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蚯蚓纤溶酶新基因EfP-0的电子克隆及其编码区序列RT-PCR验证
引用本文:赵晓瑜,高珊,崔大岺,耿风廷. 蚯蚓纤溶酶新基因EfP-0的电子克隆及其编码区序列RT-PCR验证[J]. 生物工程学报, 2006, 22(6): 897-901. DOI: 10.1016/S1872-2075(06)60062-9
作者姓名:赵晓瑜  高珊  崔大岺  耿风廷
作者单位:河北大学生命科学学院,保定,071002
基金项目:河北省生物工程重点学科项目
摘    要:利用生物信息学手段,以期获得蚯蚓纤溶酶F-Ⅰ-0组分的基因。根据从粉正蚓(Lumbricusrubellus)中分离的F-Ⅰ-0组分的N端氨基酸序列VVGGSDTTIGQYPHQL,利用DNAMAN软件通过电子克隆方法,从Lumbricidae的dbEST中获得该组分的核酸序列信息,设计特异引物,经过RT-PCR,成功地从赤子爱胜蚓(Eiseniafoetida)中克隆到一条蚯蚓纤溶酶新基因,命名为EfP-0。EfP-0基因全长678bp,编码225个氨基酸的成熟肽,属丝氨酸蛋白酶,胰蛋白酶家族,与F-Ⅰ-0组分的氨基酸组成非常接近。BLAST证明,EfP-0与已报道的蚯蚓纤溶酶基因之间的相似性均低于40%,因此为蚯蚓纤溶酶中的一个新基因,GenBank登录号为DQ836917。构建的pMAL-c2x-EfP-0重组质粒,在大肠杆菌TB1中获得融合蛋白MBP-EfP-0的可溶性表达,表达产物有酪蛋白平板溶解活性。

关 键 词:蚯蚓纤溶酶  电子克隆  EfP-0
文章编号:1000-3061(2006)06-0897-05
收稿时间:2006-07-26
修稿时间:2006-09-04

In silico cloning of EfP-0, a novel earthworm fibrinolytic enzyme gene, and verification of its coding region by RT-PCR
ZHAO Xiao-Yu,GAO Shan,CUI Da-Ling,GENG Feng-Ting. In silico cloning of EfP-0, a novel earthworm fibrinolytic enzyme gene, and verification of its coding region by RT-PCR[J]. Chinese journal of biotechnology, 2006, 22(6): 897-901. DOI: 10.1016/S1872-2075(06)60062-9
Authors:ZHAO Xiao-Yu  GAO Shan  CUI Da-Ling  GENG Feng-Ting
Affiliation:College of Life Sciences, Hebei University, Baoding 071002, China
Abstract:There are four different types of N-terminal amino acid sequences (F-I-0, F-I, F-II, F-III) in the multicomponents of earthworm fibrinolytic enzymes (EFE). In GenBank 21 nucleic acid sequences of EFE have been reported. Among them, most of the N-terminal amino acid sequences belong to the F-III type,few belong to the F-II type. Only one is similar to the F-I type, but none to F-I-0. In this research we hoped to obtain the gene encoding component F-I-0 of EFE by the bioinformatics tools. Based on the N-terminal amino acid sequence VVGGSDTTIGQYPHQL of the F-I-0 type from Lumbricus rubellus, a nucleic acid sequence was obtained by in silico cloning from dbEST of Lumbricidae using the software DNAMAN. A new gene of EFE from Eisenia foetida was successfully obtained by RT-PCR using specific primers designed according to this sequence. The new gene named EfP-0 was cloned in pMAL-c2x and expressed as the fusion protein MBP-EfP-0 in the supernatant of lysate. The fusion protein MBP-EfP-0 purified by affinity chromatography had hydrolytic activity on casein plate. Sequencing result shows, EfP-0 has 678bp and encodes a protein of 225 amino acids. The protein is a serine protease belonging to trypsin family. It has similar amino acid composition to F-I-0. BLAST in GenBank shows that the similarity is lower than 40% between EJP-0 gene and other EFE genes. By this we conclude that EfP-0 gene of EFE is a novel gene and it is the first time to be reported, its accession number for Genbank is DQ836917.
Keywords:earthworm fibrinolytic enzymes  in silico cloning  EfP-0
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