Free Standard AU & NZ Shipping For All Book Orders Over $80!
Register      Login
Functional Plant Biology Functional Plant Biology Society
Plant function and evolutionary biology
RESEARCH ARTICLE

Early accumulation of non-enzymatically synthesised oxylipins in Arabidopsis thaliana after infection with Pseudomonas syringae

Christoph Grun A , Susanne Berger A , Daniel Matthes A and Martin J. Mueller A B
+ Author Affiliations
- Author Affiliations

A Julius-von-Sachs-Institute for Biosciences, Pharmaceutical Biology, University of Wuerzburg, Julius-von-Sachs-Platz 2, D-97082 Würzburg, Germany.

B Corresponding author. Email: martin.mueller@biozentrum.uni-wuerzburg.de

Functional Plant Biology 34(1) 65-71 https://doi.org/10.1071/FP06205
Submitted: 23 August 2006  Accepted: 3 November 2006   Published: 19 January 2007

Abstract

The formation of non-enzymatic oxylipins is catalysed by reactive oxygen species. Reactive oxygen species are produced in response to pathogen attack. In this study, the accumulation of non-enzymatically formed hydroxy fatty acids and F1-phytoprostanes in leaves of Arabidopsis thaliana (L.) Heyhn upon infection with Pseudomonas syringae was investigated and compared with the accumulation of the enzymatically formed oxylipins jasmonic acid and 12-oxo-phytodienoic acid. Levels of all oxylipins increased after infection with a virulent and with an avirulent strain of P. syringae. Inoculation of the avirulent strain resulted in a biphasic accumulation with a first maximum around 5 h which was missing after inoculation of the virulent strain. Levels of free and esterified hydroxy fatty acids and F1-phytoprostanes increased after pathogen treatment; however, esterified compounds were 30 times more abundant than free oxylipins. The increase of the free compounds occurred later than the increase of the esterified compounds suggesting that non-enzymatic lipid oxidation occurs predominantly in membranes from which oxidised lipids can be released.

Additional keywords: hydroxy fatty acids, phytoprostanes.


Acknowledgements

We are grateful to M. Krischke for helpful discussion. This work was supported by the SFB 567.


References


Almeras E, Stolz S, Vollenweider S, Reymond P, Mene-Saffrane L, Farmer EE (2003) Reactive electrophile species activate defense gene expression in Arabidopsis. The Plant Journal 34, 205–216.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Apel K, Hirt H (2004) Reactive oxygen species: metabolism, oxidative stress, and signal transduction. Annual Review of Plant Biology 55, 373–399.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Bate N, Rothstein S (1998) C6-volatiles derived from the lipoxygenase pathway induce a subset of defense-related genes. The Plant Journal 16, 561–569.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Berger S, Weichert H, Porzel A, Wasternack C, Kuhn H, Feussner I (2001) Enzymatic and non-enzymatic lipid peroxidation in leaf development. Biochimica et Biophysica Acta 1533, 266–276.
PubMed | open url image1

Block A, Schmelz E, Jones JB, Klee HJ (2005) Coronatine and salicylic acid: the battle between Arabidopsis and Pseudomonas for phytohormone control. Molecular Plant Pathology 6, 79–83.
Crossref | GoogleScholarGoogle Scholar | open url image1

Feussner I, Wasternack C (2002) The lipoxygenase pathway. Annual Review of Plant Physiology and Plant Molecular Biology 53, 275–297. open url image1

Goebel C, Feussner I, Hamberg M, Rosahl S (2002) Oxylipin profiling in pathogen-infected potato leaves. Biochimica et Biophysica Acta 1584, 55–64.
PubMed | open url image1

Grant JJ, Loake GL (2000) Role of reactive oxygen intermediates and cognate redox signaling in disease resistance. Plant Physiology 124, 21–30.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Heath MC (2000) Hypersensitive response-related death. Plant Molecular Biology 44, 321–334.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Imbusch R, Mueller MJ (2000) Formation of isoprostane F2-like compounds (phytoprostanes F1) from alpha-linolenic acid in plants. Free Radical Biology and Medicine 28, 720–726.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Iqbal M, Evans P, Lledo A, Verdaguer X, Pericàs MA, Riera A, Loeffler C, Sinha AK, Mueller MJ (2005) Total synthesis and biological activity of 13,14-dehydro-12-oxo-phytodienoic acids (deoxy-J1-phytoprostanes). ChemBioChem 6, 276–280.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Loeffler C, Berger S, Guy A, Durand T, Bringmann G, Dreyer M, von Rad U, Durner J, Mueller MJ (2005) B1-phytoprostanes trigger plant defense and detoxification responses. Plant Physiology 137, 328–340.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Montillet JL, Cacas JL, Garnier L, Montane MH, Douki T , et al. (2004) The upstream oxylipin profile of Arabidopsis thaliana: a tool to scan for oxidative stresses. The Plant Journal 40, 439–451.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Montillet JL, Chamnongpol S, Rusterucci C, Dat J, van de Cotte B, Agnel JP, Battesti C, Inze D, van Breusegem F, Triantaphylides C (2005) Fatty acid hydroperoxides and H2O2 in the execution of hypersensitive cell death in tobacco leaves. Plant Physiology 138, 1516–1526.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Mueller MJ (2004) Archetype signals in plants: the phytoprostanes. Current Opinion in Plant Biology 7, 441–448.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Mueller MJ, Mene-Saffrane L, Grun C, Karg K, Farmer EE (2006) Oxylipin analysis methods. The Plant Journal 45, 472–489.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Ochsenbein C, Przybyla D, Danon A, Landgraf F, Gobel C, Imboden A, Feussner I, Apel K (2006) The role of EDS1 (enhanced disease susceptibility) during singlet oxygen-mediated stress responses of Arabidopsis. The Plant Journal 47, 445–456.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

op den Camp RG, Przybyla D, Ochsenbein C, Laloi C, Kim C, Danon A, Wagner D, Hideg E, Gobel C, Feussner I, Nater M, Apel K (2003) Rapid induction of distinct stress responses after the release of singlet oxygen in Arabidopsis. The Plant Cell 15, 2320–2332.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Parchmann S, Mueller M (1998) Evidence for the formation of dinor isoprostanes E1 from alpha-linolenic acid in plants. Journal of Biological Chemistry 273, 32650–32655.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Tao Y, Xie Z, Chen W, Glazebrook J, Chang HS, Han B, Zhu T, Zou G, Katagiri F (2003) Quantitative nature of Arabidopsis responses during compatible and incompatible interactions with the bacterial pathogen Pseudomonas syringae. The Plant Cell 15, 317–330.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Thoma I, Loeffler C, Sinha AK, Gupta M, Krischke M, Steffan B, Roitsch T, Mueller MJ (2003) Cyclopentenone isoprostanes induced by reactive oxygen species trigger defense gene activation and phytoalexin accumulation in plants. The Plant Journal 34, 363–375.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Torres MA, Dangl JL (2005) Functions of the respiratory burst oxidase in biotic interactions, abiotic stress and development. Current Opinion in Plant Biology 8, 397–403.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Weber H, Chételat A, Reymond P, Farmer EE (2004) Selective and powerful stress gene expression in Arabidopsis in response to malondialdehyde. The Plant Journal 37, 877–888.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1

Whalen M, Innes RW, Bent AF, Staskawicz B (1991) Identification of Pseudomonas syringae pathogens of Arabidopsis thaliana and bacterial gene determining avirulence on both Arabidopsis and soybean. The Plant Cell 3, 49–59.
Crossref | GoogleScholarGoogle Scholar | PubMed | open url image1