Colombo V, Fernández-de-Heredia M, Malpartida F
Centro Nacional de Biotecnologia, Campus de la Universidad Autónoma de Madrid, 28049 Cantoblanco, Madrid, Spain.
Microbiology (Reading). 2001 Nov;147(Pt 11):3083-92. doi: 10.1099/00221287-147-11-3083.
In the search for Type II polyketide synthases (PKSs) a DNA fragment was isolated from Streptomyces antibioticus ATCC 11891 (a producer of oleandomycin). DNA sequencing of the cloned fragment revealed six complete ORFs whose deduced products showed similarities to those of other genes known to be involved in polyketide biosynthesis. Several S. coelicolor strains mutated in different steps of actinorhodin biosynthesis (actI, actIII, actV(A) and actVII) were complemented by the cloned genes, suggesting that the isolated genes encode an aromatic polyketide of unknown structure and function. The cluster also contains a putative LysR-type transcriptional regulator (ORF0), which controls PKS gene expression in a heterologous host. DNA binding assays and transcriptional analysis suggest that the pathway-specific regulator for actinorhodin biosynthesis (actII-ORF4) is also involved in the expression of the cloned PKS in the host strain.
在寻找II型聚酮合酶(PKSs)的过程中,从抗生链霉菌ATCC 11891(竹桃霉素的产生菌)中分离出一个DNA片段。对克隆片段进行DNA测序,发现有六个完整的开放阅读框(ORF),其推导产物与已知参与聚酮生物合成的其他基因的产物具有相似性。在放线紫红素生物合成不同步骤(actI、actIII、actV(A)和actVII)发生突变的几种天蓝色链霉菌菌株被克隆基因互补,这表明分离出的基因编码一种结构和功能未知的芳香族聚酮。该基因簇还包含一个假定的LysR型转录调节因子(ORF0),它在异源宿主中控制PKS基因的表达。DNA结合试验和转录分析表明,放线紫红素生物合成的途径特异性调节因子(actII-ORF4)也参与宿主菌株中克隆的PKS的表达。