Gibberellins inhibitors

Uses Plant growth regulator gibberellin inhibitor... 

Bismuth subgallate gibberellin inhibitor Paclobutrazol gingivitis control agent Chlorhexidine glass... 

In addition to inhibitory chemicals which enter the plant from the external environment, many endogenous inhibitors appear to function as regulators of seed germination and plant growth and development. The interrelationships between endogenous inhibitors and growth promoters such as the auxins, gibberellins, and kinins remain to be elucidated. 

Bioassay procedures for the determination of gibberellic acid have been developed (2, 5), but more recent chemical fluorometric assay methods are equally specific. However, both assay methods show a low response with samples containing less than 10 /x/xg. of the gibberellins. Consequently, in determining residual amounts within the part per billion (p.p.b.) range, relatively large samples must be extracted and extracts partially purified to satisfy the assay conditions. These operations are usually accompanied by some material losses or degradation, which impair quantitative interpretation of the results. Natural inhibitors can influence the results in the bioassay method (2), and fluorescent contaminants can interfere with the spectrophotometric analysis. 

Many compounds have been tested simultaneously with (2-chloroethyl)tri-methylammonium chloride on Thatcher wheat, to ascertain, if possible, whether these chemicals were affecting a particular metabolic process. Other cholinesterase inhibitors such as eserine, diisopropyl fluorophosphate, and nitrogen mustard, neither negated the effect from (2-chloroethyl)trimethylammonium chloride nor altered the growth of the plant themselves. Many other substances were also without effect on the action of (2-chloroethyl)trimethylammonium chloride. A very slight reversal of the alteration by (2-chloroethyl)trimethylam-monium chloride was obtained by 10 2 and 10 3 M choline, betaine, and adenine. Only gibberellin completely and rapidly reversed the shorter growth pattern of a plant which had been treated with (2-chloroethyl)trimethylammonium chloride. 

Kim, H. Y., and Suzuki, Y. (1989). Changes in assimilated BC distribution and soluble acid invertase activity of Zinnia elegans induced by Uniconazol an inhibitor of gibberellin biosynthesis. Plant Physiol. 90, 316-321. 

Aphidicolin is a diterpenoid metabolite of Cephalosporium aphidicola and Phoma betae. The strueture of aphidieolin (5.126) was established in 1972 through a eombination of ehemieal, spectroseopie and X-ray crystallographic studies. Unlike the ent-kaurene and gibberellin metabolites of G. fujikuroi, aphidicolin possesses an absolute stereochemistry that is steroid-like . It has attracted considerable interest as a specific inhibitor of DNA polymerase a and as a potential anti-viral and anti-tumour agent. 

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