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作 者:吴升山[1,2] 蔡慧农[1,2] 苏文金[1,2] 倪辉 李利君[1] 肖安风[1]
机构地区:[1]集美大学生物工程学院,福建厦门361021 [2]厦门市食品生物工程技术研究中心,福建厦门361021
出 处:《中国食品学报》2010年第4期193-201,共9页Journal of Chinese Institute Of Food Science and Technology
基 金:福建省青年人才创新基金项目(2007F3073);科技人员服务企业项目(SQ2009GJC4000525);福建省科技计划重点项目(No.2009N0044);厦门市科技项目(3502Z20093023)
摘 要:目的:优化黑曲霉DB056产α-鼠李糖苷酶和柚苷酶的培养基,提高这两种酶的产量。方法:以α-鼠李糖苷酶活力和柚苷酶活力为指标,研究碳源、氮源和乳化剂TritonX-100对α-鼠李糖苷酶活力和柚苷酶活力的影响,优化黑曲霉DB056摇瓶发酵α-鼠李糖苷酶和柚苷酶的培养基。结果:碳氮源的种类与浓度,乳化剂Tri-tonX-100的浓度对黑曲霉DB056产α-鼠李糖苷酶和柚苷酶有重要影响;黑曲霉DB056产酶的优化培养基是:柚皮苷3.5g/L,玉米浆4g/L,MgSO4·7H2O1.0g/L,KH2PO41.0g/L,KCl0.5g/L,无水CaCl20.1g/L,乳化剂TritonX-1001.0%。此时α-鼠李糖苷酶活力和柚苷酶活力分别为994U/mL和276U/mL,分别比发酵初始培养基提高了42.3%和147.8%。结论:通过培养基优化,大幅度提高了黑曲霉DB056液态深层发酵α-鼠李糖苷酶活力和柚苷酶活力。Objective:To optimize the culture medium of Aspergillus niger DB056 for increasing the yields of α-rhamnosidase and naringinase.Methods:The medium with different composition and concentration of carbon source,nitrogen source and emulsifier Triton X-100 were used in shaking culture Aspergillus niger DB056.The activities of α-rhamnosidase and naringinase were detected to evaluate the effect of medium constituents and their concentrations.Results:Both the types and concentrations of carbon source and nitrogen source and the concentration of emulsifier Triton X-100 showed important impact on the activities of α-rhamnosidase and naringinase.The optimum culture medium was consisted of naringin 3.5 g/L,corn steep liquor 4.0 g/L,MgSO4·7H2O 1.0 g/L,KH2PO4 1.0 g/L,KCl 0.5 g/L,CaCl2 0.1 g/L,emulsifier Triton X-100 1%.Using the optimum medium,the activities of α-rhamnosidase and naringinase increased 1.42fold and 2.48-fold,and the enzyme activity of α-rhamnosidase and naringinase reached to 994 U/mL and 276 U/mL,respectively.Conclusion:After the optimization of medium,the activity of α-rhamnosidase and naringinase were increased significently in liquid deep layer fermentation using Aspergillus niger DB056.
关 键 词:黑曲霉 发酵培养基 α-鼠李糖苷酶 柚苷酶 高效液相色谱法
分 类 号:TQ925[轻工技术与工程—发酵工程]
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