Production Of microcystin-LR Research Articles

Impact of butylparaben on growth dynamics and microcystin-LR production in Microcystis aeruginosa

The presence of butylparaben (BP), a prevalent pharmaceutical and personal care product, in surface waters has raised concerns regarding its impact on aquatic ecosystems. Despite its frequent detection, the toxicity of BP to the cyanobacterium Microcystis aeruginosa remains poorly understood. This study investigates the influence of BP on the growth and physiological responses of M. aeruginosa. Results indicate that low concentrations of BP (below 2.5 mg/L) have negligible effects on M. aeruginosa growth, whereas higher concentrations (5 mg/L and 10 mg/L) lead to significant growth inhibition. This inhibition is attributed to the severe disruption of photosynthesis, evidenced by decreased Fv/Fm values and chlorophyll a content. BP exposure also triggers the production of reactive oxygen species (ROS), resulting in elevated activity of antioxidant enzymes. Excessive ROS generation stimulates the production of microcystin-LR (MC-LR). Furthermore, lipid peroxidation and cell membrane damage indicate that high BP concentrations cause cell membrane rupture, facilitating the release of MC-LR into the environment. Transcriptome analysis reveals that BP disrupts energy metabolic processes, particularly affecting genes associated with photosynthesis, carbon fixation, electron transport, glycolysis, and the tricarboxylic acid cycle. These findings underscore the profound physiological impact of BP on M. aeruginosa and highlight its role in stimulating the production and release of MC-LR, thereby amplifying environmental risks in aquatic systems.

Microcystin-LR, a cyanotoxin, modulates division of higher plant chloroplasts through protein phosphatase inhibition and affects cyanobacterial division

Microcystin-LR (MC-LR) is a harmful cyanotoxin that inhibits 1 and 2A serine-threonine protein phosphatases. This study examines the influence of MC-LR on chloroplast division and the underlying mechanisms and consequences in Arabidopsis. MC-LR increased the frequency of dividing chloroplasts in hypocotyls in a time range of 1–96 h. At short-term exposures to MC-LR, small-sized chloroplasts (longitudinal diameters ≤6 μm) were more sensitive to these stimulatory effects, while both small and large chloroplasts showed stimulations at long-term exposure. After 48 h, the cyanotoxin increased the frequency of small-sized chloroplasts, indicating the stimulation of division. MC-LR inhibited protein phosphatases in whole hypocotyls and isolated chloroplasts, while it did not induce oxidative stress. We show for the first time that total cellular phosphatases play important roles in chloroplast division and that particular chloroplast phosphatases may be involved in these processes. Interestingly, MC-LR has a protective effect on cyanobacterial division during methyl-viologen (MV) treatments in Synechococcus PCC6301. MC-LR production has harmful effects on ecosystems and it may have an ancient cell division regulatory role in stressed cyanobacterial cells, the evolutionary ancestors of chloroplasts. We propose that cytoplasmic (eukaryotic) factors also contribute to the relevant effects of MC-LR in plants.

Visualization of microcystin-LR and sulfides in plateau lakes

In eutrophic water bodies, sulfides are closely related to the growth of cyanobacteria and the production of microcystin-LR (MC-LR). To date, the underlying interaction mechanism between a sulfides and MC-LR remains controversial. Thus, visually presenting the distribution characteristics of sulfides and MC-LR in contaminated water is crucial. Here, we propose a novel and expeditious practical approach, utilizing fluorescence probe technology, to assess the distribution characteristics of MC-LR and sulfur in natural lakes. We have developed novel probes, pib2, to detect HSO3– and HS–, and pib18, to simultaneously identify MC-LR and sulfides. Through correlation analysis of fluorescence data and physicochemical indicators at sampling points, it is found that fluorescence data has good correlation with sulfides and MC-LR, and speculated that pib2 and pib18 may be able to detect sulfides and MC-LR in lakes. Using this method, we rapidly obtained the distribution of MC-LR and sulfur in Qilu and Erhai Lakes. Notably, for the first time, we rapidly displayed the distributions of sulfides and MC-LR across lakes by the fluorescent probe technology.

