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酒花苦味酸诱导的活的非可培养状态的转录组分析

Transcriptome Analysis of Viable but Non-Culturable Induced by Hop Bitter Acids.

作者信息

He Yang, Zhao Junfeng, Yin Hua, Deng Yuan

机构信息

State Key Laboratory of Biological Fermentation Engineering of Beer, Tsingtao Brewery Co. Ltd., Qingdao, China.

College of Food Science and Engineering, Henan University of Science and Technology, Luoyang, China.

出版信息

Front Microbiol. 2022 May 30;13:902110. doi: 10.3389/fmicb.2022.902110. eCollection 2022.

Abstract

The viable but non-culturable (VBNC) state has been studied in detail in bacteria. However, it has received much less attention in eukaryotic cells. The induction of a VBNC beer-spoilage yeast () by hop bitter acids with different concentrations and its recovery were studied in this work. cells were completely induced into the VBNC state by treatment of 250 mg/L hop bitter acids for 2 h. The addition of catalase at a concentration of 2,000 U/plate on YPD agars enabled these VBNC cells to recover their culturability within 2 days. Moreover, the transcriptome profiling revealed that 267 and 197 genes were significantly changed upon VBNC state entry and resuscitation, respectively. The differentially expressed genes involved in the peroxisome activities, ABC transporter, organic acid metabolism, and TCA cycle were mainly downregulated in the VBNC cells. In contrast, the amino acid and carbohydrate metabolism, cell division, and DNA replication were promoted. This study supplies a theoretical basis for microbial risk assessment in the brewing industry.

摘要

细菌中的活的非可培养(VBNC)状态已得到详细研究。然而,它在真核细胞中受到的关注要少得多。本研究考察了不同浓度的啤酒花苦味酸对啤酒腐败酵母诱导形成VBNC状态及其复苏情况。用250mg/L啤酒花苦味酸处理2小时可使细胞完全进入VBNC状态。在YPD琼脂平板上添加浓度为2000U/平板的过氧化氢酶可使这些VBNC细胞在2天内恢复可培养性。此外,转录组分析表明,分别有267个和197个基因在进入VBNC状态和复苏时发生了显著变化。参与过氧化物酶体活性、ABC转运蛋白、有机酸代谢和三羧酸循环的差异表达基因在VBNC细胞中主要下调。相反,氨基酸和碳水化合物代谢、细胞分裂和DNA复制则得到促进。本研究为酿造工业中的微生物风险评估提供了理论依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8242/9189414/00ff505ab675/fmicb-13-902110-g0001.jpg

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