Senior Research Group for Genome Research of Industrial Microorganisms, Center for Biotechnology, Bielefeld University, Universitätsstraße 27, 33615 Bielefeld, Germany.
J Biotechnol. 2013 Aug 20;167(2):166-77. doi: 10.1016/j.jbiotec.2012.10.019. Epub 2012 Nov 8.
Actinoplanes sp. SE50/110 is known as the producer of the alpha-glucosidase inhibitor acarbose, a potent drug in the treatment of type-2 diabetes mellitus. We conducted the first whole transcriptome analysis of Actinoplanes sp. SE50/110, using RNA-sequencing technology for comparative gene expression studies between cells grown in maltose minimal medium, maltose minimal medium with trace elements, and glucose complex medium. We first studied the behavior of Actinoplanes sp. SE50/110 cultivations in these three media and found that the different media had significant impact on growth rate and in particular on acarbose production. It was demonstrated that Actinoplanes sp. SE50/110 grew well in all three media, but acarbose biosynthesis was only observed in cultures grown in maltose minimal medium with and without trace elements. When comparing the expression profiles between the maltose minimal media with and without trace elements, only few significantly differentially expressed genes were found, which mainly code for uptake systems of metal ions provided in the trace element solution. In contrast, the comparison of expression profiles from maltose minimal medium and glucose complex medium revealed a large number of differentially expressed genes, of which the most conspicuous genes account for iron storage and uptake. Furthermore, the acarbose gene cluster was found to be highly expressed in maltose-containing media and almost silent in the glucose-containing medium. In addition, a putative antibiotic biosynthesis gene cluster was found to be similarly expressed as the acarbose cluster.
放线菌属 SE50/110 是一种能够产生阿卡波糖(一种治疗 2 型糖尿病的有效药物)的α-葡萄糖苷酶抑制剂的产生菌。我们利用 RNA 测序技术对放线菌属 SE50/110 进行了首次全转录组分析,以比较其在麦芽糖最低培养基、含微量元素的麦芽糖最低培养基和葡萄糖复杂培养基中生长的细胞的基因表达情况。我们首先研究了三种培养基中放线菌属 SE50/110 的培养行为,发现不同的培养基对生长速率有显著影响,特别是对阿卡波糖的生产有显著影响。结果表明,放线菌属 SE50/110 在三种培养基中均生长良好,但仅在含微量元素的麦芽糖最低培养基和不含微量元素的麦芽糖最低培养基中观察到阿卡波糖的生物合成。当比较含微量元素和不含微量元素的麦芽糖最低培养基之间的表达谱时,只发现了少数表达差异显著的基因,这些基因主要编码在微量元素溶液中提供的金属离子摄取系统。相比之下,麦芽糖最低培养基和葡萄糖复杂培养基的表达谱比较揭示了大量表达差异的基因,其中最显著的基因是铁的储存和摄取。此外,发现阿卡波糖基因簇在含麦芽糖的培养基中高度表达,而在含葡萄糖的培养基中几乎沉默。此外,还发现了一个假定的抗生素生物合成基因簇,其表达与阿卡波糖簇相似。