Abstract:Jasmonic acid (jA) is rapidly biosynthesized from a-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, 1 2-0x0-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 allo… Show more
“…For instance, conventional -oxidation of the C 18 precursor to jasmonate would involve 15 steps, including the initial activation of the carboxyl group and the final release of jasmonate by acylCoA thioesterase activity (Mueller, 1997). The compartment in which these transformations take place is not known (Mueller, 1997;Parchmann et al, 1997). It would obviously be of great interest to determine whether the enzymes involved are mitochondrial or peroxisomal.…”
The existence in higher plants of an additional -oxidation system in mitochondria, besides the well-characterized peroxisomal system, is often considered controversial. Unequivocal demonstration of -oxidation activity in mitochondria should rely on identification of the enzymes specific to mitochondrial -oxidation. Acylcoenzyme A dehydrogenase (ACAD) (EC 1.3.99.2,3) activity was detected in purified mitochondria from maize (Zea mays L.) root tips and from embryonic axes of early-germinating sunflower (Helianthus annuus L.) seeds, using as the enzyme assay the reduction of 2,6-dichlorophenolindophenol, with phenazine methosulfate as the intermediate electron carrier. Subcellular fractionation showed that this ACAD activity was associated with mitochondrial fractions. Comparison of ACAD activity in mitochondria and acylcoenzyme A oxidase activity in peroxisomes showed differences of substrate specificities. Embryonic axes of sunflower seeds were used as starting material for the purification of ACADs. Two distinct ACADs, with medium-chain and long-chain substrate specificities, respectively, were separated by their chromatographic behavior, which was similar to that of mammalian ACADs. The characterization of these ACADs is discussed in relation to the identification of expressed sequenced tags corresponding to ACADs in cDNA sequence analysis projects and with the potential roles of mitochondrial -oxidation in higher plants.
“…For instance, conventional -oxidation of the C 18 precursor to jasmonate would involve 15 steps, including the initial activation of the carboxyl group and the final release of jasmonate by acylCoA thioesterase activity (Mueller, 1997). The compartment in which these transformations take place is not known (Mueller, 1997;Parchmann et al, 1997). It would obviously be of great interest to determine whether the enzymes involved are mitochondrial or peroxisomal.…”
The existence in higher plants of an additional -oxidation system in mitochondria, besides the well-characterized peroxisomal system, is often considered controversial. Unequivocal demonstration of -oxidation activity in mitochondria should rely on identification of the enzymes specific to mitochondrial -oxidation. Acylcoenzyme A dehydrogenase (ACAD) (EC 1.3.99.2,3) activity was detected in purified mitochondria from maize (Zea mays L.) root tips and from embryonic axes of early-germinating sunflower (Helianthus annuus L.) seeds, using as the enzyme assay the reduction of 2,6-dichlorophenolindophenol, with phenazine methosulfate as the intermediate electron carrier. Subcellular fractionation showed that this ACAD activity was associated with mitochondrial fractions. Comparison of ACAD activity in mitochondria and acylcoenzyme A oxidase activity in peroxisomes showed differences of substrate specificities. Embryonic axes of sunflower seeds were used as starting material for the purification of ACADs. Two distinct ACADs, with medium-chain and long-chain substrate specificities, respectively, were separated by their chromatographic behavior, which was similar to that of mammalian ACADs. The characterization of these ACADs is discussed in relation to the identification of expressed sequenced tags corresponding to ACADs in cDNA sequence analysis projects and with the potential roles of mitochondrial -oxidation in higher plants.
“…As shown in Table I, the function of LOX in the defense against pests seems to be related to the synthesis of a number of different compounds with signaling functions (Creelman and Mullet, 1997;Parchmann et al, 1997), antimicrobial activity (Croft et al, 1993;Weber et al, 1999), or to the development of the HR (Rustérucci et al, 1999).…”
Section: Pathogen Attackmentioning
confidence: 99%
“…JA and OPDA levels increase upon wounding (Creelman and Mullet, 1997;Parchmann et al, 1997). JA or OPDA treatment induces the synthesis of molecules that function in the defense against herbivores (Creelman and Mullet, 1997).…”
Section: Different Oxylipins Are Required For the Defense Of Plants Wmentioning
“…JA signaling can be induced by a range of abiotic stresses, including osmotic stress (Kramell et al, 1995), wounding, drought, and exposure to "elicitors," which include chitins, oligosaccharides, oligogalaturonides (Doares et al, 1995), and extracts from yeast (Parchmann et al, 1997;Leon et al, 2001). JA biosynthesis in Arabidopsis is also regulated by cues in the developing stamen, where jasmonic acid is required for pollen development.…”
Section: Perception Of the Stimulus And Production Of The Signal Thatmentioning
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