Complete biosynthesis of nicotine
Summary
Nicotine, tobacco's addictive and potent insecticidal alkaloid, has shaped human history, agriculture, and the plants that produce it. However, the enzymatic steps and reaction mechanisms involved in nicotine biosynthesis remain elusive. Here, we reveal that the final coupling reaction is stabilized by glycosylation via a uridine diphosphate (UDP)-glycosyltransferase, reduced and activated by an A622, condensed through a stereoselective intermolecular Mannich-like reaction, sequentially ox
Content
# Complete biosynthesis of nicotine
*Published: 2026 Apr 30*
Nicotine, tobacco's addictive and potent insecticidal alkaloid, has shaped human
history, agriculture, and the plants that produce it. However, the enzymatic
steps and reaction mechanisms involved in nicotine biosynthesis remain elusive.
Here, we reveal that the final coupling reaction is stabilized by glycosylation
via a uridine diphosphate (UDP)-glycosyltransferase, reduced and activated by an
A622, condensed through a stereoselective intermolecular Mannich-like reaction,
sequentially oxidized by a berberine bridge enzyme-like (BBL), and finally
deglycosylated by a β-glucosidase to yield nicotine. A 5-component metabolon
assembles at vacuolar membranes to channel both nicotine biosynthesis and its
transport. We reconstituted this metabolon both in vitro and heterologously in
vivo. Abrogating any of these components depletes nicotine accumulations. A
multidrug and toxic compound extrusion (MATE) transporter is essential for
efficiently engineering nicotine production in heterologous plant species, which
confers pest resistance. This work completes the nicotine biosynthesis pathway
and provides critical insights into the intermolecular Mannich-like reaction, a
fundamental mechanism for scaffold formation in many plant alkaloids.
DOI: 10.1016/j.cell.2026.03.034