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Comparative Transcriptome Analysis Shows Conserved Metabolic Regulation during Production of Secondary Metabolites in Filamentous Fungi

机译:比较转录组分析显示丝状真菌次生代谢产物生产过程中保守的代谢调控。

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Filamentous fungi possess great potential as sources of medicinal bioactive compounds, such as antibiotics, but efficient production is hampered by a limited understanding of how their metabolism is regulated. We investigated the metabolism of six secondary metabolite-producing fungi of the Penicillium genus during nutrient depletion in the stationary phase of batch fermentations and assessed conserved metabolic responses across species using genome-wide transcriptional profiling. A coexpression analysis revealed that expression of biosynthetic genes correlates with expression of genes associated with pathways responsible for the generation of precursor metabolites for secondary metabolism. Our results highlight the main metabolic routes for the supply of precursors for secondary metabolism and suggest that the regulation of fungal metabolism is tailored to meet the demands for secondary metabolite production. These findings can aid in identifying fungal species that are optimized for the production of specific secondary metabolites and in designing metabolic engineering strategies to develop high-yielding fungal cell factories for production of secondary metabolites. IMPORTANCE Secondary metabolites are a major source of pharmaceuticals, especially antibiotics. However, the development of efficient processes of production of secondary metabolites has proved troublesome due to a limited understanding of the metabolic regulations governing secondary metabolism. By analyzing the conservation in gene expression across secondary metabolite-producing fungal species, we identified a metabolic signature that links primary and secondary metabolism and that demonstrates that fungal metabolism is tailored for the efficient production of secondary metabolites. The insight that we provide can be used to develop high-yielding fungal cell factories that are optimized for the production of specific secondary metabolites of pharmaceutical interest.
机译:丝状真菌作为药用生物活性化合物(如抗生素)的来源具有巨大潜力,但由于对其代谢调控的了解有限,阻碍了有效生产。我们在分批发酵的固定阶段营养耗竭期间调查了青霉属的六个次生代谢产物真菌的代谢,并使用全基因组转录谱评估了跨物种的保守代谢反应。共表达分析表明,生物合成基因的表达与与负责次级代谢的前体代谢产物生成途径的基因表达相关。我们的结果突出了二级代谢前体供应的主要代谢途径,并提出了调节真菌代谢的方法,以满足二级代谢产物的生产需求。这些发现可以帮助鉴定针对特定次级代谢产物生产而优化的真菌种类,并设计代谢工程策略以开发用于次级代谢产物生产的高产真菌细胞工厂。重要事项次生代谢产物是药物(尤其是抗生素)的主要来源。然而,由于对控制次级代谢的代谢调控的了解有限,已证明开发有效的次级代谢产物生产方法是很麻烦的。通过分析跨次要代谢物的生产真菌物种的基因表达保守性,我们确定了连接主要代谢和次要代谢的代谢特征,并表明真菌代谢是为有效生产次要代谢产物量身定制的。我们提供的见解可用于开发高产真菌细胞工厂,这些工厂针对生产特定的药用次生代谢产物进行了优化。

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