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作 者:万小飞[1] 伦璇[2] 程璐[3] 钟毅敏[2] 陆东雯[2] 吴冰[4] 蔡俊鹏[1]
机构地区:[1]华南理工大学轻工与食品学院,广东广州510640 [2]华南农业大学生命科学学院,广东广州510641 [3]中山大学东校区教学实验中心,广东广州510006 [4]华南理工大学分析测试中心,广东广州510640
出 处:《现代食品科技》2008年第5期415-419,共5页Modern Food Science and Technology
摘 要:副溶血弧菌C20发酵液经离心,超滤浓缩,盐析,DEAE-SepharoseFastFlow和SephardexG-100分离纯化得到电泳纯的褐藻胶裂解酶,其分子量为40kD。酶的最适温度为30℃,在此温度下保温3.5h,相对酶活仍保持在90%;酶的最适pH为7.2,在pH7.0~7.6范围内稳定;Mg2+、Na+、NH4+、Ca2+、甲醇和适量浓度的Tween-80对酶有激活作用;Zn2+、Cu2+、Fe2+、Al3+、乙醇、丙三醇、DTT、尿素和SDS等对酶有较强的抑制作用;此褐藻胶裂解酶对聚古罗糖醛酸有很强的底物专一性,其Km值为1.38mg/mL,Vmax为0.052mg/(mL-min)。Alginate lyase was successfully purified from fermented broth of 14. parahaemolyticus C20 by ultra-filtration, ammonium sulfate precipitation, ion exchange chromatography and size exclusion chromatography. The purified alginate lyase with molecular mass of 40 kD had optimal temperature of 30℃ and maintained 90% of its activity after 3.5-hour incubation at 30℃. The enzyme with optimal pH of 7.2 was stable within the pH value range of 7.0 to 7.6. Mg^2+, Na^+, NH^4+, Ca^2+, methanol and Tween-80 with certain concentration had activation of the enzyme while ethanol, acetone, DTT, urea, SDS, Zn^2+, Cu^2+, Fe^2+ and Al^3+ showed inhibition. This enzyme specifically degraded polyguluronate with K,,of 1.38 mg/mL and Vmax of 0.052 mg/(ml.min).
分 类 号:TQ920.1[轻工技术与工程—发酵工程]
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