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作 者:鞠建松[1] 马宁[1] 赵冉冉[1] 刘景伟[2] 徐书景[3] 赵宝华[1]
机构地区:[1]河北师范大学生命科学学院,石家庄050024 [2]邢台医学高等专科学校,邢台054000 [3]河北师范大学旅游学院,石家庄050024
出 处:《微生物学报》2013年第4期363-371,共9页Acta Microbiologica Sinica
基 金:河北省自然科学基金(C2011205045);河北省科技支撑项目(10205521D);河北省留学回国人员资助项目(20100705);河北省高等学校科学技术研究青年基金项目(2011102);河北师范大学博士启动基金项目(L2009B13)~~
摘 要:【目的】研究假坚强芽胞杆菌OF4中乙醇脱氢酶和乙醛脱氢酶的酶学特性。【方法】通过引物设计,采用PCR技术从嗜碱芽胞杆菌OF4的基因组DNA中扩增获得乙醇脱氢酶(adh)基因和乙醛脱氢酶(aldh)基因,构建表达载体,通过异源原核表达,Ni-NTA柱层析纯化酶蛋白,分析其酶学特性。【结果】乙醛脱氢酶的最适反应温度为35℃,最适反应pH值为8.0,酶蛋白的活力为979.6 U/mg,其稳定性在25℃和35℃下比45℃稍好;尽管由于乙醇脱氢酶的表达量低而未能纯化获得酶蛋白,但通过双基因共表达及乙醇耐受性实验发现乙醇脱氢酶也具备较高的催化活性。【结论】成功地从假坚强芽胞杆菌OF4中克隆获得了乙醇脱氢酶和乙醛脱氢酶基因,二者共同作用能够较大提高宿主对乙醇的耐受性。[Objective] To clone and characterize the alcohol dehydrogenase (ADH) and aldehyde dehydrogenase (ALDH) from Bacillus pseudofirmus OF4. [Methods]Genes of adh and aldh were cloned by PCR; expression vectors pET-Ahd and pET-Aldh were constructed and expressed in Escherichia coli BL21 (DE3).After Ni-NTA column chromatography purification,the protein was characterized.[Results]The optimal temperature and pH of ALDH was 35℃ and 8. 0,the specific activities of ALDH was 979.6 U/mg protein,the thermostability at 25℃ and 35℃ was better than at 45℃ . Although the expression level of ADH was too low to purify,but it was found that ADH had high catalytic activities by experiments of co-expression and ethanol tolerance.[Conclusion]Adh and aldh from B. pseudofirmus OF4 were cloned successfully. Co-expression of double genes could greatly increase the host strain on ethanol tolerance.
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