Cloning of a Gene Encoding Dextranase from Lipomyces starkeyi and its Expression in Pichia pastoris

被引:11
|
作者
Kang, Hee-Kyoung [1 ,2 ,3 ]
Park, Ji-Young [4 ]
Ahn, Joon-Seob [5 ]
Kim, Seung-Heuk [6 ]
Kim, Doman [1 ,2 ,3 ]
机构
[1] Chonnam Natl Univ, Sch Biol Sci & Technol, Kwangju 500757, South Korea
[2] Chonnam Natl Univ, Res Inst Catalysis, Kwangju 500757, South Korea
[3] Chonnam Natl Univ, Bioind Technol Ctr, Kwangju 500757, South Korea
[4] Korea Res Inst Biosci & Biotechnol, Jeonbuk Branch Inst, Jeonbuk 580185, South Korea
[5] Gang Jin City Agr Technol Extens Ctr, Gang Jin 527853, South Korea
[6] Lifenza Co Ltd, Gyeonggi Do 431062, South Korea
关键词
Dextranase; Lipomyces starkeyi; Pichia pastoris; expression; dextran; PURIFICATION; OVEREXPRESSION; MINIOLUTEUM;
D O I
10.4014/jmb.0802.100
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
A gene (lsd1) encoding dextranase from Lipomyces starkeyi KSM22 has been previously cloned, sequenced, and expressed in Saccharomyces cerevisiae. The gene consisting of 1,824 base pairs and encoding a protein of 608 amino acids was then cloned into and secretively expressed in Pichia pastoris under the control of the AOX1 promoter. The dextranase productivity of the P pastoris transformant (pPIC9K-LSD1, 134,000 U/l) was approximately 4.2-fold higher than that of the S. cerevisiae transformant (pYLSD1, 32,000 U/l) cultured in an 8-1 fermentor. Over 0.63 g/l of active dextranase was secreted into the medium after methanol induction. The dextranase of the P pastoris transformant, as analyzed by SDS-PAGE and Western blotting, showed only one homogeneous band. This dextranase of the R pastoris transformant showed a broad band near 73 kDa. Rabbit monoclonal antibodies against a synthetic LSD1 peptide mix also recognized approximately 73 kDa.
引用
收藏
页码:172 / 177
页数:6
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