Yin Jia, Hoffmann Michael, Bian Xiaoying, Tu Qiang, Yan Fu, Xia Liqiu, Ding Xuezhi, Stewart A Francis, Müller Rolf, Fu Jun, Zhang Youming
Shandong University-Helmholtz Institute of Biotechnology, State Key Laboratory of Microbial Technology, School of Life Science, Shandong University, Shanda Nanlu 27, Jinan, 250100, People's Republic of China.
Department of Genomics, Dresden University of Technology, BioInnovations-Zentrum, Tatzberg 47-51, Dresden, 01307, Germany.
Sci Rep. 2015 Oct 13;5:15081. doi: 10.1038/srep15081.
Linear plus linear homologous recombination-mediated recombineering (LLHR) is ideal for obtaining natural product biosynthetic gene clusters from pre-digested bacterial genomic DNA in one or two steps of recombineering. The natural product salinomycin has a potent and selective activity against cancer stem cells and is therefore a potential anti-cancer drug. Herein, we separately isolated three fragments of the salinomycin gene cluster (salO-orf18) from Streptomyces albus (S. albus) DSM41398 using LLHR and assembled them into intact gene cluster (106 kb) by Red/ET and expressed it in the heterologous host Streptomyces coelicolor (S. coelicolor) A3(2). We are the first to report a large genomic region from a Gram-positive strain has been cloned using LLHR. The successful reconstitution and heterologous expression of the salinomycin gene cluster offer an attractive system for studying the function of the individual genes and identifying novel and potential analogues of complex natural products in the recipient strain.
线性加线性同源重组介导的重组工程(LLHR)非常适合通过一到两步重组工程从预先消化的细菌基因组DNA中获得天然产物生物合成基因簇。天然产物沙利霉素对癌症干细胞具有强大且选择性的活性,因此是一种潜在的抗癌药物。在此,我们使用LLHR从白色链霉菌(S. albus)DSM41398中分别分离出沙利霉素基因簇(salO-orf18)的三个片段,并通过Red/ET将它们组装成完整的基因簇(106 kb),并在异源宿主天蓝色链霉菌(S. coelicolor)A3(2)中进行表达。我们首次报道了使用LLHR克隆革兰氏阳性菌株的一个大基因组区域。沙利霉素基因簇的成功重建和异源表达为研究单个基因的功能以及鉴定受体菌株中复杂天然产物的新型和潜在类似物提供了一个有吸引力的系统。