Algal Cell Membrane Research Articles

Oxidation effects on Microcystis aeruginosa inactivation through various reactive oxygen species: Degradation efficiency, mechanisms, and physiological properties

The study investigated the inactivation of Microcystis aeruginosa using a combined approach involving thermally activated peroxyacetic acid (Heat/PAA) and thermally activated persulfate (Heat/PDS). The Heat/PDS algal inactivation process conforms to first-order reaction kinetics. Both hydroxyl radical (•OH) and sulfate radical (SO4-•) significantly impact the disruption of cell integrity, with SO4-• assuming a predominant role. PAA appears to activate organic radicals (RO•), hydroxyl (•OH), and a minimal amount of singlet oxygen (1O2). A thorough analysis underscores persulfate's superior ability to disrupt algal cell membranes. Additionally, SO4-• can convert small-molecule proteins into aromatic hydrocarbons, accelerating cell lysis. PAA can accelerate cell death by diffusing into the cell membrane and triggering advanced oxidative reactions within the cell. This study validates the effectiveness of the thermally activated persulfate process and the thermally activated peroxyacetic acid as strategies for algae inactivation.

Anticyanobacterial effect of p-coumaric acid on Limnothrix sp. determined by proteomic and metabolomic analysis

Regulating photosynthetic machinery is a powerful but challenging strategy for selectively inhibiting bloom-forming cyanobacteria, in which photosynthesis mainly occurs in thylakoids. P-coumaric acid (p-CA) has several biological properties, including free radical scavenging and antibacterial effects, and studies have shown that it can damage bacterial cell membranes, reduce chlorophyll a in cyanobacteria, and effectively inhibit algal growth at concentrations exceeding 0.127 g/L. Allelochemicals typically inhibit cyanobacteria by inhibiting photosynthesis; however, research on inhibiting harmful algae using phenolic acids has focused mainly on their inhibitory and toxic effects and metabolite levels, and the molecular mechanism by which p-CA inhibits photosynthesis remains unclear. Thus, we examined the effect of p-CA on the photosynthesis of Limnothrix sp. in detail. We found that p-CA inhibits algal growth and damages photosynthesis-related proteins in Limnothrix sp., reduces carotenoid and allophycocyanin levels, and diminishes the actual quantum yield of Photosystem II (PSII). Moreover, p-CA significantly altered algal cell membrane protein systems, and PSII loss resulting from p-CA exposure promoted reactive oxygen species production. It significantly altered algae cell membrane protein systems. Finally, p-CA was found to be environmentally nontoxic; 80 % of 48-h-old Daphnia magna larvae survived when exposed to 0.15 g/L p-CA. These findings provide insight into the mechanism of cyanobacterial inhibition by p-CA, providing a more practical approach to controlling harmful algal blooms.

Integrating transcriptomics and biochemical analysis to understand the interactive mechanisms of the coexisting exposure of nanoplastics and erythromycin on Chlorella pyrenoidosa

Nanoplastics and antibiotics frequently co-exist in water polluted by algal blooms, but little information is available about interaction between substances. Erythromycin, as a representative of antibiotics, has been frequently detected in aquatic environments. This investigation attempted to reveal the interaction mechanism of nanoplastics and erythromycin on Chlorella pyrenoidosa. Results demonstrated that the joint toxicity of erythromycin and nanoplastics was dynamic and depended on nanoplastics concentration. Antagonistic effects of 1/2 or 1 EC50 erythromycin and nanoplastic concentration (10 mg/L) on the growth of C. pyrenoidosa was observed. The joint toxicity of 1/2 or 1 EC50 erythromycin and nanoplastic concentration (50 mg/L) was initially synergistic during 24–48 h and then turned to antagonistic during 72–96 h. Consequently, antagonistic effect was the endpoint for joint toxicity. Integration of transcriptomics and physiological biochemical analysis indicated that the co-existence of nanoplastics and erythromycin affected the signal transduction and molecular transport of algal cell membrane, induced intracellular oxidative stress, and hindered photosynthetic efficiency. Overall, this study provided a theoretical basis for evaluating the interactive mechanisms of nanoplastics and antibiotics.

