Study of the antibacterial activity of essential oils of three moroccan and aromatics plants on four bacterial strains

The aim of this work is the in vitro evaluation of the antibacterial activities of essential oils extracted from three aromatic and Moroccan plants: Thymus vulgaris, Mentha spicata and Citrus limonum, on four bacterial strains: Staphylococcus aureus, Escherichia coli, Pseudomonas aerations and Klebsiella pneumoniae. These strains have been chosen for their pathological impact due to their pathogen city in relation to problems of resistance to common antibiotics. The results obtained showed that for the strains of Escherichia coli and Pseudomonas aerations, the essential oil of Thymus vulgaris, showed the highest antibacterial activity, while for the strains of Staphylococcus aureus and Klebsiella pneumonia, the essential oil of Menthe spicata which proved to be the most active. Published by the International journal of Microbiology and Mycology (IJMM

Etude De L’Activité Antioxydante Des Huiles Essentielles De Plantes Aromatiques Et Médicinales Marocaines

Morocco is a traditional supplier of medicinal and aromatic plants to the world. This activity has resulted to the exploitation of wild plants than dried plants for herbal needs and food flavors. Many species are used for the production of plant extracts and other aromatic essences mainly for the pharmaceutical and cosmetics industry. Among these metabolites, there are essential oils that are mixtures of aromatic substances present in the form of tiny droplets in the leaves, fruit peel, resin, branches, and wood. These oils, however, is endowed with antioxidant properties. This study aims to evaluate the antioxidant activity of essential oils of three moroccan aromatic and medicinal plants: Thymus vulgaris, Mentha spicata, and Citrus limonum. The oil extraction was performed by steam distillation in a Clevenger type apparatus. Also, the antioxidant activity of these oils was evaluated by the method of DPPH (2,2-diphenyl-1-picrylhydrazyl), in comparison with the antioxidant synthetic, ascorbic acid. In the present work, the results showed that the antioxidant activity of three essential oils studied by the trapping method of free radical is moderate. Also, the oil of Thymus vulgaris has a strong activity which exceeds that of ascorbic acid. This was followed by the oil of Mentha spicata, while the lowest activity was observed in Citrus limonum

Deep eutectic solvent-ultrasound assisted extraction as a green approach for enhanced extraction of naringenin from Searsia tripartita and retained their bioactivities

BackgroundNaringenin (NA) is a natural flavonoid used in the formulation of a wide range of pharmaceutical, fragrance, and cosmetic products. In this research, NA was extracted from Searsia tripartita using an environmentally friendly, high efficiency extraction method: an ultrasound-assisted extraction with deep eutectic solvents (UAE-DES).MethodsSix natural deep eutectic solvent systems were tested. Choline chloride was used as the hydrogen bond acceptor (HBA), and formic acid, ethylene glycol, lactic acid, urea, glycerol, and citric acid were used as hydrogen bond donors (HBD).ResultsBased on the results of single-factor experiments, response surface methodology using a Box-Behnken design was applied to determine the optimal conditions for UAE-DES. According to the results, the optimal NA extraction parameters were as follows: DES-1 consisted of choline chloride (HBA) and formic acid (HBD) in a mole ratio of 2:1, an extraction time of 10 min, an extraction temperature of 50°C, an ultrasonic amplitude of 75 W, and a solid-liquid ratio of 1/60 g/mL. Extracted NA was shown to inhibit the activity of different enzymes in vitro, including α-amylase, acetylcholinesterase, butyrylcholinesterase, tyrosinase, elastase, collagenase, and hyaluronidase.ConclusionThus, the UAE-DES technique produced high-efficiency NA extraction while retaining bioactivity, implying broad application potential, and making it worthy of consideration as a high-throughput green extraction method

Reactions des diarylnitrilimines avec des derives de la quinoleine et de l'isoquinoleine. Problemes de regio et de stereochimie

SIGLEINIST T 77062 / INIST-CNRS - Institut de l'Information Scientifique et TechniqueFRFranc

