4.6 Article

Hydroxymethylated Phyllobilins: A Puzzling New Feature of the Dioxobilin Branch of Chlorophyll Breakdown

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 20, Issue 1, Pages 87-92

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201303398

Keywords

Arabidopsis thaliana; bilin; chlorophyll; cytochrome P450; phyllobilin

Funding

  1. Austrian Science Foundation (FWF) [L-472, I-563]
  2. Swiss Science Foundation (SNF) [31003A_132603]
  3. Swiss National Science Foundation (SNF) [31003A_132603] Funding Source: Swiss National Science Foundation (SNF)
  4. Austrian Science Fund (FWF) [I 563] Funding Source: researchfish

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Colorless nonfluorescent chlorophyll (Chl) catabolites (NCCs) are formyloxobilin-type phyllobilins, which are considered the typical products of Chl breakdown in senescent leaves. However, in degreened leaves of some plants, dioxobilin-type Chl catabolites (DCCs) predominate, which lack the formyl group of the NCCs, and which arise from Chl catabolites by oxidative removal of the formyl group by a P450 enzyme. Here a structural investigation of the DCCs in the methylesterase16 mutant of Arabidopsis thaliana is reported. Eight new DCCs were identified and characterized structurally. Strikingly, three of these DCCs carry stereospecifically added hydroxymethyl groups, and represent bilin-type linear tetrapyrroles with an unprecedented modification. Indeed, DCCs show a remarkable structural parallel, otherwise, to the bilins from heme breakdown.

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