[1]刘嘉,贺淹才,施腾鑫,等.重组粘质沙雷氏菌几丁质酶C的纯化及酶学性质[J].华侨大学学报(自然科学版),2010,31(5):552-556.[doi:10.11830/ISSN.1000-5013.2010.05.0552]
 LIU Jia,HE Yan-cai,SHI Teng-xin,et al.Purification and Enzyme Properties of Recombinant Serratia marcescens Chitinase C[J].Journal of Huaqiao University(Natural Science),2010,31(5):552-556.[doi:10.11830/ISSN.1000-5013.2010.05.0552]
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重组粘质沙雷氏菌几丁质酶C的纯化及酶学性质()
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《华侨大学学报(自然科学版)》[ISSN:1000-5013/CN:35-1079/N]

卷:
第31卷
期数:
2010年第5期
页码:
552-556
栏目:
出版日期:
2010-09-20

文章信息/Info

Title:
Purification and Enzyme Properties of Recombinant Serratia marcescens Chitinase C
文章编号:
1000-5013(2010)05-0552-05
作者:
刘嘉贺淹才施腾鑫李梓君王珍珠
华侨大学化工学院
Author(s):
LIU Jia HE Yan-cai SHI Teng-xin LI Zi-jun WANG Zhen-zhu
College of Chemical Engineering, Huaqiao University, Quanzhou 362021, China
关键词:
粘质沙雷氏菌 重组 几丁质酶C 分离纯化 酶学性质
Keywords:
Serratia marcescens recombinant chitinase C isolation and purification enzyme properties
分类号:
Q78
DOI:
10.11830/ISSN.1000-5013.2010.05.0552
文献标志码:
A
摘要:
为从已构建的重组大肠杆菌pET-22b-chiC获得高纯的几丁质酶C,通过降低培养温度,提高粘质沙雷氏菌几丁质酶C的可溶性表达.表达产物经镍柱亲和层析(IMAC)和Phenyl-Sepharose疏水层析(HIC)分离纯化后,得到电泳纯的几丁质酶.酶学性质研究表明,纯化的几丁质酶C为单体蛋白,相对分子质量为51.8ku; 最适pH值为5.0,最适温度为55℃,在55℃的条件下保温4 h后仍有90%以上的酶活力.研究结果还表明,Cu2+,Hg2+,Co2+,Mg2+对酶活力均有明显抑制作用,而Fe2+,Zn2+,Sn2+,Ba2+对酶活力有一定促进作用,Mn2+对酶活力明显促进作用.
Abstract:
To obtain high pure chitinase C from constructed recombinant E.coli pET-22b-chiC,we decreased culture temperature to increase soluble expression of Serratia marcescens chitinase C.The expressed product was purified to electrophoretic homogeneity by immobilized metal ion affinity chromatography(IMAC)and Phenyl-Sepharose hydrophobic interaction chromatography(HIC).The enzyme properties research indicated that the purified chitinase C was a monomeric protein with a molecular weight of 51.8 ku.The optimum pH was 5.0 and the optimum temperature was 55 ℃.And its activity still kept above 90% after 1 h at 55 ℃.Results also showed that the activity of chitinase was significantly inhibited by Cu2+,Hg2+,Co2+,Mg2+,while promoted by Fe2+,Zn2+,Sn2+,Ba2+ and also significantly promoted by Mn2+.

参考文献/References:

[1] SUZUKI K, SUGAWARA N, SUZUKI M. Chitinase A, B, and C1 of Serratia marcescens 2170 produced by recombinant Escherichia coli:Enzymatic properties and synergism on chitin degradation [J]. Bioscience, Biotechnology, and Biochemistry, 2002(5):1075-1083.
[2] BRURBERG M, SYNSTAD B, KLEMSDAL S S. Chitinases from Serratia marcescens [EB/OL]. http://davapc1.bioch.dundee.ac.uk/pdf/chirev.pdf, 2000.
[3] GAL S W, CHOI Y J KIM Y C. Cloning of the 52-kDa chitinase gene from Serratia marcescens KCTC2172 and its proteolytic cleavage into an active 35-kDa enzyme [J]. FEMS Microbiology Letters, 1998(1):151-158.
[4] 魏巍, 贺淹才, 方柏山. 粘质沙雷氏菌几丁质酶(ChiC)基因克隆及其生物信息学分析 [J]. 江西农业大学学报, 2006(3):444-448.doi:10.3969/j.issn.1000-2286.2006.03.027.
[5] SUZUKI K, TAIYOJI M, SUGAWARA N. The third chitinase gene (chiC) of Serratia marcescens 2170 and the relationship of its product to other bacterial chitinases [J]. Biochemical Journal, 1999(3):587-596.doi:10.1042/0264-6021:3430587.
[6] 贺淹才, 刘爱花, 张荣奎. 嗜麦芽窄食单胞菌产生的几丁质酶的特性 [J]. 华侨大学学报(自然科学版), 2008(2):245-249.
[7] 萨姆布鲁克·J, 拉塞尔 D W, 黄培堂. 分子克隆实验指南 [M]. 北京:科学出版社, 2002.
[8] SYNSTAD B, VAAJE-KOLSTAD G, CEDERKVIST F. Expression and characterization of endochitinase C from Serratia marcescens BJL200 and its purification by a one-step general chitinase purification method [J]. Bioscience, Biotechnology, and Biochemistry, 2008(3):715-723.doi:10.1271/bbb.70594.
[9] TSAFFRIR Z, ZVI S. Linearization of the bradford protein assay increases its sensitivity:Theoretical and experimental studies [J]. Analytical Biochemistry, 1996(2):302-308.
[10] 唐亚雄, 赵建, 丁诗华. 产气肠杆菌几丁质酶的分离纯化及性质研究 [J]. 微生物学报, 2001(1):82-86.doi:10.3321/j.issn:0001-6209.2001.01.015.
[11] SYNSTAD B, GASEIDNES S, AALTEN D M F. Mutational and computational analysis of the role of conserved residues in the active site of a family 18 chitinase [J]. European Journal of Biochemistry, 2004(2):253-262.doi:10.1046/j.1432-1033.2003.03923.x.

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备注/Memo

备注/Memo:
福建省自然科学基金资助项目(C04010011)
更新日期/Last Update: 2014-03-23