Sharma Vasudha, Kelly Gilbert T, Foulke-Abel Jennifer, Watanabe Coran M H
Department of Chemistry, Texas A&M University, College Station, Texas 77843, USA.
Org Lett. 2009 Sep 3;11(17):4006-9. doi: 10.1021/ol9016639.
Experiments reveal that the metabolic precursor aminoacetone is a key intermediate in the production of the antitumor agent azinomycin A relative to the structurally and functionally related agent, azinomycin B. Azinomycin A and B arise through bifurcation of the biosynthetic pathway and competition between metabolic substrates. The availability of the biosynthetic precursors in vivo, aminoacetone for azinomycin A and threonine for azinomycin B, controls the overall ratio of azinomycin A to B produced.