Combatting cyanobacteria: unraveling the potency of 316L-Cu stainless steel in inhibiting Microcystis aeruginosa growth.

Harmful algal blooms, particularly those of Microcystis aeruginosa, present significant ecological and health risks. To address this issue, this study utilized a custom static algal growth assessment apparatus to investigate the anti-algal performance of a copper-alloyed 316L stainless steel (SS), named 316L-Cu SS. This material was compared with traditional 316L SS, which is widely utilized in freshwater systems for its corrosion resistance. Algal growth dynamics were monitored through optical density (OD) and chlorophyll A concentration measurements. Notably, 316L-Cu SS exhibited superior inhibitory effects on Microcystis aeruginosa growth compared to 316L SS and control groups. Inductively coupled plasma mass spectrometry (ICP-MS) confirmed that the copper ion release from 316L-Cu SS played a critical role in this algal suppression, which interfered with photosynthesis, induced oxidative stress, and damaged algal cell membranes. In contrast, other metal ions (Ni, Cr, Fe) had a negligible impact on algal growth. The study highlights 316L-Cu SS as a promising material for mitigating harmful algal blooms, thereby offering potential benefits for both aquatic ecosystem conservation and public health protection.

Length-dependent toxic effects of microplastic fibers on Chlorella pyrenoidosa

Microplastics (MPs), a pervasive pollutant in aquatic environments, are increasingly recognized for their detrimental effects on aquatic organisms. However, the present understanding of their impact on phytoplankton, particularly freshwater microalgae, remains limited. Furthermore, previous studies have predominantly focused on MP particles, largely overlooking the most prevalent form of MPs in aquatic settings-fibers. In this study, we scrutinized the toxicological implications of microplastic fibers (MFs) spanning four distinct lengths (50 μm, 100 μm, 150 μm, and 200 μm) on the protein-nucleated algae Chlorella pyrenoidosa over a six-day period. The study unequivocally demonstrated that MFs markedly impeded C. pyrenoidosa growth, diminished photosynthetic pigment content, and induced oxidative stress, with all observed effects exhibiting a length-dependent correlation. Electron microscopy further revealed notable damage to algal cell membranes. Cell membrane shrinkage, cytoplasm outflow, and abnormalities in cell division were observed in the 150 μm and 200 μm groups. Furthermore, C. pyrenoidosa clustered around the 200 μm MF were notably denser compared to other groups. The present study demonstrated that MFs had length-dependent toxic effects on C. pyrenoidosa. These findings offer novel insights into the deleterious impact of MFs on aquatic organisms, underscoring the pivotal role of length in influencing their toxicity.

Elimination of Microcystis aeruginosa through Leuconostoc mesenteroides DH and its underlying mechanism

Microcystis aeruginosa is ubiquitously found in various water bodies and can produce microcystins (MCs), which threaten the health of aquatic animals and human beings. The elimination of excessive M. aeruginosa is beneficial for the protection of the ecosystems and public health. In this regard, algae-lysing bacteria have been extensively studied as an effective measure for their eradication. However, the active substances generated by algae-lysing bacteria are limited. For this study, we reveal that the phenyllactic acid (PLA) produced by Leuconostoc mesenteroides DH exhibits high efficacy for the removal of M. aeruginosa, and explore the elimination mechanism of strain DH on M. aeruginosa. It was found that a cell-free supernatant of strain DH possessed high removal activities against M. aeruginosa. Abundant reactive oxygen species were induced in algal cells following exposure to strain DH supernatant, as well as superoxide dismutase and catalase responses. Furthermore, the integrity of algal cell membranes and photosynthesis was seriously damaged. Interestingly, added exogenous eugenol significantly inhibited the synthesis of active substance produced by strain DH, which further identified that PLA is one of the active substances that contribute to the eradication of M. aeruginosa on the basis of metabolomics analysis. Our finding demonstrated, for the first time, that PLA (as an anti-cyanobacterial compound) can be used for the removal of M. aeruginosa, which provides a theoretical basis for the control of M. aeruginosa.

