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首页> 外文期刊>Journal of Biotechnology >Revelation and cloning of valinomycin synthetase genes in Streptomyces lavendulae ACR-DA1 and their expression analysis under different fermentation and elicitation conditions
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Revelation and cloning of valinomycin synthetase genes in Streptomyces lavendulae ACR-DA1 and their expression analysis under different fermentation and elicitation conditions

机译:在不同发酵和诱导条件下,链霉素植物植物植物素合成酶基因的启示与克隆及其表达分析

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Streptomyces species are amongst the most exploited microorganisms due to their ability to produce a plethora of secondary metabolites with bioactive potential, including several well known drugs. They are endowed with immense unexplored potential and substantial efforts are required for their isolation as well as characterization for their bioactive potential. Unexplored niches and extreme environments are host to diverse microbial species. In this study, we report Streptomyces lavendulae ACR-DA1, isolated from extreme cold deserts of the North Western Himalayas, which produces a macrolactone antibiotic, valinomycin. Valinomycin is a K+ ionophoric non-ribosomal cyclodepsipeptide with a broad range of bioactivities including antibacterial, antifungal, antiviral and cytotoxic/anticancer activities. Production of valinomycin by the strain S. lavendulae ACR-DA1 was studied under different fermentation conditions like fermentation medium, temperature and addition of biosynthetic precursors. Synthetic medium at 10 degrees C in the presence of precursors i.e. valine and pyruvate showed enhanced valinomycin production. In order to assess the impact of various elicitors, expression of the two genes viz. vlm1 and vlm2 that encode components of heterodimeric valinomycin synthetase, was analyzed using RT-PCR and correlated with quantity of valinomycin using LC-MS/MS. Annelid, bacterial and yeast elicitors increased valinomycin production whereas addition of fungal and plant elicitors down regulated the biosynthetic genes and reduced valinomycin production. This study is also the first report of valinomycin biosynthesis by Streptomyces lavendulae.
机译:Streptomyces物种是由于它们生产具有生物活性潜力的血液活性潜力的血液活性潜力的能力,包括几种次要地代谢物,包括几种众所周知的药物。他们赋予了巨大的未开发的潜在潜力,并且孤立所需的实质性努力以及对其生物活跃潜力的表征。未探索的利基和极端环境是多种微生物物种的宿主。在这项研究中,我们报告了Streptomyces Lavendulae ACR-DA1,从北西部喜马拉雅山的极端寒冷沙漠中分离出来,它产生了致癌物质抗生素的valinomycin。 Valinomycin是一种K +离子非核糖体环己二肽,具有广泛的生物活性,包括抗菌,抗真菌,抗病毒和细胞毒性/抗癌活性。在不同发酵条件下,在不同发酵条件下,在发酵培养基,温度和添加生物合成前体的不同发酵条件下研究了Lawendulae ACR-DA1的制剂。在前体的存在下10℃的合成培养基,缬氨酸和丙酮酸含量增强的缬氨酸霉素产生。为了评估各种elicetors的影响,两种基因的表达。使用RT-PCR分析非二二聚霉素合成酶组分的VLM1和VLM2,并使用LC-MS / MS与价值霉素的量相关。环菌,细菌和酵母菌株增加了缬氨酸霉素生产,而药物和植物的加入下调生物合成基因并降低缬氨酸霉素生产。本研究也是链霉菌淡紫色的缬氨酸霉素生物合成的第一份报告。

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