Gu Di, Zhai Rui, Daymo Bailey, Xie Yuxin, Luo Caroline, Zhang Wenjun
Department of Chemistry, University of California, Berkeley, California 94720, United States.
Department of Chemical and Biomolecular Engineering, University of California, Berkeley, California 94720, United States.
Biochemistry. 2024 Dec 17;63(24):3213-3219. doi: 10.1021/acs.biochem.4c00515. Epub 2024 Dec 4.
Salivabactin is a newly identified polyketide/nonribosomal peptide (PK/NRP) from a human oral probiotic, possessing a unique chemical structure and outstanding antibiotic activities. Although the biosynthetic gene cluster for salivabactin is known, the enzymatic logic that governs the synthesis of salivabactin has not yet been fully studied. In this work, we dissected the biosynthetic pathway for salivabactin using biochemical analysis. We successfully reconstituted the enzymatic synthesis of salivabactin in vitro, identified the minimal set of enzymes required for its biosynthesis, and revealed an unusual thioesterase domain involved in terminal olefin formation.
唾液杆菌素是一种新发现的来自人类口腔益生菌的聚酮化合物/非核糖体肽(PK/NRP),具有独特的化学结构和出色的抗菌活性。尽管唾液杆菌素的生物合成基因簇已为人所知,但控制唾液杆菌素合成的酶学逻辑尚未得到充分研究。在这项工作中,我们通过生化分析剖析了唾液杆菌素的生物合成途径。我们成功地在体外重建了唾液杆菌素的酶促合成,确定了其生物合成所需的最小酶集,并揭示了一个参与末端烯烃形成的不寻常硫酯酶结构域。