Characterization and activities of S-adenosyl-l-methionine:cyanidin 3-glucoside 3′-O-methyltransferase in relation to anthocyanin accumulation in Vitis vinifera cell suspension cultures

Autor: Chi Bao Do, François Cormier, Christophe Bailly
Rok vydání: 1997
Předmět:
Zdroj: Plant Science. 122:81-89
ISSN: 0168-9452
Popis: A cell suspension of Vitis vinifera cv Gamay Freaux was grown in a maintenance and an anthocyanin-promoting medium (APM). Time-course changes in anthocyanin accumulation and S -adenosyl- l -methionine:cyanidin 3-glucoside 3′- O -methyltransferase (CGMT) activity were examined throughout the growth cycle. An increase in anthocyanin accumulation mainly due to peonidin 3-glucoside and peonidin 3- p -coumaroylglucoside i.e. 3′-methylated derivatives of cyanidin 3-glucoside (Cy3G), of cells grown in APM was observed. The higher activity of CGMT in cells grown in the APM might be responsible for the enhanced formation of 3′-methylated anthocyanins. CGMT isolated from cell suspension cultures has been purified approx. 35-fold with 3.4% enzyme activity recovery using anion exchange, chromatofocusing and gel filtration liquid chromatography. Mg 2+ ions strongly enhanced the reaction rate at a concentration of 5 mM. Optimal pH of CGMT ranged from 7.75 to 9.75. Michaelis-Menten kinetics were observed at pH 8.75 with respect to the substrates Cy3G and S -adenosyl- l -methionine with K m values of 199 and 18 μM respectively. S -adenosyl- l -homocysteine showed a non-competitive inhibition with an approx. K i value of 50 μM. Relative to Cy3G, the activity of CGMT was 13% with cyanidin. No activity was observed with delphinidin or cyanidin 3- p -coumaroylglucoside.
Databáze: OpenAIRE