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Article Addendum
Role of Peroxisomal β-Oxidation in the Production of Plant Signaling Compounds
Abraham J.K. Koo and Greg A. Howe
volume 2 | issue 1
january/february 2007Pages: 20 - 22
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The lipid-derived signaling compound jasmonic acid (JA) regulates a wide variety of developmental and defense-related processes in higher plants. JA synthesis is initiated in the plastid and completed in peroxisomes. The peroxisomal reactions involve reduction of 12-oxo-phytodienoic acid (OPDA) to 3-oxo-2-(2’-pentenyl)-cyclopentane-1-octanoic acid (OPC-8:0), which is subsequently converted to JA by three rounds of β-oxidation. It is widely assumed that JA precursors are activated to their CoA derivatives prior to entering the β-oxidation cycle. However, acyl-activating enzymes (AAEs) that catalyze this reaction in vivo have remained elusive, owing in part to the large size and functional redundancy of the AAE gene family. In a recent issue of J. Biol. Chem., we reported the use of co-expression analysis to identify an AAE gene that is coordinately regulated with known JA biosynthetic components in Arabidopsis. A combination of genetic, biochemical, and cellular approaches were used to demonstrate that this gene, called OPC-8:0 CoA Ligase1 (OPCL1), has a physiological role in activating JA precursors in the peroxisome. Similar approaches may be useful for identifying additional components of the jasmonate pathway, as well as AAEs that participate in the synthesis of other plant signaling compounds.
Authors
Abraham J.K. Koo
Michigan State University, East Lansing, MI
Greg A. Howe
Michigan State University, East Lansing, MI
We now provide open access to journal articles published online for one year or more. This article may be downloaded at the following link:
Download PDF If the document does not open, please right-click on the link (control-click on a Macintosh) and select the option to save the file to disk.