Proteomic analysis of Antarctic sea-ice yeast Rhodotorula mucilaginosa AN5 responding to hyper- and hyposalinity stress.

IF 4 3区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Guangfeng Kan, Yan Zhang, Hong Zhang, Kai Yu, Yanxiao Jiang, Jie Jiang, Lina Qiao, Cuijuan Shi
{"title":"Proteomic analysis of Antarctic sea-ice yeast Rhodotorula mucilaginosa AN5 responding to hyper- and hyposalinity stress.","authors":"Guangfeng Kan, Yan Zhang, Hong Zhang, Kai Yu, Yanxiao Jiang, Jie Jiang, Lina Qiao, Cuijuan Shi","doi":"10.1007/s11274-025-04472-x","DOIUrl":null,"url":null,"abstract":"<p><p>Antarctic sea-ice microorganism lives in polar sea-ice channels, in which the salinity can be three times that of seawater in winter and close to freshwater in summer. Here, we investigated the survival and adaptive strategies of Antarctic yeast Rhodotorula mucilaginosa AN5 treated individually with high (150‰) and low (0‰) salinity to simulate the natural environment. The results showed that salinity changes did not significantly affect the growth of yeast AN5. Scanning electron microscope (SEM) observation revealed that the cell size increased under both hyper- and hyposalinity compared to control, and more extracellular substances were observed, especially under hypersalinity stress. Biochemical factors determination indicated that after high salinity exposure, the increased antioxidant systems eliminated the induced ROS, while under low salinity stress, ROS and the antioxidant system were decreased. The proteomic analysis based on iTRAQ and PRM technology revealed that 86 proteins were up-regulated and 388 were down-regulated. Under high salinity stress, the most predominant enrichment pathway was nucleocytoplasmic transport. In addition, high salinity exposure inhibited fatty acid metabolism, the one-carbon pool by folate, and ubiquitin-mediated proteolysis. Under low salinity stress, the glyoxylate cycle pathway was induced, and aldolase was down-regulated, indicating that the energy demand in yeast survival was supplied by the catabolism of lipids. Meanwhile, low salinity also limited the synthesis of RNA, DNA, and protein by inhibiting the ribosome biogenesis and pyrimidine metabolism pathways. Generally, these results provide comprehensive insights into the molecular mechanisms underlying the adaptation of Antarctic sea-ice yeast R. mucilaginosa to high and low salt stress.</p>","PeriodicalId":23703,"journal":{"name":"World journal of microbiology & biotechnology","volume":"41 7","pages":"249"},"PeriodicalIF":4.0000,"publicationDate":"2025-07-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"World journal of microbiology & biotechnology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1007/s11274-025-04472-x","RegionNum":3,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Antarctic sea-ice microorganism lives in polar sea-ice channels, in which the salinity can be three times that of seawater in winter and close to freshwater in summer. Here, we investigated the survival and adaptive strategies of Antarctic yeast Rhodotorula mucilaginosa AN5 treated individually with high (150‰) and low (0‰) salinity to simulate the natural environment. The results showed that salinity changes did not significantly affect the growth of yeast AN5. Scanning electron microscope (SEM) observation revealed that the cell size increased under both hyper- and hyposalinity compared to control, and more extracellular substances were observed, especially under hypersalinity stress. Biochemical factors determination indicated that after high salinity exposure, the increased antioxidant systems eliminated the induced ROS, while under low salinity stress, ROS and the antioxidant system were decreased. The proteomic analysis based on iTRAQ and PRM technology revealed that 86 proteins were up-regulated and 388 were down-regulated. Under high salinity stress, the most predominant enrichment pathway was nucleocytoplasmic transport. In addition, high salinity exposure inhibited fatty acid metabolism, the one-carbon pool by folate, and ubiquitin-mediated proteolysis. Under low salinity stress, the glyoxylate cycle pathway was induced, and aldolase was down-regulated, indicating that the energy demand in yeast survival was supplied by the catabolism of lipids. Meanwhile, low salinity also limited the synthesis of RNA, DNA, and protein by inhibiting the ribosome biogenesis and pyrimidine metabolism pathways. Generally, these results provide comprehensive insights into the molecular mechanisms underlying the adaptation of Antarctic sea-ice yeast R. mucilaginosa to high and low salt stress.

南极海冰酵母黏胶红酵母AN5对高、低盐度胁迫响应的蛋白质组学分析。
南极海冰微生物生活在极地海冰通道中,冬季盐度可达海水的3倍,夏季接近淡水。为了模拟自然环境,研究了高盐度(150‰)和低盐度(0‰)条件下南极酵母Rhodotorula mucilaginosa AN5的生存和适应策略。结果表明,盐度变化对酵母菌AN5的生长影响不显著。扫描电镜(SEM)观察发现,高盐和低盐胁迫下的细胞体积均比对照增大,细胞外物质增多,尤其是高盐胁迫下。生化因子测定表明,高盐胁迫后,抗氧化系统的增加消除了诱导的ROS,而低盐胁迫下,ROS和抗氧化系统的减少。基于iTRAQ和PRM技术的蛋白质组学分析显示,86个蛋白上调,388个蛋白下调。在高盐度胁迫下,最主要的富集途径是核质转运。此外,高盐度暴露抑制脂肪酸代谢、叶酸单碳池和泛素介导的蛋白质水解。低盐度胁迫诱导了乙醛酸循环途径,醛缩酶下调,表明酵母生存所需能量由脂质分解代谢提供。同时,低盐度还通过抑制核糖体生物发生和嘧啶代谢途径,限制了RNA、DNA和蛋白质的合成。总的来说,这些结果为南极海冰酵母mucilaginosa适应高盐和低盐胁迫的分子机制提供了全面的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
World journal of microbiology & biotechnology
World journal of microbiology & biotechnology 工程技术-生物工程与应用微生物
CiteScore
6.30
自引率
2.40%
发文量
257
审稿时长
2.5 months
期刊介绍: World Journal of Microbiology and Biotechnology publishes research papers and review articles on all aspects of Microbiology and Microbial Biotechnology. Since its foundation, the Journal has provided a forum for research work directed toward finding microbiological and biotechnological solutions to global problems. As many of these problems, including crop productivity, public health and waste management, have major impacts in the developing world, the Journal especially reports on advances for and from developing regions. Some topics are not within the scope of the Journal. Please do not submit your manuscript if it falls into one of the following categories: · Virology · Simple isolation of microbes from local sources · Simple descriptions of an environment or reports on a procedure · Veterinary, agricultural and clinical topics in which the main focus is not on a microorganism · Data reporting on host response to microbes · Optimization of a procedure · Description of the biological effects of not fully identified compounds or undefined extracts of natural origin · Data on not fully purified enzymes or procedures in which they are applied All articles published in the Journal are independently refereed.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信