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Design, manufacture, and application of DNA microarrays to study gene expression phenotypes of lysine-producing Corynebacterium glutamicum

机译:设计,制造和应用DNa微阵列研究产赖氨酸的谷氨酸棒杆菌的基因表达表型

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摘要

Corynebacterium glutamicum partial genome DNA microarrays were constructed that were capable of assaying the transcriptional profile of the genes of pathways involved in central carbon metabolism and lysine biosynthesis. It was found that to ensure arrays of high quality, protocols applying the arrays should include DNase treatment of RNA samples. additional RNA filtration purification steps, and the use of gene specific primers in the formation of labeled cDNA through reverse transcription. After implementing these procedures, the accuracy and reproducibility of the array data were validated. The microarrays were used to explore the effects of the over-expression of the key anaplerotic enzyme pyruvate carboxylase and the use of different medium carbon source compositions, both of which have been shown to influence the yields of biomass on carbon and of lysine on biomass. Three different strains of C. glutamicum that were grown on six different minimal medium formulations that varied in their balance of glucose and lactate were assayed by isolating total mRNA samples from cultures in three different phases of growth and lysine production. Genes associated with glycolysis and the pentose phosphate pathway showed decreased transcript concentrations as the available carbon source was shifted from glucose to lactate, while those associated with the TCA cycle and the glyoxylate bypass demonstrated increased transcription. As the cultures stopped generating biomass and began generating lysine, mRNA of genes associated with lysine synthesis and export was measured at elevated concentrations.
机译:构建了谷氨酸棒杆菌部分基因组DNA微阵列,其能够分析参与中央碳代谢和赖氨酸生物合成的途径的基因的转录谱。发现为了确保高质量的阵列,应用该阵列的方案应包括RNA样品的DNase处理。额外的RNA过滤纯化步骤,以及通过逆转录在标记的cDNA形成中使用基因特异性引物。在执行这些步骤后,验证了阵列数据的准确性和可重复性。该微阵列用于探索关键的过磷酸酶丙酮酸羧化酶的过表达的影响以及使用不同的中等碳源组成的影响,这两者均已显示出影响碳上生物量和赖氨酸上生物量的产量。通过在生长和赖氨酸生产的三个不同阶段从培养物中分离出总mRNA样品,分析了在六种不同的基本培养基制剂上生长的三种不同的谷氨酸棒状杆菌菌株,这些制剂在葡萄糖和乳酸的平衡方面各不相同。与糖酵解和戊糖磷酸途径相关的基因显示转录物浓度降低,因为可用的碳源从葡萄糖转移至乳酸,而与TCA循环和乙醛酸旁路相关的基因表明转录增加。当培养物停止产生生物质并开始产生赖氨酸时,在升高的浓度下测量了与赖氨酸合成和输出有关的基因的mRNA。

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