Microcystis aeruginosa

铜绿微囊藻
  • 文章类型: Journal Article
    藻华已成为人们广泛关注的饮用水生产问题,威胁生态系统和人类健康。光催化,一种有前途的高级氧化工艺(AOP)废水处理技术,被认为是原位修复藻华的潜在措施。然而,传统的光催化剂通常遭受有限的可见光响应和光生电子-空穴对的快速重组。在这项研究中,我们使用共沉淀法制备了具有优异可见光吸收性能的Z-schemeAgBr/NH2-MIL-125(Ti)复合材料,以有效灭活铜绿微囊藻。可见光照射180min后AgBr/NH2-MIL-125(Ti)对叶绿素a的降解效率为98.7%,显著超过AgBr和NH2-MIL-125(Ti)的降解速率效率分别为3.20和36.75倍。此外,即使重复使用五次,去除率仍保持在91.1%。实验结果表明,超氧自由基(•O2-)是主要的活性氧。光催化反应改变了藻类细胞的形态和表面电荷,抑制了它们的新陈代谢,破坏了它们的光合和抗氧化系统.总之,本研究为光催化技术在藻华修复中的应用提供了一种有前途的材料。
    Algal blooms have become a widespread concern for drinking water production, threatening ecosystems and human health. Photocatalysis, a promising advanced oxidation process (AOP) technology for wastewater treatment, is considered a potential measure for in situ remediation of algal blooms. However, conventional photocatalysts often suffer from limited visible-light response and rapid recombination of photogenerated electron-hole pairs. In this study, we prepared a Z-scheme AgBr/NH2-MIL-125(Ti) composite with excellent visible light absorption performance using co-precipitation to efficiently inactivate Microcystis aeruginosa. The degradation efficiency of AgBr/NH2-MIL-125(Ti) for chlorophyll a was 98.7 % after 180 min of visible light irradiation, significantly surpassing the degradation rate efficiency of AgBr and NH2-MIL-125(Ti) by factors of 3.20 and 36.75, respectively. Moreover, the removal rate was maintained at 91.1 % even after five times of repeated use. The experimental results indicated that superoxide radicals (•O2-) were the dominant reactive oxygen species involved. The photocatalytic reaction altered the morphology and surface charge of algal cells, inhibited their metabolism, and disrupted their photosynthetic and antioxidant systems. In conclusion, this study presents a promising material for the application of photocatalytic technology in algal bloom remediation.
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  • 文章类型: Journal Article
    淡水中浮游植物的生长通常受到磷(P)的可利用性的限制,彻底了解磷的可用性对于防止藻类繁殖至关重要。然而,不同P形式的生物利用度和利用机制的差异尚不清楚,特别是有机磷是否可以用作P源。本研究调查了0.5、1.0和2.0mg/LP对铜绿微囊藻的影响。包括溶解的有机P(DOP)(1-羟基乙烷1,1-二膦酸)和溶解的无机P(DIP)(磷酸二钾)。与DIP相比,在DOP处理中吸收的细胞内P含量明显降低。DOP更有利于可溶性蛋白的合成和胞外聚合物的释放。碱性磷酸酶活性通常响应于DIP缺乏而增强。DIP和DOP均在相同程度上促进碳吸收。DOP基团吸收碳来合成能量和蛋白质以响应压力,而DIP组主要用于生长的碳。它们都降低了微囊藻毒素释放到水环境中的含量,从而降低了微囊藻毒素引起的生态风险。与DIP相比,DOP组光合作用相关基因表达显著下调,而核苷磷酸分解代谢的表达,P运输车,在缺磷环境和1.0mg/LDOP浓度的胁迫下,氨基酸的生物合成和代谢显着上调。总之,不同P形式对蓝藻的生物利用度不同,因此,仅使用总P来评估环境风险是不够的。在淡水生态系统的风险管理中也应考虑使用P形式。
    Phytoplankton growth in freshwater is often limited by the availability of phosphorus (P), and thorough understandings of P availability are essential to prevent algal blooms. However, the differences in bioavailability and utilization mechanisms of different P forms remain unclear, especially whether organophosphorus could be used as P sources. This study investigated the effects of 0.5, 1.0, and 2.0 mg/L P on Microcystis aeruginosa, including dissolved organic P (DOP) (1-hydroxyethane 1,1-diphosphonic acid) and dissolved inorganic P (DIP) (dipotassium phosphate). Compared with DIP, intracellular P content absorbed in DOP treatment was significantly lower. DOP was more conducive to the synthesis of soluble protein and the release of extracellular polymeric substances. Alkaline phosphatase activity was generally enhanced in response to DIP deficiency. Both DIP and DOP promoted carbon uptake to the same extent. DOP groups absorbed carbon to synthesize energy and proteins in response to stress, while DIP groups were mainly used carbon for growth. They all reduced the content of microcystin releasing into the aquatic environment and therefore reduced ecological risk caused by microcystin. Compared with DIP, the expressions of photosynthesis-related genes were significantly down-regulated in DOP group, while the expressions of nucleoside phosphate catabolism, P transporter, and amino acid biosynthesis and metabolism were significantly up-regulated in response to P deficiency environment and the stress of 1.0 mg/L DOP concentration. In summary, the bioavailability of different P forms on cyanobacteria is different, so it is not sufficient to only use total P for assessing environmental risk. P forms should also be considered for risk management of freshwater ecosystems.
