胍
生物化学
烟草
异源表达
酶
细菌
化学
天然产物
异源的
生物合成
丙炔基转移酶
预酸化
生物
生物有机化学
作者
Dominik Kolling,Katharina Stemwedel,Daghan Taser,Tom Jentsch,Svenja Schwoerer,Henry Struwe,Arne Bültemeier,Jonas Freiberg,Claus‐Peter Witte,Jakob Franke,Andriy N. Luzhetskyy,Andreas Kirschning,Sophia Rudorf,Jesko Koehnke
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2026-10-22
卷期号:394 (6822): 413-418
标识
DOI:10.1126/science.aeg1821
摘要
Guanidine exists almost exclusively as a resonance-stabilized cation, making its direct enzymatic functionalization challenging. We identified the cyanobacterial enzyme NosH, which catalyzes direct prenyl transfer to free guanidine. Structural and mechanistic analyses revealed guanidine activation by a two-aspartate clamp coupled to prenyl-donor binding through a distinct catalytic architecture. Guided by these features, we identified a large family of guanidine prenyltransferases across bacteria and plants. Plant enzymes produced guanidine alkaloids such as galegine in vitro and heterologous expression of a plant ortholog in Nicotiana benthamiana produced galegine in planta, providing a direct enzymatic link to plant-specialized metabolism.
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