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食品研究与开发:2016,37(1):184-189
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培养条件对八角内生真菌发酵液抗氧化活性的 影响
李海云1,2,袁志林2,李子院2,阮贵华2,郝再彬2,3,韩卫东3
(1. 桂林理工大学 广西矿冶与环境科学实验中心,广西 桂林 541004; 2. 桂林理工大学 化学与生物工程 学院,广西 桂林 541004;3. 广西壮药产业化工程院,广西 柳州 545200)
Effect of Culture Conditions on Antioxidative Activity of Fermentation Broth of Endophytic Fungal Isolated from Illicium verum
LI Hai-yun1,2, YUAN Zhi-lin2, LI Zi-yuan2, RUAN Gui-hua2, HAO Zai-bin2,3, HAN Wei-dong3
(1. Guangxi Scientific Experiment Center of Minin, Metallurgy and Environment,Guilin University of Technology, Guilin 541004, Guangxi, China; 2. College of Chemistry & Bioengineering, Guilin University of Technology, Guilin 541004, Guangxi, China; 3. Guangxi Zhuang Medicine Industrial Engineering Institute, Liuzhou 545200, Guangxi, China)
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投稿时间:2014-08-09    
中文摘要: 对八角内生真菌 Chaetomium globosum BJEF13 产抗氧化活性物质的培养条件进行了研究。 在筛选确定基础培 养基的基础上,采用单因素试验方法考察了培养基组成及摇瓶发酵条件对菌株发酵液抗氧化活性、菌株生长的影响。基 础培养基的筛选结果表明,马铃薯葡萄糖培养基、察氏培养基、马丁培养基、豆芽汁蔗糖培养基等 4 种常用真菌培养基 中,察氏培养基优于其他 3 种。培养基组成和发酵条件的研究结果表明,当以 4 %葡萄糖、0.4 %的蛋白胨、0.1 %K2HPO4、0.05 %KCl、0.05 %MgSO4 和 0.001 %FeSO4 作为摇瓶发酵培养基时,接种量为 10 %,装液量为 100 mL/250 mL,在初始 pH 为 7.5、28℃、150 r/min 条件下振荡培养 7 d,该菌株的生长和培养液的抗氧化活性可以达到较好的水平,其生物量平均 干重达 0.682 6 g/100 mL,5 倍稀释的乙酸乙酯萃取液对 DPPH 自由基的清除率可达 57.51 %。
中文关键词: 内生真菌  球毛壳菌  八角  抗氧化  培养条件
Abstract:Influences of cultural conditions on the production of antioxidant materials by the endophytic fungal Chaetomium globosum BJEF13 isolated from Illicium verum were studied. After screening the basic culture medium, influences of compositions of the cultural medium and fermentation conditions to the dry weight of mycelia and DPPH· scavenging activity were investigated using single factor experiment. The basic culture medium screening results indicated that Czapek culture medium was more suitable for the strain than the other three media, the PD culture medium, Martin culture medium and BSS culture medium. The results of single factor experiments for components of Czapek culture medium indicated that the suitable cultural conditions for the mycelia growth and production of antioxidant materials were as followed: 4 % glucose, 0.4 % peptone, 0.1 % K2HPO4, 0.05 % KCl, 0.05 % MgSO4, 0.001 % FeSO4, initial pH 7.5, temperature 28 ℃, inoculation amount 10 %, liquid volume 100 mL/250 mL, shaking speed 150 r/min and cultural time 7 days. Under the suitable cultural conditions, the dry weight of mycelia and DPPH· scavenging activity of 5 -fold dilution of acetate extract of the broth were 0.682 6 g/100 mL and 57.51 %, respectively.
文章编号:201601045     中图分类号:    文献标志码:A
基金项目:国家自然科学基金项目(31460409);广西矿冶与环境科学实验中心资助项目(KH2013YB013);广西壮药产业化工程院科研项目 (2014GXZYCYH03)
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