Losey F G, Engel N
Institute of Organic Chemistry, University of Fribourg, Chemin du Musée 9, CH-1700 Fribourg, Switzerland.
J Biol Chem. 2001 Mar 23;276(12):8643-7. doi: 10.1074/jbc.M009288200. Epub 2000 Dec 13.
A new type of chlorophyll catabolite was isolated from extracts of de-greened primary leaves of barley (Hordeum vulgare cv. Lambic). Its constitution was elucidated by one-dimensional and two-dimensional [(1)H,(13)C]-homo- and heteronuclear NMR spectroscopic techniques and by high resolution mass spectroscopy. The isolated catabolite, a water-soluble, colorless, and nonfluorescent linear tetrapyrrole, resembles urobilinogen in which one of the propionic side chains forms a five membered isocylic ring system, indicating its origin from the chlorophylls.