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


Molecular cloning of the promoter region of the glyceraldehyde-3-phosphate dehydrogenase gene that contributes to the construction of a new transformation system in <Emphasis Type="Italic">Coriolus versicolor</Emphasis>
Authors:Email author" target="_blank">Yumi?NittaEmail author  Yasumasa?Miyazaki  Masaya?Nakamura  Yosuke?Iimura  Kazuo?Shishido  Shinya?Kajita  Noriyuki?Morohoshi
Institution:(1) Koshida Corporation, 2-2-9 Higashi-shinbashi, Minato-ku, Tokyo, 105-8642, Japan;(2) Forestry and Forest Products Research Institute, Tsukuba, Japan;(3) National Institute of Advanced Industrial Science and Technology, Tsukuba, Japan;(4) Graduate School and School of Bioscience and Biotechnology, Tokyo Institute of Technology, Yokohama, Japan;(5) Graduate School of Bio-Applications and Systems Engineering, Tokyo University of Agriculture and Technology, Tokyo, Japan
Abstract:The white-rot basidiomycete Coriolus versicolor secretes several enzymes that participate in the degradation of lignin and various persistent organic pollutants. In this study, we attempted to establish a genetic transformation system with a homogenous promoter sequence for driving the gene for antibiotic resistance. We succeeded in cloning the promoter sequence of the gene for glyceraldehyde-3-phosphate dehydrogenase (gpd), which is expressed at high levels in C. versicolor. The expression vector pT7GPTHPT was constructed, which included a gene for resistance to hygromycin B under control of the gpd promoter. The successful selection of transformants on medium that contained hygromycin B indicated that the system should be useful not only for the genetic transformation of C. versicolor, but also for the overproduction of useful fungal enzymes such as laccase and peroxidase.
Keywords:Coriolus versicolor  Glyceraldehyde-3-phosphate dehydrogenase  Homologous transformation  Hygromycin B  Promoter
本文献已被 SpringerLink 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