Phosphorus conditions change the cellular responses of Microcystis aeruginosa to perfluorooctanoic acid

Perfluorooctanoic acid (PFOA), a widespread and emerging organic contaminant of aquatic environments, has high bioaccumulation potential and high toxicity. Consequently, major concerns have been raised worldwide regarding the management of this pollutant in aquatic ecosystems. To thoroughly understand PFOA's toxic effects on aquatic organisms, systematic investigations were conducted on the cellular responses of Microcystis aeruginosa to the environmental concentrations of PFOA under various concentrations as well as phosphorus (P) conditions (concentrations and forms). The results showed that P conditions remarkably affected cyanobacterial growth as well as photosynthetic pigment content, triggered oxidative stress to disrupt the function and structure of the cell membrane, and caused changes in the extracellular and intracellular contents of microcystin-LR (MC-LR). Furthermore, PFOA (100 μg/L) was absorbed by cyanobacterial cells through the stimulation of the secretion of extracellular polymeric substances (EPS) by M. aeruginosa. After entering the cyanobacterial cells, PFOA inhibited photosynthesis, reduced P absorption, induced oxidative damage, lead to a loss of cell integrity evident in scanning electron microscope images, and increased mcyA gene expression to promote MC-LR production. Moreover, the limited P concentration and forms conditions led to increased PFOA absorption by cyanobacterial cells, which further upregulated mcyA gene expression and increased the risk of MC-LR diffusion into the aquatic environment. Our present study provided a theoretical basis and new ideas for understanding and addressing safety issues related to the presence of PFOA in aquatic environments with varying nutritional statuses.

Reconstitution and expression of mcy gene cluster in the model cyanobacterium Synechococcus 7942 reveals a role of MC-LR in cell division.

Cyanobacterial blooms pose a serious threat to public health due to the presence of cyanotoxins. Microcystin-LR (MC-LR) produced by Microcystis aeruginosa is the most common cyanotoxins. Due to the limitation of isolation, purification, and genetic manipulation techniques, it is difficult to study and verify insitu the biosynthetic pathways and molecular mechanisms of MC-LR. We reassembled the biosynthetic gene cluster (mcy cluster) of MC-LR invitro by synthetic biology, designed and constructed the strong bidirectional promoter biPpsbA2 , transformed it into Synechococcus 7942, and successfully expressed MC-LR at a level of 0.006-0.018 fg cell-1 d-1 . We found the expression of MC-LR led to abnormal cell division and cellular filamentation, further using various methods proved that by irreversibly competing its GTP-binding site, MC-LR inhibits assembly of the cell division protein FtsZ. The study represents the first reconstitution and expression of the mcy cluster and the autotrophic production of MC-LR in model cyanobacterium, which lays the foundation for resolving the microcystins biosynthesis pathway. The discovered role of MC-LR in cell division reveals a mechanism of how blooming cyanobacteria gain a competitive edge over their nonblooming counterparts.

Toxicity effects of microplastics and nanoplastics with cadmium on the alga Microcystis aeruginosa.

The extensive spread of microplastics (MPs) and nanoplastics (NPs) in the aquatic environment has attracted widespread attention. The toxicity of cadmium (Cd) combined with microplastics (MPs) and nanoplastics (NPs) toward freshwater algae Microcystis aeruginosa (M. aeruginosa) was investigated to evaluate the environmental behavior of the Cd complexation in fresh water. Cd alone has the highest toxicity to algae. Both MPs and NPs also have a negative effect on the growth of algae as individual components due to their adsorption of nutrients and disruption of the alga's activity in a single MPs/NPs system. Compared with the single system, the toxicity of compound pollution including MPs + Cd and NPs + Cd becomes stronger, which presents a synergistic effect. In the presence of NPs, more extracellular polymeric substances (EPS) appeared, which helped to reduce the toxic effect on the algal cells. Moreover, MPs/NPs + Cd stimulate the production of microcystin-LR (MC-LR) under different treatments. Overall, the aquatic environmental assessment shows potentially elevated risks associated with combined MPs/NPs with Cd, which should be considered.

