Identification of an unexpected shunt pathway product provides new insights into tirandamycin biosynthesis

Tetrahedron Lett. 2016 Dec 28;57(52):5919-5923. doi: 10.1016/j.tetlet.2016.11.080. Epub 2016 Nov 19.

Abstract

Tirandamycin K (7), the first linear 7,13;9,13-diseco-tirandamycin derivative, was isolated from the tamI (encoding the TamI P450 monooxygenase) disruption mutant strain (ΔtamI) of marine Streptomyces sp. 307-9. Its chemical structure with relative and absolute configurations was elucidated by a combination of extensive spectroscopic analyses and biosynthetic inferences. Structural elucidation of this unusual compound provides new insights into tirandamycin biosynthesis. Moreover, examination of the biological activity of 7 confirms the essential function of the bicyclic ketal ring for antibiotic activities of tirandamycins.

Keywords: Biosynthesis; Natural product; Streptomyces; Tetramic acid; Tirandamycin.