Glyphosate-based herbicides (GBHs) are the most widely used pesticides for weed control. In parallel with the renewal of the active ingredient, polyethoxylated POE(15) containing GBHs were banned in the EU in 2016. Since then, co-formulants were changed and numerous GBHs are marketed with different excipients declared as inert substances. In our study, we focused to determine acute and chronic cytotoxicity (by Aliivibrio fischeri assay) and direct hormonal activity (estrogenic and androgenic effects measured by Saccharomyces cerevisiae BLYES/BLYAS strains, respectively) of glyphosate, AMPA, polyethoxylated POE(15) and 13 GBHs from which 11 formulations do not contain polyethoxylated POE(15). Among the pure substances, neither glyphosate nor AMPA had any effects, while polyethoxylated POE(15) exhibited pronounced toxicity and was also estrogenic but not androgenic. Regarding the acute and chronic cytotoxicity and hormonal activity of GBHs, dilution percentages calculated from EC₅₀ values were in the most cases by one or two order of magnitude lower than the minimum recommended dilution for agricultural and household use. Relation could not be observed between the biological effects and type of glyphosate-salts; hence toxicity could be linked to the co-formulants, which are not even declared in 3 GBHs. Toxicological evaluation must focus on these substances and free accessibility of GBHs should be reconsidered.

Environment can be affected by a variety of micropollutants. In this paper, we develop a system to assess the toxicity on an environmental sample, based on the expression of a nanoluciferase under the control of the STB5 promotor in a yeast. The STB5 gene encodes for a transcription factor involved in a pleiotropic drug resistance and in the oxidative stress response. The response of the modified yeast was assessed using 42 micropollutants belonging to different families (antibiotics, pain killers, hormones, plasticizers, pesticides, etc.). Among them, 26 induced an increase of the bioluminescence for concentration ranges from pg.L⁻¹ to ng.L⁻¹. Surprisingly, for concentrations higher than 100 ng.L⁻¹, no response can be observed, suggesting that other mechanisms are involved when the stress increases. Analyzing the different responses obtained, we highlighted six nonmonotonic types of responses. The type of response seems to be independent of the properties of the compounds (polarity, toxicology, molecular weight) and of their family. In conclusion, we highlighted that a cellular response exists for very low exposition to environmental concentration of micropollutants and that it was necessary to explore the cellular mechanisms involved at very low concentration to provide a better risk assessment.

Assessment of the impact of pharmaceutical residues on living organisms is a very complex subject. Apart from taking into account the toxicity of individual compounds, environmental factors should also be taken into account. In this paper, attempts were made to assess the impact of coexisting inorganic ions and changes in pH on the toxicity of ten selected pharmaceuticals. Two bioassays were used to measure the estrogenic and androgenic effects (XenoScreen YES/YAS – Saccharomyces cerevisiae) and acute toxicity (Microtox® – Vibrio fischeri).The Microtox® test gave the most definitive outputs concerning the determination of interaction type between drugs and chemical species. Synergism was proven for almost all drugs and chemical species, and only two cases of antagonism were found. Significant drug/pH interactions were rare.Regarding the XenoScreen YES/YAS bioassay, when estrogenic and androgenic agonistic effects (YES+ and YAS+, respectively) were studied, many cases of well-expressed synergism for all inorganic ions with limited number of drugs (diazepam, fluoxetine, estrone, chloramphenicol for the YES+ test and diazepam, progesterone, androstenedione, and estrone for the YAS+ test) were found. Antagonism was also proven for the YES+ test, especially for diclofenac and androstenedione interacting with cations. On the other hand, the YES- and YAS- tests (estrogenic and androgenic, respectively, antagonistic effects) did not indicate cases of synergetic interaction except for the couples Br−/diazepam and NH4+/ketoprofen. Antagonistic drug/ion interactions were detected only with diclofenac and fluoxetine. It is interesting that well-expressed (antagonism or synergism) drug/pH interactions were rare.Both tests were found utilizable in performing studies on impact of ions/pH fluctuations on drugs mixtures' toxicity confirming in most cases synergic impact of parameters studied on toxicity. The approach proposed in the paper seems to be proven as a reliable tool in assessing impact of abiotic factors on toxicity and endocrine potential of complex mixtures of pharmaceuticals' mixtures.

