Related Experiment Video
Updated: May 3, 2026

A Flexible Low Cost Hydroponic System for Assessing Plant Responses to Small Molecules in Sterile Conditions
Published on: August 25, 2018
Structural modification of gibberellins by in-vitro hydroxylating systems
R L Jones1, J L Stoddart, J Macmillan
1Department of Botany, University of California, Berkeley, U.S.A..
Abstract:
The behaviour of gibberellins A4, A5 and A7 (GA4, GA5 and GA7) has been studied in various in vitro hydroxylating systems. Incubation of GA4 and GA7 in peroxidase/dihydroxyfumarate or tyrosinase/ascorbate formulations resulted in the production of additional biologically-active zones on thin-layer chromatograms of the reaction mixtures. The product from GA7/peroxidase incubations was conclusively identified as GA7 norketone by gas/liquid chromatography-mass spectrometry and nuclear magnetic resonance spectrometry. A similar reaction is inferred for GA4 in the same system and for both GA4 and GA7 with tyrosinase/ascorbate. By analogy, the product derived from GA5 in the non-enzymatic ascorbate/ferrous iron system may be GA5 norketone. The reaction kinetics and the biological activity of the products are discussed.
Related Concept Videos
Hydrolysis
Hydrolysis is a chemical reaction in which the addition of water breaks down a polymer into its simpler monomer units. For example, peptides break into amino acids, carbohydrates into simple sugars, and DNA into nucleotides. Enzymes often facilitate these processes.
Hydrolysis Reverses Dehydration Synthesis
Complex carbohydrates can be broken down by breaking the bonds between individual sugar units. The reaction breaks a glycosidic bond as water is added to the compound. The...
Alkynes to Aldehydes and Ketones: Hydroboration-Oxidation
One of the convenient methods for the preparation of aldehydes and ketones is via hydration of alkynes. Hydroboration-oxidation of alkynes is an indirect hydration reaction in which an alkyne is treated with borane followed by oxidation with alkaline peroxide to form an enol that rapidly converts into an aldehyde or a ketone. Terminal alkynes form aldehydes, whereas internal alkynes give ketones as the final product.
Aldehydes and Ketones with Water: Hydrate Formation
The formation of hydrates is a reversible reaction. Hydrate formation is influenced by steric and electronic factors accompanying the alkyl substituents on the carbonyl group: The rate of hydrate formation increases with a decrease in the number of alkyl groups attached to the carbonyl carbon. Hence,...