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  • 文章类型: Journal Article
    有害藻华(HAB)是水生有毒微藻的爆发,是由营养富集驱动的全球性问题。全球气候变化和入侵物种。我们独特地描述了一个前所未有的持续时间的HAB,2023年在Neagh湖的范围和大小;英国和爱尔兰最大的淡水湖,使用无与伦比的卫星图像组合,营养分析,16SrRNA基因测序和氰基毒素分析。病原体铜绿微囊藻占水样中DNA的三分之一以上,尽管常见的浮游细菌物种也大量繁殖。水磷酸盐水平肥大并驱动当地藻类生物量。HAB遍布整个生态系统,在码头周围积聚了藻类垫,码头和锁门。从藻类垫样品中分离出的超过80%的细菌DNA由与野禽或牲畜粪便和人类废水相关的物种组成,包括13种可能导致严重人类疾病的潜在病原体,包括:大肠杆菌,沙门氏菌,肠杆菌和梭菌等。十种微囊藻毒素,结节蛋白和两种anabaenoptin毒素被证实存在(进一步怀疑微囊藻毒素和四种anabaenoptin),在某些位置(1,137-18,493μg/L),MC-RR和-LR的浓度很高,在所有采样的藻类垫中,MC-LR超过了世界卫生组织(WHO)休闲暴露指南。这是爱尔兰岛上任何水体中首次检测到anabaenopeptin。尽管有生态影响,这个HAB代表了环境和公共卫生风险,减少湖内外的娱乐活动,破坏当地企业。减少农业径流和人类废水处理的排放,以管理养分负荷,和公共卫生风险,应该是利益相关者的首要任务,尤其是政府。主要建议包括基于自然的解决方案,以避免与农业部门的生产力和盈利能力发生冲突,从而提高可持续性。我们希望这会激发现实世界的行动,以解决困扰这个国际重要生态系统的问题。
    Harmful Algal Blooms (HABs) are outbreaks of aquatic toxic microalgae emerging as a global problem driven by nutrient enrichment, global climate change and invasive species. We uniquely describe a HAB of unprecedented duration, extent and magnitude during 2023 in Lough Neagh; the UK and Ireland\'s largest freshwater lake, using an unparalleled combination of satellite imagery, nutrient analysis, 16S rRNA gene sequencing and cyanotoxin profiling. The causative agent Microcystis aeruginosa accounted for over a third of DNA in water samples though common bacterioplankton species also bloomed. Water phosphate levels were hypertrophic and drove local algal biomass. The HAB pervaded the entire ecosystem with algal mats accumulating around jetties, marinas and lock gates. Over 80 % of bacterial DNA isolated from algal mat samples consisted of species associated with wildfowl or livestock faeces and human-effluent wastewater including 13 potential pathogens that can cause serious human illness including: E. coli, Salmonella, Enterobacter and Clostridium among others. Ten microcystins, nodularin and two anabaenopeptin toxins were confirmed as present (with a further microcystin and four anabaenopeptins suspected), with MC-RR and -LR in high concentrations at some locations (1,137-18,493 μg/L) with MC-LR exceeding World Health Organisation (WHO) recreational exposure guidelines in all algal mats sampled. This is the first detection of anabaenopeptins in any waterbody on the island of Ireland. Notwithstanding the ecological impacts, this HAB represented an environmental and public health risk, curtailing recreational activities in-and-around the lake and damaging local businesses. Reducing agricultural runoff and discharge from human-effluent wastewater treatment to manage nutrient loading, and the public health risk, should be the top priority of stakeholders, especially government. Key recommendations include Nature-based Solutions that avoid conflict with the productivity and profitability of the farming sector enhancing sustainability. We hope this stimulates real-world action to resolve the problems besetting this internationally important ecosystem.