Algicidal bacteria in phycosphere regulate free-living Symbiodinium fate via triggering oxidative stress and photosynthetic system damage

Free-living Symbiodinium, which forms symbiotic relationships with many marine invertebrates, plays an important role in the vast ocean. Nutrient levels have been shown to significantly impact microbial community structure and regulate algal communities. In this study, the bacterial community structure within the phycosphere of free-living Symbiodinium underwent significant changes in response to nutrient stimulation. Alteromonas exhibited dominance in Zobell 2216E broth nutrient stimulation concomitant with the demise of algal cells. Alteromonas abrolhosensis JY-JZ1, a marine bacterium isolated from the phycosphere of Symbiodinium, demonstrated an algicidal effect on Symbiodinium cells. Optical and scanning electron microscopy revealed that the algal cell membrane structure was disrupted, leading to intracellular leakage. Strain JY-JZ1 exerted its cytotoxicity by producing and secreting bioactive compounds into the supernatant. The marked declines in the chlorophyll a content, photosynthetic efficiency (Fv/Fm) and the electron transport rate (rETR) indicated that the photosynthetic system of Symbiodinium was damaged by JY-JZ1 supernatant. The observed elevation in levels of malondialdehyde (MDA), glutathione (GSH), superoxide dismutase (SOD), peroxidase (POD) and catalase (CAT) content suggested that the algal cells experienced oxidative stress. Moreover, the supernatant exhibited remarkable adaptability to temperature and pH. Additionally, it displayed exceptional algicidal efficacy against various harmful algae species. To the best of our knowledge, this study represents the first successful isolation of an algicidal bacterial strain from the phycosphere of free-living Symbiodinium and subsequent investigation into its mechanism for controlling Symbiodinium growth, thereby providing novel insights into algae-bacteria interactions. The remarkable algicidal efficacy exhibited by strain JY-JZ1 against other harmful algae species suggests its significant potential for harmful algal blooms (HABs) control.

Efficient inactivation of harmful algae K. mikimotoi by a novel algicidal bacterium via a rare direct contact pathway: Performances and mechanisms

Harmful algal blooms (HABs) caused by Karenia mikimotoi have posed great threats to marine ecosystems, and algal inactivation by symbiotic bacteria has been recognized as environmental benign methods for controlling HABs. However, the identified algicidal bacteria for K. mikimotoi is limited and exclusively based on indirect algicidal pathways, which may cause secondary pollution due to releasing toxic algicidal agents. In this study, a novel strain of algicidal bacteria Tenacibaculum sp. GD3 was isolated from the phycosphere of K. mikimotoi. The bacterial strain GD3 could achieve 92.6 % of inactivation efficiency against K. mikimotoi within 8 h of co-culturing period, which outperformed those in existing literatures reported so far. The algicidal mechanisms were revealed to be a rare direct cell-to-cell contact pathway, and the GD3 could grow by utilizing metabolites from K. mikimotoi, exhibiting excellent bacterial adaptability in the phycosphere. Cell morphology changes were monitored by live cell imaging system combined with SEM and TEM observations, which showed that the GD3 was first attached to the algal cell membrane, followed by lipid peroxidation and lysis of membrane protein. Oxidative stress responses were induced as reveled by up-regulation of intracellular ROSs and antioxidant enzyme activity. Photosynthetic parameters including rETRmax, Fv/Fm, YII and NPQ were reduced, and expression of functional genes involved in decomposition of chlorophyll and cell wall was significantly suppressed. Moreover, the intracellular release profile and acute toxicity assessment indicated that the GD3 could also detoxify the K. mikimotoi cultures and the released biomolecules would not cause adverse effect to marine environment. This study not only provides a novel algicidal bacterium against K. mikimotoi via a rare direct mode, but also helps to better understand the algicidal mechanisms at physiological and genetic level, thus moving forward the areas of HABs control by microbiological strategies.

