Phytoalexin synthesis in soybean cells: Elicitor induction of reductase involved in biosynthesis of 6′-deoxychalcone

Abstract

Chromatofocusing on Mono P proved to be an efficient purification procedure for the NADPH-dependent reductase from soybean ( Glycine max L.) cell cultures which acts together with chalcone synthase in the biosynthesis of 2′,4′,4-trihydroxychalcone (6′-deoxychalcone). By isoelectric focusing the p I of reductase was determined to be 6.3. Addition of pure soybean reductase to cell-free extracts from stimulated cell cultures of parsley and bean ( Phaseolus vulgaris) and from young flowers of Dahlia variabilis caused in each case synthesis of 6′-deoxychalcone. When 4-coumaroyl-CoA was replaced by caffeoyl-CoA in the reductase assay, formation of 2′,4′,3,4-tetrahydrochalcone (butein) was observed. A polyclonal antireductase antiserum was raised in rabbits and proved to be specific in Ouchterlony diffusion experiments, Western blots and immunotitration. The reductase antiserum showed no cross-reactivity with soybean chalcone synthase (CHS). A biotin/[ 125I]streptavidin system provided a quantitative Western blot for the reductase. Changes in the activities, amounts of protein, and mRNA activities of reductase and CHS were determined after challenge of soybean cell cultures by elicitor (from Phytophthora megasperma f.sp. glycinea or yeast). For both enzymes a pronounced and parallel increase in activity and amounts of protein was observed after elicitor addition with a maximum at about 16 h after challenge. Parallel increases in mRNA activities occurred earlier. The results indicate a parallel induction of de novo synthesis of reductase and CHS which coact in synthesis of 6′-deoxychalcone.