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Fast Isolation of Highly Active Photosystem Ⅱ Core Complexes from Spinach
作者单位:Zhao-Gai Wang(Key Laboratory of Photobiology, Institute of Botany, the Chinese Academy of Sciences, Beijing 100093, China;Graduate University of the Chinese Academy of Sciences, Beijing 100049, China;Institute of Farm Product Processing, Henan Academy of Agricultural Sciences, Zhengzhou 450002, China);Tian-Hua Xu(Key Laboratory of Photobiology, Institute of Botany, the Chinese Academy of Sciences, Beijing 100093, China;Graduate University of the Chinese Academy of Sciences, Beijing 100049, China);Cheng Liu,Chun-Hong Yang(Key Laboratory of Photobiology, Institute of Botany, the Chinese Academy of Sciences, Beijing 100093, China) 
基金项目:the,National,Natural,Science,Foundation,of,China
摘    要:

收稿时间:2010-01-05

Fast Isolation of Highly Active Photosystem II Core Complexes from Spinach
Authors:Zhao-Gai Wang  Tian-Hua Xu  Cheng Liu  Chun-Hong Yang
Institution:1.Key Laboratory of Photobiology, Institute of Botany, Chinese Academy of Sciences, Beijing, 100093, China;2.Graduate University of Chinese Academy of Sciences, Beijing, 100049, China;3.Institute of Farm Product Processing, Henan Academy of Agricultural Sciences, Zhengzhou 450002, China
Abstract:Purification of photosystem Ⅱ (PSII) core complexes is a time-consuming and low-efficiency process. In order to isolate pure and active PSII core complexes in large amounts, we have developed a fast method to isolate highly active monomeric and dimeric PSII core complexes from spinach leaves by using sucrose gradient ultracentrifugation. By using a vertical rotor the process was completed significantly faster compared with a swing-out rotor. In order to keep the core complexes in high activity, the whole isolation procedure was performed in the presence of glycine betain and pH at 6.3. The isolated pigment-protein complexes were characterized by sodium dodecyl sulfate-polyacrylamide gel electrophoresis, absorption spectroscopy, 77 K fluorescence spectroscopy and high performance liquid chromatography. Our results show that this method is a better choice for quick and efficient isolation of functionally active PSII core complexes.
Keywords:
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