首页 | 本学科首页   官方微博 | 高级检索  
   检索      

马铃薯α-淀粉酶基因的克隆及生物信息学分析(英文)
引用本文:王玉丽,王永刚,马建忠,王倩,陶鹏飞,苏移.马铃薯α-淀粉酶基因的克隆及生物信息学分析(英文)[J].基因组学与应用生物学,2010,29(6).
作者姓名:王玉丽  王永刚  马建忠  王倩  陶鹏飞  苏移
摘    要:本研究利用RT-PCR从马铃薯(Solanum tuberosum)茎段总RNA中扩增、克隆了一cDNA分子。该cDNA分子含有一长为1224bp的开放读框,可编码一含407个氨基酸残基的多肽、理论分子量为46.40kD、可能为亲水性的胞外酶。因其氨基酸序列同源于α-淀粉酶,故将该基因命名为amyA1(NCBI收录号:GQ406048.1)。采用半定量RT-PCR方法检测了amyA1基因在马铃薯茎、叶等不同组织中的表达强度,表明在茎组织中的表达丰度略高。利用生物信息学软件分析了amyA1密码子的偏好性,以期为选择适宜的表达系统提供依据;同时对amyA1的理化性质、细胞内定位、保守结构及高级结构进行了预测。基于NCBI数据库中有物种代表性的29种α-淀粉酶基因序列构建了基因进化树。与NCBI收录的马铃薯α-淀粉酶基因(NCBI收录号:M79328.1)的核苷酸及氨基酸序列同源性达98%。第20至第348范围内的氨基酸残基含有与淀粉酶13家族及亚家族相似的催化活性域(PF00128、SM00624),第349至第407范围内的氨基酸残基含有α-淀粉酶C-末端β折叠区域(PF07821)。蛋白质结构预测表明氨基酸残基序列有维持淀粉酶活性的(β/α)8桶状结构以及其它几个功能域结构。所构建的基因进化树表明,2个马铃薯α-淀粉酶基因与木薯、苹果的序列同源性较高,与菜豆的次之,与水稻、大麦和玉米等单子叶植物的序列同源性较低。

关 键 词:马铃薯  α-淀粉酶基因  克隆  生物信息学

Cloning and Bioinformatic Analysis of Potato α-Amylase Gene amyA1
Wang Yuli,Wang Yonggang,Ma Jianzhong,Wang Qian,Tao Pengfei,Su Yi.Cloning and Bioinformatic Analysis of Potato α-Amylase Gene amyA1[J].Genomics and Applied Biology,2010,29(6).
Authors:Wang Yuli  Wang Yonggang  Ma Jianzhong  Wang Qian  Tao Pengfei  Su Yi
Abstract:In this research, we amplified a cDNA for potato α-amylase by RT-PCR and cloned it. Sequence analysis showed that the cDNA had a 1 224 bp open reading frame and was referred to as amyA1, which encodes for an α-amylase with 407 amino acid residues (GenBank accession number: GQ406048.1) with the MW 46.40 kD.After that we used semi-quantitative RT-PCR assay to detective the expression of the amyA1 gene in potato leaves and stems. The result showed that the expression in stems is a little stronger than in leaves. Then we analyzed the amino acid sequence bioinformatically, including its codon usage bias, physical and chemical properties, subcellular localization, and conserved structures. 29 α-amylase genes from same or different species were taken from the GenBank for constructing a phylogenetic tree. The bioinformatical analyses showed that the putative protein shared 98% identity with a published potato α-amylase (GenBank accession number: M79328.1) at the amino acid level. The deducted α-amylase also contains a catalytic domain (PF00128、 SM00624) between 20 to 348 and a C-terminal beta-sheet domain (PF07821)between 349~407, which are similar to ones of the amylase family 13.The postulated eight-stranded alpha/beta barrel was also found in the enzyme, which was thought as an active site of α-amylase. According to the phylogenetic tree, the two genes from potato presents more close homology to those from cassava and apple than from barley, rice and maize.
Keywords:Potato  α-amylase  Clone  Bioinformatic analysis
本文献已被 CNKI 万方数据 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号