The evaluation of biogenic silica in brackish and freshwater strains reveals links between phylogeny and silica accumulation in picocyanobacteria.

IF 3.9 2区 生物学 Q2 BIOTECHNOLOGY & APPLIED MICROBIOLOGY
Applied and Environmental Microbiology Pub Date : 2025-04-23 Epub Date: 2025-03-27 DOI:10.1128/aem.02527-24
Anabella Aguilera, Daniel Lundin, Evangelia Charalampous, Yelena Churakova, Christian Tellgren-Roth, Sylwia Śliwińska-Wilczewska, Daniel J Conley, Hanna Farnelid, Jarone Pinhassi
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引用次数: 0

Abstract

Through biosilicification, organisms incorporate dissolved silica (dSi) and deposit it as biogenic silica (bSi), driving the silicon (Si) cycle in aquatic systems. While Si accumulation in marine picocyanobacteria has been recently observed, its mechanisms and ecological implications remain unclear. This study investigates biosilicification in marine and brackish picocyanobacteria of the Synechococcus clade and two model freshwater coccoid cyanobacteria. Brackish strains showed significantly higher Si quotas when supplemented with external dSi (100 µM) compared to controls (up to 60.0 ± 7.3 amol Si.cell-1 versus 9.2 to 16.3 ± 2.9 amol Si.cell-1). Conversely, freshwater strains displayed no significant differences in Si quotas between dSi-enriched treatments and controls, emphasizing that not all phytoplanktons without an obligate Si requirement accumulate this element. The Si-accumulating marine and brackish picocyanobacteria clustered within the Synechococcus clade, whereas their freshwater counterparts formed a distinct sister group, suggesting a link between phylogeny and silicification. Rapid culture growth caused increased pH and led to dSi precipitation, influencing apparent dSi uptake; this was mitigated by pH control through bubbling. This phenomenon has significant implications for natural systems affected by phytoplankton blooms. In such environments, pH-induced silicon precipitation may reduce dSi availability impacting Si-dependent populations like diatoms. Our findings suggest brackish picocyanobacteria could significantly influence the Si cycle through at least two mechanisms: cellular Si accumulation and biologically induced changes in dSi concentrations.IMPORTANCEThis work provides the first evidence of biogenic silica accumulation in brackish picocyanobacteria and uncovers a link between phylogeny and biosilicification patterns. Our findings demonstrate that picocyanobacterial growth induces pH-dependent silica precipitation, which could lead to overestimations of cellular Si quotas by up to 85%. This process may drive substantial silica precipitation in highly productive freshwater and coastal marine systems, with potential effects on silica cycling and the population dynamics of Si-dependent phytoplankton. The extent of biosilicification in modern picocyanobacteria offers insights into the rock record, shedding light on the evolutionary and ecological dynamics that influence sedimentary processes and the preservation of biosilicification signatures in geological formations. Overall, this research adds to the significant impact that microorganisms lacking an obligate silica requirement may have on silica dynamics.

咸淡水和淡水菌株中生物源二氧化硅的评价揭示了系统发育与picocyanobacteria中二氧化硅积累之间的联系。
通过生物硅化作用,生物体吸收溶解的二氧化硅(dSi)并将其沉积为生物源二氧化硅(bSi),从而驱动水生系统中的硅(Si)循环。虽然最近观察到海洋picocyanobacteria中的Si积累,但其机制和生态意义尚不清楚。本研究研究了海水和咸淡半咸水蓝藻中的聚藻球菌分支和两种模式淡水球藻蓝藻的生物硅化作用。与对照组(高达60.0±7.3 amol Si)相比,当添加100µM外部dSi时,咸淡水菌株的Si配额显著增加。cell-1对比9.2 ~ 16.3±2.9 mol Si.cell-1)。相反,淡水菌株的Si配额在富Si处理和对照之间没有显着差异,这表明并非所有不需要Si的浮游植物都积累了这种元素。聚硅的海洋和咸淡picocyanobacteria聚集在聚藻球菌分支中,而它们的淡水同类形成了一个独特的姐妹群,这表明系统发育与硅化之间存在联系。快速培养导致pH升高,导致dSi沉淀,影响dSi表观吸收量;通过鼓泡控制pH值可以缓解这一问题。这一现象对受浮游植物大量繁殖影响的自然系统具有重要意义。在这样的环境中,ph诱导的硅沉淀可能会降低dSi的可用性,影响硅藻等依赖si的种群。我们的研究结果表明,微咸picocyanobacteria可以通过至少两种机制显著影响Si循环:细胞Si积累和生物诱导的dSi浓度变化。重要意义:这项工作提供了在微咸picocyanobacteria中生物源二氧化硅积累的第一个证据,并揭示了系统发育和生物硅化模式之间的联系。我们的研究结果表明,花青菌的生长诱导ph依赖性二氧化硅沉淀,这可能导致细胞硅配额高估高达85%。这一过程可能在高产淡水和沿海海洋系统中驱动大量二氧化硅沉淀,对二氧化硅循环和依赖硅的浮游植物种群动态具有潜在影响。现代picocyanobacteria的生物硅化程度提供了对岩石记录的见解,揭示了影响沉积过程和地质构造中生物硅化特征保存的进化和生态动力学。总的来说,这项研究增加了微生物缺乏专性二氧化硅需求可能对二氧化硅动力学的重大影响。
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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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