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紫孢侧耳Ps-mnp1基因克隆与蛋白结构预测(PDF)

《广西植物》[ISSN:1000-3142/CN:45-1134/Q]

期数:
2015年03期
页码:
393-400
栏目:
遗传与育种
出版日期:
2015-05-20

文章信息/Info

Title:
Cloning and protein structure prediction of Ps-mnp1 from Pleurotus sapidus
文章编号:
1000-3142(2015)03-0393-08
作者:
尹立伟1* 杨春成1 朱 玉1 伦志明2 张 静2
1. 安庆师范学院 生命科学学院, 安徽 安庆 246011; 2. 黑龙江农业经济职业学院, 黑龙江 牡丹江 157041
Author(s):
YIN Li-Wei1* YANG Chun-Cheng1 ZHU Yu1 LUN Zhi-Ming2 ZHANG Jing2
1. School of Life Sciences, Anqing Teachers College, Anqing 246011, China; 2. Heilong Jiang Agricultural Economy Vocational College, Mudanjiang 157041, China
关键词:
紫孢侧耳 锰过氧化物酶 蛋白结构 生物信息学 同源模建
Keywords:
Pleurotus sapidus manganese peroxidase protein structure bioinformatics homology modeling
分类号:
S718.81
DOI:
10.11931/guihaia.gxzw201501024
文献标识码:
A
摘要:
克隆紫孢侧耳PS1菌株锰过氧化物酶基因Ps-mnp1,具有生物降解木质素的活性,可用于分析锰过氧化物酶的蛋白功能与结构,并对深入了解紫孢侧耳Ps-mnp1基因功能和转录调控具有重要意义。基于ITS序列分析,明确了该菌株的分类地位。根据GenBank中白腐菌MnPs保守序列设计引物,采用染色体步移法和逆转录PCR法获得Ps-mnp1基因,GenBank登录号为(KP189358.1)。在克隆Ps-mnp1基因并分析蛋白结构时,采用多种现代生物信息学技术,经染色体步移法克隆的DNA全长序列后,利用contigexpress拼接软件预测Ps-mnp1基因的cDNA全长序列; 使用BioEdit分析软件对DNA和cDNA核苷酸序列比对; 通过Augustus网站预测RNA的剪接位点并在NCBI上进行同源序列比对校正; 采用基因结构软件对比了解白腐菌MnPs基因的内含子/外显子的组成。序列分析表明Ps-mnp1 的DNA全长序列1 854 bp,具有外显子14条和内含子13条。从Ps-mnp1与其它白腐菌MnPs基因的内含子/外显子组成分析来看,紫孢侧耳和糙皮侧耳同属于侧耳属,但它们之间的MnPs基因结构完全不同。Ps-mnp1开放阅读框为1 095 bp,起始密码子ATG,终止密码子TAA,编码364 aa,含有20 aa残基构成的信号肽序列。采用MEGA 5.1软件构建的蛋白系统进化树表明Ps-mnp1与6株白腐菌蛋白聚类在短枝MnPs,区分了含有5个二硫键组成的长枝MnPs组群; 此外,构建的蛋白同源模型表明,与刺芹侧耳多功能过氧化物酶相似度为72.51%,蛋白配体中结合位点有1个含铁血红素、2个钙离子、1个锰离子等,这些结合位点为不守恒。该研究为紫孢侧耳锰过氧化物酶的结构,蛋白功能Ps-mnp1奠定了基础,并进一步为Ps-mnp1的蛋白质工程改造提供借鉴作用。
Abstract:
To clone the manganese peroxidase gene Ps-mnp1 from Pleurotus sapidus PS1 contributing a lot to the lignin biodegradation activity is important for the analysis of protein structure and functions of MnP and the understanding of manganese peroxidase gene function and transcriptional regulation of Pleurotus sapidus. Based on the analysis of ribosomal rDNA Intenal Transcribed Spacer(ITS)sequences,the classification status of the strain PS1 was defined. Ps-mnp1 was cloned by using the methods of Genome Walking-PCR and Reverse transcription-PCR with primers designed from some white-rot fungi which contains the conserved sequences of the known manganese peroxidase genes(GenBank No. KP189358.1). We used a variety of modern bioinformatics technology softwares to clone the manganese peroxidase gene and analyze the protein structure of Ps-mnp1. For example, after the cloning full length DNA sequence of genome walking method, prediction of the full cDNA sequence of manganese peroxidase gene by using contigexpress splicing software; comparison the DNA and cDNA nucleotide sequences alignment analysis by using BioEdit software; prediction the RNA splice site through Augustus website,following the comparison and correction of Ps-mnp1 sequences by using the the NCBI database; understanding the compositions of the intron and exon by using online software Gene Structure Display Server contrast of white rot fungus manganese peroxidase gene. The results obtained in the sequence analysis of Ps-mnp1 from Pleurotus sapidus indicated that the full length of the DNA was 1 854 bp containing 14 exons and 13 introns. Meanwhile, exons and introns composition analysis of the genes Ps-mnp1 from Pleurotus sapidus, compared to other white-rot fungi manganese peroxidase genes, suggested that P. ostreatus and P. sapidus belonged to the same genus Pleurotus, but the manganese peroxidase gene structures between them were entirely different. The Ps-mnp1 gene included a signal peptide of 20 amino acids and held Open Reading Frame of 1 095 bp,with start codon ATG and stop codon TAA,encoding 364 amino acids. The results of protein phylogenetic analysis by MEGA 5.1 software revealed that Ps-mnp1 and 6 strains of white rot fungus protein clustered on short branches MnPs,and differentiated 5 long branches of MnPs group formed by disulphide bond. In addition,the 3D structures of Ps-mnp1 were built using homology modelling technique, and the results showed that the binding sites of the protein ligand included 1 Fe heme,2 Ca ions and 1 Mn(II),and the those sites were non-conservation. The results also suggested that the modelling similarity was 72.51% compared with P. eryngii VPs. This paper could establish the basis of the study in the structure and function of the Ps-nmp1. It is further helpful to offer reference on the variation of protein engineering of the Ps-mnp1.

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备注/Memo

备注/Memo:
收稿日期: 2015-01-20修回日期: 2015-03-26
基金项目: 安徽省自然科学基金(AQKJ2014B008); 安庆师范学院科研启动项目(044-K05000130030)。
作者简介: 尹立伟(1981-),女,黑龙江双鸭山人,博士,讲师,主要从事植物病理学,分子真菌学等教学与研究,(E-mail)kaixinliwei@163.com。
更新日期/Last Update: 2015-05-20