Sinapic Acid Ester Metabolism in Wild Type and a Sinapoylglucose-Accumulating Mutant of Arabidopsis
Open Access
- 1 December 1996
- journal article
- Published by Oxford University Press (OUP) in Plant Physiology
- Vol. 112 (4) , 1625-1630
- https://doi.org/10.1104/pp.112.4.1625
Abstract
Sinapoylmalate is one of the major phenylpropanoid metabolites that is accumulated in the vegetative tissue of Arabidopsis thaliana. A thin-layer chromatography-based mutant screen identified two allelic mutant lines that accumulated sinapoylglucose in their leaves in place of sinapoylmalate. Both mutations were found to be recessive and segregated as single Mendelian genes. These mutants define a new locus called SNG1 for sinapoylglucose accumulator. Plants that are homozygous for the sng1 mutation accumulate normal levels of malate in their leaves but lack detectable levels of the final enzyme in sinapate ester biosynthesis, sinapoylglucose:malate sinapoyltransferase. A study of wild-type and sng1 seedlings found that sinapic acid ester biosynthesis in Arabidopsis is developmentally regulated and that the accumulation of sinapate esters is delayed in sng1 mutant seedlings.Keywords
This publication has 8 references indexed in Scilit:
- Ferulate-5-hydroxylase from Arabidopsis thaliana defines a new family of cytochrome P450-dependent monooxygenases.Proceedings of the National Academy of Sciences, 1996
- Arabidopsis Mutants Lacking Phenolic Sunscreens Exhibit Enhanced Ultraviolet-B Injury and Oxidative DamagePlant Physiology, 1995
- Analysis of Arabidopsis mutants deficient in flavonoid biosynthesisThe Plant Journal, 1995
- Altered Growth and Cell Walls in a Fucose-Deficient Mutant of ArabidopsisScience, 1993
- Arabidopsis Flavonoid Mutants Are Hypersensitive to UV-B Irradiation.Plant Cell, 1993
- An Arabidopsis mutant defective in the general phenylpropanoid pathway.Plant Cell, 1992
- Effects of ionizing radiation on a plant genome: analysis of two Arabidopsis transparent testa mutations.Plant Cell, 1992
- A Rapid and Sensitive Method for the Quantitation of Microgram Quantities of Protein Utilizing the Principle of Protein-Dye BindingAnalytical Biochemistry, 1976