Quinone is the important redox functional group for electron transfer capacity (ETC) of humic acid (HA). Lignin, as major component in corn straw, can be decomposed into phenol monomers, then oxidation into quinones for synthesis of HA during composting process. However, it is still unclear that the effects of type and variation characteristics of phenol monomers on redox characteristics of HA during straw composting process. In this study, p-hydroxybenzoic acid (P1), vanillic acid (P2), syringic acid (P3), p-hydroxy benzaldehyde (P4), 4-coumaric acid (P5), 4-hydroxyacetophenone (P6), ferulic acid (P7) and 4-hydroxy-3-methylacetophenone (P8) were recognized and clustered into three groups. The concentration of polyphenol presented a significant downward trend during the straw composting process. Based on the relationships among phenol monomers to ETC, electron donating capacity (EDC), electron accepting capacity (EAC) and quinone, we found that P1, P2, P3, P5 and P7 were significantly related to ETC, EDC and EAC of HA (P < 0.05). Furthermore, NH₄⁺-N and NO₃⁻-N were the main micro-environmental factors linking to ETC-related phenol monomers and redox characteristics of HA in straw composts (P < 0.05). Finally, two groups of core microflora that promoting the ETC-related phenol monomers and NH₄⁺-N, and ETC-related phenol monomers and NO₃⁻-N were identified by Mantel test, respectively. This study contributes a new insight for polyphenol way for redox capacity of HA in traditional composting and utilization of straw compost in contaminated environments.

Type 2 diabetes mellitus is a complicated metabolic disorder with no definite treatment. Cyperus iria (Cyperaceae) possess several traditional therapeutic uses. According to the folklore tales, the whole plant of Cyperus iria possesses antihyperglycemic activity. The present study was undertaken to investigate whether aqueous-ethanol extract of Cyperus iria can ameliorate the altered activities of carbohydrate metabolism in streptozotocin (STZ)-induced diabetic rats along with appraisal of inflammatory and stress markers involved in endocrine dysfunction. Presence of biophenolics and flavonoids might be responsible for the antidiabetic potential. STZ-induced diabetic rats were treated orally with Cyperus iria extract (125, 250, and 500 mg/kg) for 15 days. Blood samples were collected. Metformin was used as positive control. Significantly higher quantities of phenolic (82.79±0.003 mg/g GAE) and flavonoid (13.61±0.002 mg/g QE) contents were present. Inhibitory concentration (IC50) exhibited an excellent potential for both antioxidant (IC50= 3.22 μg/mL) and alpha amylase (IC50=36.29 μg/mL) inhibitory assays. High-performance liquid chromatography (HPLC) confirmed the existence of myercetin, quercetin, kaempferol, and ferulic acid. Cyperus iria aqueous-ethanol extract exhibits good tolerance against glucose at 90 min in normal rats. Streptozotocin-induced hyperglycemia declined significantly at day 9 (265 mg/dL) along with improvement in inflammatory (TNF-α=15.6± 0.2 g/l, COX-2=357±0.396 U/l, IL-6= 572±0.99 pg/l) and oxidative stress markers (SOD= 163±0.616 and GSH-ST= 95.8±0.44 U/mL) along with biochemical parameters in a dose-dependent manner. Present study suggests that Cyperus iria aqueous-ethanol extract possesses hypoglycemic potential which might be attributed to the decrease in oxidative stress and inflammatory markers.

