Mode of Action of Jasmonates
Search narrowed by
Advanced Search
- Type of publication
- Books and chapters (1)
- Publication (1)
- Year
- Journal / Volume / Preprint Server Sorted by frequency and by alphabetical order
- 0 (1)
- Acta Biol. Szeged. (1)
- Author Sorted by frequency and by alphabetical order
- Wasternack, C. (166)
- Miersch, O. (80)
- Hause, B. (66)
- Feussner, I. (47)
- Kramell, R. (24)
- Stenzel, I. (23)
- Parthier, B. (20)
- Atzorn, R. (13)
- Maucher, H. (13)
- Ziegler, J. (12)
- Kühn, H. (11)
- Strnad, M. (11)
- Weichert, H. (10)
- Abdala, G. (9)
- Porzel, A. (8)
- Schmidt, J. (8)
- Demuth, H.-U. (6)
- Floková, K. (6)
- Novák, O. (6)
- Schilling, S. (6)
- Apel, K. (5)
- Feussner, K. (5)
- Göbel, C. (5)
- Schneider, G. (5)
- Strack, D. (5)
- Stumpe, M. (5)
- Vigliocco, A. (5)
- Alemano, S. (4)
- Bohlmann, H. (4)
- Brandt, W. (4)
- Delker, C. (4)
- Hamberg, M. (4)
- Hause, G. (4)
- Hoffmann, T. (4)
- Mik, V. (4)
- Ortel, B. (4)
- Vörös, K. (4)
- Willmitzer, L. (4)
- Balkenhohl, T. J. (3)
- Boland, W. (3)
- Brunoni, F. (3)
- Forner, S. (3)
- Goetz, S. (3)
- Hertel, S. C. (3)
- Hilpert, B. (3)
- Kogel, K.-H. (3)
- Kohlmann, M. (3)
- Kombrink, E. (3)
- Kutchan, T. M. (3)
- Kutter, C. (3)
- Köck, M. (3)
- Lange, P. R. (3)
- Lehmann, J. (3)
- Leopold, J. (3)
- Monostori, T. (3)
- Rosahl, S. (3)
- Schulze, J. (3)
- Sharma, V. K. (3)
- Wermann, M. (3)
- Široká, J. (3)
- Ammer, C. (2)
- BERGER, S. (2)
- Bachmann, A. (2)
- Bartsch, M. (2)
- Beale, M. (2)
- Bittner, F. (2)
- Blée, E. (2)
- Brückner, C. (2)
- Castro, G. (2)
- Dorka, R. (2)
- Dunaeva, M. (2)
- Eschen-Lippold, L. (2)
- Facchini, P. J. (2)
- Felix, G. (2)
- Fisahn, J. (2)
- Geißler, R. (2)
- Gershenzon, J. (2)
- Gesell, A. (2)
- Graner, A. (2)
- Groß, N. (2)
- Grúz, J. (2)
- Guranowski, A. (2)
- Görschen, E. (2)
- Hellwege, A. (2)
- Herde, O. (2)
- Hornung, E. (2)
- Hänsch, R. (2)
- Kenton, P. (2)
- Kienow, L. (2)
- Knöfel, H.-D. (2)
- Kolbe, A. (2)
- Küster, H. (2)
- Ludwig-Müller, J. (2)
- Manhart, S. (2)
- Mendel, R. R. (2)
- Mur, L. A. J. (2)
- Neumerkel, J. (2)
- Nožková, V. (2)
- O'Donnell, P. J. (2)
- Otto, M. (2)
Displaying results 1 to 2 of 2.
Sharma, V. K.; Monostori, T.; Hause, B.; Maucher, H.; Göbel, C.; Hornung, E.; Hänsch, R.; Bittner, F.; Wasternack, C.; Feussner, I.; Mendel, R. R.; Schulze, J.; Genetic transformation of barley to modify expression of a 13-lipoxygenase Acta Biol. Szeged. 49, 33-34, (2005)
Immature scutella of barley were transformed with cDNA coding for a 13-lipoxygenase of barley (LOX-100) via particle bombardment. Regenerated plants were tested by PAT-assay, Western-analysis and PCR-screening. Immunocytochemical assay of T0 plants showed expression of the LOX cDNA both in the chloroplasts and in the cytosol, depending on the presence of the chloroplast signal peptide sequences in the cDNA. A few transgenic plants containing higher amounts of LOX-derived products have been found. These are the candidates for further analysis concerning pathogen resistance.
Weichert, H.; Maucher, H.; Hornung, E.; Wasternack, C.; Feussner, I.; Shift in Fatty Acid and Oxylipin Pattern of Tomato Leaves Following Overexpression of the Allene Oxide Cyclase 275-278, (2003) DOI: 10.1007/978-94-017-0159-4_64
Polyunsaturated fatty acids (PUFAs) are a source of numerous oxidation products, the oxylipins. In leaves, α-linolenic acid (α-LeA) is the preferential substrate for lipid peroxidation reactions. This reaction may be catalyzed either by a 9-lipoxygenase (9-LOX) or by a 13-LOX and oxygen is inserted regioselectively as well as stereospecifically leading to formation of 13S- or 9S-hydroperoxy octadecatrienoic acid (13-/9-HPOT; Brash, 1999). At least, seven different enzyme families or reaction branches within the LOX pathway can use these HPOTs or other hydroperoxy PUFAs leading to (i) keto-PUFAs (LOX); (ii) epoxy hydroxy-PUFAs (epoxy alcohol synthase, EAS); (iii) octadecanoids and jasmonates (allene oxide synthase, AOS); (iv) leaf aldehydes and leaf alcohols (hydroperoxide lyase, HPL); (v) hydroxy PUFAs (reductase); (vi) divinyl ether PUFAs (divinyl ether synthase, DES); and (vii) epoxy- or dihydrodiol-PUFAs (peroxygenase, PDX; Fig. 1; Feussner and Wasternack, 2002).