Functional characterization of a chalcone synthase from the liverwort Plagiochasma appendiculatum
Flavonoids
Hepatophyta
Models, Molecular
0303 health sciences
Molecular Sequence Data
Gene Expression
Cyclopentanes
Acetates
Recombinant Proteins
Biosynthetic Pathways
Anthocyanins
03 medical and health sciences
Chalcones
Plant Growth Regulators
Flavanones
Marchantia
Amino Acid Sequence
Oxylipins
Salicylic Acid
Acyltransferases
Phylogeny
Abscisic Acid
DOI:
10.1007/s00299-014-1702-8
Publication Date:
2014-11-21T11:31:10Z
AUTHORS (6)
ABSTRACT
A chalcone synthase gene ( PaCHS ) was isolated and functionally characterized from liverwort. The ectopic expression of PaCHS in Marchantia paleacea callus raised the flavonoids content. Chalcone synthase (CHS; EC 2.3.1.74) is pivotal for the biosynthesis of flavonoid and anthocyanin pigments in plants. It produces naringenin chalcone by condensing one p-coumaroyl- and three malonyl-coenzyme A thioesters through a polyketide intermediate that is cyclized by intramolecular Claisen condensation. Although CHSs of higher plants have been extensively studied, enzyme properties of the CHSs in liverworts have been scarcely characterized. In this study, we report the cloning and characterization of CHS (designated as PaCHS) from the liverwort Plagiochasma appendiculatum. The gene product was 60-70 % identical with chalcone synthases from other species, and contained the characteristic conserved Cys-His-Asn catalytic triad. The recombinant PaCHS was able to catalyze p-coumaroyl-CoA and malonyl-CoA to generate naringenin in vitro. Heterologously expressed PaCHS protein showed similar kinetic properties to those of higher plant CHS. The ectopic expression of PaCHS in Marchantia paleacea callus raised the content of the total flavonoids. These results suggested that PaCHS played a key role in the flavonoids biosynthesis in liverworts. Furthermore, when the thallus of P. appendiculatum was treated with abiotic stress inducers methyl jasmonate, salicylic acid and abscisic acid, PaCHS expression was enhanced. This is the first time that a CHS in liverworts has been functionally characterized.
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