The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kemitorvet 220, 2800 Kgs. Lyngby, Denmark.
Fundación MEDINA, Centro de Excelencia en Investigación de Medicamentos Innovadores en Andalucía, Avenida del Conocimiento, 34 Parque Tecnológico de Ciencias de la Salud, 18016 Armilla, Granada, Spain.
ACS Chem Biol. 2022 Sep 16;17(9):2411-2417. doi: 10.1021/acschembio.2c00480. Epub 2022 Aug 30.
Actinomycetes make a wealth of complex, structurally diverse natural products, and a key challenge is to link them to their biosynthetic gene clusters and delineate the reactions catalyzed by each of the enzymes. Here, we report the biosynthetic gene cluster for pyracrimycin A, a set of nine genes that includes a core nonribosomal peptide synthase () that utilizes serine and proline as precursors and a monooxygenase () that catalyzes Baeyer-Villiger oxidation. The cluster is similar to the one for brabantamide A; however, pyracrimycin A biosynthesis differs in that feeding experiments with isotope-labeled serine and proline suggest that a ring opening reaction takes place and a carbon is lost from serine downstream of the oxidation reaction. Based on these data, we propose a full biosynthesis pathway for pyracrimycin A.
放线菌产生了丰富多样的复杂天然产物,其中一个关键挑战是将它们与其生物合成基因簇联系起来,并阐明每个酶所催化的反应。在这里,我们报告了吡拉西罗霉素 A 的生物合成基因簇,该基因簇由九个基因组成,其中包括一个核心非核糖体肽合酶(NRPS),它利用丝氨酸和脯氨酸作为前体,以及一个单加氧酶(Monooxygenase),它催化 Baeyer-Villiger 氧化反应。该基因簇与布拉班塔米胺 A 的基因簇相似;然而,吡拉西罗霉素 A 的生物合成不同之处在于,用同位素标记的丝氨酸和脯氨酸进行的饲喂实验表明,开环反应发生,并且在氧化反应的下游,丝氨酸失去一个碳原子。基于这些数据,我们提出了吡拉西罗霉素 A 的完整生物合成途径。