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  • 文章类型: Journal Article
    供水系统中的蓝细菌被认为是一个新的威胁,当一些物种产生有毒代谢物时,氰毒素,其中最广泛和研究最充分的是微囊藻毒素。饮用受污染的水是一种常见的氰毒素暴露途径,使研究饮用水中的蓝藻成为保护公众健康的优先事项。在饮用水处理厂,氯化化合物的预氧化被广泛用于抑制蓝细菌的生长,尽管存在对其降低氰基毒素含量的功效的担忧。此外,氯化对丰富但研究较少的氰基代谢物(例如毒性尚不清楚的氰基吡啶)的影响仍未得到充分研究。这里,两种氯化氧化剂,次氯酸钠(NaClO)和二氧化氯(ClO2),对有毒的蓝细菌铜绿微囊藻进行了测试,评估它们对细胞活力的影响,毒素概况和含量。内外微囊藻毒素和其他氰基代谢物,包括它们的降解产物,使用非靶向LC-HRMS方法进行鉴定。两种氧化剂都能够在低剂量(0.5mgL-1)时灭活铜绿分枝杆菌细胞,并大大降低细胞内毒素含量(>90%),无论治疗时间(1-3小时)。相反,NaClO处理后,细胞外毒素增加了两倍,表明细胞损伤。根据LC-HRMSn(n=2,3)证据,鉴定了一种新的代谢产物,命名为氰基吡啶型肽-1029,两种氧化剂对它的影响不同。NaClO导致其细胞外浓度从2增加到80-100μgL-1,ClO2诱导其氧化衍生物的形成,氰洞素型肽-1045。总之,对被有毒蓝细菌污染的原水进行预氧化处理可能导致饮用水中氰基毒素浓度增加,取决于化学剂,其剂量和治疗持续时间,也是氧化代谢物。由于这些代谢物对人类健康的影响仍然未知,参与饮用水管理的水安全机构应极其谨慎地处理这一问题。
    Cyanobacteria in water supplies are considered an emerging threat, as some species produce toxic metabolites, cyanotoxins, of which the most widespread and well-studied are microcystins. Consumption of contaminated water is a common exposure route to cyanotoxins, making the study of cyanobacteria in drinking waters a priority to protect public health. In drinking water treatment plants, pre-oxidation with chlorinated compounds is widely employed to inhibit cyanobacterial growth, although concerns on its efficacy in reducing cyanotoxin content exists. Additionally, the effects of chlorination on abundant but less-studied cyanometabolites (e.g. cyanopeptolins whose toxicity is still unclear) remain poorly investigated. Here, two chlorinated oxidants, sodium hypochlorite (NaClO) and chlorine dioxide (ClO2), were tested on the toxic cyanobacterium Microcystis aeruginosa, evaluating their effect on cell viability, toxin profile and content. Intra- and extracellular microcystins and other cyanometabolites, including their degradation products, were identified using an untargeted LC-HRMS approach. Both oxidants were able to inactivate M. aeruginosa cells at a low dose (0.5 mg L-1), and greatly reduced intracellular toxins content (>90%), regardless of the treatment time (1-3 h). Conversely, a two-fold increase of extracellular toxins after NaClO treatment emerged, suggesting a cellular damage. A novel metabolite named cyanopeptolin-type peptide-1029, was identified based on LC-HRMSn (n = 2, 3) evidence, and it was differently affected by the two oxidants. NaClO led to increase its extracellular concentration from 2 to 80-100 μg L-1, and ClO2 induced the formation of its oxidized derivative, cyanopeptolin-type peptide-1045. In conclusion, pre-oxidation treatments of raw water contaminated by toxic cyanobacteria may lead to increased cyanotoxin concentrations in drinking water and, depending on the chemical agent, its dose and treatment duration, also of oxidized metabolites. Since the effects of such metabolites on human health remain unknown, this issue should be handled with extreme caution by water security agencies involved in drinking water management.
