IBG-1: Biotechnology, Institute of Bio- and Geosciences, Forschungszentrum Jülich, D-52425, Jülich, Germany.
IBG-4: Bioinformatics, Institute of Bio- and Geosciences, Forschungszentrum Jülich, D-52425, Jülich, Germany.
Sci Data. 2022 Oct 1;9(1):594. doi: 10.1038/s41597-022-01706-7.
Corynebacterium glutamicum is the major host for the industrial production of amino acids and has become one of the best studied model organisms in microbial biotechnology. Rational strain construction has led to an improvement of producer strains and to a variety of novel producer strains with a broad substrate and product spectrum. A key factor for the success of these approaches is detailed knowledge of transcriptional regulation in C. glutamicum. Here, we present a large compendium of 927 manually curated microarray-based transcriptional profiles for wild-type and engineered strains detecting genome-wide expression changes of the 3,047 annotated genes in response to various environmental conditions or in response to genetic modifications. The replicates within the 927 experiments were combined to 304 microarray sets ordered into six categories that were used for differential gene expression analysis. Hierarchical clustering confirmed that no outliers were present in the sets. The compendium provides a valuable resource for future fundamental and applied research with C. glutamicum and contributes to a systemic understanding of this microbial cell factory. Measurement(s) Gene Expression Analysis Technology Type(s) Two Color Microarray Factor Type(s) WT condition A vs. WT condition B • Plasmid-based gene overexpression in parental strain vs. parental strain with empty vector control • Deletion mutant vs. parental strain Sample Characteristic - Organism Corynebacterium glutamicum Sample Characteristic - Environment laboratory environment Sample Characteristic - Location Germany.
谷氨酸棒杆菌是工业生产氨基酸的主要宿主,已成为微生物生物技术中研究最深入的模式生物之一。合理的菌株构建导致了生产菌株的改进,并产生了各种具有广泛底物和产物谱的新型生产菌株。这些方法成功的关键因素是对谷氨酸棒杆菌转录调控的详细了解。在这里,我们展示了一个由 927 个手动整理的基于微阵列的转录谱组成的大型汇编,用于野生型和工程菌株,以检测 3047 个注释基因对各种环境条件或遗传修饰的全基因组表达变化。927 个实验中的重复实验被组合成 304 个微阵列集,分为六个类别,用于差异基因表达分析。层次聚类证实这些集中没有异常值。该汇编为未来与谷氨酸棒杆菌的基础和应用研究提供了宝贵的资源,并有助于系统地了解这个微生物细胞工厂。