Toxicity effects of disinfection byproduct chloroacetic acid to Microcystis aeruginosa: Cytotoxicity and mechanisms

Chlorine-based disinfectants are widely used for disinfection in wastewater treatment. The mechanism of the effects of chlorinated disinfection by-products on cyanobacteria was unclear. Herein, the physiological effects of chloroacetic acid (CAA) on Microcystis aeruginosa (M. aeruginosa), including acute toxicity, oxidative stress, apoptosis, production of microcystin-LR (MC-LR), and the microcystin transportation-related gene mcyH transcript abundance have been investigated. CAA exposure resulted in a significant change in the cell ultrastructure, including thylakoid damage, disappearance of nucleoid, production of gas vacuoles, increase in starch granule, accumulation of lipid droplets, and disruption of cytoplasm membranes. Meanwhile, the apoptosis rate of M. aeruginosa increased with CAA concentration. The production of MC-LR was affected by CAA, and the transcript abundance of mcyH decreased. Our results suggested that CAA poses acute toxicity to M. aeruginosa, and it could cause oxidative damage, stimulate MC-LR production, and damage cell ultrastructure. This study may provide information about the minimum concentration of CAA in the water environment, which is safe for aquatic organisms, especially during the global coronavirus disease 2019 pandemic period.

Salt-alkalization may potentially promote Microcystis aeruginosa blooms and the production of microcystin-LR

The development of saline-alkali lands has contributed to the increasing discharge of alkaline salt-laden wastewater, which poses a threat to aquatic organisms. However, the comprehensive effect of alkaline salt on Microcystis aeruginosa, a harmful cyanobacterium, remains unclear. In this study, the growth, physiology, cell ultrastructure and production of microcystin-LR (MC-LR) in Microcystis aeruginosa exposed to four levels of alkaline salt stress were evaluated. The growth of Microcystis aeruginosa was stimulated at an electrical conductivity (EC) of 2.5 mS/cm compared to the control, as supported by the increased cell density, photosynthetic pigment and protein contents. Microcystis aeruginosa could tolerate a certain level of alkaline salt (i.e., EC of 5 mS/cm) via increasing photosynthetic pigment contents to protect cells from alkaline salt stress, but the antioxidant defence system and cell ultrastructure were not affected. When EC increased to 7.5 mS/cm, alkaline salt caused oxidative stress and toxicity in Microcystis aeruginosa, as evidenced by analysis of the integrated biomarker response (IBR). Furthermore, the photosynthetic pigment and protein contents decreased, and cell apoptosis associated with ultrastructural changes was observed. Therefore, we propose that EC of 7.5 mS/cm is a threshold for growth of Microcystis aeruginosa. Additionally, the intracellular MC-LR content was stimulated by alkaline salt, and the highest value was observed at EC of 2.5 mS/cm. The extracellular MC-LR content increased with the increasing alkaline salt concentration. When EC was 7.5 mS/cm, the extracellular MC-LR content was significantly higher than in the control and was associated with the upregulated mcyH gene. This study recommends that more attention should be paid to the risk of Microcystis aeruginosa bloom and microcystin-LR pollution in lakes located in salinization regions.

Morphological, molecular, and biochemical study of cyanobacteria from a eutrophic Algerian reservoir (Cheffia).

The cyanobacteria management in water bodies requires a deep knowledge of the community composition. Considering the reliable and thorough information provided by the polyphasic approach in cyanobacteria taxonomy, here we assess the cyanobacterial community structure of the Cheffia reservoir from Algeria. Cyanobacteria were identified on the basis of morphological traits and next-generation sequencing (NGS); toxins-related genes were localized in addition to the identification of toxins; temperature and nutrient level of water samples were also determined. The polyphasic approach was essential for cyanobacteria investigation; 28 genera were identified through 16S rRNA metabarcoding with the dominance of taxa from Microcystis (34.2%), Aphanizomenon (20.1%), and Planktothrix (20.0%), and morphological analysis revealed the association in this water body of five species within the genus Microcystis: M. aeruginosa, M. novacekii, M. panniformis, M. ichthyoblabe, and M. flos-aquae. The presence of mcyE genotypes was detected; moreover, HPLC-PDA and LC-ESI-MS/MS revealed the production of microcystin-LR. Results obtained in our study are very important since this ecosystem is used for water supply and irrigation; as a consequence, a good water management plan is essential.

