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来自链霉菌菌株WP 4669的PD 116740以及来自龟裂链霉菌NRRL 3016的四方醇和四方霉素的整个基因簇的克隆及异源表达。

Cloning and heterologous expression of the entire gene clusters for PD 116740 from Streptomyces strain WP 4669 and tetrangulol and tetrangomycin from Streptomyces rimosus NRRL 3016.

作者信息

Hong S T, Carney J R, Gould S J

机构信息

Department of Biochemistry and Biophysics, Oregon State University, Corvallis 97331-4003, USA.

出版信息

J Bacteriol. 1997 Jan;179(2):470-6. doi: 10.1128/jb.179.2.470-476.1997.

Abstract

The genes for the complete pathways for two polycyclic aromatic polyketides of the angucyclinone class have been cloned and heterologously expressed. Genomic DNAs of Streptomyces rimosus NRRL 3016 and Streptomyces strain WP 4669 were partially digested with MboI, and libraries (ca. 40-kb fragments) in Escherichia coli XL1-Blue MR were prepared with the cosmid vector pOJ446. Hybridization with the actI probe from the actinorhodin polyketide synthase genes identified two clusters of polyketide genes from each organism. After transfer of the four clusters to Streptomyces lividans TK24, expression of one cluster from each organism was established through the identification of pathway-specific products by high-performance liquid chromatography with photodiode array detection. Peaks were identified from the S. rimosus cluster (pksRIM-1) for tetrangulol, tetrangomycin, and fridamycin E. Peaks were identified from the WP 4669 cluster (pksWP-2) for tetrangulol, 19-hydroxytetrangulol, 8-O-methyltetrangulol, 19-hydroxy-8-O-methyltetrangulol, and PD 116740. Structures were confirmed by 1H nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry.

摘要

已克隆并异源表达了环内酯类两种多环芳香聚酮化合物完整生物合成途径的基因。用MboI对龟裂链霉菌NRRL 3016和链霉菌菌株WP 4669的基因组DNA进行部分酶切,并用黏粒载体pOJ446在大肠杆菌XL1-Blue MR中构建文库(约40 kb片段)。用来自放线紫红素聚酮合酶基因的actI探针进行杂交,从每个生物体中鉴定出两个聚酮基因簇。将这四个基因簇转移到变铅青链霉菌TK24后,通过用光电二极管阵列检测的高效液相色谱法鉴定途径特异性产物,确定了每个生物体中一个基因簇的表达。从龟裂链霉菌基因簇(pksRIM-1)中鉴定出了四棱菌素、四棱霉素和弗氏霉素E的峰。从WP 4669基因簇(pksWP-2)中鉴定出了四棱菌素、19-羟基四棱菌素、8-O-甲基四棱菌素、19-羟基-8-O-甲基四棱菌素和PD 116740的峰。通过1H核磁共振光谱和高分辨率质谱对结构进行了确认。

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Appl Environ Microbiol. 1993 Jul;59(7):2220-8. doi: 10.1128/aem.59.7.2220-2228.1993.
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