| Literature DB >> 28374305 |
María A Luján1, Patricia Lorente1, Valter Zazubovich2, Rafael Picorel3.
Abstract
Using a single size-exclusion chromatography we were able to isolate highly pure dimers and monomers of the Cyt b 6 f complex from spinach from a bulk preparation of that protein complex obtained with a standard procedure. At higher protein/detergent ratio during the chromatography most of the Cyt b 6 f complex remained as dimers. In contrast, at lower protein/detergent ratio (around 15 times lower), most dimers became monomerized. As a bonus, this chromatography also allowed the elimination of potential Chl a contaminant to the Cyt b 6 f preparations. SDS-PAGE protein analysis with 18% (w/v) acrylamide revealed the loss of the ISP subunit in our monomeric preparation. However, it fully retained the content of Chl a, a prerequisite to perform any spectroscopic study involving this unique pigment.Entities:
Keywords: Cytochrome b 6 f; Photosynthesis; Plant; Protein; Purification; SDS-PAGE
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Year: 2017 PMID: 28374305 DOI: 10.1007/s11120-017-0375-x
Source DB: PubMed Journal: Photosynth Res ISSN: 0166-8595 Impact factor: 3.573