Glyphosate-based herbicides, the most extensively used herbicides in the world, are available in an enormous number of commercial formulations with varying additives and adjuvants. Here, we study the effects of one such formulation, Credit41, in two genetically diverse yeast strains. A quantitative trait loci (QTL) analysis between a sensitive laboratory strain and a resistant strain linked mitochondrial function to Credit41 resistance. Two genes encoding mitochondrial proteins identified through the QTL analysis were HFA1, a gene that encodes a mitochondrial acetyl CoA carboxylase, and AAC3, which encodes a mitochondrial inner membrane ATP/ADP translocator. Further analysis of previously studied whole-genome sequencing data showed that, although each strain uses varying routes to attain glyphosate resistance, most strains have duplications of mitochondrial genes. One of the most well-studied functions of the mitochondria is the assembly of Fe–S clusters. In the current study, the expression of iron transporters in the transcriptome increased in cells resistant to Credit41. The levels of iron within the cell also increased in cells exposed to Credit41 but not pure glyphosate. Hence, the additives in glyphosate-based herbicides have a significant contribution to the negative effects of these commercial formulations on biological systems.

Pharmaceuticals and analogs of bisphenol A (BPA) are increasingly threatening environmental pollutants. In this study, mixtures of selected pharmaceuticals (diclofenac sodium salt, chloramphenicol, oxytetracycline hydrochloride, fluoxetine hydrochloride, estrone, ketoprofen, progesterone, gemfibrozil and androstenedione) were prepared with BPA and its two analogs (namely, bisphenols F and S) at such ratios to reflect environmentally detectable levels. Then, the mixture solutions were studied with a XenoScreen YES/YAS assay to determine the variations in the initial hormonal response of each pharmaceutical compound due to the presence of a bisphenol analog. The results obtained were modeled with the concentration addition (CA) and independent action (IA) approaches, the trueness of which was studied with model deviation ratios (MDR). The estrogenic agonistic activity of the drugs studied was most strongly affected by the presence of BPA in solution (twenty-one cases of synergy observed for CA models versus twelve cases of antagonism in the case of IA predictions). BPS shows a strong agonistic estrogenic impact on most of the drugs studied at medium and high concentration levels; androgenic agonistic activity was also impaired with elevated concentrations of BPS. Increasing the concentration of BPF in a reaction mixture also increased the number of YES + synergism incidences (for CA modeling). Estrone, progesterone and androstenedione were mostly affected by the highest BPF concentrations studied in the case of androgenic agonistic research performed.

The textile industry is responsible for the disposal of a large volume of effluents containing synthetic dyes, which are considered to be highly toxic compounds for both human health and the environment. The aim of the present study was to test potential use of a renewable, low-cost product—Luffa cylindrica in disk and powder form—as adsorbent material for the treatment of textile effluents containing dyes. Saccharomyces cerevisiae cells were also immobilized on L. cylindrica to increase the adsorbent capacity. Batch experiments were conducted for the evaluation of the removal of the azo dye Direct Red 23. The Langmuir, Freundlich, and Temkin isotherms were used for a better interpretation of the data. The results showed that adsorption is more efficient at acidic pH and all adsorbent materials best fit the Langmuir model, indicating the formation of a monolayer. The isotherm results also demonstrated that the materials immobilized with the yeast had a greater sorption rate, but the cell-free L. cylindrica powder had a higher adsorbate/adsorbent interaction. The comparison with a spectrophotometrically defined standard revealed that the powder without and with yeast cells was able to achieve an acceptable removal rate of the dye from the solution. Moreover, the difference in adsorption between the powder without and with yeast cells was very small. Thus, the application of the cell-free L. cylindrica powder is economically more feasible. The findings demonstrate the potential use of L. cylindrica powder as an adsorbent for the treatment of effluents containing textile dyes.

Since the last century, humanity has sought ways to minimize the impact of the industrial growth in the environment. The textile industry, as one of the major contributors to water pollution, has been dumping coloured effluents which cause great impact in water bodies. The electrolytic process not only degrades the colour of the effluent but also transforms recalcitrant substances by direct or indirect oxidation. The ecotoxicological tests are used nowadays as a way to verify the toxicity degree of water bodies polluted by industrial and farming activities. The ecotoxicological tests consist in exposing determined organisms to the samples with the intention to evaluate their toxicity by observing the organisms’ responses. This study had the objective to degrade, by electrolytic process, a simulated textile effluent containing a mixture of Acid Blue 40 and Acid Red 151 dyes and the toxicity evaluation of the treated effluent by ecotoxicological tests. The bioassays used were tests with seeds of Lactuca sativa (lettuce), Eruca sativa (rocket), and Cucumis sativus (cucumber). Tests with the micro crustaceous Artemia salina and the yeast Saccharomyces cerevisiae were also conducted. The electrolytic treatment degraded the initial colour of the textile effluent, and the ecotoxicological tests indicated low toxicity to the treatment.

