Abstract
2-Carboxyarabinitol-1-phosphate, the nocturnal inhibitor of ribulose-1,5-bisphosphate carboxylase/oxygenase is identical with d-hamamelonic acid-21-phosphate. Reasoning is based on theoretical considerations as well as on mass spectra and 1H- and 13C-NMR spectra of the phosphate-free compounds. d-Hamamelonic acid-21-phosphate is interpreted as a metabolic derivative of d-hamamelose-21,5-bisphosphate which originates in the chloroplast from fructose-1,6-bisphosphate. A simple method for the synthesis of the inhibitor is suggested.
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