Improved Method for DNA Extraction and Purification from <i>Tetrahymena pyriformis</i>

Tetrahymena pyriformis (protozoa) is intensely investigated as a model organism, offering numerous advantages in comprehensive and multidisciplinary studies using morphologic or molecular methods. Since DNA extraction is a vital step of any molecular experiment, here a new mixed surfactant (Sodium dodecyl sulfate (SDS) 20%/Triton X-100) was adopted for effective DNA extraction from Tetrahymena pyriformis under an easy, fast protocol. The efficiency of this technique was then compared with three widely-used alternative techniques, namely the Chelex 100 matrix, Ammonium pyrrolidine dithiocarbamate (APD) complex and SDS&#8211;chloroform methods. DNA extraction was analyzed by pulsed-field gel electrophoresis, spectral measurement, fluorometry (Qubit), restriction enzyme digestion, and polymerase chain reaction. Data analysis revealed that the quantity and quality of the recovered DNA varied depending on the applied DNA extraction method. The new method (SDS 20%/Triton X-100) was the most efficient for extracting DNA from Tetrahymena pyriformis with high integrity and purity, affordable cost, less time, and suitability for molecular applications

A Comparative Study between Conventional and Advanced Extraction Techniques: Pharmaceutical and Cosmetic Properties of Plant Extracts

This study aimed to compare the influence of extraction methods on the pharmaceutical and cosmetic properties of medicinal and aromatic plants (MAPs). For this purpose, the dried plant materials were extracted using advanced (microwave (MAE), ultrasonic (UAE), and homogenizer (HAE) assisted extractions) and conventional techniques (maceration, percolation, decoction, infusion, and Soxhlet). The tyrosinase, elastase, &alpha;-amylase, butyryl, and acetylcholinesterase inhibition were tested by using L-3,4 dihydroxy-phenylalanine, N-Succinyl-Ala-Ala-p-nitroanilide, butyryl, and acetylcholine as respective substrates. Antioxidant activities were studied by ABTS, DPPH, and FRAP. In terms of extraction yield, advanced extraction techniques showed the highest values (MAE &gt; UAE &gt; HAE). Chemical profiles were dependent on the phenolic compounds tested, whereas the antioxidant activities were always higher, mainly in infusion and decoction as a conventional technique. In relation to the pharmaceutical and cosmetic properties, the highest inhibitory activities against &alpha;-amylase and acetylcholinesterase were observed for Soxhlet and macerated extracts, whereas the highest activity against tyrosinase was obtained with MAE &gt; maceration &gt; Soxhlet. Elastase and butyrylcholinesterase inhibitory activities were in the order of Soxhlet &gt; maceration &gt; percolation, with no activities recorded for the other tested methods. In conclusion, advanced methods afford an extract with high yield, while conventional methods might be an adequate approach for minimal changes in the biological properties of the extract

Biological activities of Schottenol and Spinasterol, two natural phytosterols present in argan oil and in cactus pear seed oil, on murine miroglial BV2 cells

International audienceThe objective of this study was to evaluate the biological activities of the major phytosterols present in argan oil (AO) and in cactus seed oil (CSO) in BV2 microglial cells. Accordingly, we first determined the sterol composition of AO and CSO, showing the presence of Schottenol and Spinasterol as major sterols in AO. While in CSO, in addition to these two sterols, we found mainly another sterol, the Sitosterol. The chemical synthesis of Schottenol and Spinasterol was performed. Our results showed that these two phytosterols, as well as sterol extracts from AO or CSO, are not toxic to microglial BV2 cells. However, treatments by these phytosterols impact the mitochondrial membrane potential. Furthermore, both Schottenol and Spinasterol can modulate the gene expression of two nuclear receptors, liver X receptor (LXR)-alpha and LXR beta, their target genes ABCA1 and ABCG1. Nonetheless, only Schottenol exhibited a differential activation vis-a-vis the nuclear receptor LXR beta. Thus Schottenol and Spinasterol can be considered as new LXR agonists, which may play protective roles by the modulation of cholesterol metabolism