首页 | 期刊介绍 | 编委会 | 道德声明 | 投稿指南 | 常用下载 | 过刊浏览 | In English
引用本文:于坤,汝少国,邴欣,潘宗保,王蔚.大菱鲆卵黄原蛋白的分离纯化及Native-PAGE、SDS-PAGE性质鉴定[J].海洋科学,2009,33(9):71-75.
【打印本页】   【HTML】   【下载PDF全文】   查看/发表评论  下载PDF阅读器  关闭
←前一篇|后一篇→ 过刊浏览    高级检索
本文已被:浏览 2289次   下载 1625 本文二维码信息
码上扫一扫!
分享到: 微信 更多
大菱鲆卵黄原蛋白的分离纯化及Native-PAGE、SDS-PAGE性质鉴定
于坤1, 汝少国1, 邴欣1, 潘宗保1, 王蔚1
中国海洋大学
摘要:
采用5 mg /kg 17β-雌二醇对大菱鲆(Scophthalmus maximus)进行肌肉注射,一周后尾静脉取血,离心分离获得血浆,经Sephacryl S-300 (高分辨)分子筛纯化卵黄原蛋白,对卵黄原蛋白进行常规聚丙烯酰胺凝胶电泳,考马斯亮蓝染色和糖、磷、脂的特征性基团染色。结果表明,17β-雌二醇能诱导大菱鲆产生卵黄原蛋白,以Native-PAGE方法计算得到大菱鲆卵黄原蛋白的分子质量为538 ku,以SDS-PAGE方法得出其两种亚基的分子质量分别为100 ku和82 ku。分子筛凝胶过滤能较好地纯化大菱鲆血浆中的卵黄原蛋白。
关键词:  大菱鲆(Scophthatmus maximus  卵黄原蛋白  分离纯化  Native-PAGE  SDS-PAGE
DOI:
分类号:
基金项目:国家自然科学基金资助项目(30200211,30671618)
Purification and partial characterization of turbot(Scophthatmus maximus) vitellogenin
YU Kun,RU Shao-guo,BING Xin,PAN Zong-bao,WANG Wei
Abstract:
Vitellogenin was induced in turbot (Scophthatmus maximus) by intramuscular injections of 17β-estradiol(5 mg/kg BW). After one week induction, the blood was collected from caudal vessel and then centrifuged. The blood plasma was loaded onto a Sephacryl S-300 high resolution column to purify the vitellogenin. Then the fraction was applied to Native-PAGE and the vitellogenin band was confirmed by the stainability with CBB G250-, phospho-, lipo- and glyco-staining methods. The result of Native-PAGE showed that the vitellogenin in turbot was significantly induced by treatment of 17β-estradiol for one week. Moreover, the vitellogenin showed a molecular weight of approximately 538 ku by Native-PAGE, and it was cleaved into two monomers in SDS-PAGE, with molecular weight of approximately 100 and 82 ku, respectively. Thus, the purification of vitellogenin in S. maximus was effectively established in this paper.
Key words:  Scophthatmus maximus  vitellogenin  purification  Native-PAGE  SDS-PAGE
版权所有 《海洋科学》 Copyright©2008 All Rights Reserved
主管单位:中国科学院 主办单位:中国科学院海洋研究所
地址:青岛市市南区福山路32号  邮编:266071  电话:0532-82898755  E-mail:marinesciences@qdio.ac.cn
技术支持:北京勤云科技发展有限公司