Enzyme Profiles in Seedling Development and the Effect of Itaconate, an Isocitrate Lyase-directed Reagent
- PMID: 16660938
- PMCID: PMC543060
- DOI: 10.1104/pp.64.2.228
Enzyme Profiles in Seedling Development and the Effect of Itaconate, an Isocitrate Lyase-directed Reagent
Abstract
Changes in levels of isocitrate lyase, malate synthase, and catalase have been investigated during germination of flax (Linum usitatissimum L.) in the presence and absence of itaconate. Germination was accompanied by a rapid increase in these enzymes during the first 3 days. The presence of 38 millimolar itaconate inhibited the incidence of seed germination and the growth of embryo axes as well as the appearance of isocitrate lyase but did not alter the levels of malate synthase, catalase, or NADP(+)-isocitrate dehydrogenase. The specific activity for the latter enzyme was constant throughout germination. Oxalate or succinate, each at 38 millimolar, had no effect upon germination of flax seeds. Itaconate did not inhibit the activities of malate synthase, catalase, or NADP(+)-isocitrate dehydrogenase in vitro but was a potent noncompetitive inhibitor of isocitrate lyase (K(i):17 micromolar at 30 C, pH 7.6). Itaconate (at 38 millimolar) did not alter the appearance of malate synthase but reduced the incidence of germination, onset of germination, and growth of the embryo axis as well as the specific activity of isocitrate lyase in seedlings of Zea mays, Vigna glabra, Glycine hispida, Vigna sinensis, Trigonella foenumgraecum, Lens culinaris, and Medicago sativa. The incidence and onset of germination of wheat seeds were unaltered by the same concentration of itaconate but seedlings did not contain isocitrate lyase or malate synthase. The data suggest that itaconate may be isocitrate lyase-directed in inhibiting the germination of fatty seeds.
Similar articles
-
Regulation of glyoxysomal enzymes during germination of cucumber. Temporal changes in translatable mRNAs for isocitrate lyase and malate synthase.Eur J Biochem. 1980 Dec;112(3):469-77. Eur J Biochem. 1980. PMID: 6161814
-
Isocitrate lyase and malate synthase in Pseudomonas indigofera. I. Suppression and stimulation during growth.J Bacteriol. 1962 Dec;84(6):1216-21. doi: 10.1128/jb.84.6.1216-1221.1962. J Bacteriol. 1962. PMID: 13955177 Free PMC article.
-
Regulation of acetate metabolism in Corynebacterium glutamicum: transcriptional control of the isocitrate lyase and malate synthase genes.Arch Microbiol. 1997 Oct;168(4):262-9. doi: 10.1007/s002030050497. Arch Microbiol. 1997. PMID: 9297462
-
Advances in mycobacterial isocitrate lyase targeting and inhibitors.Curr Med Chem. 2012;19(36):6126-37. doi: 10.2174/092986712804485782. Curr Med Chem. 2012. PMID: 23092127 Review.
-
Regulation of acetate metabolism by protein phosphorylation in enteric bacteria.Annu Rev Microbiol. 1998;52:127-64. doi: 10.1146/annurev.micro.52.1.127. Annu Rev Microbiol. 1998. PMID: 9891796 Review.
Cited by
-
Gene isolation and characterization of two acyl CoA oxidases from soybean with broad substrate specificities and enhanced expression in the growing seedling axis.Plant Mol Biol. 2001 Nov;47(4):519-31. doi: 10.1023/a:1011825114301. Plant Mol Biol. 2001. PMID: 11669577
-
Comparison of the glyoxysomes and the glyoxysomal enzymes in maize lines with high or low oil content.Plant Physiol. 1983 Mar;71(3):447-50. doi: 10.1104/pp.71.3.447. Plant Physiol. 1983. PMID: 16662846 Free PMC article.
-
The crystal structure of mouse IRG1 suggests that cis-aconitate decarboxylase has an open and closed conformation.PLoS One. 2020 Dec 1;15(12):e0242383. doi: 10.1371/journal.pone.0242383. eCollection 2020. PLoS One. 2020. PMID: 33259501 Free PMC article.
-
Imidazolinones and acetohydroxyacid synthase from higher plants: properties of the enzyme from maize suspension culture cells and evidence for the binding of imazapyr to acetohydroxyacid synthase in vivo.Plant Physiol. 1987 Feb;83(2):451-6. doi: 10.1104/pp.83.2.451. Plant Physiol. 1987. PMID: 16665267 Free PMC article.
References
LinkOut - more resources
Full Text Sources