The role of gibberellin biosynthesis in the control of growth and flowering in Matthiola incana

Abstract

Recently, it was found that stem elongation and flowering of stock Matthiola incana (L.) R. Br. are promoted by exogenous gibberellins (GAs), including GA4, and also by acylcyclohexanedione inhibitors of GA biosynthesis, such as prohexadione‐calcium (PCa) and trinexapac‐ethyl (TNE). Here, because it was unclear how GA biosynthetic inhibitors could promote stem elongation and flowering, their effect on GA biosynthesis has been examined by quantifying endogenous GA levels; also, the sensitivity of stem elongation and flowering to various GAs in combination with the inhibitors was examined. Stem elongation and flowering were most effectively promoted by GA4 when combined with PCa and, next in order, by 2,2‐dimethyl‐GA4, PCa, GA4+TNE, TNE, GA9+PCa and by GA4. There was little or no promotion by GA1, GA3, GA9, GA13, GA20 and 3‐epi‐2,2‐dimethyl‐GA4. Both the promotive effects of the acylcyclohexanediones on stem elongation and flowering, particularly when applied with GA4, and the fact that TNE caused a build‐up of endogenous GA4 imply that one effect of TNE at the lower dose involved an inhibition of 2β‐hydroxylation of GA4 rather than an inhibition of 20‐oxidation and 3β‐hydroxylation of GAs which were precursors of GA4. Overall, these results indicate that: (1) GAs with 3β‐OH and without 13‐OH groups (e.g. GA4) are the most important for stem elongation and flowering in M. incana; (2) growth promotion rather than inhibition can result if an acylcyclohexanedione acts predominantly to slow 2β‐hydroxylation and so slows inactivation of active gibbberellins, including GA4. It follows that a low dose of an acylcyclohexanedione can be a ‘growth enhancer’ for any applied GA that is liable to inactivation by 2β‐hydroxylation.