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  • 文章类型: Journal Article
    光合固碳和微生物碳代谢是藻类-细菌相互作用的主要过程,影响污染物降解以及水生系统中基本的生物地球化学循环。人类引起的土地利用变化极大地改变了内陆湖泊中陆地溶解有机质(DOM)的分子组成和输入。然而,DOM的起源如何导致对藻圈微生物群落或DOM分子组成的不同影响,例如,通过碳代谢,很少在淡水中进行研究。这里,我们将蓝藻铜绿微囊藻和天然湖泊中的细菌群落进行孵育,以建立藻类细菌模型系统。这使我们能够研究来自不同来源的DOM如何影响藻圈微生物多样性和DOM多样化。我们证明了苏万尼河富里酸(SRFA),Suwannee河天然有机物(SRNOM)和农田湖泊DOM促进藻类生长,而来自城市湖泊的DOM抑制藻类生长。藻类代谢产物和DOM共同形成了藻圈群落的趋化反应。高分辨率质谱分析表明,在多种DOM源与藻类-细菌共生系统相互作用后,DOM化学多样性趋于均匀。基于底物显式模型的DOM的分子热力学分析进一步验证了微生物相互作用使DOM的生物可利用性降低,从而增加了顽固的DOM形成。代谢组分析发现,DOM添加会增强与不稳定和顽固DOM利用相关的代谢途径(主要是木质素/富含羧基的脂环分子(CRAM)-likeDOM,不饱和烃),辅因子和维生素代谢在所有代谢途径中都表现出非常强的活性。我们的结果强调了DOM与微生物代谢在分子水平上的共变和相互作用,并扩展了我们对微生物介导的DOM形成水生碳循环的理解。
    Photosynthetic carbon sequestration and microbial carbon metabolism are major processes of algae-bacteria interactions, affecting pollutant degradation as well as fundamental biogeochemical cycles in aquatic systems. Human-induced land-use changes greatly alter the molecular composition and input of terrestrial dissolved organic matter (DOM) in inland lakes. However, how the origin of DOM leads to varying effects on phycosphere microbial communities or molecular composition of DOM, e.g., via carbon metabolism, has been little studied in freshwater. Here, we incubated the cyanobacterium Microcystis aeruginosa and a bacterial community from natural lakes to establish an alga-bacteria model system. This allowed us to investigate how DOM from different sources affects phycosphere microbial diversity and DOM diversification. We showed that Suwannee River fulvic acid (SRFA), Suwannee River natural organic matter (SRNOM) and cropland lake DOM promote algal growth, whereas DOM from an urban lake inhibits algal growth. Algal metabolites and DOM together shaped the chemotaxis response of phycosphere communities. High-resolution mass spectrometry analysis demonstrated that DOM chemo-diversity tended to become uniform after interactions of diverse DOM sources with the algae-bacteria symbiosis system. Molecular thermodynamic analysis of DOM based on a substrate-explicit model further verified that microbial interactions render DOM less bioavailable and thus increase recalcitrant DOM formation. Metabolome analysis uncovered that DOM addition intensifies metabolic pathways related to labile and recalcitrant DOM utilization (mainly lignin/carboxyl-rich alicyclic molecule (CRAM)-like DOM, unsaturated hydrocarbon), whereby cofactor and vitamin metabolism represented an extremely strong activity in all metabolic pathways. Our results highlight covariation and interactions of DOM with microbial metabolism at the molecular level and expands our understanding of microbially mediated DOM shaping aquatic carbon cycling.
