
doi: 10.1271/bbb.65.1849
pmid: 11577726
The natural quinone, hydroxydietrichequinone (3-heptadec-8-enyl-2-hydroxy-5-methoxy-[1,4]benzoquinone) is a secondary metabolite of Cyperus javanicus. We found that this quinone inhibited both mitochondrial respiration and photosynthesis in their electron transportation systems. The quinone was found to have a mode of action against the ubiquinone reductase site from the results of different electron donor experiments on intact mitochondria from rat liver. The electron transport system, photosystem-II (PS-II), in chroloplast from spinach leaves was inhibited by the quinone in a similar way to that of the triazin sires herbicide, atrazin, with its mode of action against PS II. This natural quinone has a long aliphatic chain (C17) including an unsaturated bond at its midpoint. We recognized 8-9 unsaturated bonds in the aliphatic chain from an MS analysis of the methylthio-addact, and spectral data presumed a configuration of cis. form.
photosynthesis, Magnetic Resonance Spectroscopy, Plants, Medicinal, Spectrophotometry, Infrared, Mitochondria, Liver, In Vitro Techniques, Mass Spectrometry, Rats, Electron Transport, Oxygen Consumption, Liver, Cyperus javanicus, Benzoquinones, Animals, electron transport inhibitor, Chromatography, Thin Layer, Cyperaceae, Rats, Wistar, hydroxydietrichequinone, respiration
photosynthesis, Magnetic Resonance Spectroscopy, Plants, Medicinal, Spectrophotometry, Infrared, Mitochondria, Liver, In Vitro Techniques, Mass Spectrometry, Rats, Electron Transport, Oxygen Consumption, Liver, Cyperus javanicus, Benzoquinones, Animals, electron transport inhibitor, Chromatography, Thin Layer, Cyperaceae, Rats, Wistar, hydroxydietrichequinone, respiration
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