化学
生物合成
天然产物
酶
产品(数学)
生物化学
立体化学
有机化学
酶催化
自然(考古学)
水解
键裂
组合化学
作者
Jingkun Shi,Guiyun Zhao,Yi‐Ling Du
出处
期刊:Chemical Reviews
[American Chemical Society]
日期:2026-04-22
卷期号:126 (9): 5518-5584
被引量:1
标识
DOI:10.1021/acs.chemrev.5c01091
摘要
Nitrogen–nitrogen (N–N) bonds constitute essential structural motifs in numerous bioactive natural products and pharmaceuticals. Recent advances in genomics and biochemistry have unveiled diverse enzymatic strategies employed by nature to forge these chemically challenging linkages. This review highlights the discovery and mechanistic elucidation of key enzyme families responsible for N–N bond formation, including heme-dependent hydrazine synthases, zinc-dependent hydrazine synthetases, ATP-dependent diazotases or N -nitrosylases, and membrane-bound hydrazine synthases and diazotase. We summarize the biosynthetic pathways of representative N–N-containing natural products, emphasizing the catalytic logic and chemical ingenuity of these enzymes. Understanding these biological routes not only expands the enzymology of N–N bond formation but also provides a foundation for biocatalyst development and genome-driven discovery of novel bioactive compounds.
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