Assessment of exogenous application of plant growth regulators on Cress seed germination and ?-Galactosidase activity

Plant growth regulators (PGRs) were involved in several types of abiotic stress responses by means of improving seed germination and modifying the growth and development of medicinally important Lepidium sativum via alleviating the negative effects of abiotic stresses. Therefore, the present research was carried out to investigate the effects of exogenous application of PGRson seed germination, protein content and ?-galactosidase activity of L. sativum. Germination of L. sativum seeds was monitored for a short interval after the start of incubation until growth became 100%. While cytokinin treatment showed a positive effect on seed germination more than Gibberellic acid (GA), salicylic acid (SA) produced a higher negative effect than auxins. Quantifying changes in total protein content during seed germination as influenced by PGRs revealed that all PGRs have to exert a positive effect arranged in the following order: SA ? auxin ? cytokinin ? GA. Parallel to changes in germination percentage and total protein content of seed, a negative effect was attainedon ?-galactosidase specific activity in response to PGRs with the following arrangement: SA ? auxin ? cytokinin ? GA.In conclusion, the present study proposed the potential importance of the type and magnitude of exogenously applied PGRs during the germination of easily or even more difficult-to-germinate seeds

Antibacterial synergy of Tritirachium oryzae-produced silver nanoparticles with different antibiotics and essential oils derived from Cupressus sempervirens and Asteriscus graveolens (Forssk)

Purpose: To carry out eco-friendly biosynthesis of fungi-derived silver nanoparticles (AgNPs) and investigate their antibacterial synergies with essential oils (EOs) of Asteriscus graveolens (Forssk.) Less. and Cupressus sempervirens. Methods: Biosynthesis of AgNPs was carried out using a cell-free filtrate of Tritirachium oryzae. The biosynthesized AgNPs characteristics were assessed using different methods, including ultravioletvisible spectrophotometry (UV), Fourier-transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) with energy-dispersive x-ray spectroscopy (EDS) and transmission electron microscopy (TEM). Results: Obvious synergistic effects were observed between AgNPs and chloramphenicol, vancomycin, nitrofurantoin or tetracycline with Pseudomonas aeruginosa, through increases in fold area of inhibition (IFAs) within the range of 2.4 to 9.0. Synergistic interactions were also seen between AgNPs and the antibiotics used, depending on the strain. Increase in IFA ranged from 1- to 3-fold for S. aureus, E. coli and P. aeruginosa. Similarly, combinations of AgNPs, EO of A. graveolens and cefotaxime, nitrofurantoin or amoxicillin against P. aeruginosa led to 10-, 3- and 10-fold synergy, respectively. In contrast, the use of AgNPs and trimethoprim, tetracycline or amoxicillin against E. coli led to 1 to 6-fold synergy. The best synergistic capacity resulted from AgNPs and the EO of C. sempervirens and trimethoprim against S. epidermidis, which yielded 29-fold increase in IFA. The use of combination of AgNPs and vancomycin against P. aeruginosa led to 16.4-fold enhancement of IFA. Conclusion: The findings can potentially lead to the development of a new perception of antibacterial agents (innovative medications) involving the incorporation of nanoparticles (NPs) or new materials that potentially synergize with antibiotics, NPs and the EOs of different plants

Antioxidant and Antihyperglycemic Effects of <i>Ephedra foeminea</i> Aqueous Extract in Streptozotocin-Induced Diabetic Rats

