Lombó F, Braña A F, Méndez C, Salas J A
Departamento de Biología Funcional e Instituto Universitario de Biotecnología de Asturias, Universidad de Oviedo, 33006 Oviedo, Spain.
J Bacteriol. 1999 Jan;181(2):642-7. doi: 10.1128/JB.181.2.642-647.1999.
Sequencing of a 4.3-kb DNA region from the chromosome of Streptomyces argillaceus, a mithramycin producer, revealed the presence of two open reading frames (ORFs). The first one (orfA) codes for a protein that resembles several transport proteins. The second one (mtmR) codes for a protein similar to positive regulators involved in antibiotic biosynthesis (DnrI, SnoA, ActII-orf4, CcaR, and RedD) belonging to the Streptomyces antibiotic regulatory protein (SARP) family. Both ORFs are separated by a 1.9-kb, apparently noncoding region. Replacement of the mtmR region by an antibiotic resistance cassette completely abolished mithramycin biosynthesis. Expression of mtmR in a high-copy-number vector in S. argillaceus caused a 16-fold increase in mithramycin production. The mtmR gene restored actinorhodin production in Streptomyces coelicolor JF1 mutant, in which the actinorhodin-specific activator ActII-orf4 is inactive, and also stimulated actinorhodin production by Streptomyces lividans TK21. A 241-bp region located 1.9 kb upstream of mtmR was found to be repeated approximately 50 kb downstream of mtmR at the other end of the mithramycin gene cluster. A model to explain a possible route for the acquisition of the mithramycin gene cluster by S. argillaceus is proposed.
来自光神霉素产生菌泥质链霉菌染色体的一段4.3 kb DNA区域的测序结果显示存在两个开放阅读框(ORF)。第一个(orfA)编码一种类似于几种转运蛋白的蛋白质。第二个(mtmR)编码一种与参与抗生素生物合成的正调控因子(属于链霉菌抗生素调控蛋白(SARP)家族的DnrI、SnoA、ActII-orf4、CcaR和RedD)相似的蛋白质。两个ORF被一个1.9 kb的明显非编码区域隔开。用抗生素抗性盒替换mtmR区域完全消除了光神霉素的生物合成。在泥质链霉菌中以高拷贝数载体表达mtmR导致光神霉素产量增加了16倍。mtmR基因恢复了天蓝色链霉菌JF1突变体中放线紫红素的产生,在该突变体中放线紫红素特异性激活剂ActII-orf4无活性,并且还刺激了变铅青链霉菌TK21中放线紫红素的产生。发现在mtmR上游1.9 kb处的一个241 bp区域在光神霉素基因簇另一端的mtmR下游约50 kb处重复出现。提出了一个解释泥质链霉菌获取光神霉素基因簇可能途径的模型。