Cell density-dependent regulation of microcystin synthetase genes (mcy) expression and microcystin-LR production in Microcystis aeruginosa that mimics quorum sensing

As the secondary metabolites of cyanobacterial harmful algal blooms (Cyano-HABs), microcystins (MCs) were generated under various environmental and cellular conditions. The understanding of the causes of MCs generation is of great interest in the field of water treatment and environmental science. In this work, we studied how Microcystis aeruginosa (FACHB-905) cell densities affect the MCs synthetase genes (mcy) expression, microcystin-LR (MC-LR) and quorum sensing molecules (Acyl-homoserine lactones (AHLs)) production. An electrochemical sensor was developed here for sensitive and quantitative detection of MC-LR that cultured at different cell densities. The results showed that mcy expression and MC-LR concentration started to increase when the cell density reached ca. 22 × 106 cells/mL, and was significantly increased with increasing cell densities. Moreover, the up-regulation of AHLs with increasing cell densities revealed that MC-LR is quorum sensing-mediated. Our results undoubtedly confirmed that MC-LR was produced in a cell density-dependent way that mimics quorum sensing, and the minimum cell density (ca. 22 × 106 cells/mL) that was required to produce MC-LR was provided and offered a reference standard for the prevention and control of MCs pollution in the actual water environment.

Optimization of microcystin biodegradation by bacterial community YFMCD4 using response surface method

The increasing production of microcystin-LR (MC-LR) causing animal and human health issues is found in eutrophic water bodies, marine habitats and desert environments. The health threat posed by MC-LR has led to the establishment of World Health Organization’s water guideline value of 1 μg/mL. Combating this has increased the search for cost-effective approach to degrade MC-LR. The study aimed to optimize the MC-degrading environmental factors of bacterial community YFMCD4. Response surface methodology (RSM) was employed to evaluate the influence of varying temperatures, pH and initial MC-LR concentration on the biodegradation efficiency of MC-LR by bacterial community YFMCD4. The optimal MC-LR biodegradation environmental factors were found to be 30 °C, pH 7 and 2 μg/mL initial MC-LR. The biodegradation rate reached 100% after 10 h. YFMCD4 mainly consisted of genera Alacligenes, Sphingobacterium and Pseudomonas using High-throughput pyrosequencing technology. The mlrA gene encoding MlrA enzyme considered most important for MC-LR biodegradation was obtained from YFMCD4. Data demonstrated that the bacterial structure and biodegradation efficiency of YFMCD4 varied with the change of environmental factors including temperature, pH and MC-LR concentrations. RSM is considered a good method to examine the optimal biodegradation environmental conditions for MC-LR. To date, RSM and High-throughput pyrosequencing technology are employed to optimize the biodegradation conditions (30 °C, pH 7 and 2 μg/mL initial MC-LR) and analyze the structure of bacterial community for the first time.

Salt-Alkalization May Potentially Promote <i>Microcystis Aeruginosa</i> Blooms and the Production of Microcystin-LR

Salt-Alkalization May Potentially Promote <i>Microcystis Aeruginosa</i> Blooms and the Production of Microcystin-LR

Effects of glyphosate on microcystin-LR production and release from Microcystis aeruginosa at different temperatures.

