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深测序分析 Aspergillus oryzae 转录组对盐胁迫的响应。

Deep sequencing analysis of transcriptomes in Aspergillus oryzae in response to salinity stress.

机构信息

Jiangxi Key Laboratory of Bioprocess Engineering and Co-Innovation Center for In-vitro Diagnostic Reagents and Devices of Jiangxi Province, College of Life Sciences, Jiangxi Science & Technology Normal University, Nanchang, 330013, China.

出版信息

Appl Microbiol Biotechnol. 2018 Jan;102(2):897-906. doi: 10.1007/s00253-017-8603-z. Epub 2017 Nov 3.

Abstract

Characterization of the changes after various stimuli is crucial to comprehend the adaptation of cells to the changing condition. Aspergillus oryzae is widely used for the industrial production of soy sauce, which always encounter changes within a complex environment, such as salinity stress. However, the protective biochemical mechanisms of A. oryzae against salinity stress are poorly understood. In this study, we successfully characterized the fermentative behavior, transcriptomic profiles, and metabolite changes of A. oryzae in response to salinity stress. The results showed that salt treatment of A. oryzae inhibited the fungal development and conidia formation. Transcriptomic analysis showed an upregulated expression of the genes related to arginine accumulation and oleic acid synthesis. The results of qRT-PCR were further confirmed by the reliability and availability of the differentially expressed genes obtained from the transcriptome analysis. Metabolomic analysis revealed that the corresponding intracellular accumulation of arginine and oleic acid were also increased in response to the salinity stress. All of the results provide a global transcriptome characterization of the salt adaptation process in A. oryzae, and offer multiple target genes for salt tolerance improvement via genetic engineering.

摘要

研究曲霉属米曲霉菌种在盐胁迫下的发酵行为、转录组和代谢组变化,成功解析了其耐盐机制。结果表明,盐胁迫抑制了米曲霉的生长和分生孢子的形成。转录组分析表明,与精氨酸积累和油酸合成相关的基因表达上调。qRT-PCR 结果进一步证实了差异表达基因的可靠性和可用性,这些差异表达基因是从转录组分析中获得的。代谢组分析显示,精氨酸和油酸的相应细胞内积累也因盐胁迫而增加。这些结果为米曲霉的耐盐适应过程提供了一个全面的转录组特征,并为通过遗传工程提高耐盐性提供了多个目标基因。

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