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中国精品科技期刊2020
娄潇雨, 童群义. 超声波辅助碱液-酶解法对柚皮脱苦效果的研究[J]. 食品工业科技, 2017, (13): 206-211. DOI: 10.13386/j.issn1002-0306.2017.13.039
引用本文: 娄潇雨, 童群义. 超声波辅助碱液-酶解法对柚皮脱苦效果的研究[J]. 食品工业科技, 2017, (13): 206-211. DOI: 10.13386/j.issn1002-0306.2017.13.039
LOU Xiao-yu, TONG Qun-yi. Study on effect of debittering shaddock peel by ultrasound-assisted alkaline solution-enzymolysis method[J]. Science and Technology of Food Industry, 2017, (13): 206-211. DOI: 10.13386/j.issn1002-0306.2017.13.039
Citation: LOU Xiao-yu, TONG Qun-yi. Study on effect of debittering shaddock peel by ultrasound-assisted alkaline solution-enzymolysis method[J]. Science and Technology of Food Industry, 2017, (13): 206-211. DOI: 10.13386/j.issn1002-0306.2017.13.039

超声波辅助碱液-酶解法对柚皮脱苦效果的研究

Study on effect of debittering shaddock peel by ultrasound-assisted alkaline solution-enzymolysis method

  • 摘要: 在柚皮产品深加工中,为了使柚皮达到更好的脱苦效果,以柚皮脱苦率为指标,采用超声波辅助碱液-酶解法对柚皮进行脱苦。经单因素和正交实验得出超声波辅助碱液法优化工艺条件为:料液比1∶30(g/m L),超声时间20 min,超声温度55℃,超声功率120 W,所得脱苦率为75.31%。在超声波优化基础上,通过响应面优化实验对柚皮进行柚苷酶酶解处理,其优化条件为:酶添加量0.15%,酶解温度52℃,酶解p H4.1,酶解时间36 min,所得柚皮脱苦率为90.14%。此方法与传统柚苷酶酶解法相比,具有更高的脱苦效率。 

     

    Abstract: The ultrasound-assisted alkaline solution-enzymolysis method, which used removal rate of naringin as the index, was studied to get better debittering effect in the further-processing product of shaddock peel. By single factor experiment and orthogonal experiment, the results showed that the optimum treatment conditions of ultrasound-assisted alkaline solution were obtained as follows: material-to-liquid ratio 1 ∶ 30 ( g/m L) , ultrasonic treatment time 20 min, ultrasonic temperature 55 ℃, ultrasonic power 120 W.Under these optimum conditions, the removal rate of naringin was 75.31%.On this basis, by response surface design, the results showed that 90.14% removal rate of naringin was achieved through the use of naringinase at 0.15%, dosage for 36 min, p H4.1 and 52 ℃. The results of this study indicated that the ultrasound-assisted alkaline solution-enzymolysis method was more effective compared with the traditional naringinase enzymolysis method.

     

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