Cyanobacterial blooms and their associated toxins are growing issues for many aquatic ecosystems. Microcystin-LR (MC-LR) is a toxic and common cyanobacterial toxin, whereas glyphosate is a commonly used herbicide that is massively applied in agriculture. In this study, the effects of glyphosate on the growth of Microcystis aeruginosa and MC-LR synthesis and release from M. aeruginosa at different temperatures are investigated. In addition, the MC-LR pollution in the Huangpu River in Shanghai urban area is studied. Results indicated that the MC-LR concentration in the Huangpu River is related to water temperature. The laboratory experiments revealed that the growth of M. aeruginosa was slightly promoted at 15°C and glyphosate concentrations of 1 and 5mg/L and inhibited in the presence of glyphosate and high temperatures (20°C, 25°C, 30°C, and 35°C). The intracellular MC-LR contents were remarkably increased by glyphosate at 15°C, 20°C, 25°C, and 30°C and remarkably decreased at 35°C. Meanwhile, the extracellular MC-LR contents were remarkably increased at all temperatures and all concentrations except when treated with 1mg/L glyphosate at 35°C. The highest extracellular MC-LR content, which was 143.9% higher compared with that of the control, was observed at 30°C and treatment with 10mg/L glyphosate. These results were consistent with those of MC-LR investigation in Huangpu River. Furthermore, in accordance with the intracellular MC-LR contents, the ability of a single cell to synthesize MC-LR was enhanced at 15°C, 20°C, 25°C, and 30°C and decreased at 35°C. These results provide an understanding on the toxic effects of glyphosate on cyanobacteria and the effects of temperature on MC release. Moreover, these results will be helpful in protecting aquatic ecosystems and human health.

Assessment of water quality in eutrophized water bodies through the application of indexes and toxicity

It is essential to have tools that can be used to diagnose water resources. For this reason, this study sets out on the one hand to assess water quality in three reservoirs in Spain (Salas, A Baxe and Conchas) with Cyano-Habs problems through the application of water quality indexes: The National Sanitation Foundation Water Quality Index (NFSWQI), the General Quality Index (GQI), the Trophic State Index (TSI), and the Trophic Contamination Index (ICOTRO). On the other hand, it seeks to learn how parameters such as nitrogen and phosphorus influence the presence of cyanotoxin, specifically Microcystis aeruginosa. To that end, samples from the three reservoirs are cultured and physical-chemical parameters and the toxicity of the water are measured. The results show that Salas reservoir has the worst water quality rating (GQI is bad and NFSWQI medium), while As Conchas and A Baxe obtain very good figures for NFSWQI. This contrasts with the data obtained via the TSI of moderately eutrophic conditions for all three reservoirs, and hypereutrophic levels for As Conchas and A Baxe downstream. On the other hand, the toxicity analysis shows levels of 1.12 ± 0.06 μg/l microcystin-LR (MC-LR) for As Conchas, 0.64 ± 0.04 μg/l MC-LR for Salas, and 1.24 ± 0.05 μg/l MC-LR for A Baxe, of which 20% corresponds to free MC-LR. This study finds that nitrogen is the parameter that most favors the production of MC-LR. We conclude that the eutrophication indexes are more reliable when studying the presence of cyanobacteria. Furthermore, nitrogen and phosphorous are the most significant parameters in this regard. They are taken into account in the quality indices (GQI, NFSWI), but they are not sufficiently representative. It is recommended as a future line of research that water quality indices be adapted or designed to incorporate eutrophication levels and even water toxicity.

Characteristics of growth and microcystin production of Microcystis aeruginosa exposed to low concentrations of naphthalene and phenanthrene under different pH values

