Separation of Monovinyl and Divinyl Protochlorophyllides and Chlorophyllides from Etiolated and Phototransformed Cucumber Cotyledons
Authors:
- Paul A. CastelfrancoPCPaul A. Castelfranco
- 1 September 1983
- journal article
- research article
- Published by Oxford University Press (OUP) in Plant Physiology
- Vol. 73 (1) , 79-81
Abstract
A method was developed to separate the monovinyl and divinyl forms of protochlorophyllide and chlorophyllide by high pressure liquid chromatography using a silicic acid column coated with dodecyl residues and a moving phase containing the lipophilic cation, tetrabutyl ammonium. The solvent was 70% methyl alcohol containing varying amounts of methyl ethyl ketone. The separation was carried out at 0 degrees C. This method was used to test and confirm a previous report that, in cucumber cotyledons, divinyl protochlorophyllide is phototransformed to give divinyl chlorophyllide, which is biologically unstable and disappears rapidly in the dark.Keywords
This publication has 6 references indexed in Scilit:
- In Vitro Synthesis of the Chlorophyll Isocyclic RingPlant Physiology, 1982
- Chloroplast biogenesis. Identification of chlorophyllide a (E458f674) as a divinyl chlorophyllide a.Journal of Biological Chemistry, 1982
- Separation of Mg-Protoporphyrin IX and Mg-Protoporphyrin IX Monomethyl Ester Synthesized de novo by Developing Cucumber EtioplastsPlant Physiology, 1982
- Chloroplast biogenesis. Detection of divinyl protochlorophyllide in higher plants.Journal of Biological Chemistry, 1980
- Chloroplast biogenesis XXVII detection of novel chlorophyll and chlorophyll precursors in higher plantsBiochemical and Biophysical Research Communications, 1979
- Magnesium 2,4-divinylphaeoporphyrin a5 as a substrate for chlorophyll biosynthesis in vitroFEBS Letters, 1975