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

利用真菌纤维素结合域(CBD)保守性序列进行草菇木聚糖酶cDNA的克隆
引用本文:丁少军,J.A.BUSWELL.利用真菌纤维素结合域(CBD)保守性序列进行草菇木聚糖酶cDNA的克隆[J].中国生物化学与分子生物学报,2004,20(3):408-412.
作者姓名:丁少军  J.A.BUSWELL
作者单位:1. 南京林业大学化工学院,南京,210037
2. 香港中文大学,香港
摘    要:木聚糖是植物细胞壁的主要组分,它是木糖以β1 ,4 木糖苷键形成主链,乙酰基,阿拉伯糖基等为附链组成的复合多聚糖.木聚糖酶可以降解木聚糖主链,在木聚糖的生物降解中起着非常重要的作用1 ] .根据木聚糖酶催化域(catalyticdomain ,CD)氨基酸序列的相似性,木聚糖酶可分为两个家

收稿时间:2004-06-20
修稿时间:2003年6月27日

Cloning and Sequencing of Xylanase cDNA from Volvariella volvacea Using Conserved Sequences in Cellulose-Binding Domain
DING shao jun ,J.A.BUSWELL.Cloning and Sequencing of Xylanase cDNA from Volvariella volvacea Using Conserved Sequences in Cellulose-Binding Domain[J].Chinese Journal of Biochemistry and Molecular Biology,2004,20(3):408-412.
Authors:DING shao jun  JABUSWELL
Institution:( 1) College of Chemical Engineering,Nanjing Forestry University, Nanjing 210037, China; 2) The Chinese University of Hong Kong, Hong Kong SAR,China
Abstract:Cellulose binding domains (CBDs) are present in the majority of fungal cellulases and hemicellulases. Based on the conserved region of CBDs, degenerate primers were designed and used to amplify the 5′ end cDNA fragment of xylanase from Volvariella volvacea by 5′ RACE. Gene specific primer was then designed based on extreme region of 5′ end cDNA fragment and used to amplify the full length cDNA of xylanase. The cDNA of xyn 1 was 1 287 bp in length, including 3′ and 5′ non coding region. The xyn 1 cDNA contained an ORF of 1101 bp encoding 367 amino acids, in which there was a putative signal peptide with 19 amino acids. Alignment of the deduced amino acid sequence of xyn 1 with other xylanases showed that the homology with family 10 xylanases from Agaricus bisporus xyl1,Aspergillus sojae xyn1, Aspergillus kawachii xynA, Fusarium oxysporum f.sp xyl3 was 64%,55%,52%,55%, respectively.
Keywords:Volvariella volvacea  cellulose-binding domain(CBD)  xylanase  cDNA
本文献已被 CNKI 万方数据 等数据库收录!
点击此处可从《中国生物化学与分子生物学报》浏览原始摘要信息
点击此处可从《中国生物化学与分子生物学报》下载免费的PDF全文
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