延长的光照时间增加了渗透性褐藻的光合投资。

IF 3.7 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-07-23 Epub Date: 2025-06-24 DOI:10.1128/aem.01032-25
Xiaoqing Xu, Xiaoyu Cheng, Zhihao Shao, Zhou Yang, Lu Zhang
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引用次数: 0

摘要

光周期作为一种重要的外部环境信号,在生物体内引发一系列信号反应,显著影响自养生物的光合效率和光形态发生,同时也影响异养生物的行为模式和活动节律。尽管它很重要,但混合营养体对光周期变化的反应机制仍未得到充分研究。了解混合营养体如何通过调节其自养和渗透途径对光可用性做出反应并在昼夜转换中做出最佳决策,对于理解代谢可塑性至关重要。因此,本研究以具有光自养和渗透营养生长能力的真核原生生物gloeopara为研究对象,探讨混合营养体在光周期变化下的代谢策略。结果表明:(i)在自养条件下,Ochromonas光合效率的最佳光周期约为12 h,而超过此时间的长时间光照会减少光合投资和效率,同时增加散热以防止光损伤。(ii)在渗透营养条件下,黄貂草通过减少水分来适应长时间的光照。依赖外部有机碳源和增强光合能力,从而转向更自养的代谢模式。本研究从种群动态、光合生理和碳获取途径等方面系统阐明了混合营养植物对光周期变化的营养响应策略,加深了我们对混合营养生物对光周期变化响应的认识。这些发现为理解混合营养体在生态系统中的功能作用和准确预测全球碳循环的变化提供了重要的理论见解。重要性:混合营养体具有灵活的代谢方式和多重生态作用,对环境变化非常敏感。由于其广泛的分布和独特的营养策略,它们是海洋和淡水生态系统中的关键功能群,在全球生物地球化学循环中发挥着重要作用。光周期是调节生物昼夜节律并影响混合营养体代谢策略的关键环境信号。因此,本研究主要关注混合营养微生物gloeopara Ochromonas如何调节自养和渗透途径以响应光周期变化。这些发现强调了混合营养生物在响应光周期变化时的代谢灵活性,为混合营养生物如何调节物质流动和重塑食物网结构提供了新的见解。该研究为理解混合营养微生物在生态系统中的功能作用提供了有价值的创新视角,对提高全球碳循环预测的准确性具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prolonged light exposure time enhances the photosynthetic investment in osmotrophic Ochromonas.

The photoperiod, as a critical external environmental signal, triggers a cascade of signaling responses in organisms that significantly affect photosynthetic efficiency and photomorphogenesis in autotrophs, while also influencing behavioral patterns and activity rhythms of heterotrophs. Despite its importance, the mechanisms by which mixotrophs respond to photoperiod changes remain largely unexplored. It is crucial for understanding metabolic plasticity how mixotrophs respond to light availability and make optimal decisions during diurnal transitions by regulating their autotrophic and osmotrophic pathways. Therefore, this study focused on Ochromonas gloeopara, a eukaryotic protist capable of both photoautotrophic and osmotrophic growth, aiming to explore the metabolic strategies of mixotrophs in response to changes in photoperiod. The results showed the following. (i) Under autotrophic conditions, the optimal photoperiod for photosynthetic efficiency in Ochromonas was approximately 12 h of light exposure, while prolonged light exposure beyond this duration reduced photosynthetic investment and efficiency, accompanied by an increase in heat dissipation to prevent photodamage. (ii) Under osmotrophic conditions, O. gloeopara adapted to prolonged light exposure by reducing. The reliance on external organic carbon sources and enhancing photosynthetic capacity, thereby shifting towards a more autotrophic metabolic mode. This study systematically elucidates the nutritional strategies of mixotrophic O. gloeopara in response to photoperiod changes at the levels of population dynamics, photosynthetic physiology, and carbon acquisition pathways, deepening our understanding of the response to photoperiodic changes in mixotrophs. These findings provide important theoretical insights for understanding the functional roles of mixotrophs in ecosystems and for accurately predicting changes in global carbon cycles.

Importance: Mixotrophs possess flexible metabolism modes and multiple ecological roles, making them sensitive to environmental changes. Due to their widespread distribution and unique nutritional strategy, they serve as key functional groups in marine and freshwater ecosystems, with significant roles in global biogeochemical cycles. Photoperiod, a critical environmental cue, regulates circadian rhythms and may influence the metabolic strategies of mixotrophs. Therefore, this study focused on how the mixotrophic microorganisms Ochromonas gloeopara adjusted autotrophic and osmotrophic pathways in response to photoperiodic changes. These findings highlight the metabolic flexibility of mixotrophic organisms in response to photoperiodic changes, providing new insight on how mixotrophs regulate the flow of materials and reshape the food web structures. This research offers valuable and innovative perspectives for understanding the functional roles of mixotrophic microorganisms in ecosystems, with important implications for improving the accuracy of global carbon cycle predictions.

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来源期刊
Applied and Environmental Microbiology
Applied and Environmental Microbiology 生物-生物工程与应用微生物
CiteScore
7.70
自引率
2.30%
发文量
730
审稿时长
1.9 months
期刊介绍: Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.
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