Artificial Biosynthetic Pathway for an Unnatural Terpenoid with an Iridiumcontaining P450

18 March 2020, Version 1
This content is a preprint and has not undergone peer review at the time of posting.

Abstract

Synthetic biology enables microbial hosts to produce complex molecules that are
otherwise produced by organisms that are rare or difficult to cultivate, but the structures of these
molecules are limited to chemical reactions catalyzed by natural enzymes. The integration of
artificial metalloenzymes (ArMs) that catalyze abiotic reactions into metabolic networks could
broaden the cache of molecules produced biosynthetically by microorgansms. We report the
assembly of an ArM containing an iridium-porphyrin complex in the cytoplasm of a terpene
producing Escherichia coli by a heterologous heme transport machinery, and insertion of this ArM
into a natural biosynthetic pathway to produce an unnatural terpenoid. This work shows that
synthetic biology and synthetic chemistry, incorporated together in whole cells, can produce
molecules previously inaccessible to nature.

Keywords

artificial metalloenzyme
heterologous biosynthesis
synthetic biology
P450
cyclopropanation
terpene

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