Information on the biological responses of polyploid animals towards environmental contaminants is scarce. This study aimed to compare reproductive axis-related gene expressions in the brain, plasma biochemical responses, and the liver and gill histopathological alterations in diploid and triploid full-sibling juvenile African catfish (Clarias gariepinus). Fish were exposed for 96 h to one of the two waterborne phenanthrene (Phe) concentrations [mean measured (SD): 6.2 (2.4) and 76 (4.2) μg/L]. In triploids, exposure to 76 μg/L Phe increased mRNA level of fushi tarazu-factor 1 (ftz-f1). Expression of tryptophan hydroxylase2 (tph2) was also elevated in both ploidies following the exposure to 76 μg/L Phe compared to the solvent control. In triploids, 76 μg/L Phe increased plasma alkaline phosphatase (ALP) and lactate dehydrogenase (LDH) levels compared to the other Phe-exposed group. It also elevated lactate and glucose contents relative to the other groups. In diploids, however, biochemical biomarkers did not change. Phenanthrene exposures elevated glycogen contents and the prevalence of histopathological lesions in the liver and gills of both ploidies. This study showed substantial differences between diploids and triploids on biochemical and molecular biomarker responses, but similar histopathological alterations following acute Phe exposures.

1H-HRMAS NMR-based metabolomics was used to better understand the toxic effects on maize root tips of organochlorine pesticides (OCPs), namely lindane (γHCH) and chlordecone (CLD). Maize seedlings were exposed to 2.5 μM γHCH (mimicking basic environmental contaminations) for 7 days and compared to 2.5 μM CLD and 25 μM γHCH for 7 days (mimicking hot spot contaminations). The 1H-HRMAS NMR-based metabolomic profiles provided details of the changes in carbohydrates, amino acids, tricarboxylic acid (TCA) cycle intermediates and fatty acids with a significant separation between the control and OCP-exposed root tips. First of all, alterations in the balance between glycolysis/gluconeogenesis were observed with sucrose depletion and with dose-dependent fluctuations in glucose content. Secondly, observations indicated that OCPs might inactivate the TCA cycle, with sizeable succinate and fumarate depletion. Thirdly, disturbances in the amino acid composition (GABA, glutamine/glutamate, asparagine, isoleucine) reflected a new distribution of internal nitrogen compounds under OCP stress. Finally, OCP exposure caused an increase in fatty acid content, concomitant with a marked rise in oxidized fatty acids which could indicate failures in cell integrity and vitality. Moreover, the accumulation of asparagine and oxidized fatty acids with the induction of LOX3 transcription levels under OCP exposure highlighted an induction of protein and lipid catabolism. The overall data indicated that the effect of OCPs on primary metabolism could have broader physiological consequences on root development. Therefore, 1H-HRMAS NMR metabolomics is a sensitive tool for understanding molecular disturbances under OCP exposure and can be used to perform a rapid assessment of phytotoxicity.

The mass spectrometric analysis of the impact of sulfur dioxide and dust emission on carbon and oxygen stable isotopic compositions of glucose hydrolysed from α-cellulose samples extracted from Scots pine growing in the vicinity of “Huta Katowice” steelworks was the main aim of this study. The annual rings covered the time span from 1975 to 2012 AD. The relationships between climatic conditions, sulfur dioxide, and industrial dust emission and oxygen and carbon isotopic compositions were analyzed using correlation function methods. This study shows the first analysis of carbon and oxygen stable isotopes in glucose as the bio-indicators of CO₂, sulfur dioxide, and industrial dust emission. The anticoincidence trend of δ¹⁸O and δ¹³C and dust and sulfur dioxide confirms that the decreases of dust and sulfur dioxide industrial emission increase δ¹⁸O and δ¹³C values in glucose.

