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Abstract

Pelargonium graveoiens (rose-scented pelargonium) is a plant that belongs to the Geraniaceae family native to South Africa. It is recognized for its aroma and essential oil which is widely used in the cosmetic industry, aromatherapy and as a food flavoring agent. It is also known for its antifungal, antimicrobial, anti-inflammatory and antispasmodic properties. For this, it is interesting to study the chemical composition of the essential oil of Pelargonium graveolens from the four regions of Morocco (Er-Rachidia, Meknes, Rabat, Tetouan) by gas chromatography coupled with mass spectrometry (GC-MS), and determine the similarities and dissimilarities of the chemical composition of these four essential oils by carrying out an analysis on the one hand in main composition (ACP) and on the other hand, evaluating their antioxidant activities by two methods DPPH and CAT. The results showed that the essential oil of Pelargonium graveoiens (rose-scented pelargonium) from the four regions mainly contains p-Citronellol, geraniol, citronellyl formate, epi-y-eudesmol, geranyl tiglate and linalool. On the other hand, the antioxidant activity of Pelargonium graveolens essential oil by the measured DPPH method showed that the IC50 values of the Meknes region are lower than the IC50 values found in the Er-Rachidia, Tetouan and Rabat regions.

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... Salicylic acid-O-hexoside Multivariate data analysis of UPLC-ESI-MS data Several attempts were previously performed to study chemical composition of different Pelargonium species and/or cultivars using multivariate data analyses. [36][37][38] In this study, the UPLC-ESI-MS dataset was further analyzed using PCA and HCA to explain metabolite differences and possible discrimination between the three examined P. graveolens cultivars in an untargeted manner. The PCA score plot (Fig. 2a) for the three examined cvs. in positive ion mode explained 57% of the total variance. ...
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... Overall, the obtained results highlighted the strongest toxicity against S. oryzae for P. graveolens EO. The strong insecticidal action of EO could depend on the presence of some components contained in high amounts such as monoterpenoids [25]. These compounds are severely poisonous to insects and have repellent and antifeedant qualities; for this reason, they have been explored as possible pest control agents [57]. ...
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In vitro studies have demonstrated antibacterial activity of essential oils (EOs) against Listeria monocytogenes, Salmonella typhimurium, Escherichia coli O157:H7, Shigella dysenteria, Bacillus cereus and Staphylococcus aureus at levels between 0.2 and 10 microl ml(-1). Gram-negative organisms are slightly less susceptible than gram-positive bacteria. A number of EO components has been identified as effective antibacterials, e.g. carvacrol, thymol, eugenol, perillaldehyde, cinnamaldehyde and cinnamic acid, having minimum inhibitory concentrations (MICs) of 0.05-5 microl ml(-1) in vitro. A higher concentration is needed to achieve the same effect in foods. Studies with fresh meat, meat products, fish, milk, dairy products, vegetables, fruit and cooked rice have shown that the concentration needed to achieve a significant antibacterial effect is around 0.5-20 microl g(-1) in foods and about 0.1-10 microl ml(-1) in solutions for washing fruit and vegetables. EOs comprise a large number of components and it is likely that their mode of action involves several targets in the bacterial cell. The hydrophobicity of EOs enables them to partition in the lipids of the cell membrane and mitochondria, rendering them permeable and leading to leakage of cell contents. Physical conditions that improve the action of EOs are low pH, low temperature and low oxygen levels. Synergism has been observed between carvacrol and its precursor p-cymene and between cinnamaldehyde and eugenol. Synergy between EO components and mild preservation methods has also been observed. Some EO components are legally registered flavourings in the EU and the USA. Undesirable organoleptic effects can be limited by careful selection of EOs according to the type of food.
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Non-structural phenolic compounds perform a variety of functions in plants, including acting as antioxidants. We describe a microplate-adapted colorimetric total phenolics assay that utilizes Folin-Ciocalteu (F-C) reagent. The F-C assay relies on the transfer of electrons in alkaline medium from phenolic compounds to phosphomolybdic/phosphotungstic acid complexes, which are determined spectroscopically at 765 nm. Although the electron transfer reaction is not specific for phenolic compounds, the extraction procedure eliminates approximately 85% of ascorbic acid and other potentially interfering compounds. This assay is performed in microcentrifuge tubes and assessed in a 96-well plate reader. At least 64 samples can be processed in 1 d.
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