Investigation of Methionine Metabolism in Coccolithophore by In Situ Light-Coupled Nuclear Magnetic Resonance Spectroscopy.

IF 4.8 2区 化学 Q2 CHEMISTRY, PHYSICAL
Yi-Shan Wu, Li-Kang Chu, Tsyr-Yan Yu
{"title":"Investigation of Methionine Metabolism in Coccolithophore by <i>In Situ</i> Light-Coupled Nuclear Magnetic Resonance Spectroscopy.","authors":"Yi-Shan Wu, Li-Kang Chu, Tsyr-Yan Yu","doi":"10.1021/acs.jpclett.5c01316","DOIUrl":null,"url":null,"abstract":"<p><p>Coccolithophores play critical roles in global carbon and sulfur cycles. They contribute to the carbon cycle through photosynthesis and calcification and the sulfur cycle by producing dimethylsulfoniopropionate (DMSP). Despite their ecological importance, the details and dynamics of methionine metabolism in coccolithophores are poorly understood. Here, we introduce an <i>in situ</i> light-coupled nuclear magnetic resonance (NMR) spectroscopy setup to monitor methionine metabolism directly in coccolithophore cultures under varying environmental conditions. Combining <i>in situ</i> light-coupled NMR spectroscopy and <sup>13</sup>C magic angle spinning (MAS) spectroscopy, we observed that coccolithophores can take up methionine and convert it into 4-methylthio-2-oxobutyrate (MTOB), which is subsequently secreted into the culture medium, while DMSP was detected only intracellularly. Furthermore, environmental factors, such as elevated temperatures at 24.8 °C, which is 6.8 °C higher than the typical growth temperature for coccolithophores, and darkness, accelerated methionine consumption but reduced its incorporation into proteins and its conversion into MTOB, suggesting a shift toward alternative metabolic pathways under stress. In contrast, seawater acidification had minimal effects on the methionine metabolism. These findings provide new insights into how environmental conditions influence sulfur metabolism in coccolithophores, with potential consequences for their ecological functioning under future climate scenarios.</p>","PeriodicalId":62,"journal":{"name":"The Journal of Physical Chemistry Letters","volume":" ","pages":"5800-5805"},"PeriodicalIF":4.8000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12169660/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of Physical Chemistry Letters","FirstCategoryId":"1","ListUrlMain":"https://doi.org/10.1021/acs.jpclett.5c01316","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/6/3 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0

Abstract

Coccolithophores play critical roles in global carbon and sulfur cycles. They contribute to the carbon cycle through photosynthesis and calcification and the sulfur cycle by producing dimethylsulfoniopropionate (DMSP). Despite their ecological importance, the details and dynamics of methionine metabolism in coccolithophores are poorly understood. Here, we introduce an in situ light-coupled nuclear magnetic resonance (NMR) spectroscopy setup to monitor methionine metabolism directly in coccolithophore cultures under varying environmental conditions. Combining in situ light-coupled NMR spectroscopy and 13C magic angle spinning (MAS) spectroscopy, we observed that coccolithophores can take up methionine and convert it into 4-methylthio-2-oxobutyrate (MTOB), which is subsequently secreted into the culture medium, while DMSP was detected only intracellularly. Furthermore, environmental factors, such as elevated temperatures at 24.8 °C, which is 6.8 °C higher than the typical growth temperature for coccolithophores, and darkness, accelerated methionine consumption but reduced its incorporation into proteins and its conversion into MTOB, suggesting a shift toward alternative metabolic pathways under stress. In contrast, seawater acidification had minimal effects on the methionine metabolism. These findings provide new insights into how environmental conditions influence sulfur metabolism in coccolithophores, with potential consequences for their ecological functioning under future climate scenarios.

Abstract Image

用原位光耦合核磁共振光谱法研究球石藻中蛋氨酸代谢。
球石藻在全球碳和硫循环中起着至关重要的作用。它们通过光合作用和钙化作用促进碳循环,通过产生二甲基磺酰丙酸盐(DMSP)促进硫循环。尽管它们具有重要的生态学意义,但人们对粒石藻中蛋氨酸代谢的细节和动力学知之甚少。在这里,我们引入了一种原位光耦合核磁共振(NMR)波谱装置来直接监测不同环境条件下球石藻培养物中的蛋氨酸代谢。结合原位光耦合核磁共振光谱和13C魔角旋转(MAS)光谱,我们发现球石团可以吸收蛋氨酸并将其转化为4-甲基硫代-2-氧丁酸盐(MTOB),随后分泌到培养基中,而DMSP仅在细胞内检测到。此外,环境因素,如24.8 °C的高温(比球石藻的典型生长温度高6.8 °C)和黑暗,加速了蛋氨酸的消耗,但减少了蛋氨酸与蛋白质的结合和向MTOB的转化,这表明在胁迫下蛋氨酸向替代代谢途径的转变。相比之下,海水酸化对蛋氨酸代谢的影响很小。这些发现为了解环境条件如何影响颗石藻的硫代谢提供了新的见解,并对它们在未来气候情景下的生态功能产生了潜在影响。
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
The Journal of Physical Chemistry Letters
The Journal of Physical Chemistry Letters CHEMISTRY, PHYSICAL-NANOSCIENCE & NANOTECHNOLOGY
CiteScore
9.60
自引率
7.00%
发文量
1519
审稿时长
1.6 months
期刊介绍: The Journal of Physical Chemistry (JPC) Letters is devoted to reporting new and original experimental and theoretical basic research of interest to physical chemists, biophysical chemists, chemical physicists, physicists, material scientists, and engineers. An important criterion for acceptance is that the paper reports a significant scientific advance and/or physical insight such that rapid publication is essential. Two issues of JPC Letters are published each month.
×
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