Comparing the Effects and Mechanisms of Action of Permanganate, Chlorine, and Hydrogen Peroxide on the Membrane Integrity of Pseudanabaena sp. Cells

Preoxidation is usually used to remove cyanobacteria in drinking waterworks. However, the effects and mechanisms of action of oxidants on the membrane integrity of cyanobacterial cells are scarcely known, which may lead to cell damage and facile release of plenty of harmful metabolites. This study investigated the kinetics of Pseudanabaena cell lysis under separate exposure to potassium permanganate (KMnO4), sodium hypochlorite (NaClO), and hydrogen peroxide (H2O2). Mechanisms of interaction between them and the Pseudanabaena cell surface at the cellular and molecular levels were then defined. Results showed that cell lysis matched a two-stage kinetic model under KMnO4 or H2O2 exposure, and cells remained intact below a certain exposure threshold; in comparison, the log value of cell concentration decreased linearly with NaClO exposure. Pseudanabaena cell damage rates followed the order NaClO > KMnO4 > H2O2. Permanganate ions primarily reacted with cell-bound organic matter and then oxidized cell membrane, whereas neutral HClO produced by NaClO can permeate the membrane of algal cells and damage cell membrane quickly. As for H2O2, although H2O2 can gradually permeate the algal cell membrane, the reactivity between H2O2 and cell membranes was low. The algal cell membrane remained intact in the initial stage and then was damaged when H2O2 accumulation reached a certain level.

A novel strategy for efficient capture of intact harmful algal cells using Zinc oxide modified carbon nitride composites

The development of safe and efficient materials to remove harmful algae is continuing to be a major challenge in controlling cyanobacterial blooms in eutrophication waters. Herein, we present a novel strategy that combines Zinc oxide (ZnO) with carbon nitride composites to efficiently collect the intact Microcystis aeruginosa cells. The influence of different dosages of g-C3N4 precursors were assessed and the synthesized catalysts were characterized. The results revealed that 93.0 % of algae cells were removed by the ZnO/CN (2:1) system within 10 min at a dose of 4.0 g L−1. Regardless of the variation in initial cell density, the final removal efficiency reached >90.0 %. The integrity of the algal cell membrane was observed by K+ release and intracellular organic matter such as MC-LR during the removal process, which were further verified by SEM images. The Zeta potential values indicated that the improved effectiveness may be attributed to the electrostatic attraction and coagulation by ZnO/CN. The removal mechanism of ZnO/CN was revealed through charge neutralizing flocculation and the different types of flocculants were compared. The present work provides a new insight in using ZnO nanoparticles modified carbon-based composites in treating cyanobacterial blooms.

Efficient Microcystis aeruginosa coagulation and removal by palladium clusters doped g-C3N4 with no light irradiation

Efficient treatment of cyanobacterial blooms in eutrophication waters by safe and reliable nanomaterials is a big challenge for reducing environmental health risks. Herein, a novel strategy combining palladium clusters (Pdn) with g-C3N4 nanocomposite was presented to achieve high-efficient removal of Microcystis aeruginosa cells through coagulation and breakage. Interestingly, 95.17% of algal cells (initial concentration of 5.6 × 106 cells mL−1) were promptly removed in the Pd/g-C3N4 (5%) system within only 10 min and without visible light irradiation and persulfate activation. Both the release of potassium ion and microcystin during the removal process and the transmission electron microscope observations of Microcystis aeruginosa cells proved that the integrity of the algal cell membrane was destroyed. The removal of Microcystin-LR (MC-LR) were further confirmed in the next process. Pd metal interaction and breakage against algal cells may cause disruption of algal cells. This study describes a novel technology for the superfast removal of harmful algae and may provide a new insight into the control of cyanobacterial blooms in practical applications.

Visible-light-drivenself-floating Ag2MoO4/TACN@LF photocatalyst inactivation of Microcystis aeruginosa: Performance and mechanisms

The poor light transmittance, low recycling rate and potential secondary pollution problems of powder photocatalysts limit the practical application of photocatalytic technology. Therefore, there is an urgent need to develop stable floating photocatalysts to alleviate the problem of harmful algal blooms (HABs). In this work, a floating Ag2MoO4/TACN@LF composite was synthesized for the inactivation of Microcystis aeruginosa (M. aeruginosa) by employing a simple oscillatory impregnation method. The Ag2MoO4/TACN@LF floating photocatalyst exhibited stable algae removal performance under various conditions, and 100% chlorophyll a removal rate could be achieved within 4 h of visible light irradiation under the optimal photocatalyst loading of 6 g/L. The effects of Ag2MoO4/TACN@LF floating catalyst on algal cell membrane permeability, phycobiliprotein, intracellular antioxidant enzyme activities and algal organic matter were further studied. Moreover, the scavenging experiments demonstrated that •OH was the predominant reactive oxygen species (ROSs). Ag0 and 3g-C3N4 * also made a non-negligible contribution to the inactivation of algal cells. What's more, the Ag2MoO4/TACN@LF still exhibited 92% inactivation efficiency for M. aeruginosa after 5 cycles reused experiments, indicating its promising potential for practical application of alleviating HABs.

