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产碱假单胞菌碱性脂肪酶的克隆表达及酶学性质
引用本文:刘滔滔,刘明瑞,刘恒嘉,杜丽琴,梁智群,韦宇拓.产碱假单胞菌碱性脂肪酶的克隆表达及酶学性质[J].广西科学,2016,23(3):248-254.
作者姓名:刘滔滔  刘明瑞  刘恒嘉  杜丽琴  梁智群  韦宇拓
作者单位:广西大学生命科学与技术学院,广西南宁 530005; 亚热带农业资源保护与利用国家重点实验室,广西南宁 530005
基金项目:国家自然科学基金项目(31460437)资助。
摘    要:【目的】为获得可应用于酯类水解及合成的脂肪酶资源,本研究通过筛选分离得到能够水解长链脂肪酸酯的脂肪酶产生菌,克隆表达其脂肪酶基因并研究脂肪酶的酶学性质。【方法】从环境中筛选分离出可水解三硬脂酸甘油酯的菌株,利用16SrDNA对其进行分子鉴定,并扩增其脂肪酶基因和脂肪酶分子伴侣基因。以pET-22b(+)为表达载体,构建共表达重组质粒,转化Escherichia coli BL21(DE3)进行异源表达,并对重组酶进行酶学性质研究。【结果】经16SrDNA鉴定该菌株为产碱假单胞菌Pseudomonas alcaligenes。通过PCR成功克隆到该菌的脂肪酶基因(lipPA-9A)和脂肪酶分子伴侣基因(lipPA-9B),并构建共表达重组质粒pET22b-lipPA-9A-9B,实现脂肪酶LIP-9A的活性表达。酶学性质研究表明LIP-9A的最适反应温度为35℃,最适反应pH值为10.5,最适反应底物为对硝基苯酚辛酸酯(pNPO);同时,LIP-9A还可以催化醇和羧酸发生酯化反应产生酯类物质。【结论】LIP-9A在碱性条件下具有较高活力,且可以催化酯化反应,在洗涤行业和酯合成领域具有一定的应用价值。

关 键 词:产碱假单胞菌  碱性脂肪酶  共表达  酯化
收稿时间:2016/5/8 0:00:00
修稿时间:2016/6/19 0:00:00

Gene Cloning,Expression and Characterization of An Alkaline Lipase from Pseudomonas alcaligenes PA-9
LIU Taotao,LIU Mingrui,LIU Hengji,DU Liqin,LIANG Zhiqun and WEI Yutuo.Gene Cloning,Expression and Characterization of An Alkaline Lipase from Pseudomonas alcaligenes PA-9[J].Guangxi Sciences,2016,23(3):248-254.
Authors:LIU Taotao  LIU Mingrui  LIU Hengji  DU Liqin  LIANG Zhiqun and WEI Yutuo
Institution:College of Life Science & Technology of Guangxi University, Nanning, Guangxi, 530005, China;State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Nanning, Guangxi, 530005, China,College of Life Science & Technology of Guangxi University, Nanning, Guangxi, 530005, China;State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Nanning, Guangxi, 530005, China,College of Life Science & Technology of Guangxi University, Nanning, Guangxi, 530005, China;State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Nanning, Guangxi, 530005, China,College of Life Science & Technology of Guangxi University, Nanning, Guangxi, 530005, China;State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Nanning, Guangxi, 530005, China,College of Life Science & Technology of Guangxi University, Nanning, Guangxi, 530005, China;State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Nanning, Guangxi, 530005, China and College of Life Science & Technology of Guangxi University, Nanning, Guangxi, 530005, China;State Key Laboratory for Conservation and Utilization of Subtropical Agro-bioresources, Nanning, Guangxi, 530005, China
Abstract:Objective]In order to obtain the lipase that can be applied to the hydrolysis and syn-thesis of esters,the alkaline lipase-producing strains that hydrolyze long chain fatty acid ester were screened and isolated.The related genes were cloned and expressed,and enzyme charac-terization was studied.Methods]A strain,which degraded glycerol tristearate,was isolated from the environment,and identified based on 16S rDNA sequence analyses.Then the lipase gene and the lipase chaperone gene were amplified by PCR.The target genes lipPA-9A and lipPA-9B were introduced into expression vector pET-22b(+)and induced for expression inEscherichiacoli BL21(DE3).Finally,the char-acteristics of the recombinant enzyme were stud-ied in detail.Results]The strain was identified as the genus of Pseudomonas alcaligenes by ana-lyzing of 16S rDNA sequence.And the lipase gene (lipPA-9A ) and lipase chaperone gene (lipPA-9B)were cloned.The co-expression re-combinant plasmid of pET22b-lipPA-9A-9B was successfully constructed and expressed in E. coli BL21(DE3).The maximum activity of LIP-9A was obtained at 35℃,pH 10.5,and pNPO was the most suitable substrate.Meanwhile,the active LIP-9A could catalyze fatty alcohols and fatty acids to generate esters.Conclusion]LIP-9A is a lipase with relatively high activity in al-kaline conditions and can catalyze esterification reaction.Its characteristics are of high value in the detergent industry and biocatalytic applications.
Keywords:Pseudomonas alcaligenes  alkaline lipase  co-expression  esterification
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