Dose responses of gibberellins

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Abstract
To determine the response type, published data for the most widely used bioassays for gibberellins have been analyzed by means of a computer program for estimating sensitivity parameters, or by interpolation. The dose response data are almost uniformly subsensitive, i. e. more than an 81‐fold increase in external gibberellin concentration is required for a change from 10 to 90% of maximal response (S90/S10). Data for the interaction of gibberellins with artificial membranes are, in contrast, markedly ultrasensitive (S90/S10± 10). This difference further strengthens the view that lipid structures do not function as receptors for gibberellins. Most of the subsensitive dose responses for gibberellins can be quite precisely represented by cooperative isotherms. However, available data are insufficiently detailed for an unequivocal choice among cooperative, multiphasic or more complex kinetics.