Mechanistic insight into the inhibitory effect of artemisinin sustained-release inhibitors with different particle sizes on Microcystis aeruginosa.

Environment-friendly algaecides based on allelopathy have been widely used to control harmful algal blooms. In this research, micro and nano scale artemisinin sustained-release algal inhibitor was prepared, the optimal preparation conditions were explored, and the inhibitory mechanism of artemisinin algaecides was turned perfect. The results showed that when the particle size of artemisinin sustained-release microspheres (ASMs) was 2/10,000 of artemisinin sustained-release granules (ASGs), the inhibitory effect was more remarkable. The optimal concentration of ASMs was 0.2gL-1, and the inhibitory effect reached 99% on the 10th day. The algal density and chlorophyll a both showed a downward trend, indicating that ASGs and ASMs could promote the degradation of chlorophyll a. The inhibition rate of ASGs was faster than that of ASMs on the 4th day, and the inhibitory effect of ASMs was more significant after the 5th day. The activities of superoxide dismutase (SOD), peroxidase (POD), and catalase (CAT) increased rapidly at first and then decreased, which indicated that ASGs and ASMs caused oxidative damage to Microcystis aeruginosa and inhibited the activity of antioxidant enzymes. Furthermore, the content of the oxygen free radical (O2-) and malondialdehyde (MDA) continued to rise after the 5th day, and the protein, nucleic acid, and conductivity in the culture medium increased. These results showed that lipid peroxidation occurred in the algal cell membrane, and the permeability of the membrane increased. In summary, the ASMs had a significant sustained inhibitory effect while the ASGs had a better short-term effect. The main inhibitory mechanism of artemisinin algaecides is the irreversible damage of cell membrane.

Effects of Taurine on Primary Metabolism and Transcription in a Coral Symbiodinium sp.

Coral reefs belong to the marine ecosystems and host the richest biodiversity of marine organisms. Coral reefs are formed as a result of the symbiotic relationship between the host coral animal and photosynthetic dinoflagellates, namely Symbiodinium sp. Coral animals induce the release of carbon fixation products of symbiotic Symbiodinium sp. through secreting host release factors (HRFs) such as taurine. To study the potential effect of taurine on photosynthesis and release of carbon fixation products of Symbiodinium sp., we compared the growth of Symbiodinium sp. under control and taurine-stimulated conditions. Photosynthesis parameters were detected to monitor the photosynthetic efficiency. Biomass and the contents of total soluble sugar, total insoluble sugar, total protein, total lipids, chlorophyll a were analyzed. Metabolome and transcriptome analyses were performed to analyze the potential effect of taurine on primary metabolism and mRNA transcription. The results revealed that taurine significantly increased the growth, photosynthesis efficiency, total soluble sugar, chlorophyll a, and chlorophyll b and free amino acid content of Symbiodinium sp. while decreased the content of total insoluble sugar. Results of metabolome and transcriptome analyses suggested that taurine might affect metabolic pathways in Symbiodinium sp. by altering the permeability of the algal cell membrane, diverting photosynthetically fixed carbon from storage compounds to translocated compounds, releasing a signal of low concentrations of nitrogen to initiate a series of response mechanisms, and controlling the density of Symbiodinium sp. through the quorum sensing effect. These results help to explore how corals control carbon metabolism in Symbiodinium sp. and to provide theoretical guidance for furthering our understanding of Symbiodinium sp. biology and coral-algal symbiosis.

