Suwa M, Sugino H, Sasaoka A, Mori E, Fujii S, Shinkawa H, Nimi O, Kinashi H
Department of Molecular Biotechnology, Hiroshima University, 1-4-1 Kagamiyama, Higashi-Hiroshima, Japan.
Gene. 2000 Apr 4;246(1-2):123-31. doi: 10.1016/s0378-1119(00)00060-3.
The 200kb linear plasmid pSLA2-L was suggested to be involved in the production of two macrolide antibiotics, lankamycin (Lm) and lankacidin (Lc), in Streptomyces rochei 7434AN4. Hybridization experiments with the polyketide synthase (PKS) genes for erythromycin and actinorhodin identified two eryAI-homologous regions and an actI-homologous region on pSLA2-L. The nucleotide sequence of a 3.6kb SacI fragment carrying one of the eryAI-homologs revealed that it codes for part of a large protein with four domains for ketoreductase, acyl carrier protein, ketosynthase, and acyltransferase. Gene disruption confirmed that the two eryAI-homologs are parts of a large type-I PKS gene cluster for Lm. A 4.8kb DNA carrying the actI-homologous region contains four open reading frames (ORF1-ORF4) as well as an additional ORF, i.e. ORF5, which might code for a thioesterase. Deletion of the ORF2-ORF4 region showed that it is not involved in the synthesis of Lm or Lc. Thus, it was confirmed that pSLA2-L contains two PKS gene clusters for Lm and an unknown type-II polyketide.
200kb的线性质粒pSLA2-L被认为参与了罗氏链霉菌7434AN4中两种大环内酯类抗生素兰卡霉素(Lm)和兰卡杀菌素(Lc)的产生。用红霉素和放线紫红素的聚酮合酶(PKS)基因进行的杂交实验在pSLA2-L上鉴定出两个eryAI同源区域和一个actI同源区域。携带其中一个eryAI同源物的3.6kb SacI片段的核苷酸序列显示,它编码一种大蛋白的一部分,该蛋白具有酮还原酶、酰基载体蛋白、酮合成酶和酰基转移酶四个结构域。基因破坏证实这两个eryAI同源物是Lm的一个大型I型PKS基因簇的组成部分。携带actI同源区域的4.8kb DNA包含四个开放阅读框(ORF1-ORF4)以及一个额外的ORF,即ORF5,它可能编码一种硫酯酶。ORF2-ORF4区域的缺失表明它不参与Lm或Lc的合成。因此,证实pSLA2-L包含两个用于Lm的PKS基因簇和一个未知的II型聚酮化合物。