4.6 Article

Hydroxymethylated Dioxobilins in Senescent Arabidopsis thaliana Leaves: Sign of a Puzzling Biosynthetic Intermezzo of Chlorophyll Breakdown

Journal

CHEMISTRY-A EUROPEAN JOURNAL
Volume 21, Issue 33, Pages 11664-11670

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201501489

Keywords

biosynthesis; chlorophyll; phyllobilin; structure elucidation; tetrapyrrole

Funding

  1. Science Foundations of Austria (FWF) [L-472, I-563]
  2. Science Foundations of Switzerland (SNF) [31003A_132603, 31003A_149389]
  3. Austrian Science Fund (FWF) [I 563] Funding Source: researchfish
  4. Swiss National Science Foundation (SNF) [31003A_132603] Funding Source: Swiss National Science Foundation (SNF)

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1-Formyl-19-oxobilin-type tetrapyrroles are characteristic, abundant products of chlorophyll breakdown in senescent leaves. However, in some leaves, 1,19-dioxobilin-type chlorophyll catabolites (DCCs) lacking the formyl group accumulate instead. A P450 enzyme was identified in in vitro studies that removed the formyl group of a primary fluorescent chlorophyll catabolite (pFCC) and generated fluorescent DCCs. These DCCs are precursors of isomeric nonfluorescent DCCs (NDCCs). Here, we report a structural investigation of the NDCCs in senescent leaves of wild-type Arabidopsis thaliana. Four new NDCCs were characterized, two of which carried a stereoselectively added hydroxymethyl group. Such formal DCC hydroxymethylations were previously found in DCCs in leaves of a mutant of A.thaliana. They are now indicated to be a feature of chlorophyll breakdown in A.thaliana, associated with the specific in vivo deformylation of pFCC en route to NDCCs.

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