生物合成
化学
酶
辅因子
铁氧还蛋白
立体化学
突变
药物发现
辅酶A
化学合成
双键
生物化学
单一债券
组合化学
生物催化
蛋白质工程
蛋白质结构
酶催化
转氨作用
肽键
作者
Yuchun Zhao,Zhihong Xiao,Xiangyang Liu,Chenxi Zhu,Xianwen Liang,Xinyi He,Shuangjun Lin,Zixin Deng,Ming Jiang
出处
期刊:Angewandte Chemie
[Wiley]
日期:2025-10-24
卷期号:64 (50): e202513778-e202513778
被引量:2
标识
DOI:10.1002/anie.202513778
摘要
A nitrogen-nitrogen (N─N) bond is a core feature of diverse natural products with interesting structural and biological properties. Kinamycin and lomaiviticin, featuring a diazobenzo[b]fluorene core, exhibit exceptional potency as chemotherapeutic agents. However, the N─N bond forming step in their biosynthesis has remained elusive. Through extensive mutagenesis and biochemical studies, we herein report that Alp1J, belonging to a new family of heme-dependent enzymes, catalyzes the N─N bond formation in kinamycin biosynthesis. Interestingly, Alp1J forms a stable complex with its partner ferredoxin Alp1I, which can protect the cofactors and is critical for the N─N bond formation activity. With its partner ferredoxin, Alp1J catalyzes formation of the hydrazine intermediate directly from l-aspartate and nitrite by a pathway involving four-electron reduction. Our findings expand the knowledge of enzymatic N─N bond formation and show the potential for the discovery and development of novel N─N bond containing natural products through genome mining and synthetic biology.
科研通智能强力驱动
Strongly Powered by AbleSci AI