Here, Microcystis aeruginosa (M. aeruginosa) was studied to analyze the effects of 0.5 mg L−1 naphthalene and 0.05 mg L−1 phenanthrene on profiles of cell growth, chlorophyll-a content and Microcystin-LR (MC-LR) production at different pH values. The results indicated that for both the naphthalene and phenanthrene treatments, the specific growth rates were higher in pH 10.0 than in either pH 7.0 or pH 5.0. In the presence of low concentrations of naphthalene or phenanthrene, chlorophyll-a in medium increased significantly more in pH 10.0 than pH 5.0. chlorophyll-a in cell was significantly lowered when exposed to naphthalene in both pH 10.0 and pH 7.0, and was higher when exposed to phenanthrene in pH 10.0 than pH 5.0. HPLC analysis revealed that the extracellular MC-LR concentrations in M. aeruginosa exposed to either naphthalene or phenanthrene were lower than in control M. aeruginosa at pH 5.0. The intracellular MC-LR levels in toxic M. aeruginosa cells exposed to naphthalene or phenanthrene were higher than in the controls at pH 10.0. Our study suggests that the MC-LR production of M. aeruginosa was affected by the pH value when low concentrations of either naphthalene or phenanthrene were present in the water. These results indicate that the pH value should not be ignored when evaluating the risk of chemicals that promote MC-LR production in eutrophic waters.

Ultrasensitive Detection of Hepatotoxic Microcystin Production from Cyanobacteria Using Surface-Enhanced Raman Scattering Immunosensor.

Microcystin-LR (MC-LR) is considered the most common hazardous toxin produced during harmful algal blooms. In addition to potential risk of long-term exposure to low concentrations in drinking water, acute toxicity due to MC-LR resulting from algal blooms could result in fatalities in rare cases. Although several methods are currently available to detect MC-LR, development of a low-cost, ultrasensitive measurement method would help limit exposure by enabling early detection and continuous monitoring of MC-LR. Here, we develop a surface-enhanced Raman scattering (SERS) spectroscopic immunosensor for detection and quantification of the hepatotoxic MC-LR toxin in aquatic settings with excellent robustness, selectivity, and sensitivity. We demonstrate that the developed SERS sensor can reach a limit of detection (0.014 μg/L) at least 1 order of magnitude lower and display a linear dynamic detection range (0.01 μg/L to 100 μg/L) 2 orders of magnitude wider in comparison to the commercial enzyme-linked immunosorbent assay test. The superior analytical performance of this SERS immunosensor enables monitoring of the dynamic production of MC-LR from a Microcystis aeruginosa culture. We believe that the present method could serve as a useful tool for detection of hepatotoxic microcystin toxins in various aquatic settings such as drinking water, lakes, and reservoirs. Further development of this technique could result in single-cell microcystin resolution or real-time monitoring to mitigate the associated toxicity and economic loss.

Impacts of Identified Bacterium Ensifer adhaerens on Microcystis aeruginosa and Subsequent Microcystin Release

The release of microcystin and dissolved organic matter (DOM) during algae-lysing process draws much attention. In this study, Ensifer adhaerens (bacterium r23) was screened for algicidal activity against Microcystis aeruginosa (MA). The effects of dosage (2.04 × 106, 3.90 × 106, and 7.15 × 106 CFU ml−1) and dosing modes (single, double, and quadruple treatments totaling 7.15 × 106 CFU ml−1) on the release of microcystin-LR (MC-LR) and DOM were investigated. Besides cell density, intra/extra-cellular, and total MC-LR were measured during the lysing treatment. The DOM components were analyzed by parallel factor analysis (PARAFAC). Results show that the lowest dosage (2.04 × 106 CFU ml−1) not only stimulated MA growth during the initial 4 days but also triggered the production of more toxins, resulting in higher total MC-LR than the controls on 2–16 days. The higher dosages suppressed MA growth and MC-LR production simultaneously, and the total MC-LR content was substantially lower than those of the controls during the whole experimental period. The total MC-LR for the double and quadruple treatments were lower than the controls after 30-day treatment, but still higher than the single dosage. Both intracellular and extracellular DOM (IDOM, EDOM) of MA had five components, namely tyrosine-like (C1), tryptophan-like (C2 and C3), fulvic acid-like (C4), and humic acid-like (C5) substances. C1 and C3 in the EDOM resulted from MA lysis and increased along with the treatment. C2 in the EDOM came from the nutrient broth and could be consumed by r23. C4 and C5 in the EDOM mainly resulted from the growth of r23.

