Journal of Integrative Plant Biology · 2010 · 12 citations · 30 references
Life SciencesBiochemistryPlant BiologyPhotosynthesisPlant BiochemistryPlant Molecular BiologyLight HarvestingPhotosynthesis BiochemistryPhotosynthetic PigmentsPhotosystem IiProtein PurificationProtein SeparationHigh-performance Liquid ChromatographyIsolationLight Harvesting Complex IiPolyacrylamide Gel ElectrophoresisProtein Separation TechniquesSodium Dodecyl Sulfate-polyacrylamide Gel ElectrophoresisSucrose Gradient CentrifugationUltracentrifugation
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.
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Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Ulrich K. Laemmli · Nature · 1970 · 251.6K citations
COPPER ENZYMES IN ISOLATED CHLOROPLASTS. POLYPHENOLOXIDASE IN <i>BETA VULGARIS</i>
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