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作 者:郝荣华 张晓元 王羽 刘飞 陈勉[1] 朱希强 凌沛学 HAO Rong-hua1, ZHANG Xiao-yuan1, WANG Yu3, LIU Fei1,2, CHEN Mian1, ZHU Xi-qiang1,2,4, LING Pei-xue1,2,4(1. Key Laboratory of Biopharmaceuticals, Engineering Laboratory of Polysaccharide Drugs, National-Local Joint Engineering Laboratory of Polysaccharide Drugs, Shandong Academy of Pharmaceutical Sciences, Jinan 250101, China; 2. School of Pharmaceutical Sciences, Shandong University, Jinan 250012, China; 3. School of Environmental Science and Engineering, Shandong Agriculture and Engineering University, Jinan 250100, China; 4. Shandong Freda Pharmaceutical Group Co., Ltd., Jinan 250101, Chin)
机构地区:[1]山东省药学科学院,山东省生物药物重点实验室,山东省多糖类药物工程实验室,多糖类药物发酵与精制国家地方联合工程实验室,山东济南250101 [2]山东大学药学院,山东济南250012 [3]山东农业工程学院环境科学与工程学院,山东济南250100 [4]山东福瑞达医药集团有限公司,山东济南250101
出 处:《食品与药品》2018年第3期168-173,共6页Food and Drug
基 金:山东省重点研发计划(2016GSF121012);山东省科技重大专项(重大关键技术)(2015ZDJS04002);山东省自然科学基金企业先导技术联合基金资助项目(ZR2015QL007)
摘 要:目的研究枯草芽孢杆菌来源的木聚糖酶基因在大肠杆菌BL2l中的高效分泌表达并对其产木聚糖酶进行酶学性质分析。方法全基因合成枯草芽孢杆菌木聚糖酶基因序列并进行密码子优化,经大肠杆菌BL2l表达后获得基因工程菌株,通过SDS-PAGE电泳检测、硫酸铵分级沉淀和AKTA系统分离纯化,分析表达产物的酶学性质。结果重组木聚糖酶为胞外分泌性表达,相对分子质量约43×103;酶促反应最适温度为65℃,最适p H为10.0,最适条件下酶活最高可达1201.5 IU/ml。结论成功获得高效分泌表达重组木聚糖酶的基因工程菌株,该木聚糖酶具较好的耐热性和耐碱性。Objective To construct an engineering strain in E. coli BL21 with high production of thermo-alkaliphilic xylanase and analyze the properties of the secreted xylanase. Methods The optimized sequence from Bacillus subtilis encoding thermo-alkaliphilic xylanase(xyn) was synthesized and introduced into Escherichia coli. The recombinant protein was identified by SDS-PAGE and purified by ammonium sulfate precipitation and AKTA system, then the enzymatic properties of the recombinant xylanase were analyzed. Results The recombinant xylanase was successfully expressed and secreted into the medium, and SDS-PAGE analysis revealed that the relative molecular mass of the protein is determined about 43×103. The optimum temperature and p H for enzymatic reaction were 65 ℃ and 10.0, respectively. The maximum enzymatic activity under optimal condition reached 1201.5 IU/ml. Conclusion The genetic engineering strain gene with high level of secretory expression of thermo-alkaliphilic xylanase is obtained.
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