Effects of arginine on the growth and microcystin-LR production of Microcystis aeruginosa in culture

Although toxic cyanobacterial blooms and their toxins threaten drinking water and ecology and are promoted by nutrient loading, the precise nutrient regime that increases cyanobacterial populations and toxin production is poorly understood. Here, the influences of arginine (Arg), as a common amino acid with high nitrogen content, on the growth and microcystins (MCs) production of Microcystis aeruginosa (M. aeruginosa) were investigated by an isotope method (15N). The results showed that the biomass and production of microcystin-LR (MC-LR) increased with an increase in initial Arg concentrations in the range of 0.3–1.4 mmol-N L−1, whereas a higher Arg concentration (3.6 mmol-N L−1) inhibited the growth. MC-LR on different days (days 0, 6, 12, and 18) was detected by liquid chromatography with tandem mass spectrometry (LC-MS/MS) after incubation with 15N-Arg. The MC-LR molecular weight increased from 995 to 1004 with 100% relative abundance with 10 15N atoms bound by the Adda, Arg (4 15N), Glu, Mdha, Ala, Leu, and MeAsp residues on day 18. It seems that there was a sequential order when M. aeruginosa assimilated Arg to synthesize MC-LR. The Arg residue in the molecule of MC-LR was the last one to be labeled by 15N from 15N-arginine. This study not only presents a deeper insight into the biosynthesis of free amino acids that are incorporated into MCs but also reminds us of the potential risk caused by Arg, which should arouse concerns.

Environmental risks of ZnO nanoparticle exposure on Microcystis aeruginosa: Toxic effects and environmental feedback

The vast majority of studies measure the toxic effect of organisms exposed to nanoparticles (NPs) while there is still a lack of knowledge about the influence of NPs on the aquatic environment. It is unknown whether or not the interaction between NPs and algae will result in the variation of algal organic matter (AOM) and stimulate the production of more algal toxins. In this study, zinc oxide nanoparticles (nano-ZnO) as a typical representative of metal oxide NPs were used to evaluate the toxic effects and environmental feedback of Microcystis aeruginosa. Reactive oxygen species (ROS) and malondialdehyde (MDA) were measured to explain the toxicity mechanism. Changes of AOM, including the production of toxins, the molecular weight distribution and the excitation-emission matrices of algal solution were also studied as environmental feedback indicators after nano-ZnO destroyed the algae. As the nano-ZnO exceeded the comparable critical concentration (1.0 mg/L), the algae were destroyed and intracellular organic matters were released into the aquatic environment, which stimulated the generation of microcystin-LR (MC-LR). However, it is worth noting that the concentration of nano-ZnO would need to be high (at mg/L range) to stimulate more MC-LR production. These findings are expected to be beneficial in interpreting the toxicity and risks of the releasing of NPs through the feedback between algae and the aquatic environment.

The influence of temperature on Radiocystis fernandoi strain (cyanobacteria) growth and microcystin production

Radiocystis fernandoi Komarek and Komarkova-Legnerova has great ecological importance in tropical regions, due to its widespread occurrence in freshwaters in the American continent, besides its ability to form blooms and to produce toxins. Global warming has a very important and positive role on cyanobacterial development considering that the growth rate of these organisms increases at temperatures above 25 °C. Considering that there is no information in the literature about the effects of temperature on the development of R. fernandoi, we performed an experimental study on its effects on growth and microcystin-LR production, employing a tropical microcystin-producer R. fernandoi. The selected strain was tested at three temperatures: 20, 25 and 30 °C and sampled at intervals of 2 days including different growth phases. Our results show that the strain presents greater growth rates and the smaller cell size at 25 and 30 °C. Differently from Microcystis aeruginosa (Kutzing) Kutzing that presents the greatest microcystin production at the end of the exponential growth phase, R. fernandoi produced microcystin only in the stationary phase. This result emphasizes the importance of monitoring Radiocystis blooms for a long period of time considering that these toxins remain in the water for up to 42 days. Thus, besides the morphological differences between M. aeruginosa and R. fernandoi, our results reveal that physiologically these cyanobacterial species also present different strategies that allow them to co-occur in nature forming long-lasting blooms.