华北农学报 ›› 2007, Vol. 22 ›› Issue (2): 14-17. doi: 10.3321/j.issn:1000-7091.2007.02.004

所属专题: 生物技术

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植酸酶基因PhyB1的克隆及序列分析

柯晓静, 郭润芳, 于宏伟, 贾英民   

  1. 河北农业大学食品科技学院, 河北 保定 071001
  • 收稿日期:2007-03-01 出版日期:2007-04-28
  • 通讯作者: 贾英民(1961-),男,河北唐县人,教授,博士生导师,主要从事食品微生物研究工作。
  • 作者简介:柯晓静(1980-),女,河北张家口人,在读硕士,主要从事酶工程及食品资源开发研究工作。
  • 基金资助:
    河北省“十一五”科技攻关项目资助(06220106D)

Cloning and Sequence Analysis of the PhyB Gene of Aspergillus niger WP1

KE Xiao-jing, GUO Run-fang, YU Hong-wei, JIA Ying-min   

  1. College of Food Science, Agriculture University of Hebei, Baoding 071001, China
  • Received:2007-03-01 Published:2007-04-28

摘要: 为了进一步研究多种植酸酶之间的相互作用,利用PCR技术,从黑曲霉WP1中克隆出植酸酶PhyB基因,该基因长1560 bp,含有3段内含子,共编码460个氨基酸,与已报道的ALKO243的植酸酶Aph基因(GeneBank Acces-sion:L02420)相比较,编码的氨基酸序列同源性为99.13%,因此将其命名为PhyB1。该基因含有植酸酶保守序列“RHGXRXP”和“HD”。黑曲霉WP1植酸酶PhyB1基因序列已在国际基因库中注册,注册号为:DQ836360。

关键词: 黑曲霉, PhyB基因, PCR, 序列分析

Abstract: The PhyB1 encoding phytase of Aspergillus niger WP1 was amplified by the polymerase Chain reaction (PCR) with primers designed according to the sequences in GeneBank. The amplified fragment was cloned and sequenced. The results showed that the coding region was 1560 bp in size, includes 3 introns, and encoded a peptide of 460 amino acid residues. Comparison of this sequence with the Aph of the nature A. niger ALKO243 (GeneBank Accession: L02420), shows that the nucleotide homology is 96.79%, and the amino acid homology comes up to 99.13%. The PhyB1 ofA. niger WP1 strain in this paper its sequence has been accessed by GeneBank (Accession: DQ836360).

Key words: Aspergillus niger, PhyB gene, PCR, Sequence analysis

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引用本文

柯晓静, 郭润芳, 于宏伟, 贾英民. 植酸酶基因PhyB1的克隆及序列分析[J]. 华北农学报, 2007, 22(2): 14-17. doi: 10.3321/j.issn:1000-7091.2007.02.004.

KE Xiao-jing, GUO Run-fang, YU Hong-wei, JIA Ying-min. Cloning and Sequence Analysis of the PhyB Gene of Aspergillus niger WP1[J]. ACTA AGRICULTURAE BOREALI-SINICA, 2007, 22(2): 14-17. doi: 10.3321/j.issn:1000-7091.2007.02.004.

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