氮、磷限制下原绿球藻的生理响应及分子机制OA
Physiological response and molecular mechanisms of Prochlorococcus under nitrogen and phosphorus limitation
[目的]原绿球藻(Prochlorococcus)是寡营养大洋中最小且丰度最高的光合自养生物,氮(N)、磷(P)营养盐是影响其生长的关键要素.本研究旨在探究营养盐限制条件对原绿球藻生理表型的影响及其分子机制.[方法]以HLⅡ型原绿球藻株系AS9601为实验对象,构建营养盐限制[N限制c(NH4+)∶c(PO43-)=1.6,P限制c(NH4+)∶c(PO43-)=160,对照组c(NH4+)∶c(PO43-)=16]的培养实验体系,并在此基础上进行多项生理指标测定,同时针对N限制体系开展转录组学分析.[结果]当原绿球藻面临N限制时,可利用的无机N减少,以无机N为原料的有机物合成受到抑制,尤其是需要大量N元素的捕光色素合成显著下降约62%;色素含量下降会削弱其光合固碳能力,CO2固定速率下降约65%,从而导致胞内有机碳积累减少约41%,生物量增长受限,最终表现为最大比生长速率下降72%,细胞体积减小10%.与N限制相比,原绿球藻在P限制下有相似的生理表型变化,但变化程度相对较弱;P缺乏使原绿球藻细胞的最大比生长速率下降27%,细胞体积减小8%.进一步通过转录组分析发现,原绿球藻在N限制条件下会将有限资源优先用于核苷酸合成,减少光合系统和核糖体相关基因表达,体现出其在营养盐限制下调整细胞资源分配的适应策略.[结论]综上,N、P限制均会削弱原绿球藻的多项生理表型,包括固碳和生长速率显著下降及细胞体积减小等,其中N限制的影响更显著,并伴随转录水平上资源分配的调整,反映出其在营养盐限制环境下的生理与分子响应特征.
[Objective]Prochlorococcus is the smallest and most abundant photoautotrophic organism in the oligotrophic ocean,playing a crucial role in global primary production and biogeochemical cycling.Among the environmental factors affecting its growth,nitrogen(N)and phosphorus(P)nutrients are recognized as the most critical,as they serve as essential elements for the synthesis of key cellular components.This study aims to investigate the effects of N and P limitation on the physiological traits of Prochlorococcus,as well as to elucidate its molecular response mechanisms,with a particular focus on how N and P scarcity influences key physiological parameters,including growth,carbon fixation capacity,pigment content,and global gene expression patterns.[Methods]In this study,the HL Ⅱ P.marinus AS9601 strain was selected as the experimental model.A nutrient-limited culture system was established,including a N-limited condition[c(NH4+)∶c(PO43-)=1.6],a P-limited condition[c(NH4+)∶c(PO43-)=160],and a control group with balanced nutrient availability[c(NH4+)∶c(PO43-)=16].Multiple physiological parameters were systematically measured,including growth rate,cell volume,pigment content,particulate organic carbon(POC)accumulation,and dissolved organic carbon(DOC)release.In addition,transcriptomic analysis was performed under N-limited conditions to investigate genome-wide changes in gene expression.This analysis identified genes that were significantly up-or down-regulated,providing insights into the molecular responses of P.marinus AS9601 to N limitation.[Results]Under N limitation,the availability of inorganic N decreased significantly,resulting in a pronounced inhibition of organic compound synthesis that depends on inorganic N as a substrate.Among these,the synthesis of light-harvesting pigments,which require substantial N investment,decreased by approximately 62%.This reduction in pigment content led to a substantial impairment of photosynthetic carbon fixation,with CO2 fixation rate declining by 65%.Consequently,intracellular organic carbon accumulation decreased by approximately 41%,biomass growth was limited,and the cells exhibited 72%reduction in maximum specific growth rate and 10%decrease in cell volume.Compared with N limitation,P.marinus AS9601 displayed similar physiological changes under P limitation,although the magnitude of these changes was smaller,with P deficiency causing 27%reduction in maximum specific growth rate and 8%decrease in cell volume.Transcriptomic analysis further revealed that under N limitation,P.marinus AS9601 preferentially allocated limited cellular resources to the synthesis of genetic material while downregulating the expression of genes associated with the photosynthetic apparatus and ribosomal machinery,suggesting an adaptive strategy to reallocate cellular resources under nutrient stress.[Conclusion]In summary,both N and P limitation resulted in the weakening of multiple physiological phenotypes in P.marinus AS9601,including decreased growth rate,reduced cell volume,diminished pigment content,and impaired carbon fixation capacity.N limitation exhibited more pronounced effects,accompanied by adjustments in resource allocation at the transcriptomic level.These findings comprehensively reflect the physiological and molecular response characteristics of Prochlorococcus under nutrient-limited conditions and provide valuable insights into its adaptive strategies for coping with nutrient scarcity in oligotrophic marine environments.
曾函清;李梦芸;张瑶
厦门大学海洋与地球学院,海洋生物地球化学全国重点实验室,福建厦门 361102厦门大学海洋与地球学院,海洋生物地球化学全国重点实验室,福建厦门 361102厦门大学海洋与地球学院,海洋生物地球化学全国重点实验室,福建厦门 361102
海洋科学
原绿球藻氮限制磷限制生理表型转录组
Prochlorococcusnitrogen limitationphosphorus limitationphysiological phenotypetranscriptome
《厦门大学学报(自然科学版)》 2026 (3)
418-426,9
国家重点研发计划(2023YFF0805002)
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