Cercosporin-bioinspired photoinactivation of harmful cyanobacteria under natural sunlight via bifunctional mechanisms

Harmful cyanobacterial blooms (HCBs), mainly caused by eutrophication, have deleterious impacts on water resources and pose a great threat to human health and natural ecosystems. Thus, an environmentally-friendly method to inhibit HCBs is urgently needed. Learning from nature, herein, natural product cercosporin, produced by the fungi Cercospora to damage plant cells under natural sunlight, was developed as a powerful photosensitive algicidal reagent to inhibit HCBs. Microcystis aeruginosa could be severely inactivated by 20 μM cercosporin in 36 h with 95% inhibition ratio under 23 W compact fluorescent light irradiation. Further mechanism investigation showed that algal cell walls and membranes along with the antioxidant and photosynthetic systems were damaged via two mechanisms, those being, reactive oxygen species generation and cell adsorption. More importantly, the practical applicability of cercosporin was demonstrated by its effectiveness in a 2 L-scale photoinactivation experiment using cyanobacterial blooms from Taihu Lake, China under natural sunlight with a lower dosage of cercosporin (7.5 μM). This study established the bifunctional mechanisms by which cercosporin inactivates HCBs, opening design possibilities for the development of novel photosensitive algicidal reagents to control HCBs.

Release and removal of algal organic matter during prechlorination and coagulation treatment of cyanobacteria-laden water: Are we on track?

A better understanding of the physicochemical properties and fate of algae-derived organic matter (AOM) in water treatments significantly benefits the control of algae-derived disinfection byprodcuts and process parameter optimization. In this study, we conducted a comprehensive investigation of the release and treatability of dissolved organic matter during prechlorination and postcoagulation treatments of cyanobacteria-laden source water via size-exclusion chromatography-tandem diode array detector, fluorescence detector and organic carbon detector. The results revealed that the allochthonous humic substances could protect algal cell membrane from damage during prechlorination at a low level of chlorine dose. Due to the release and oxidation of biopterins during prechlorination of M. aeruginosa cells, the variation of the humic-like fluorescence can be used to indicate the chlorine dose for a sufficient membrane damage of algae cells. The prechlorination of M. aeruginosa cells induced minimal release of large MW biopolymer fractions but much more release of low MW fractions E1 and E2 (i.e., unknown carbonaceous substances and fluorescent nitrogenous biopterins). The physically extracted AOM contained a large proportion of biopolymers and could not well represent those released during prechlorination treatment. During coagulation, the negative effect of humic substances on the coagulant demand to achieve algae removal was more remarkable than AOM released by prechlorination. The high-MW biopolymers and humic substances can be removed over 50% by coagulation. Among the low-MW carbonaceous fractions, E1 released by prechlorination can also be effectively removed via coagulation while fractions C, D (possibly oligopeptides or secondary aromatic metabolites & low MW acids) and nitrogenous biopterins were recalcitrant to coagulation. This study highlights the differences of AOM properties between physical extraction and prechlorination and provides a basis for drinking water treatment plants to give more attention to the recalcitrant low MW fractions in coagulation when treating algae-laden source water.

Antifouling performance of in situ synthesized chitosan-zinc oxide hydrogel film against alga M. aeruginosa

The undesirable settlement and growth of microalgae on submerged installations is a universal problem in water environment. Soft hydrogels are promising fouling-resistant materials due to the inherent surface properties. Herein, a kind of chitosan hydrogels with increasing zinc oxide (ZnO) mineral phase content were prepared by in situ sol–gel and solvent casting method, to prevent growth of algae Microcystis. aeruginosa. Incorporation with ZnO mineral phase improved mechanical property, water absorption, and stability of the obtained chitosan-zinc oxide (CS@ZnO) hydrogel films in Zn dose-dependent manner. The highest strength and growth inhibition (63.45 ± 8.93%) were observed by CS@ZnO-1.5 hydrogel films with the concentrations of 1.5% precursor in comparison with other hydrogel films. During this process, algal cell membrane was slightly damaged (24.5 ± 1.57%) and accompanied by significantly synthesis inhibition such as chlorophyll a (55.22 ± 2.72%) and total soluble protein (42.97 ± 1.66%). To sum up, synthesis inhibition of algal cell is the main mechanism of CS@ZnO hydrogel films inhibiting algal growth, which has the potential in antibiofouling application.