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  • 文章类型: Journal Article
    蓝细菌的快速生长,特别是铜绿微囊藻,对全球水安全构成重大威胁。有毒的铜绿微囊藻的增殖由于其对人类健康和社会经济影响的潜在危害而引起人们的关注。密集的花朵有助于时空无机碳消耗,促进对碳浓缩机制(CCM)在竞争性碳吸收中的作用的兴趣。尽管HCO3-转运蛋白很重要,铜绿分枝杆菌的遗传评估和功能预测仍然不足。在这项研究中,我们探索了46株铜绿假单胞菌基因组中HCO3-转运蛋白的多样性,评估每个人的积极选择。有趣的是,尽管微囊藻BicA转运蛋白在46个基因组菌株中有23个成为部分基因,我们观察到显著的阳性位点。结构分析,包括预测的2D和3D模型,证实了微囊藻BicA转运蛋白的结构保守性。我们的研究结果表明,微囊藻BicA运输可能在竞争性碳吸收中起着至关重要的作用。强调其生态意义。在蓝藻水华期间,微囊藻BicA运输在竞争性生长中的生态功能提出了重要问题。未来的研究需要实验确认,以更好地了解微囊藻BicA转运蛋白在蓝藻水华动力学中的作用。
    The rapid growth of cyanobacteria, particularly Microcystis aeruginosa, poses a significant threat to global water security. The proliferation of toxic Microcystis aeruginosa raises concerns due to its potential harm to human health and socioeconomic impacts. Dense blooms contribute to spatiotemporal inorganic carbon depletion, promoting interest in the roles of carbon-concentrating mechanisms (CCMs) for competitive carbon uptake. Despite the importance of HCO3- transporters, genetic evaluations and functional predictions in M. aeruginosa remain insufficient. In this study, we explored the diversity of HCO3- transporters in the genomes of 46 strains of M. aeruginosa, assessing positive selection for each. Intriguingly, although the Microcystis BicA transporter became a partial gene in 23 out of 46 genomic strains, we observed significant positive sites. Structural analyses, including predicted 2D and 3D models, confirmed the structural conservation of the Microcystis BicA transporter. Our findings suggest that the Microcystis BicA transport likely plays a crucial role in competitive carbon uptake, emphasizing its ecological significance. The ecological function of the Microcystis BicA transport in competitive growth during cyanobacterial blooms raises important questions. Future studies require experimental confirmation to better understand the role of the Microcysits BicA transporter in cyanobacterial blooms dynamics.
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  • 文章类型: Journal Article
    陆地溶解有机物(tDOM)有望通过流域管理控制蓝藻水华。为了识别可能抑制生长的tDOM,光合作用和集落形成,单细胞铜绿微囊藻Kützing(FACHB-469)培养并用不同浓度的没食子酸处理,脯氨酸和茶多酚中不同含量的铁。结果表明,没食子酸和茶多酚可以通过抑制光合作用和减少胞外多糖(EPS)分泌来抑制微囊藻的生长。然而,脯氨酸对生长没有显著影响,光合作用,微囊藻的菌落大小和EPS含量。转录组分析表明,微囊藻可能通过不同铁水平下的藻胆体变化来优化光合作用的内部能量转移模式。此外,微囊藻通过调节与铁摄取和转运相关基因的表达来适应不同的铁浓度环境。这些发现表明,在流域植树造林中应考虑植物物种对藻华的影响。这种考虑需要在使用tDOM控制蓝藻水华的成本和收益之间找到平衡。
    Terrestrial dissolved organic matter (tDOM) holds great promise for controlling cyanobacteria blooms through watershed management. To identify tDOM that could inhibit the growth, photosynthesis and colony formation, unicellular Microcystis aeruginosa Kützing (FACHB-469) was cultivated and treated with varying concentrations of gallic acid, proline and tea polyphenols at different levels of iron. The results indicated that gallic acid and tea polyphenols could inhibit Microcystis growth by suppressing photosynthesis and colony formation by reducing extracellular polysaccharides (EPS) secretion. However, proline had no significant effect on the growth, photosynthesis, colony size and EPS content of Microcystis. Transcriptome analysis showed Microcystis may optimize the internal energy transfer mode of photosynthesis through the change of phycobilisome at different levels of iron. In addition, Microcystis adapted to different iron concentration environments by regulating the expression of genes associated with iron uptake and transport. These findings suggest that the effects of plant species on algal blooms should be considered in reforestation of watershed. This consideration necessitates finding a balance between the costs and benefits of controlling cyanobacteria blooms using tDOM.
