Haydock Stephen F, Mironenko Tatiana, Ghoorahoo Haroun I, Leadlay Peter F
Department of Biochemistry, University of Cambridge, Tennis Court Road, CB2 1TN, UK.
J Biotechnol. 2004 Sep 30;113(1-3):55-68. doi: 10.1016/j.jbiotec.2004.03.022.
A type I PKS gene probe obtained from RAPB of the rapamycin producer Streptomyces hygroscopicus, strongly hybridised to 92 out of 1120 cosmids from a genomic library of the elaiophylin-producing strain Streptomyces sp. DSM4137. Partial cosmid sequencing suggested the presence of 10 separate sequences encoding type I PKS genes. One entire DNA sequence was obtained and found exactly to match the gene organisation expected for the biosynthesis of the unusual macrodiolide polyketide elaiophylin. The putative elaiophylin gene cluster contains five large open-reading frames encoding typical modular polyketide synthases, which together catalyse the synthesis of the octaketide monomer of elaiophylin. Other genes were identified that would be required for provision of the ethylmalonate extender unit, for the synthesis and attachment of 2-deoxy-L-fucose and in regulation, or in export of the product. Immediately adjacent to the putative elaiophylin biosynthetic gene cluster is a 30-kbp region containing the gene for adenosylcobalamin-dependent methylmalonyl CoA mutase and also genes involved in the biosynthesis of the cobalamin cofactor. Analysis of the latter gene set confirms the view that cbiD of the anaerobic pathway and cobF in the aerobic pathway catalyse the same methylation of precorrin-5. The proximity of these genes to the putative elaiophylin gene cluster can best be rationalised if in this organism succinyl-CoA is a significant source of the methylmalonate units for complex polyketide biosynthesis.
从雷帕霉素产生菌吸水链霉菌的RAPB中获得的I型聚酮合酶(PKS)基因探针,与产伊索霉素菌株链霉菌DSM4137基因组文库的1120个黏粒中的92个发生了强烈杂交。黏粒部分测序表明存在10个独立的编码I型PKS基因的序列。获得了一个完整的DNA序列,发现其与不寻常的大环二萜聚酮化合物伊索霉素生物合成预期的基因组织完全匹配。推测的伊索霉素基因簇包含五个大的开放阅读框,编码典型的模块化聚酮合酶,它们共同催化伊索霉素八酮单体的合成。还鉴定出了其他一些基因,这些基因是提供乙基丙二酸延伸单元、合成和连接2-脱氧-L-岩藻糖以及调控或输出产物所必需的。紧邻推测的伊索霉素生物合成基因簇的是一个30 kbp的区域,该区域包含腺苷钴胺素依赖性甲基丙二酰辅酶A变位酶的基因以及参与钴胺素辅因子生物合成的基因。对后一组基因的分析证实了这样一种观点,即厌氧途径的cbiD和好氧途径的cobF催化预咕啉-5的相同甲基化反应。如果在这种生物体中琥珀酰辅酶A是复杂聚酮生物合成中甲基丙二酸单元的重要来源,那么这些基因与推测的伊索霉素基因簇的接近性就最能说得通。