Toxicity mechanism of Nylon microplastics on Microcystis aeruginosa through three pathways: Photosynthesis, oxidative stress and energy metabolism

Nylon has been widely used all over the world, and most of it eventually enters the aquatic environment in the form of microplastics (MPs). However, the impact of Nylon MPs on aquatic ecosystem remains largely unknown. Thus, the long-term biological effects and toxicity mechanism of Nylon MPs on Microcystis aeruginosa (M. aeruginosa) were explored in this study. Results demonstrated that Nylon MPs had a dose-dependent growth inhibition of M. aeruginosa at the initial stage, and the maximum inhibition rate reached to 47.62% at the concentration of 100 mg/L. Meanwhile, Nylon MPs could obstruct photosynthesis electron transfer, reduce phycobiliproteins synthesis, destroy algal cell membrane, enhance the release of extracellular polymeric substances, and induce oxidative stress. Furthermore, transcriptomic analysis indicated that Nylon MPs dysregulated the expression of genes involved in tricarboxylic acid cycle, photosynthesis, photosynthesis-antenna proteins, oxidative phosphorylation, carbon fixation in photosynthetic organisms, and porphyrin and chlorophyll metabolism. According to the results of transcriptomic and biochemical analysis, the growth inhibition of M. aeruginosa is inferred to be regulated by three pathways: photosynthesis, oxidative stress, and energy metabolism. Our findings provide new insights into the toxicity mechanism of Nylon MPs on freshwater microalgae and valuable data for risk assessment of MPs.

Sulfur vacancies affect the environmental fate, corona formation, and microalgae toxicity of molybdenum disulfide nanoflakes

Sulfur vacancy (SV) defects have been engineered in two-dimensional (2D) transition metal dichalcogenides (TMDs) for high performance applications in various fields involving environmental protection. Understanding the influence of SVs on the environmental fate and toxicity of TMDs is critical for evaluating their risk. Our work discovered that SVs (with S/Mo ratios of 1.65 and 1.32) reduced the dispersibility and promoted aggregation of 2H phase molybdenum disulfide (2H-MoS2, a hot TMD) in aqueous solution. The generation capability of •O2- and •OH was increased and the dissolution of 2H-MoS2 was significantly accelerated after SVs formation. Different with pristine form, S-vacant 2H-MoS2 preferentially harvested proteins (i.e., forming protein corona) involved in antioxidation, photosynthetic electron transport, and the cytoskeleton structure of microalgae. These proteins contain a higher relative number of thiol groups, which exhibited stronger affinity to S-vacant than pristine 2H-MoS2, as elucidated by density functional theory calculations. Notably, SVs aggravated algal growth inhibition, oxidative damage, photosynthetic efficiency and cell membrane permeability reduction induced by 2H-MoS2 due to increased free radical yield and the specific binding of functional proteins. Our findings provide insights into the roles of SVs on the risk of MoS2 while highlighting the importance of rational design for TMDs application.

Cell Cycle Control of Nanoplastics Internalization in Phytoplankton.

Nanoparticles (NPs) for delivering chemotherapeutic drugs are now in clinical trials, and cellular uptake of NPs plays an important role in determining the drug delivery efficiency. Herein, we reported that the bioaccumulation and internalization of NPs were governed by the cell cycle. Specifically, we found that the bioaccumulation of NPs was more favored in the G2/M stages, followed by the S and G0/G1 stages. We demonstrated that three key parameters-clathrin-mediated endocytosis capacity, algal cell membrane permeability, and exopolymer substance (EPS) thickness-were critical in the bioaccumulation of NPs during the cell cycling process. Over the 24-h average duration of cell cycle, clathrin-mediated endocytosis capacity was much higher at the S stage than that at the G0/G1 and G2/M stages. Besides, cell membrane permeability was measured to be higher in S and G2/M stages while the lowest in G0/G1 stage. We have also identified the change of EPS thickness during the 24-h cell cycle. Transition from G0/G1 to S and G2/M induced the attenuation in EPS thickness, and the thinnest EPS was found at the end of mitosis. The cell cycle control NPs internalization were further verified by exposing Ag nanoparticles to algae at different cell cycle stages, confirming the important roles of EPS thickness and cell cycle control in the dynamic internalization processes. The present study highlights the important roles of cell cycle controlling the NPs bioaccumulation and internalization, with possible implications in maximizing NPs internalization efficiency while reducing the cost.