Arabidopsis thaliana - OPUS - Universität Würzburg

Arabidopsis thaliana - OPUS - Universität Würzburg Arabidopsis thaliana - OPUS - Universität Würzburg

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Schaller F., Zerbe P., Reinbothe S., Reinbothe C., Hofmann E., Pollmann S. 2008. The allene oxide cyclase family of Arabidopsis thaliana: localization and cyclization. FEBS Journal (275): 2428-2441. Schweizer P., Gees R., Mosinger E. 1993. Effect of Jasmonic Acid on the Interaction of Barley (Hordeum-Vulgare L) with the Powdery Mildew Erysiphe- Graminis F Sp Hordei. Plant Physiology (102): 503-511. Seltmann M. A., Stingl N. E., Lautenschlaeger J. K., Krischke M., Mueller M. J., Berger S. 2010. Differential Impact of Lipoxygenase 2 and Jasmonates on Natural and Stress-Induced Senescence in Arabidopsis. Plant Physiology (152): 1940-1950. Sembdner G., Parthier B. 1993. The biochemistry and the physiological and molecular actions of jasmonates. Annual Review of Plant Physiology and Plant Molecular Biology (44): 569–589. Seo H. S., Song J. T., Cheong J. J., Lee Y. H., Lee Y. W., Hwang I., Lee J. S., Choi Y. D. 2001. Jasmonic acid carboxyl methyltransferase: a key enzyme for jasmonate-regulated plant responses. Proceedings of the National Academy of Sciences of the United States of America (98): 4788-4793. Seo Y. S., Kim E. Y., Kim J. H., Kim W. T. 2009. Enzymatic characterization of class I DAD1-like acylhydrolase members targeted to chloroplast in Arabidopsis. FEBS Letters (583): 2301-2307. Sigal E. 1991. The Molecular-Biology of Mammalian Arachidonic-Acid Metabolism. American Journal of Physiology (260): L13-L28. Staswick P. E., Tiryaki I. 2004. The oxylipin signal jasmonic acid is activated by an enzyme that conjugates it to isoleucine in Arabidopsis. The Plant Cell (16): 2117-2127. Staswick P. E., Su W., Howell S. H. 1992. Methyl jasmonate inhibition of root growth and induction of a leaf protein are decreased in an Arabidopsis thaliana 142

mutant. Proceedings of the National Academy of Sciences of the United States of America (89): 6837-6840. Stelmach B. A., Muller A., Hennig P., Gebhardt S., Schubert-Zsilavecz M., Weiler E. W. 2001. A novel class of oxylipins, sn1-O-(12-oxophytodienoyl)-sn2-O- (hexadecatrienoyl)-monogalactosyl Diglyceride, from Arabidopsis thaliana. The Journal of Biological Chemistry (276): 12832-12838. Stenzel I., Hause B., Miersch O., Kurz T., Maucher H., Weichert H., Ziegler J., Feussner I., Wasternack C. 2003. Jasmonate biosynthesis and the allene oxide cyclase family of Arabidopsis thaliana. Plant Molecular Biology (51): 895-911. Stintzi A., Browse J. 2000. The Arabidopsis male-sterile mutant, opr3, lacks the 12-oxophytodienoic acid reductase required for jasmonate synthesis. Proceedings of the National Academy of Sciences of the United States of America (97): 10625-10630. Stintzi A., Weber H., Reymond P., Browse J., Farmer E. E. 2001. Plant defense in the absence of jasmonic acid: the role of cyclopentenones. Proceedings of the National Academy of Sciences of the United States of America (98): 12837- 12842. Szyroki A., et al. 2001. KAT1 is not essential for stomatal opening. Proceedings of the National Academy of Sciences of the United States of America (98): 2917-2921. Taki N., et al. 2005. 12-oxo-phytodienoic acid triggers expression of a distinct set of genes and plays a role in wound-induced gene expression in Arabidopsis. Plant Physiology (139): 1268-1283. Thaler J. S., Owen B., Higgins V. J. 2004. The role of the jasmonate response in plant susceptibility to diverse pathogens with a range of lifestyles. Plant Physiology (135): 530-538. 143

mutant. Proceedings of the National Academy of Sciences of the United States<br />

of America (89): 6837-6840.<br />

Stelmach B. A., Muller A., Hennig P., Gebhardt S., Schubert-Zsilavecz M., Weiler<br />

E. W. 2001. A novel class of oxylipins, sn1-O-(12-oxophytodienoyl)-sn2-O-<br />

(hexadecatrienoyl)-monogalactosyl Diglyceride, from <strong>Arabidopsis</strong> <strong>thaliana</strong>. The<br />

Journal of Biological Chemistry (276): 12832-12838.<br />

Stenzel I., Hause B., Miersch O., Kurz T., Maucher H., Weichert H., Ziegler J.,<br />

Feussner I., Wasternack C. 2003. Jasmonate biosynthesis and the allene oxide<br />

cyclase family of <strong>Arabidopsis</strong> <strong>thaliana</strong>. Plant Molecular Biology (51): 895-911.<br />

Stintzi A., Browse J. 2000. The <strong>Arabidopsis</strong> male-sterile mutant, opr3, lacks the<br />

12-oxophytodienoic acid reductase required for jasmonate synthesis.<br />

Proceedings of the National Academy of Sciences of the United States of<br />

America (97): 10625-10630.<br />

Stintzi A., Weber H., Reymond P., Browse J., Farmer E. E. 2001. Plant defense<br />

in the absence of jasmonic acid: the role of cyclopentenones. Proceedings of<br />

the National Academy of Sciences of the United States of America (98): 12837-<br />

12842.<br />

Szyroki A., et al. 2001. KAT1 is not essential for stomatal opening. Proceedings<br />

of the National Academy of Sciences of the United States of America (98):<br />

2917-2921.<br />

Taki N., et al. 2005. 12-oxo-phytodienoic acid triggers expression of a distinct<br />

set of genes and plays a role in wound-induced gene expression in<br />

<strong>Arabidopsis</strong>. Plant Physiology (139): 1268-1283.<br />

Thaler J. S., Owen B., Higgins V. J. 2004. The role of the jasmonate response in<br />

plant susceptibility to diverse pathogens with a range of lifestyles. Plant<br />

Physiology (135): 530-538.<br />

143

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