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作 者:杨江科[1] 张正平[1] 刘立营[1] 闫云君[1]
机构地区:[1]分子生物物理教育部重点实验室,华中科技大学生命科学与技术学院,武汉430074
出 处:《微生物学报》2009年第8期1095-1101,共7页Acta Microbiologica Sinica
基 金:"十一五"863计划(2007AA05Z417;2006AA020203)~~
摘 要:【目的】本研究拟克隆新型的黑曲霉(Aspergillus niger)脂肪酶(EC3.1.1.3)基因,实现其在大肠杆菌(Escherichia coli)的高效表达,并对表达产物进行系统的酶学性质分析,为该脂肪酶的工业化生产及应用奠定基础。【方法】通过PCR和RT-PCR克隆脂肪酶基因,并将其开放式阅读框(ORF)克隆入融合表达载体pET28a;表达产物经Ni-agarose纯化后对LipB进行酶学性质分析,并通过圆二色谱进行结构分析。【结果】成功地从A.nigerF044中克隆了一个新型的脂肪酶基因lipB,获得了该基因的全基因组序列和cDNA序列(GenBank:FJ536287、FJ536288),并实现了其在E.coli中的高效表达。LipB分子量约为43.0kDa,最适底物为pNPC(C8),酶学动力学常数Km=5.98mmol/L,最适反应温度为50℃,最适pH为6.0;该酶能在40℃条件下保持稳定,在60℃条件下处理1h后残余酶活仅为18.8%;该酶对Ca2+敏感,当脂肪酶经2mmol/L Ca2+处理1h后,酶活提高了2.6倍。圆二色谱分析表明,该酶在Ca2+处理前后具有明显的结构变化。【结论】新型A.niger脂肪酶lipB基因的克隆不仅积累了脂肪酶基因资源,而且为高效基因工程菌的构建及规模化应用奠定基础;对LipB的酶学性质分析表明,该酶在食品和油酯化工等领域具有广阔的应用前景。[ Objective] We cloned, expressed and characterized a novel lipase gene lipB from Aspergillus niger FO44, to facilitate the large scale production and application of that enzyme. [Method] We cloned lipB gene and the cDNA sequence by PCR and RT-PCR, and then cloned the open reading frame of lipB into pET28a vector and expressed by isopropyl β-D-l- thiogalactopyranoside (IPTG) induction. After Ni-agarose purification, the characteristics were determined and the conformation change was checked by circular dichroism methods. [ Results] The novel lipase genes cDNA of lipB were cloned from Aspergillus niger FO44 (GenBank: FJ536287, FJ536288) and expressed in Escherichia coll. The molecular weight of LipB was about 43 kDa. The optimal substrate of this enzyme is 4-nitrophenyl octanoate (pNPC-C8) with Km = 5.98 mmol/L. The optimal temperature and pH was 50℃ and pH 6.0. The enzyme was stable below 40℃ . After incubated at 60℃ for 1 h,only 18.8% activity remained. After treated by 2 mmol/L Ca^2+ for 1 h, the activity improved 2.6-fold. [ Conclusion] Enzymatic characteristics of LipB determined showed this enzyme might have potential in industrial applications.
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