Biosurfactants have been considered as promising candidates for oil spill cleanup as they are generally more biodegradable, less toxic, and better in enhancing biodegradation than chemical surfactants. This study targeted the marine microbial biosurfactants to examine their enhanced production methods and application for the removal of crude oil from soil. The biosurfactants generated by Bacillus subtilis, which was isolated from the Atlantic Ocean, were investigated in this study. The economic production medium using different carbon (n-hexadecane, diesel oil, glycerol, glucose, starch, and sucrose) and nitrogen sources (NaNO₃, (NH₄)₂SO₄, and yeast extract) was studied. The best performance of biosurfactant production was achieved when using glycerol as carbon source and sodium nitrate and yeast extract as nitrogen sources in the substrate. The production rate was enhanced five times compared with that of the original screening recipe. The fermentative production of the generated biosurfactants could reduce the surface tension of water to 27 mN/m and with strong surface activity (∼36.4 mN/m) even after dilution for 10 times. The critical micellar concentration (CMC) of the product was 507 mg/L. A thin layer chromatography (TLC) analysis indicated that the purified product was a mixture of lipopeptide and glycolipid. The microbially produced biosurfactants were further examined as a soil-washing agent to enhance crude oil removal in a soil column system. The removal rates of 58 and 65 % were achieved using the biosurfactant solution with concentrations of 4 and 8 g/L, respectively. The results demonstrated the potential of marine microbial biosurfactants in cleaning crude oil-contaminated soil.

In this study, the decolorization of a dye solution via bio-Fenton process with in situ generation of H₂O₂ by enzymatic catalyzed oxidation of glucose was investigated. For this purpose, magnetite was synthesized and was used as the support for glucose oxidase immobilization. The particle size of the magnetite was estimated to be around 42 nm according to the obtained scanning electron microscope images. The magnetite crystal size was obtained approximately 26 nm by X-ray diffraction spectrum. Effective variables on immobilization were investigated. The best immobilization conditions were achieved at pH 6, temperature of 10 °C, glucose oxidase/support ratio of 1800 U/g, and time of 2.5 h. In these conditions, 450 U of glucose oxidase was immobilized per grams of magnetite. The immobilized glucose oxidase was used for the decolorization of acid yellow 12 in batch experiments. Decolorization conditions were optimized by response surface methodology. Four parameters including pH, temperature, glucose, and Fe²⁺ concentrations in five levels were investigated. The optimum conditions were obtained as follows: pH = 4.5, T = 29 °C, initial glucose concentration of 1.5 g/L, and Fe⁺² concentration of 1.4 g/L. Decolorization efficiency after 120 min at optimal conditions in the presence of 0.3 g immobilized enzyme (450 U/g) in 100 cm³ solution was observed to be equal to 62.27 %.

Environmental pollution by pentachlorophenol (PCP) is a critical concern worldwide, and microbial bioremediation could constitute an ecologically friendly solution. The main objectives of this study were at first to clarify the factors, affecting the ability and efficiency of PCP biodegradation by the bacterium isolate P6, and secondly to optimize the condition of using P6 for PCP bioremediation. The PCP mineralizing bacterium was isolated from the contaminated forest soil of Tunisia, and it was identified as Citrobacter freundii (C. freundii), by using conventional and molecular characteristics. The HPLC and spectroscopic analysis were used to investigate the PCP degradation and the biomass formation by this isolate P6. The main results showed that P6 was able to degrade or to transform more than 98 % of 640 mg/l PCP afterwards 168 h in mineral salt medium (MSM). As well, the optimal aerobic growth conditions of P6 in MSM include essentially the range of pH (4 ≤ pH ≤ 9) and of temperature (25 °C < temperature < 30 °C). The addition of glucose as extra carbon sources has an effect to enhance the PCP biodegradation. On the other side, this isolate of C. freundii is capable to remove or transform around 95.33 % of PCP added in the sterilized soil suspension supplemented with PCP and adjusted to a final concentration of around 400 mg/l during 2 weeks of incubation at 25 °C. This last result argues in favor of the use of this strain P6 of C. freundii as a microbial tool of remediation of PCP-contaminated site.

Tributyltin (TBT) is a species of organotin compound (OTC), used as antifouling biocide in boat and ship paints to prevents the attachment of marine organism on their hull surfaces. Tributyltin was found to be very toxic to a variety of targeted and non-targeted organisms and has high persistence in sediments even after the total global ban by the International Maritime Organization (IMO) in 2008. Therefore, there is an urgent need to clean up TBT-polluted environments after the global banning due to the significant risks it poses to the human and aquatic organisms for its slow degradation rate. In selecting bioremediation agents, indigenous bacteria were documented to be of great potentials compared to non-indigenous. In this study, comparison was made between a bacterial isolate Klebsiella sp. FIRD 2, isolated from TBT-contaminated surface sediment and Pseudomonas specie isolated from non-TBT-contaminated soil. Previously, we isolated, screened, and identified Klebsiella sp. FIRD 2 as a TBT-resistant bacterium from TBT-contaminated surface sediment of Kong Kong Laut, Johor, Malaysia. The isolate was able to resist TBT up to 1500 μg/L without addition of carbon source in minimal salt medium (MSM). Pseudomonas sp., isolated from non-TBT-contaminated soil was tested in MSM treated with different concentration of TBT. The bacterium did not endure to survive in TBT-treated media without addition of carbon source; thus, the strain has no ability to utilize TBT as source carbon. Growth of Pseudomonas sp. was observed in MSM treated with TBT at concentration of 500 μg/L and 1000 μg/L along with addition of glucose as carbon source. No growth of Pseudomonas sp. was observed in MSM with higher TBT concentration even with additional of carbon source. This study equally endorses the potentials of indigenous bacteria in bioremediation of TBT contamination.

