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作 者:万月佳[1] 马江锋[1] 徐蓉[1] 贺爱永[1] 姜岷[1] 陈可泉[1] 姜引[1]
机构地区:[1]南京工业大学生物与制药工程学院材料与化学工程国家重点实验室,江苏南京211816
出 处:《生物工程学报》2012年第12期1450-1459,共10页Chinese Journal of Biotechnology
基 金:国家自然科学基金(No.21076105);国家重点基础研究发展计划(973计划)(No.2009CB724701);江苏高校优势学科建设工程项目资助~~
摘 要:利用重组大肠杆菌EscherichiacoliRosetta(DE3)/pET-SPase发酵生产蔗糖磷酸化酶(EC2.4.1.7,Sucrosephosphorylase,SPase)。收集的菌体经高压破碎后离心得到粗酶液,通过镍NTA亲和层析、超滤除盐后得到电泳纯的SPase,纯化后的SPase的比酶活是原来的2.1倍,酶活回收率达到82.7%。经SDS.PAGE电泳测定,重组SPase的分子量约为59kDa。该酶在不高于37℃,pH6.0~6.7的条件下比较稳定,最适催化温度与最适催化pH分别为37℃,pH6.7,该酶对蔗糖的米氏常数(Km)为7.3mmol/L,最大反应速率(Vmax)为0.2/μmol/(min·mg)。此外文中还以蔗糖和氢醌为底物,利用重组SPase催化合成a-熊果苷。其最佳反应条件为:20%蔗糖,200U/mL的酶液,1.6%氢醌,pH6.0~6.5,25℃,反应21h。a-熊果苷的摩尔产率为78.3%,a-熊果苷的产量为31g/L。Sucrose phosphorylase (EC 2.4.1.7, Sucrose phosphorylase, SPase) can be produced by recombinant strain Escherichia coli Rosetta(DE3)/Pet-SPase. Crude enzyme was obtained from the cells by the high pressure disruption and centrifugation. Sucrose phosphorylase was purified by Ni-NTA affinity column chromatography and desalted by ultrafiltration. The specific enzyme activity was 1.1-fold higher than that of the crude enzyme, and recovery rate was 82.7%. The purified recombinant SPase had a band of 59 kDa on SDS-PAGE. Thermostability of the enzyme was shown at temperatures up to 37 ℃, and pH stability between pH 6.0 and 6.7. The optimum temperature and pH were 37 ℃ and 6.7, respectively. The Km of SPase for sucrose was 7.3 mmol/L, and Vmax was 0.2 μmol/(min.mg). Besides, a-arbutin was synthesized from sucrose and hydroquinone by transglucosylation with recombinant SPase. The optimal conditions for synthesis of a-arbutin were 200 U/mL of recombinant SPase, 20% of sucrose, and 1.6% hydroquinone at pH 6-6.5 and 25 ℃ for 21 h. Under these conditions, a-arbutin was obtained with a 78.3% molar yield with respect to hydroquinone, and the concentration of a-arbutin was about 31 g/L.
分 类 号:TQ929[轻工技术与工程—发酵工程]
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