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黑曲霉 3.316 热应激下的蛋白质组学分析。

Proteomic analysis of Aspergillus niger 3.316 under heat stress.

机构信息

Hebei Normal University of Science and Technology, College of Food Science and Technology, Qinhuangdao, China.

出版信息

Microbiologyopen. 2020 May;9(5):e1012. doi: 10.1002/mbo3.1012. Epub 2020 Feb 27.

Abstract

β-Glucosidase production by Aspergillus niger is accompanied by an inevitable temperature increase in the industrial fermentation environment. Hence, the synthetic process of β-glucosidase is negatively affected. However, our understanding of the heat stress response (HSR) mechanism in A. niger is still incomplete. The current study explored the intracellular proteome profile of A. niger 3.316 in group T (50°C stress) and group C (30°C control) using two proteomic approaches (isobaric tags for relative and absolute quantitation [iTRAQ] and label-free) and examined the expression of four proteins using a parallel reaction monitoring (PRM) approach. Based on the result of the iTRAQ proteomic analysis, 1,025 proteins were differentially expressed in group T compared to group C. Using the label-free approach, we only focused on 77 proteins with significant changes in their protein expression levels. In addition, we performed bioinformatics analysis on all these proteins and obtained detailed gene ontology (GO) enrichment and Kyoto encyclopedia of genes and genomes (KEGG) pathway results. Under heat stress conditions, the relative expression levels of proteins with protection and repair functions were upregulated in A. niger 3.316. These proteins were involved in metabolic pathways, oxidative phosphorylation, porphyrin and chlorophyll metabolism, pyruvate metabolism, and the citrate cycle (TCA cycle). The insights obtained from the presented proteomics and bioinformatics analyses can be used to further explore the HSR mechanism of A. niger.

摘要

黑曲霉β-葡萄糖苷酶的生产伴随着工业发酵环境中不可避免的温度升高,因此,β-葡萄糖苷酶的合成过程受到负面影响。然而,我们对黑曲霉热应激反应(HSR)机制的理解仍不完整。本研究采用两种蛋白质组学方法(相对和绝对定量同位素标记[itraq]和无标记)研究了黑曲霉 3.316 在组 T(50°C 应激)和组 C(30°C 对照)中的细胞内蛋白质组谱,并使用平行反应监测(PRM)方法检测了四种蛋白质的表达。基于 itraq 蛋白质组学分析的结果,与组 C 相比,组 T 中有 1025 种蛋白质表达差异。使用无标记方法,我们只关注了 77 种蛋白质表达水平有显著变化的蛋白质。此外,我们对所有这些蛋白质进行了生物信息学分析,并获得了详细的基因本体(GO)富集和京都基因与基因组百科全书(KEGG)途径结果。在热应激条件下,黑曲霉 3.316 中具有保护和修复功能的蛋白质的相对表达水平上调。这些蛋白质参与代谢途径、氧化磷酸化、卟啉和叶绿素代谢、丙酮酸代谢和柠檬酸循环(TCA 循环)。本研究提供的蛋白质组学和生物信息学分析的见解可用于进一步探索黑曲霉的 HSR 机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c2c3/7221434/a6236415cbf9/MBO3-9-e1012-g001.jpg

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