Proteome trait regulation of marine Synechococcus elemental stoichiometry under global change.

IF 10.8 1区 环境科学与生态学 Q1 ECOLOGY ISME Journal Pub Date : 2024-01-08 DOI:10.1093/ismejo/wrae046
Nathan S Garcia, Mingyu Du, Michele Guindani, Matthew R McIlvin, Dawn M Moran, Mak A Saito, Adam C Martiny
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Abstract

Recent studies have demonstrated regional differences in marine ecosystem C:N:P with implications for carbon and nutrient cycles. Due to strong co-variance, temperature and nutrient stress explain variability in C:N:P equally well. A reductionistic approach can link changes in individual environmental drivers with changes in biochemical traits and cell C:N:P. Thus, we quantified effects of temperature and nutrient stress on Synechococcus chemistry using laboratory chemostats, chemical analyses, and data-independent acquisition mass spectrometry proteomics. Nutrient supply accounted for most C:N:Pcell variability and induced tradeoffs between nutrient acquisition and ribosomal proteins. High temperature prompted heat-shock, whereas thermal effects via the "translation-compensation hypothesis" were only seen under P-stress. A Nonparametric Bayesian Local Clustering algorithm suggested that changes in lipopolysaccharides, peptidoglycans, and C-rich compatible solutes may also contribute to C:N:P regulation. Physiological responses match field-based trends in ecosystem stoichiometry and suggest a hierarchical environmental regulation of current and future ocean C:N:P.

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全球变化下海洋 Synechococcus 元素配比的蛋白质组特征调控。
最近的研究表明,海洋生态系统的 C:N:P 存在区域差异,对碳和营养物质循环有影响。由于共变异性很强,温度和营养压力同样可以解释 C:N:P 的变化。还原法可以将单个环境驱动因素的变化与生化特征和细胞 C:N:P 的变化联系起来。因此,我们利用实验室恒温器、化学分析和数据独立获取质谱蛋白质组学,量化了温度和营养物质胁迫对 Synechococcus 化学性质的影响。养分供应造成了大部分 C:N:Pcell 变异,并导致养分获取和核糖体蛋白之间的权衡。高温会引发热休克,而只有在 P-胁迫下才能看到通过 "翻译补偿假说 "产生的热效应。非参数贝叶斯局部聚类算法表明,脂多糖、肽聚糖和富含 C 的兼容溶质的变化也可能有助于 C:N:P 的调节。生理反应与基于实地的生态系统化学计量趋势相吻合,表明环境对当前和未来海洋 C:N:P 的调控是分层的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ISME Journal
ISME Journal 环境科学-生态学
CiteScore
22.10
自引率
2.70%
发文量
171
审稿时长
2.6 months
期刊介绍: The ISME Journal covers the diverse and integrated areas of microbial ecology. We encourage contributions that represent major advances for the study of microbial ecosystems, communities, and interactions of microorganisms in the environment. Articles in The ISME Journal describe pioneering discoveries of wide appeal that enhance our understanding of functional and mechanistic relationships among microorganisms, their communities, and their habitats.
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