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  • 文章类型: Journal Article
    传统的饮用水处理除藻方法,如凝结和沉淀,由于藻类细胞表面的负电荷而面临挑战,导致无效的去除。超声空化已显示出通过破坏细胞外聚合物结构并通过诸如剪切力和自由基反应的各种机制改善蓝细菌去除来增强凝血性能的希望。然而,常规超声处理中自由基的短寿命和有限的传质距离导致高能耗,限制了广泛应用。为了克服这些限制并提高能源效率,开发和测试了先进的碳基材料。发现纳米金刚石表面上的氮掺杂官能团通过增加超声增敏剂-水界面处活性氧的产生来提高超声敏感性。利用低功率超声(0.12W/mL)结合N-ND治疗5分钟,水体中铜绿微囊藻细胞的去除率超过90%,增强了水中藻类有机物和微囊藻毒素的去除。通过共聚焦显微镜的可视化强调了带正电荷的氮掺杂纳米金刚石在聚集藻类细胞中的作用。细胞捕获和N-ND催化之间的协同作用表明,自由基从声敏剂表面到微藻表面的有效传质对于促进蓝藻絮凝物的形成至关重要。这项研究强调了采用低强度超声和N-ND系统有效改善水处理过程中藻类去除的潜力。
    Traditional methods for algae removal in drinking water treatment, such as coagulation and sedimentation, face challenges due to the negative charge on algae cells\' surfaces, resulting in ineffective removal. Ultrasonic cavitation has shown promise in enhancing coagulation performance by disrupting extracellular polymer structures and improving cyanobacteria removal through various mechanisms like shear force and free radical reactions. However, the short lifespan and limited mass transfer distance of free radicals in conventional ultrasonic treatment lead to high energy consumption, limiting widespread application. To overcome these limitations and enhance energy efficiency, advanced carbon-based materials were developed and tested. Nitrogen-doped functional groups on nanodiamond surfaces were found to boost sonosensitivity by increasing the production of reactive oxygen species at the sonosensitizer-water interface. Utilizing low-power ultrasound (0.12 W/mL) in combination with N-ND treatment for 5 min, removal rates of Microcystis aeruginosa cells in water exceeded 90 %, with enhanced removal of algal organic matters and microcystins in water. Visualization through confocal microscopy highlighted the role of positively charged nitrogen-doped nanodiamonds in aggregating algae cells. The synergy between cell capturing and catalysis of N-ND indicates that efficient mass transfer of free radicals from the sonosensitizer\'s surface to the microalgae\'s surface is critical for promoting cyanobacteria floc formation. This study underscores the potential of employing a low-intensity ultrasound and N-ND system in effectively improving algae removal in water treatment processes.
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  • 文章类型: Journal Article
    有害藻华对生态安全和人类健康构成巨大威胁。在这项研究中,模拟太阳光(SSL)辐照用于激活高碘酸盐(PI),以灭活铜绿微囊藻和降解微囊藻毒素-LR(MC-LR)。我们发现PI-SSL系统可以在180min内有效灭活5×106个细胞·mL-1的藻类细胞,低于检测限。·PI-SSL系统中产生的OH和碘(IO3·和IO4·)自由基可以破坏细胞膜,释放细胞内物质,包括MC-LR进入反应系统。然而,释放的MC-LR可以通过PI-SSL系统中的羟基化和环裂解过程降解为无毒小分子,降低环境风险。PI-SSL系统在宽pH范围(3-9)的溶液中的高藻类灭活性能,与共存的阴离子(Cl-,NO3-和SO42-)以及天然有机物(腐殖酸和富里酸)的共存,真正的水(湖水和河水),以及在连续流动反应器(14小时)也实现。此外,在自然阳光照射下,有效的藻类灭活也可以在扩大的反应器(1L)中实现。总的来说,我们的研究表明,PI-SSL系统可以避免背景物质的推断,可以用作处理藻类水华水的可行技术。
    Harmful algal blooms pose tremendous threats to ecological safety and human health. In this study, simulated solar light (SSL) irradiation was used to activate periodate (PI) for the inactivation of Microcystis aeruginosa and degradation of microcystin-LR (MC-LR). We found that PI-SSL system could effectively inactivate 5 × 106 cells·mL-1 algal cells below the limit of detection within 180 min. ·OH and iodine (IO3· and IO4·) radicals generated in PI-SSL system could rupture cell membranes, releasing intracellular substances including MC-LR into the reaction system. However, the released MC-LR could be degraded into non-toxic small molecules via hydroxylation and ring cleavage processes in PI-SSL system, reducing their environmental risks. High algae inactivation performance of PI-SSL system in solution with a wide pH range (3-9), with the coexisting anions (Cl-, NO3- and SO42-) and the copresence of natural organic matters (humic acid and fulvic acid), real water (lake water and river water), as well as in continuous-flow reactor (14 h) were also achieved. In addition, under natural sunlight irradiation, effective algae inactivation could also be achieved in an enlarged reactor (1 L). Overall, our study showed that PI-SSL system could avoid the inference by the background substances and could be employed as a feasible technique to treat algal bloom water.