Background: Ephedra foeminea is known in Jordan as Alanda and traditionally. It is used to treat respiratory symptoms such as asthma and skin rashes as an infusion in boiling water. The purpose of this study was to determine the antidiabetic property of Ephedra foeminea aqueous extract in streptozotocin-induced diabetic rats. Methods: The aqueous extract of Ephedra foeminea plant was used to determine the potential of its efficacy in the treatment of diabetes, and this extract was tested on diabetic rats as a model. The chemical composition of Ephedra foeminea aqueous extract was determined using liquid chromatography–mass spectrometry (LC-MS). Antioxidant activity was assessed using two classical assays (ABTS and DPPH). Results: The most abundant compounds in the Ephedra foeminea extract were limonene (6.3%), kaempferol (6.2%), stearic acid (5.9%), β-sitosterol (5.5%), thiamine (4.1%), riboflavin (3.1%), naringenin (2.8%), kaempferol-3-rhamnoside (2.3%), quercetin (2.2%), and ferulic acid (2.0%). The antioxidant activity of Ephedra foeminea aqueous extract was remarkable, as evidenced by radical scavenging capacities of 12.28 mg Trolox/g in ABTS and 72.8 mg GAE/g in DPPH. In comparison to control, induced diabetic rats treated with Ephedra foeminea extract showed significant improvement in blood glucose levels, lipid profile, liver, and kidney functions. Interleukin 1 and glutathione peroxidase levels in the spleen, pancreas, kidney, and liver of induced diabetic rats treated with Ephedra foeminea extract were significantly lower than in untreated diabetic rats. Conclusions: Ephedra foeminea aqueous extract appears to protect diabetic rats against oxidative stress and improve blood parameters. In addition, it has antioxidant properties that might be very beneficial medicinally

Growth Kinetics and Toxicity of Pseudomonas fredriksbergsis Grown on Phenol as Sole Carbon Source

Phenol is one of the main pollutants that have a serious impact on the environment and can even be very critical to human health. The biodegradation of phenol can be considered an increasingly important pollution control process. In this study, the degradation of phenol by Pseudomonas fredriksbergsis was investigated for the first time under different growth conditions. Six different initial concentrations of phenol were used as the primary substrate. Culture conditions had an important effect on these cells' ability to biodegrade phenol. The best growth of this organism and its highest biodegradation level of phenol were noticed at pH 7, temperature 28 °C, and periods of 36 and 96 h, respectively. The highest biodegradation rate was perceived at 700 mg/L initial phenol concentration. Approximately 90% of the phenol (700 mg/L) was removed in less than 96 hours of incubation time. It was found that the Haldane model best fitted the relationship between the specific growth rate and the initial phenol concentration, whereas the phenol biodegradation profiles time could be adequately described by the modified Gompertz model. The parameters of the Haldane equation are: $0.062 h^{−1}$, 11 ppm, and 121 ppm for Haldane’s maximum specific growth rate, the half-saturation coefficient, and the Haldane’s growth kinetics inhibition coefficient, respectively. The Haldane equation fitted the experimental data by minimizing the sum of squared error (SSR) to $1.36×10^{-3}$

Effect of <i>Matricaria aurea</i> Essential Oils on Biofilm Development, Virulence Factors and Quorum Sensing-Dependent Genes of <i>Pseudomonas aeruginosa</i>

The emergence of drug-resistant microorganisms presents a substantial global public health threat. The increase in pathogens resistant to commonly prescribed antibiotics underscores the urgent requirement to explore alternative treatment strategies. This study adopts a novel approach by harnessing natural resources, specifically essential oils (EO), to combat bacterial pathogenicity. The primary aim of this research was to analyze the chemical composition of the aerial part of the Matricaria aurea (M. aureas) EO and evaluate its potential for inhibiting quorum sensing (QS) and disrupting biofilm formation in Pseudomonas aeruginosa (P. aeruginosa). The gas chromatography-mass spectrometry (GCMS) analysis unveiled that α-bisabolol oxide A constituted the predominant portion, comprising 64.8% of the total, with β-bisabolene at 6.3% and α-farnesene at 4.8% following closely behind. The antibiofilm efficacy was observed at concentrations of 0.3, 0.15, and 0.08 mg/mL, demonstrating negligible effects on cell viability. Furthermore, the EO from M. aurea effectively inhibited the formation of P. aeruginosa biofilms by diminishing aggregation, hydrophobicity, and swarming motility. Significantly, the EO treatment resulted in a conspicuous decrease in the production of pyocyanin, rhamnolipid, and extracellular polymeric substances (EPS), along with a reduction in the enzymatic activity of protease and chitinase. The EO effectively hindered QS by disrupting QS mechanisms, resulting in a marked decline in the secretion of N-Acyl homoserine lactone (AHL) molecules and the expression of phazA1 and aprA genes. This investigation offers compelling evidence supporting the potential of M. aurea EO as a promising therapeutic candidate for addressing infectious diseases induced by biofilm formation