Textile industry is responsible for a large amount of polluted water released daily, mainly due to the dyes used. This article has aimed to study and improve methodologies for degrading textile effluents containing the dyes Acid Red 151 and Acid Blue 40 using an electrolytic reactor. Different solutions were prepared for the experiments in the electrolytic reactor with a 70 % TiO₂/30 % RuO₂anode. The textile effluents underwent 0 (control), 3, and 30 min treatment intervals. A suspension of Saccharomyces cerevisiae cells was used for toxicity tests and performed at the same day that samples were collected. The same test was applied to the samples after 15 days resting in order to verify changes in toxicity. The electrolytic treatment successfully removed the color in all effluents. However, the process efficiency varies according to the dye used and the experimental conditions, such as current and NaCl concentration. Also, it was observed that treatments longer than 30 min are very toxic to S. cerevisiae cells because of the high concentration of Cl₂.

Chemical reagents used by the textile industry are very diverse in their composition, ranging from inorganic compounds to polymeric compounds. Strong color is the most notable characteristic of textile effluents, and a large number of processes have been employed for color removal. In recent years, attention has been directed toward various natural solid materials that are able to remove pollutants from contaminated water at low cost, such as sugarcane bagasse. Cell immobilization has emerged as an alternative that offers many advantages in the biodegradation process, including the reuse of immobilized cells and high mechanical strength, which enables metabolic processes to occur under adverse conditions of pH, sterility, and agitation. Support treatment also increases the number of charges on the surface, thereby facilitating cell immobilization processes through adsorption and ionic bonds. Polyethyleneimine (PEI) is a polycationic compound known to have a positive effect on enzyme activity and stability. The aim of the present study was to investigate a low-cost alternative for the biodegradation and bioremediation of textile dyes, analyzing Saccharomyces cerevisiae immobilization in activated bagasse for the promotion of Acid Black 48 dye biodegradation in an aqueous solution. A 1 % concentration of a S. cerevisiae suspension was evaluated to determine cell immobilization rates. Once immobilization was established, biodegradation assays with free and immobilized yeast in PEI-treated sugarcane bagasse were evaluated for 240 h using UV–vis spectrophotometry. The analysis revealed significant relative absorbance values, indicating the occurrence of biodegradation in both treatments. Therefore, S. cerevisiae immobilized in sugarcane bagasse is very attractive for use in biodegradation processes for the treatment of textile effluents.

Several laccase-based products have been launched on the market over the years. However, there is little information about their toxicity and/or the toxicity of their residues. We evaluated the toxicity of a simulated denim-laundry wastewater containing Biolite BSN, a laccase-based product used for denim bleaching. The evaluation included a viability test with Saccharomyces cerevisiae, a phytotoxicity test with Sorghum vulgare, and a toxicity test with Daphnia magna. The viability of S. cerevisiae was reduced to 40%. The radicle and plumule growth of S. vulgare was reduced to 62 and 66%, respectively. The CL₅₀ for D. magna was 29.7%, which classified this water as toxic (according to the percent rank method). Biolite BSN was identified as the main cause of the toxic effects; furthermore, the chemical oxygen demand (COD) of the wastewater was significantly high (3346.2 mg/L), and more than 90% of the COD corresponded to Biolite BSN. The anaerobic biodegradability tests showed that the denim-laundry wastewater could be treated anaerobically; therefore, it was treated in an upflow anaerobic sludge blanket (UASB) reactor. The treatment reduced the toxicity and COD in 50 and 77%, respectively, and a methane yield of 311.1 mL CH₄/g of CODᵣₑₘₒᵥₑd was obtained. Based on these results, we recommend to analyze the toxicity of all textile chemicals, regardless of whether they are enzyme-based products. A UASB reactor can be used as the first treatment stage for similar effluents in order to reduce the COD and the toxicity and recover methane as an added benefit.