Related Experiment Video
Updated: Jul 23, 2026

Metabolic Labeling of Newly Transcribed RNA for High Resolution Gene Expression Profiling of RNA Synthesis, Processing and Decay in Cell Culture
Published on: August 8, 2013
Synthesis and biochemical properties of Z- and E-4,5-dehydrodethiobiotin
E Jestin1, F Moreau, D Florentin
1Laboratoire de Chimie Organique Biologique, Université P. et M. Curie, URA CNRS 493, Paris, France.
Abstract:
Radical species are postulated intermediates in the formation of the carbon-sulfur bonds of biotin. It was of interest to examine the behaviour of unsaturated analogues which should give rise to allylic radicals. The two isomers of 4,5-dehydrodethiobiotin have been synthesized and labelled with 14C on their carboxylic acid group. When incubated with an in vitro system capable of transforming dethiobiotin into biotin, they covalently label biotin synthase.
Related Concept Videos
E2 Reaction: Stereochemistry and Regiochemistry
When a substrate with two different β hydrogens undergoes an E2 elimination, the presence of a strong base can yield two regioisomeric alkenes. The more-substituted alkene is the major product and...
E1 Reaction: Stereochemistry and Regiochemistry
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Biosynthesis of Nucleic Acids
Production of Pharmaceuticals

