耐放射异常球菌海藻糖合成酶基因的克隆及功能鉴定
DOI:
作者:
作者单位:

作者简介:

通讯作者:

中图分类号:

基金项目:

国家高技术“863”计划资助项目(2001AA214171).


Cloning and Identification of a Gene Encoding Novel Trehalose Synthase From Deinococcus radiodurans
Author:
Affiliation:

Fund Project:

This work was supported by a grant from The State 863 High Technology R&D Project of China(2001AA214171).

  • 摘要
  • |
  • 图/表
  • |
  • 访问统计
  • |
  • 参考文献
  • |
  • 相似文献
  • |
  • 引证文献
  • |
  • 资源附件
  • |
  • 文章评论
    摘要:

    利用生物信息学手段,在GenBank中进行氨基酸序列的同源性比较分析,检索到来自于耐放射异常球菌(Deinococcus radiodurans)基因组序列中一功能未确定的开放阅读框(ORF),其氨基酸序列和已报道的海藻糖合成酶的氨基酸序列有约60%的同源性.将这段ORF克隆到大肠杆菌进行表达,并进行功能鉴定.实验表明这段ORF序列所编码的是一种海藻糖合成酶,它能将麦芽糖分子转化成海藻糖分子,以30%的麦芽糖为底物时能将约65%的麦芽糖转化成海藻糖.重组酶性质初步研究表明,在pH 7.0,最佳温度30℃转化麦芽糖效率最高.

    Abstract:

    An open reading frame (ORF) was annotated as putative trehalose synthase in Deinococcus radiodurans sequenced genome, which has been found in GenBank database through amino homology blast base on combination of bioinformatics. Blasting against the database indicates that amino acid sequence of this ORF has less than 60% homology with the reported terhalose synthases. The function, which was identified by expressing this ORF in Escherichia coli, proves this ORF is a novel trehalose synthase gene. Using the 30% maltose as substrate, about 65% maltose can be converted into trehalose by this enzyme. Recombinant enzyme showed optimal activity at pH 7.0 and 30℃ when it converts maltose into trehalose.

    参考文献
    相似文献
    引证文献
引用本文

韦宇拓,朱绮霞,罗兆飞,陈发忠,李桂媛,黄鲲,黄日波.耐放射异常球菌海藻糖合成酶基因的克隆及功能鉴定[J].生物化学与生物物理进展,2004,31(11):1018-1023

复制
分享
文章指标
  • 点击次数:
  • 下载次数:
  • HTML阅读次数:
  • 引用次数:
历史
  • 收稿日期:2004-05-27
  • 最后修改日期:2004-06-30
  • 接受日期:
  • 在线发布日期:
  • 出版日期: