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巴西橡胶树叶片蛋白样品的制备及质谱初步分析 被引量:2

Preparation and Mass Spectrometry Primary Analysis of Protein Samples of Rubber Tree Leaves
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摘要 采用TCA-丙酮沉淀法并稍做改进提取巴西橡胶树叶片总蛋白,蛋白溶解后,用试剂盒对蛋白上清液进行纯化和浓度测定。十二烷基磺酸钠-聚丙烯酰胺凝胶电泳(SDS-PAGE)和双向凝胶电泳(2-DE)的结果均表明,所制得的蛋白样品质量较高,并且纯化过的蛋白样品2-DE(双向电泳)图谱效果更好(7cm,考染)。根据预实验结果,选用17cmIPG预制干胶条对纯化的蛋白样品进行2-DE实验,采用快速银染法进行染色,随机挖取银染胶上6个蛋白点进行MALDI-TOFMS分析和数据库检索,鉴定了3个蛋白,它们是:1-氨基环丙烷-1羧酸合酶2,核酮糖-1,5-二磷酸羧化酶/加氧酶大亚基和F11O4.2。本实验为进一步对巴西橡胶树叶片中具有重要生物学功能蛋白的筛选和鉴定打下了方法学基础。 The method for improved TCA-acetone precipitation was used to extract proteins from rubber tree (Hevea brasilie.nsis) leaves, and the protein supernatant samples were purified and quantified by kits (Bio-Rad). The result of SDS-PAGE and two-dimensional gel electrophoresis (2-DE) both showed that the protein samples prepared were good in quality and that the purified protein samples had a better 2-DE map when compared with the nonpurified one (7 cm, Coomassie brilliant blue stained). Purified protein samples were separated by 2-DE with 17 cm IPG strips, and the protein spots were detected by fast silver staining. Six protein spots were randomly excised from the silver stained gel for primary analysis by MALDI-TOF MS. Four proteins were identified, and they were 1-aminocyclopropane-l-carboxylate synthase 2, ribulose-1, 5-bisphosphate carboxylase/oxygenase large subunit, FllO4.2 and Rubisco small subunit. This experiment has provided a methodological foundation for screening and identification of biologically important functional proteins in rubber tree leaves.
出处 《热带农业科学》 2009年第4期1-6,共6页 Chinese Journal of Tropical Agriculture
基金 中国热带农业科学院科技基金(No.RKY0609) 中央级公益性科研院所基本科研业务费专项(No.xjszx-12) 公益性行业科研专项经费(No.nyhyzx07-033-1)
关键词 巴西橡胶树 蛋白样品 双向凝胶电泳(2-DE) MALDI-TOF MS Hevea brasiliensis protein samples 2-DE MALDI-TOF MS
作者简介 林秀琴(1983-),女,福建华安人,硕士生,主要从事巴西橡胶树逆境胁迫蛋白质组学研究。电话:0898-23307303;E-mail:linxiuqin07@163.com。 通讯作者:杨礼富(1967-),男,副研究员,硕士生导师,主要从事植物和微生物分子生物学和蛋白质组学研究。电话:0898-23300595;E-mail:ylfri@126.com。
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