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  • 文章类型: Journal Article
    铜绿微囊藻是蓝藻水华中的主要毒株,其温度相关的季节性演替中的募集阶段被认为是其随后生长的关键。在这项研究中,为了研究和确认化感物质在招募阶段对铜绿分枝杆菌的优异抑制作用,开发了具有特定温度设置的方案作为模拟招募阶段.最常见的化感物质之一,没食子酸(GA)(10mg/L,20mg/L)用于在初始低温条件(15°C)下处理铜绿假单胞菌,然后中间(20°C)和最后正常(26°C),对应于蓝藻募集和生长的临界温度。增长,新陈代谢,光合活性,胞外多糖(EPS)和微囊藻毒素(MCs)的释放进行了分析和讨论,并且在20天的时间内获得了更持续和更好的抑制作用。值得注意的是,GA(10mg/L)显著延缓了低温下铜绿假单胞菌的募集,抑制效率为85.71%,并抑制Fv/Fm和光合色素的产生。还观察到铜绿假单胞菌在募集阶段对化感处理表现出更高的敏感性和更差的抗性。不同的反应表明最佳剂量可能会改变。抗氧化酶活性在长期胁迫下仍然很高,并刺激了EPS的分泌,表明蓝细菌更倾向于形成菌落。虽然基于实验室的抑制机制似乎增加了单个细胞中微囊藻毒素的释放,微囊藻毒素在自然水生环境中的实际浓度需要进一步研究。
    Microcystis aeruginosa is the main toxic strain in cyanobacterial blooms, and the recruitment stage in its temperature-dependent seasonal succession is considered as the key to its subsequent growth. In this study, a protocol with specific temperature settings was developed as the simulated recruitment stage in order to investigate and confirm the superior inhibitory effects of allelochemicals on M. aeruginosa at that stage of recruitment. One of the most common allelochemicals, gallic acid (GA) (10 mg/L, 20 mg/L) was employed to treat M. aeruginosa under initially low temperature condition (15 °C), then intermediate (20 °C) and last normal (26 °C), which corresponds to the critical temperatures for cyanobacterial recruitment and growth. Growth, metabolism, photosynthetic activity, extracellular polysaccharides (EPS) and microcystins (MCs) release were analyzed and discussed in this study, and a more sustained and better inhibitory effect over a 20-day period was achieved. Notably, GA (10 mg/L) markedly delayed the recruitment of M. aeruginosa from low temperature, with an inhibition efficiency of 85.71 %, and suppressing Fv/Fm and photosynthetic pigments production. It is also observed that M. aeruginosa at recruitment stage exhibited higher sensitivity and poorer resistance to allelochemical treatment, with variable responses suggesting that optimal dosages may alter. The antioxidant enzyme activities remained high under prolonged stress, and the secretion of EPS was stimulated, indicating that cyanobacteria were more inclined to form colonies. While the laboratory-based inhibitory mechanism appeared to increase the release of microcystins in individual cells, the actual concentration of microcystins in natural aquatic environments requires further investigation.
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