Use of herbicides is one of the most preferred options for crop protection against weeds. Imazamox is an imidazolinone (IMI)-group herbicide, and even low concentrations of imazamox might exhibit high biological activities on soil and plants. Therefore, in contrast to the conventional types of sunflowers that are sensitive to IMI-group herbicides, sunflowers that are resistive to IMI-group herbicides were also developed in recent years. In this study, the effect of imazamox on some physiological and genetic parameters of two types of sunflowers that are sensitive and resistant to IMI-group herbicides is comparatively investigated. For this purpose, three concentrations of imazamox (0.82, 1.64 and 2.45 mM, respectively) were applied on the two types of sunflower (i.e. SN:8 as IMI-sensitive type and SN:9 as IMI-resistant type, respectively). In addition, the physiological and molecular effects of IMI on antioxidant enzymes (such as superoxide dismutase (SOD), catalase, glutathione S-transferase (GST)), heat shock proteins (such as HSP26, HSP60, HSP70), phenolic contents (coumaric acid, caffeic acid, ferulic acid), phytohormone levels (indole-3-acetic acid, jasmonic acid (JA), salicylic acid (SA)) and accumulation of pesticides in the leaf tissue of sunflowers were analysed by qRT-PCR and LC MS/MS analysis. In this study, the pesticide concentration of resistant-type SN9 was significantly greater than that of SN8 with the application of 1.64–2.45 mM of imazamox, and the total pesticide amounts were 1.6 and 1.8 times significantly higher in leaf tissues, respectively. This pesticide accumulation led to an imbalance in the phytohormone and phenolic levels, increased levels of unfolded or misfolded proteins, and selective reduction of the GST, SA and JA levels in the two types of sunflowers. However, SN9 significantly responded to the pesticide accumulation via the overexpression of mitochondrial chaperone HSP60 (16.15-fold) and stress-specific HSP70 (54.46-fold), as well as higher SOD expression and SA and JA levels. In particular, by the application of high-dose IMI, our data revealed strong protein chaperone response, a high level of SOD expression, and finally the crosstalk of SA and JA, and these physiological and molecular phenomena can be indicative of pesticide-induced stress in SN9. The study suggested that high-concentration imazamox treatment induces some physiological and genetic changes at the phytotoxic level on not only IMI sensitive type but also resistant type.

In an effort to customize biochars for soil amendments, multiple feedstocks have been combined in various ratios prior to pyrolysis. The resulting variation in the chemistry and structure can affect a biochar’s adsorption capacity, which influences the bioavailability of many chemical compounds in the soil system including phenolic acids. This study characterizes the sorption of 14C-labeled ferulic acid, syringic acid, and chlorocatechol to four biochars prepared from individual feedstocks and four from mixed feedstocks using batch equilibration. Pure feedstock biochar sorption followed switchgrass< swine solids< poultry litter< pine chip for both ferulic (Kd= 1.4-75) and syringic acid (Kd= 0.07-6.03), and appeared to be influenced by the properties of the biochars as well as the chemicals themselves. All biochar Kd values, except pine chip, were lower than that of the reference soil (Waukegan silt loam). The sorptive properties of the combined feedstock biochars could not be predicted from their pure feedstock components and sorption coefficients were both unexpectedly higher and lower than the individual parent materials’ biochars. Further research is necessary to understand the characteristics of these combination biochars, particularly their sorption, which this study has shown is not merely an intermediary of its components.

The present study explores the antioxidant, anti-microbial, and hepatoprotective potentials of flavonoid-rich fractions from Fumaria officinalis against permethrin-induced liver damage ex vivo/in vivo in rat. However, HPLC-DAD analysis revealed the richness of 6 components in ethyl acetate fraction (EAF) where ferulic acid, rosmarinic acid, and myricetin are the most abundant. The in vitro assays showed that EAFs have impressive antioxidant and anti-microbial properties. Ex vivo, permethrin (PER) (100 μM) induced a decrease of hepatic AST and ALT activities and 25-OH vitamin D and vitamin C levels and an increase of ALP and LDH activities, TBARS, and ϒ-GT levels with a disturbance of oxidative status. The hepatoprotective effect of EAF (1 mg/mL) against PER was confirmed by the amelioration of oxidative stress profile. In vivo, permethrin was found to increase absolute and relative liver weights, plasma transaminase activities, lactate-to-pyruvate ratio, hepatic and mitochondrial lipid peroxidation, and protein oxidation levels. This pesticide triggered a decrease of Ca²⁺ and Mg²⁺-ATPases and mitochondrial enzyme activities. The co-treatment with EAF reestablished the hepatic and mitochondrial function, which could be attributed to its richness in phenolic compounds.

