Biosynthesis and metabolism of jasmonates

被引:172
作者
Schaller, F [1 ]
Schaller, A
Stintzi, A
机构
[1] Ruhr Univ Bochum, Lehrstuhl Pflanzenphysiol, D-44780 Bochum, Germany
[2] Univ Hohenheim, Inst Physiol & Biotechnol Pflanzen 260, D-70593 Stuttgart, Germany
关键词
jasmonates; octadecanoid pathway; oxylipins; plant defense; plant development; plant hormones; signaling;
D O I
10.1007/s00344-004-0047-x
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Jasmonates are derived from oxygenated fatty acids via the octadecanoid pathway and characterized by a pentacyclic ring structure. They have regulatory function as signaling molecules in plant development and adaptation to environmental stress. Until recently, it was the cyclopentanone jasmonic acid (JA) that attracted most attention as a plant growth regulator. It becomes increasingly clear, however, that biological activity is not limited to JA but extends to, and may even differ between its many metabolites and conjugates as well as its cyclopentenone precursors. The enzymes of jasmonate bio-synthesis and metabolism may thus have a regulatory function in controlling the activity and relative levels of different signaling molecules. Such a function is supported by both the characterization of loss of function mutants in Arabidopsis, and the biochemical characterization of the enzymes themselves.
引用
收藏
页码:179 / 199
页数:21
相关论文
共 200 条
[51]   THE LIPOXYGENASE PATHWAY IN GARLIC (ALLIUM-SATIVUM L) BULBS - DETECTION OF THE NOVEL DIVINYL ETHER OXYLIPINS [J].
GRECHKIN, AN ;
FAZLIEV, FN ;
MUKHTAROVA, LS .
FEBS LETTERS, 1995, 371 (02) :159-162
[52]   JASMONIC ACID IS A SIGNAL TRANSDUCER IN ELICITOR-INDUCED PLANT-CELL CULTURES [J].
GUNDLACH, H ;
MULLER, MJ ;
KUTCHAN, TM ;
ZENK, MH .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (06) :2389-2393
[53]   Biological activity and biosynthesis of pentacyclic oxylipins: The linoleic acid pathway [J].
Gundlach, H ;
Zenk, MH .
PHYTOCHEMISTRY, 1998, 47 (04) :527-537
[54]   Structure-activity relationships of synthetic analogs of jasmonic acid and coronatine on induction of benzo[c]phenanthridine alkaloid accumulation in Eschscholzia californica cell cultures [J].
Haider, G ;
von Schrader, T ;
Füsslein, M ;
Blechert, S ;
Kutchan, TM .
BIOLOGICAL CHEMISTRY, 2000, 381 (08) :741-748
[55]   Antisense LOX expression increases herbivore performance by decreasing defense responses and inhibiting growth-related transcriptional reorganization in Nicotiana attenuata [J].
Halitschke, R ;
Baldwin, IT .
PLANT JOURNAL, 2003, 36 (06) :794-807
[56]   New cyclopentenone fatty acids formed from linoleic and linolenic acids in potato [J].
Hamberg, M .
LIPIDS, 2000, 35 (04) :353-363
[57]   FATTY-ACID ALLENE OXIDES .3. ALBUMIN-INDUCED CYCLIZATION OF 12,13(S)-EPOXY-9(Z),11-OCTADECADIENOIC ACID [J].
HAMBERG, M ;
HUGHES, MA .
LIPIDS, 1988, 23 (05) :469-475
[58]   ALLENE OXIDE CYCLASE - A NEW ENZYME IN PLANT LIPID-METABOLISM [J].
HAMBERG, M ;
FAHLSTADIUS, P .
ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1990, 276 (02) :518-526
[59]   Inhibition of wound-induced accumulation of allene oxide synthase transcripts in flax leaves by aspirin and salicylic acid [J].
Harms, K ;
Ramirez, I ;
Peña-Cortés, H .
PLANT PHYSIOLOGY, 1998, 118 (03) :1057-1065
[60]  
HARMS K, 1995, PLANT CELL, V7, P1645, DOI 10.1105/tpc.7.10.1645