Imai Yu, Sato Seizo, Tanaka Yukinori, Ochi Kozo, Hosaka Takeshi
Interdisciplinary Graduate School of Science and Technology, Shinshu University, Nagano, Japan.
Central Research Laboratory, Nippon Suisan Kaisha, Ltd., Tokyo Innovation Center, Tokyo, Japan.
Appl Environ Microbiol. 2015 Jun;81(11):3869-79. doi: 10.1128/AEM.04214-14. Epub 2015 Mar 27.
Antibiotics have either bactericidal or bacteriostatic activity. However, they also induce considerable gene expression in bacteria when used at subinhibitory concentrations (below the MIC). We found that lincomycin, which inhibits protein synthesis by binding to the ribosomes of Gram-positive bacteria, was effective for inducing the expression of genes involved in secondary metabolism in Streptomyces strains when added to medium at subinhibitory concentrations. In Streptomyces coelicolor A3(2), lincomycin at 1/10 of its MIC markedly increased the expression of the pathway-specific regulatory gene actII-ORF4 in the blue-pigmented antibiotic actinorhodin (ACT) biosynthetic gene cluster, which resulted in ACT overproduction. Intriguingly, S. lividans 1326 grown in the presence of lincomycin at a subinhibitory concentration (1/12 or 1/3 of its MIC) produced abundant antibacterial compounds that were not detected in cells grown in lincomycin-free medium. Bioassay and mass spectrometry analysis revealed that some antibacterial compounds were novel congeners of calcium-dependent antibiotics. Our results indicate that lincomycin at subinhibitory concentrations potentiates the production of secondary metabolites in Streptomyces strains and suggest that activating these strains by utilizing the dose-response effects of lincomycin could be used to effectively induce the production of cryptic secondary metabolites. In addition to these findings, we also report that lincomycin used at concentrations for markedly increased ACT production resulted in alteration of the cytoplasmic protein (FoF1 ATP synthase α and β subunits, etc.) profile and increased intracellular ATP levels. A fundamental mechanism for these unique phenomena is also discussed.
抗生素具有杀菌或抑菌活性。然而,当以亚抑制浓度(低于最低抑菌浓度)使用时,它们也会在细菌中诱导相当程度的基因表达。我们发现,林可霉素通过与革兰氏阳性菌的核糖体结合来抑制蛋白质合成,当以亚抑制浓度添加到培养基中时,它能有效诱导链霉菌菌株中参与次级代谢的基因表达。在天蓝色链霉菌A3(2)中,林可霉素在其最低抑菌浓度的1/10时,显著增加了蓝色色素抗生素放线紫红素(ACT)生物合成基因簇中途径特异性调控基因actII-ORF4的表达,这导致了ACT的过量产生。有趣的是,在亚抑制浓度(其最低抑菌浓度的1/12或1/3)的林可霉素存在下生长的变铅青链霉菌1326产生了丰富的抗菌化合物,而在无林可霉素培养基中生长的细胞中未检测到这些化合物。生物测定和质谱分析表明,一些抗菌化合物是钙依赖性抗生素的新型同系物。我们的结果表明,亚抑制浓度的林可霉素能增强链霉菌菌株中次级代谢产物的产生,并表明利用林可霉素的剂量反应效应激活这些菌株可有效诱导隐秘次级代谢产物的产生。除了这些发现,我们还报告说,以显著增加ACT产量的浓度使用林可霉素会导致细胞质蛋白(F0F1 ATP合酶α和β亚基等)谱的改变和细胞内ATP水平的升高。还讨论了这些独特现象的基本机制。