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一株Sanguibacter sp.C4产几丁质酶基因的克隆与表达
引用本文:陶勇,金虹,龙章富,张丽,丁秀琼,陶科,刘世贵.一株Sanguibacter sp.C4产几丁质酶基因的克隆与表达[J].遗传学报,2006,33(11):1037-1046.
作者姓名:陶勇  金虹  龙章富  张丽  丁秀琼  陶科  刘世贵
作者单位:1. 四川大学生命学院教育部生物资源与生态环境重点实验室,成都,610064
2. 成都医学院,成都,610081
3. 四川大学生命学院教育部生物资源与生态环境重点实验室,成都,610064;四川大学生物技术创新所,成都,610064
摘    要:Chi58是Sanguibacter sp.strain C4产生的一种胞外几丁质酶。通过chiA的特异性PCR引物探测到菌株C4中存在几丁质酶,并将扩增到的几丁质酶基因片段(chiA-F)克隆、测序后,提交GenBank数据库进行同源性搜索。对从GenBank中获得的高同源性序列进行比对,并根据保守区域设计2对PCR引物进行嵌套PCR,扩增出Chi58基因的开放阅读框(ORF)。测序结果表明该酶的ORF由1692个核苷酸组成,编码563个氨基酸,在N端有23个氨基酸的信号肽,其成熟蛋白的分子量应为58.544kDa。对其推导氨基酸的序列分析表明Chi58与沙雷氏菌的几丁质酶(如徂)有高度同源性(88.9%-99.6%),其结构主要包括信号肽序列、PKD结构域和18家族糖苷水解酶结构域。将该基因克隆到pET32a(+)载体构建重组质粒pChi58,转入大肠杆菌BL-21(DE3)进行融合表达。经IPTG诱导后,可见分子量约81.1kDa的融合蛋白的表达。

关 键 词:几丁质酶  克隆  表达  融合蛋白
收稿时间:2006-01-25
修稿时间:2006-01-252006-04-02

Cloning and Expression of a Chitinase Gene from Sanguibacter sp. C4
TAO Yong,JIN Hong,LONG Zhang-Fu,ZHANG Li,DING Xiu-Qiong,TAO Ke,LIU Shi-Gui.Cloning and Expression of a Chitinase Gene from Sanguibacter sp. C4[J].Journal of Genetics and Genomics,2006,33(11):1037-1046.
Authors:TAO Yong  JIN Hong  LONG Zhang-Fu  ZHANG Li  DING Xiu-Qiong  TAO Ke  LIU Shi-Gui
Institution:1. Key Laboratory of Bio-resources and Eco-environment, Ministry of Education, Life Science College, Sichuan University, Chengdu 610064, China; 2. Institute of Chuangxin Biotechnology, Sichuan University, Chengdu 610064, China; 3. Chengdu Medical College, Chengdu 610081, China
Abstract:The chitinase Chi58 is an extracellular chitinase produced by Sanguibacter sp.strain C4. The gene-specific PCR primers were used to detect the presence of the chiA gene in strain C4. A chiA fragment (chiA-F) was amplified from the C4 genomic DNA and was used to blast-search the related sequences from the GenBank dadabase. By alignment and selection of the highly conserved regions of the homologous sequences, two pairs of primers were designed to amplify the open reading frame (ORF) of the chitinase from strain C4 by nested PCR. The results revealed that the Chi58 ORF consisted of 1 692 nucleotides encoding a protein of 563amino acid residues. The molecular weight of the mature protein was predicted to be 58.544 kDa. The Chi58 ORF was a modular enzyme composed of a signal peptide sequence, a polycystic kidney disease Ⅰ domain, and a glycosyl hydrolase family 18 domain.The chitinase of C4 exhibited a high level of similarity to the chitinase A of Serratia (88.9%-99.6%) at the amino acid sequence level. The Chi58 gene was cloned into the expression vector pET32a to construct the recombinant plasmid pChi58 and was expressed in E. coli BL-21 (DE3) cells with IPTG induction. The molecular weight of the Trx-Chi58 fusion protein was estimated to be 81.1 kDa by SDS-PAGE.
Keywords:pET32a  Chi58  chitinase  cloning  expression  pET32a( )  Chi58  fusion protein
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