A Gram-positive bacterium, designated as strain B1(2015b), was isolated from the soil of the chemical factory “Organika-Azot” in Jaworzno, Poland. On the basis of 16S rRNA gene sequence analysis, the isolated strain was classified as a Bacillus thuringiensis species. Strain B1(2015b) is able to degrade ibuprofen and naproxen, however, these compounds are not sufficient carbon sources for this strain. In the presence of glucose, Bacillus thuringiensis B1(2015b) degrades ibuprofen and naproxen with higher efficiency. Twenty milligrams per liter of ibuprofen was degraded within 6 days and 6 mg l⁻¹ of naproxen was removed within 35 days. Simultaneously, the growth of the bacterial culture was observed. The obtained results suggest that Bacillus thuringiensis B1(2015b) appears to be a powerful and useful tool in the bioremediation of non-steroidal anti-inflammatory drugs-contaminated environment.

In earlier studies in the existing literature, concentration balance in the feeding solution has never been considered as an influencing factor when the studies were carried out under several feeding conditions to examine effects of different carbon sources on the enhanced biological phosphorus removal (EBPR) process. For a better understanding of a stable operation of an EBPR reactor, it is thought that effects of the concentration balance need to be combined and evaluated with effects of the type of carbon sources in EBPR studies. Therefore, this study was aimed at determining the effect of concentration balance on the performance stability and the phosphorus and glycogen dynamics of a sequencing batch reactor (SBR). In this study, the SBR operation was divided into two main stages. In the first stage, two different ratios of the total concentration of monovalent (M) to divalent (D) cations (in milliequivalent per liter, meq/L) (7.6 and 1.5, 30 days of operation for each) was applied in the feeding solution to investigate the effect of the concentration balance on the performance stability of the SBR. During this stage, sodium acetate was used as the sole carbon source. To investigate the effect of the type of carbon source on the EBPR process under the condition of constant M/D ratio, sodium acetate was used as the sole carbon source during the first half of the reactor operation of 120 days, and, then, the carbon source was abruptly switched to glucose in the second stage.

In this study, the effects of cypermethrin (CYP), amitraz (AMT) and combined cypermethrin-amitraz (CYP-AMT) on some serum biochemical, oxidative stress and drug-metabolising parameters were investigated in male Wistar albino rats. CYP, AMT and combined CYP-AMT were administered at doses of 80 mg kg⁻¹ bw⁻¹ of CYP and 170 mg kg⁻¹ bw⁻¹ of AMT for 1 day (single dose), and at doses of 12 mg kg⁻¹ bw⁻¹ of CYP and 25 mg kg⁻¹ bw⁻¹ of AMT for 40 days by oral gavage. Oxidative stress (malondialdehyde (MDA), nitric oxide (NO), superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GSH-Px) and glucose-6-phosphate dehydrogenase (G6PD)), serum biochemical (glucose, triglyceride, cholesterol, high-density lipoprotein (HDL), low-density lipoprotein (LDL), blood urea nitrogen (BUN), creatinine, asparatate amino transferase (AST), alanine amino transferase (ALT), alkaline phosphatase (ALP), total protein, albumin) in blood/tissues (liver, kidney, brain, spleen and testis) and hepatic drug-metabolising (cytochrome P450 2E1 (CYP2E1), NADH-cytochrome b₅ reductase (CYPb5), NADPH-cytochrome c reductase/NADPH cytocrome P450 reductase (CYTC), glutathione S-transferase (GST), glutathione (GSH)) parameters were measured in liver samples taken on days 1 and 40. In result, it was determined that CYP, AMT and their combinations led to significant changes in the parameters investigated, and it was ascertained that long-term exposure to insecticides and the administration of insecticide combinations produced greater toxic effects in comparison with the administration of insecticides alone.