海洋和海岸聚球菌对铁限制和增温相互作用的响应对比

IF 3.6 4区 生物学 Q2 ENVIRONMENTAL SCIENCES
Ran Duan, Min Xu, Xiaopeng Bian, Conner Y. Kojima, Shengwei Hou, Qiang Zheng, Seth G. John, David A. Hutchins, Fei-Xue Fu
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引用次数: 0

摘要

本研究探讨了两种南海聚球菌对铁(Fe)和升温温度相互作用的生理和转录反应的差异,这两种聚球菌分别属于开放海洋的进化支II和沿海海洋的CB5。这两种花青菌菌株利用不同的光合作用、铁吸收和养分获取策略来应对铁的限制。在铁限制条件下,适度升温上调了海洋菌株光合作用、营养物质和铁转运基因的表达,促进了其生长和光合作用。相比之下,沿海菌株在低铁条件下的基因表达受升温影响较小。海洋分离物表现出对铁获取的底物调控和对有机营养源的偏好。沿海菌株在光系统II中具有更高的铁配额,更快的D1基因周转,并且对无机氮源进行了优化。两个菌株对热休克和氧化应激均表现出多层次的铁吸收策略和一般的应激反应。总的来说,海洋菌株的基因调控对这两种压力源的反应比沿海菌株更有效。这两种菌株的铁-温度相互作用是复杂的,可能导致协同和拮抗反应,可能影响温暖海洋的全球生物地球化学循环。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Contrasting Responses of Oceanic and Coastal Synechococcus to Iron Limitation and Warming Interactions

Contrasting Responses of Oceanic and Coastal Synechococcus to Iron Limitation and Warming Interactions

This study explored the contrasting physiological and transcriptional responses to iron (Fe) and warming temperature interactions in two South China Sea Synechococcus isolates belonging to clade II from the open ocean and CB5 from the coastal ocean. The two picocyanobacterial strains utilised contrasting photosynthesis, Fe uptake, and nutrient acquisition strategies to cope with Fe limitation. In the oceanic strain, moderate warming under Fe limitation upregulated expression of photosynthesis and nutrient and Fe transport genes, increasing its growth and photosynthesis. In contrast, gene expression under low Fe in the coastal strain was less affected by warming. The oceanic isolate exhibited substrate regulation of Fe acquisition and preferred organic nutrient sources. The coastal strain had a much higher Fe quota, faster turnover of the D1 gene in photosystem II, and was optimised for inorganic nitrogen sources. Both strains showed multi-tiered Fe uptake strategies and general stress responses to heat shock and oxidative stress. In general, gene regulation in the oceanic strain responded more effectively to both stressors than in the coastal isolate. Fe-temperature interactions in both strains are complex and may lead to synergistic and antagonistic responses, potentially influencing global biogeochemical cycles in warmer oceans.

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来源期刊
Environmental Microbiology Reports
Environmental Microbiology Reports ENVIRONMENTAL SCIENCES-MICROBIOLOGY
CiteScore
6.00
自引率
3.00%
发文量
91
审稿时长
3.0 months
期刊介绍: The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side. Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following: the structure, activities and communal behaviour of microbial communities microbial community genetics and evolutionary processes microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors microbes in the tree of life, microbial diversification and evolution population biology and clonal structure microbial metabolic and structural diversity microbial physiology, growth and survival microbes and surfaces, adhesion and biofouling responses to environmental signals and stress factors modelling and theory development pollution microbiology extremophiles and life in extreme and unusual little-explored habitats element cycles and biogeochemical processes, primary and secondary production microbes in a changing world, microbially-influenced global changes evolution and diversity of archaeal and bacterial viruses new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.
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