This study proposed the optimization of a laccase-mediator system to reduce pesticide levels (bentazone, carbofuran, diuron, clomazone, tebuconazole, and pyraclostrobin) on aqueous medium. Firstly, the mediator concentration of 1 mM was established (average removal of 36%). After that, seven redox-mediating compounds, namely, 2,20-azino-bis(3-ethylbenzothiazoline-6-sulfonic acid) diammonium salt, caffeic acid, chlorogenic acid, p-coumaric acid, ferulic acid, gallic acid, protocatechuic acid, and vanillin, were compared regarding their removal efficiency. The highest removal (77%) was achieved with the laccase-vanillin system. After this screening, the optimization was carried out by a 2² full factorial design. Variables under study were the enzyme (laccase) activity and vanillin concentration. Maximum removal (53–85%) was achieved with 0.95 U/mL laccase and 1.8 mM vanillin. Pesticide removal in reaction media was fitted to the first-order kinetics equation with an average half-time life of 2.2 h. This is the first study of the use of this natural compound as a mediator in the degradation of the pesticides under investigation. The results of this study contribute, with alternative methods, to decrease pesticide levels since they are highly persistent in aqueous samples and, as a result, mitigate the environmental impact.

Acacia jacquemontii possess has numerous traditional therapeutic uses. The rationale of this study was to investigate the role of Acacia jacquemontii ethyl acetate extract (AJEAE) in the downregulation of hyperglycemia. The current study was performed in two parts, in vitro, through characterization (high-performance liquid chromatography), estimation of total phenolic content, total flavonoid content, antioxidant (2,2-diphenyl-1-picrylhydrazylassay), and α-amylase inhibitory activities of the studied extract, and in vivo using Wistar rats in which animals were divided into five groups NC, DC, GL, AJEAE 250 mg/kg, and AJEAE 500 mg/kg. The effects of AJEAE on fasting plasma glucose, plasma insulin, HOMA-IR, oral glucose tolerance test, glycated hemoglobin (HBA1c), lipid profile, inflammatory cytokines (Interleukin-6, tumor necrosis factor-alpha), and oxidative stress markers (lipid peroxidation, nitic oxide, superoxide dismutase, catalase, glutathione peroxidase) were evaluated. Our findings confirmed the presence of quercetin, kaempferol, gallic acid, vanillic acid, syringic acid, M-coumaric acid, sinapic acid, chlorogenic acid, cinnamic acid, and ferulic acid in AJEAE. Total flavonoid and phenolic contents in AJEAE were 83.83 mg GAE/g and 77.06 mg QE/g, respectively. Significant inhibition of DPPH (69.470%/1 mg/ml) and α-amylase (71.8%/1 mg/ml) activities were exhibited by AJEAE. Alloxan-injected rats showed marked hyperglycemia and hypoinsulinemia, and increased inflammatory marker levels as compared to normal control (p < 0.001). Additionally, raised levels of triglyceride (139.7 ± 2.771), total cholesterol (198.7 ± 1.856), very low-density lipoprotein (33.43 ± 0.2728), low-density lipoprotein (155.5 ± 2.754), lipid peroxidation, and nitric oxide (p < 0.001) and decreased levels of high-density lipoprotein (17.20 ± 0.1732), superoxide dismutase, catalase, and glutathione peroxidase were observed in diabetic rats (p < 0.001). AJEAE significantly (p < 0.05) improved the aforementioned parameters and the protective efficacy was comparable to glibenclamide. Histopathological findings also evidenced the anti-hyperglycemic properties of AJEAE through regeneration of pancreatic β cells. Conclusively, our findings demonstrated the antihyperglycemic, antihyperlipidemic, antioxidant, anti-inflammatory, and pancreatic beta β cell regenerative properties of AJEAE against alloxan-induced diabetes.

