peptone as the supplement medium. The defoaming substance was defoamer GPE (polyoxypropylene-polyoxyethylene glycerol ether) with 200 mg.L-1. Under the optimized fermentation conditions, the inhibitory effect of the strain W 10 against B. cinerea reached 99.5%, increasing 34.6% compared with the control.
Keywords:Bacillus licheniformis  fermentation conditions  antifungal protein  biocontrol
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