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对镉胁迫反应的转录组分析。 需注意,原文“Transcriptome analysis of the response of to cadmium stress.”中“of the response of ”和“to cadmium stress”之间缺少具体所针对的对象,译文是按照常见的表达逻辑补充完整后呈现的。

Transcriptome analysis of the response of to cadmium stress.

作者信息

Wang Yunan, Mao Chunze, Shi Yujia, Fan Xuejing, Sun Liping, Zhuang Yongliang

机构信息

Faculty of Food Science and Engineering, Kunming University of Science and Technology, Kunming, China.

出版信息

Front Microbiol. 2022 Sep 23;13:990693. doi: 10.3389/fmicb.2022.990693. eCollection 2022.

Abstract

is a fungal parasite that grows on species. One isolated strain of from was obtained and proved of strong ability to tolerate and absorb cadmium (Cd) by previous research. However, the molecular mechanisms of underlying the resistance of to Cd stress have not been investigated. This study aimed to assess the effect of Cd stress on the global transcriptional regulation of . A total of 1,839 differentially expressed genes (DEGs) were identified under 120 mg/l Cd stress. Gene ontology (GO) enrichment analysis revealed that large amounts of DEGs were associated with cell membrane components, oxidoreductase activity, and transport activity. KEGG enrichment analysis revealed that these DEGs were mainly involved in the translation, amino acid metabolism, transport and catabolism, carbohydrate metabolism, and folding/sorting and degradation pathways under Cd stress. Moreover, the expression of DEGs encoding transporter proteins, antioxidant enzymes, nonenzymatic antioxidant proteins, detoxification enzymes, and transcription factors was associated with the Cd stress response. These results provide insights into the molecular mechanisms underlying Cd tolerance in and serve as a valuable reference for further studies on the detoxification mechanisms of heavy metal-tolerant fungi. Our findings may also facilitate the development of new and improved fungal bioremediation strategies.

摘要

是一种生长在[具体物种]上的真菌寄生虫。之前的研究从[来源]中分离出了一种[真菌名称]菌株,并证明其具有很强的耐受和吸收镉(Cd)的能力。然而,[真菌名称]对镉胁迫抗性的潜在分子机制尚未得到研究。本研究旨在评估镉胁迫对[真菌名称]全局转录调控的影响。在120毫克/升镉胁迫下共鉴定出1839个差异表达基因(DEGs)。基因本体(GO)富集分析表明,大量差异表达基因与细胞膜成分、氧化还原酶活性和转运活性有关。KEGG富集分析表明,这些差异表达基因在镉胁迫下主要参与翻译、氨基酸代谢、转运与分解代谢、碳水化合物代谢以及折叠/分选和降解途径。此外,编码转运蛋白、抗氧化酶、非酶抗氧化蛋白、解毒酶和转录因子的差异表达基因的表达与镉胁迫反应有关。这些结果为[真菌名称]耐镉的分子机制提供了见解,并为进一步研究耐重金属真菌的解毒机制提供了有价值的参考。我们的研究结果也可能有助于开发新的和改进的真菌生物修复策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c708/9539689/796dc9c10f88/fmicb-13-990693-g001.jpg

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