The photocatalytic degradation effectiveness of six selected typical phytotoxic substances (ferulic, benzoic, gallic, salicylic, tannic, and acetic acid) by two levels of 10 nm TiO₂ (11 and 22 g/m²) immobilized on tiles under 254 nm of UV light irradiation was investigated. The results showed that the immobilized nano-TiO₂ significantly degraded all phytotoxic substances dissolved in distilled water, and the cumulative degradation rates of ferulic, benzoic, gallic, salicylic, tannic, and acetic acid reached 22.2, 33.6, 48.2, 56.9, 57.5, and 76.0 % after 6 h of treatment, respectively. Furthermore, the cumulative degradation rates of six phytotoxic substances by immobilized nano-TiO₂ were different remarkably, i.e., salicylic acid > benzoic acid, gallic acid > ferulic acid, acetic acid > tannic acid. The maximal photocatalytic degradation efficiencies of all phytotoxic substances appeared at the first 2 h in the three experiments. During the 6-h treatment period, the photocatalytic degradation efficiency of all phytotoxic substances decreased gradually. There was no significant difference in the photocatalytic degradation of benzoic acid and ferulic acid between the two levels of immobilized nano-TiO₂ treatments, whereas a significant difference was found in the photocatalytic degradation of salicylic acid, gallic acid, tannic acid, and acetic acid. In a word, nano-TiO₂ photocatalysis is an effective method to degrade phytotoxic substances. And the photocatalytic degradation effectiveness of six typical phytotoxic substances may be related to their structures.

Two indigenous bacterial strains, Bacillus megaterium ETLB-1 (accession no. KC767548) and Pseudomonas plecoglossicida ETLB-3 (accession no. KC767547), isolated from soil contaminated with paper mill effluent, were co-immobilized on corncob cubes to investigate their biodegradation potential against black liquor (BL). Results exhibit conspicuous reduction in color and lignin of BL upto 913.46 Co-Pt and 531.45 mg l⁻¹, respectively. Reduction in chlorophenols up to 12 mg l⁻¹was recorded with highest release of chloride ions, i.e., 1290 mg l⁻¹. Maximum enzyme activity for lignin peroxidase (LiP), manganese peroxidase (MnP), and laccase (LAC) was recorded as 5.06, 8.13, and 8.23 U ml⁻¹, respectively, during the treatment. Scanning electron microscopy (SEM) revealed successful immobilization of bacterial strains in porous structures of biomaterial. Gas chromatography/mass spectroscopy (GC/MS) showed formation of certain low molecular weight metabolites such as 4-hydroxy-benzoic acid, 3-hydroxy-4-methoxybenzaldehyde, ferulic acid, and t-cinnamic acid and removal of majority of the compounds (such as teratogenic phthalate derivatives) during the period of treatment. Results demonstrated that the indigenous bacterial consortium possesses excellent decolorization and lignin degradation capability which enables its commercial utilization in effluents treatment system.

Liver injury is one of the adverse effects of methotrexate (MTX). Ferulic acid (FA) is an antioxidant phytochemical that confers hepatoprotective efficacy; however, its effect against MTX hepatotoxicity remains unexplored. This study investigated the role of FA in modulating oxidative stress, inflammation, Nrf2/HO-1 signaling, and PPARγ in MTX-administered rats. Following oral FA supplementation for 15 days, rats received a single dose of MTX at day 16 and samples were collected at day 19. MTX provoked multiple histological manifestations, including degenerative changes, steatosis, inflammatory cells infiltration and hemorrhage, and altered serum transaminases, bilirubin, and albumin. Reactive oxygen species, lipid peroxidation, and nitric oxide were increased in the liver of rats that received MTX. FA prevented all histological alterations, ameliorated liver function markers, suppressed oxidative stress, and boosted antioxidants in MTX-induced rats. FA reduced serum TNF-α and IL-1β, and hepatic NF-κB p65, Bax, and caspase-3, whereas increased Bcl-2, Nrf2, NQO1, HO-1, and PPARγ. In conclusion, FA prevented MTX hepatotoxicity by activating Nrf2/HO-1 signaling and PPARγ, and attenuating oxidative stress, inflammation, and cell death.