Skip to main content
Plant Physiology logoLink to Plant Physiology
. 1997 Nov;115(3):1057–1064. doi: 10.1104/pp.115.3.1057

Induction of 12-oxo-phytodienoic acid in wounded plants and elicited plant cell cultures.

S Parchmann 1, H Gundlach 1, M J Mueller 1
PMCID: PMC158569  PMID: 9390438

Abstract

Jasmonic acid (JA) is rapidly biosynthesized from alpha-linolenic acid in plants upon contact with pathogens or wounding, and triggers gene activation, leading to the synthesis of defensive secondary metabolites and proteins. Despite the recent finding that its precursor, 12-oxo-phytodienoic acid (PDA), is a more powerful inducer of gene activation, interest has focused so far almost exclusively on JA. A validated negative chemical ionization-gas chromatography-mass spectrometry method has been developed that allows the simultaneous quantification of endogenous 12-oxo-PDA and JA in plant tissues. In six out of eight plant species tested maximal levels of 12-oxo-PDA exceeded peak levels of JA by approximately 3- to 5-fold after elicitation with a yeast cell wall preparation or when plants were wounded. These experiments support the hypothesis that 12-oxo-PDA acts as the predominant jasmonate signal in most plants, whereas JA remains an active metabolite of its precursor. Furthermore, JA but not 12-oxo-PDA was shown to be secreted into the medium from cultured plant cells, suggesting that JA may also act as an intercellular signal.

Full Text

The Full Text of this article is available as a PDF (775.5 KB).

Selected References

These references are in PubMed. This may not be the complete list of references from this article.

  1. Bergey D. R., Howe G. A., Ryan C. A. Polypeptide signaling for plant defensive genes exhibits analogies to defense signaling in animals. Proc Natl Acad Sci U S A. 1996 Oct 29;93(22):12053–12058. doi: 10.1073/pnas.93.22.12053. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Blechert S., Brodschelm W., Hölder S., Kammerer L., Kutchan T. M., Mueller M. J., Xia Z. Q., Zenk M. H. The octadecanoic pathway: signal molecules for the regulation of secondary pathways. Proc Natl Acad Sci U S A. 1995 May 9;92(10):4099–4105. doi: 10.1073/pnas.92.10.4099. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Dittrich H., Kutchan T. M., Zenk M. H. The jasmonate precursor, 12-oxo-phytodienoic acid, induces phytoalexin synthesis in Petroselinum crispum cell cultures. FEBS Lett. 1992 Aug 31;309(1):33–36. doi: 10.1016/0014-5793(92)80733-w. [DOI] [PubMed] [Google Scholar]
  4. Farmer E. E. Fatty acid signalling in plants and their associated microorganisms. Plant Mol Biol. 1994 Dec;26(5):1423–1437. doi: 10.1007/BF00016483. [DOI] [PubMed] [Google Scholar]
  5. Farmer E. E., Ryan C. A. Interplant communication: airborne methyl jasmonate induces synthesis of proteinase inhibitors in plant leaves. Proc Natl Acad Sci U S A. 1990 Oct;87(19):7713–7716. doi: 10.1073/pnas.87.19.7713. [DOI] [PMC free article] [PubMed] [Google Scholar]
  6. Farmer E. E., Ryan C. A. Octadecanoid-derived signals in plants. Trends Cell Biol. 1992 Aug;2(8):236–241. doi: 10.1016/0962-8924(92)90311-a. [DOI] [PubMed] [Google Scholar]
  7. Gundlach H., Müller M. J., Kutchan T. M., Zenk M. H. Jasmonic acid is a signal transducer in elicitor-induced plant cell cultures. Proc Natl Acad Sci U S A. 1992 Mar 15;89(6):2389–2393. doi: 10.1073/pnas.89.6.2389. [DOI] [PMC free article] [PubMed] [Google Scholar]
  8. Hamberg M., Gardner H. W. Oxylipin pathway to jasmonates: biochemistry and biological significance. Biochim Biophys Acta. 1992 Nov 11;1165(1):1–18. doi: 10.1016/0005-2760(92)90069-8. [DOI] [PubMed] [Google Scholar]
  9. Laudert D., Pfannschmidt U., Lottspeich F., Holländer-Czytko H., Weiler E. W. Cloning, molecular and functional characterization of Arabidopsis thaliana allene oxide synthase (CYP 74), the first enzyme of the octadecanoid pathway to jasmonates. Plant Mol Biol. 1996 May;31(2):323–335. doi: 10.1007/BF00021793. [DOI] [PubMed] [Google Scholar]
  10. Mueller M. J., Brodschelm W. Quantification of jasmonic acid by capillary gas chromatography-negative chemical ionization-mass spectrometry. Anal Biochem. 1994 May 1;218(2):425–435. doi: 10.1006/abio.1994.1202. [DOI] [PubMed] [Google Scholar]
  11. Schaller F., Weiler E. W. Enzymes of octadecanoid biosynthesis in plants--12-oxo-phytodienoate 10,11-reductase. Eur J Biochem. 1997 Apr 15;245(2):294–299. doi: 10.1111/j.1432-1033.1997.t01-1-00294.x. [DOI] [PubMed] [Google Scholar]
  12. Vick B. A., Zimmerman D. C. Biosynthesis of jasmonic Acid by several plant species. Plant Physiol. 1984 Jun;75(2):458–461. doi: 10.1104/pp.75.2.458. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Vick B. A., Zimmerman D. C. The biosynthesis of jasmonic acid: a physiological role for plant lipoxygenase. Biochem Biophys Res Commun. 1983 Mar 16;111(2):470–477. doi: 10.1016/0006-291x(83)90330-3. [DOI] [PubMed] [Google Scholar]

Articles from Plant Physiology are provided here courtesy of Oxford University Press

RESOURCES