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嗜合脂酵母葡聚糖酶编码基因的克隆及其在毕赤酵母中的表达。

Cloning of a gene encoding dextranase from Lipomyces starkeyi and its expression in Pichia pastoris.

作者信息

Kang Hee-Kyoung, Park Ji-Young, Ahn Joon-Seob, Kim Seung-Heuk, Kim Doman

机构信息

School of Biological Sciences and Technology, Chonnam National University, Gwang-ju 500-757, Korea.

出版信息

J Microbiol Biotechnol. 2009 Feb;19(2):172-7. doi: 10.4014/jmb.0802.100.

Abstract

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-l 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 P. pastoris transformant showed a broad band near 73 kDa. Rabbit monoclonal antibodies against a synthetic LSD1 peptide mix also recognized approximately 73 kDa.

摘要

之前已克隆、测序了来自斯达氏油脂酵母KSM22的编码葡聚糖酶的基因(lsd1),并在酿酒酵母中进行了表达。然后,将这个由1824个碱基对组成、编码608个氨基酸的蛋白质的基因克隆到毕赤酵母中,并在AOX1启动子的控制下进行分泌表达。在8升发酵罐中培养时,毕赤酵母转化子(pPIC9K-LSD1,134,000 U/l)的葡聚糖酶产量比酿酒酵母转化子(pYLSD1,32,000 U/l)高约4.2倍。甲醇诱导后,超过0.63 g/l的活性葡聚糖酶分泌到培养基中。通过SDS-PAGE和蛋白质免疫印迹分析,毕赤酵母转化子的葡聚糖酶仅显示出一条均一的条带。毕赤酵母转化子的这种葡聚糖酶在73 kDa附近显示出一条宽带。针对合成的LSD1肽混合物的兔单克隆抗体也识别约73 kDa的蛋白。

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