多组学揭示嗜热纳特拉纳菌适应高盐、碱性和高温联合环境的机制。

IF 3.6 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
Journal of Proteome Research Pub Date : 2025-08-01 Epub Date: 2025-07-22 DOI:10.1021/acs.jproteome.5c00395
Qinghua Xing, Xinyi Tao, Shanshan Zhang, Noha M Mesbah, Xinwei Mao, Xiaomeng Guo, Qingping Hu, Haisheng Wang, Baisuo Zhao
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引用次数: 0

摘要

嗜盐嗜碱嗜热N. thermophilus在3.3-3.9 M Na+、pH 9.5和53°C的极端组合条件下生长最佳。这项研究旨在揭示其对高盐、碱性pH值和高温组合极端环境的独特适应。由于遗传操作的困难,我们使用多组学方法来揭示在三重极端条件下嗜热乳杆菌的综合转录组学,蛋白质组学和代谢组学景观。具体来说,评估了两种不同的条件:高盐碱热(HSAT, 4 M Na+/ pH 9.8/52°C)应力和低盐碱热(LSAT, 3 M Na+/ pH 8.8/42°C)应力。在HSAT胁迫下,嗜热乳杆菌通过增加饱和脂肪酸和不带电极性脂质的水平来重塑细胞膜,增强Na+驱动的鞭毛运动,积累各种相容溶质,重定向氨基酸代谢以获取能量,调节离子转运体和伴侣蛋白的活性。这些发现在多极端生物中体现了“没有免费的午餐”原则。本研究通过检测三种极端环境同时影响下嗜热奈瑟菌基因、蛋白和代谢调节水平的变化,全面分析了多极端微生物在高盐、碱性和高温环境下的生存机制。我们的发现为了解地球上生命的起源和外星生命的可能性提供了有价值的见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multiomics Reveals the Mechanism of Natranaerobius thermophilus Adaptation to Combined Hypersaline, Alkaline, and Elevated Temperature Environments.

The halophilic alkalithermophile N. thermophilus grows optimally at the combined extremes of 3.3-3.9 M Na+, pH 9.5, and 53 °C. This study aims to uncover its unique adaptations to the combined extremes of high salt, alkaline pH, and high temperature. Due to the difficulties of genetic manipulation, we used a multiomics approach to reveal the comprehensive transcriptomic, proteomic, and metabolomic landscapes of N. thermophilus under the triple extremes. Specifically, two distinct conditions were evaluated: high salt-alkaline-thermal (HSAT, 4 M Na+/ pH 9.8/52 °C) stress and low salt-alkaline-thermal (LSAT, 3 M Na+/ pH 8.8/42 °C) stress. Under HSAT stress, N. thermophilus increased the level of saturated fatty acids and uncharged polar lipids to remodel its cell membrane, enhanced Na+-driven flagellar motility, accumulated various compatible solutes, redirected amino acid metabolism for energy, and adjusted the activity of ion transporters and chaperones. These findings exemplify the "No Free Lunch" principle in polyextremophiles. By examining changes in gene, protein, and metabolic regulation levels in N. thermophilus under the simultaneous influence of three extremes, this study provides a comprehensive analysis of the survival mechanisms of polyextremophiles in hypersaline, alkaline, and high-temperature environments. Our findings offer valuable insights into the origins of life on Earth and the potential for extraterrestrial life.

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来源期刊
Journal of Proteome Research
Journal of Proteome Research 生物-生化研究方法
CiteScore
9.00
自引率
4.50%
发文量
251
审稿时长
3 months
期刊介绍: Journal of Proteome Research publishes content encompassing all aspects of global protein analysis and function, including the dynamic aspects of genomics, spatio-temporal proteomics, metabonomics and metabolomics, clinical and agricultural proteomics, as well as advances in methodology including bioinformatics. The theme and emphasis is on a multidisciplinary approach to the life sciences through the synergy between the different types of "omics".
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