发布: 2015年12月05日第5卷第23期 DOI: 10.21769/BioProtoc.1673 浏览次数: 12608
评审: Maria SinetovaAgnieszka ZienkiewiczAnonymous reviewer(s)
相关实验方案
利用SP3珠和稳定同位素质谱技术优化蛋白质合成速率:植物核糖体的案例研究
Dione Gentry-Torfer [...] Federico Martinez-Seidel
2024年05月05日 1462 阅读
基于活性蛋白质组学和二维聚丙烯酰胺凝胶电泳(2D-PAGE)鉴定拟南芥细胞间隙液中的靶蛋白酶
Sayaka Matsui and Yoshikatsu Matsubayashi
2025年03月05日 759 阅读
Abstract
Chlamydomonas reinhardtii is a model organism for chloroplast studies. Besides other convenient features, the feasibility of chloroplast genome transformation distinguishes this unicellular alga as ideal for the manipulation of chloroplastic gene expression aiming biotechnological goals, such as improved biofuel and biomass production. Ribulose 1, 5-bisphosphate carboxylase/oxygenase (EC 4.1.1.39, Rubisco) is the photosynthetic carbon-fixing enzyme which is considered crucial for biomass accumulation in algal cultures. Purification of wild type and site-directed mutants of Rubisco in C. reinhardtii is usually performed to study its catalytic properties and assess the carbon-fixing potential of the strains. In this protocol Rubisco is extracted through sonication of cell pellets, and purified by ammonium sulfate precipitation, sucrose gradient centrifugation (Goldwaithe and Bogorad, 1975) and anion exchange chromatography.
Keywords: Ribulose 1,5-bisphosphate carboxylase/oxygenase (二磷酸核酮糖的羧化酶/加氧酶)Materials and Reagents
Equipment
Procedure
文章信息
版权信息
© 2015 The Authors; exclusive licensee Bio-protocol LLC.
如何引用
Sudhani, H. P. K., García-Murria, M. J., Marín-Navarro, J., García-Ferris, C., Peñarrubia, L. and Moreno, J. (2015). Purification of Rubisco from Chlamydomonas reinhardtii. Bio-protocol 5(23): e1673. DOI: 10.21769/BioProtoc.1673.
分类
植物科学 > 藻类学 > 蛋白质
植物科学 > 植物生物化学 > 蛋白质
您对这篇实验方法有问题吗?
在此处发布您的问题,我们将邀请本文作者来回答。同时,我们会将您的问题发布到Bio-protocol Exchange,以便寻求社区成员的帮助。
提问指南
+ 问题描述
写下详细的问题描述,包括所有有助于他人回答您问题的信息(例如实验过程、条件和相关图像等)。
Share
Bluesky
X
Copy link