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中国精品科技期刊2020
王艳, 吴鑫颖, 胡娜, 唐佳代, 王晓丹, 王啸, 邱树毅. 紫色红曲霉FBKL3.0018液态发酵产酯化酶的工艺优化[J]. 食品工业科技, 2018, 39(15): 147-153. DOI: 10.13386/j.issn1002-0306.2018.15.027
引用本文: 王艳, 吴鑫颖, 胡娜, 唐佳代, 王晓丹, 王啸, 邱树毅. 紫色红曲霉FBKL3.0018液态发酵产酯化酶的工艺优化[J]. 食品工业科技, 2018, 39(15): 147-153. DOI: 10.13386/j.issn1002-0306.2018.15.027
WANG Yan, WU Xin-ying, HU Na, TANG Jia-dai, WANG Xiao-dan, WANG Xiao, QIU Shu-yi. Optimization of Esterifying Enzyme Production Process by M.purpureus FBKL3.0018 under Liquid Fermentation[J]. Science and Technology of Food Industry, 2018, 39(15): 147-153. DOI: 10.13386/j.issn1002-0306.2018.15.027
Citation: WANG Yan, WU Xin-ying, HU Na, TANG Jia-dai, WANG Xiao-dan, WANG Xiao, QIU Shu-yi. Optimization of Esterifying Enzyme Production Process by M.purpureus FBKL3.0018 under Liquid Fermentation[J]. Science and Technology of Food Industry, 2018, 39(15): 147-153. DOI: 10.13386/j.issn1002-0306.2018.15.027

紫色红曲霉FBKL3.0018液态发酵产酯化酶的工艺优化

Optimization of Esterifying Enzyme Production Process by M.purpureus FBKL3.0018 under Liquid Fermentation

  • 摘要: 以分离自贵州某浓香型酒厂中温大曲的产酯化酶紫色红曲霉(Monascus purpureus)FBKL3.0018为研究对象,以发酵液中酯化酶活性为考察指标,通过单因素实验、Plackett-Burman实验和响应面试验对FBKL3.0018产酯化酶的发酵培养条件进行优化。由单因素实验得到FBKL3.0018产胞外酯化酶的条件为:2%牛肉膏、6%蔗糖、0.2%无水氯化钙和0.15%七水硫酸镁、初始pH4.5、发酵温度31 ℃、摇床转速160 r/min、装液量45 mL/250 mL、接种量9%和发酵时间96 h。PB结果表明,对酯化酶生产影响较显著的因素为发酵温度、发酵时间和蔗糖添加量。响应面优化实验得到的最优条件为:发酵温度31 ℃,发酵时间96 h,蔗糖浓度6%,在优化条件下,酯化酶活性为355.62 U/mL,比优化前(133.12 U/mL)提高了2.67倍,与预测值368.82 U/mL拟合率达96.4%,说明所建立的回归模型可靠。

     

    Abstract: M FBKL3.0018 selected from medium temperature Daqu was taken as the research object. The activity of esterifying enzyme in the fermentation liquor was viewed as examining index. Single factor experiment,Plackett-Burman experiment and response surface experiment were applied to opptimize the fermentation culture condition of esterifying enzyme produced by FBKL3.0018. The effect of carbon source,nitrogen source,inorganic salt,initial pH,fermentation temperature,rotate speed,culture volume,inoculation volume and fermentation time on the production of enzyme were investigated. It was turned out that the optimal medium was:2%beef extract,6% sucrose,0.2% CaCl2,0.15% MgSO4·7 H2O,initial pH4.5,culture temperature 31 ℃,rotate speed 160 r/min,culture volume 45 mL/250 mL,inoculation volume 9%,and incubation time 96 h. Furthermore,culture temperature,time and sucrose,which had obvious effects on esterifying enzyme production,were selected to conduct response surface optimization experiments. The optimized conditions were fermentation temperature 31 ℃,fermentation time 96 h,sucrose concent ration 6%,under the condition of optimization,the activity of esterifying enzyme was 355.62 U/mL,2.67 times higher than that before optimization(133.12 U/mL). At the same time,compared with the predicted value(368.82 U/mL),the fitting rate was up to 96.4%,which indicated that the established regression model was reliable.

     

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