Percorrer por autor "Haida, Mohamed"
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- Lichen extracts containing volatile compounds induce oxidative stress and modulate the growth of Microcystis aeruginosa and Chlorella sorokinianaPublication . Essadki, Yasser; Darrag, El Mehdi; Zerrifi, Soukaina El Amrani; Haida, Mohamed; Krimech, Aafaf; Martins, Rosário; Campos, Alexandre; Vasconcelos, Vitor; Bouaïcha, Noureddine; Baçaoui, Abdelaziz; Meddich, Abdelilah; Oudra, Brahim; Tazart, Zakaria; El Khallouf, Fatima; Martins, RosarioThis study evaluates volatile extracts (HE1 and HE2) from the lichen Pseudevernia furfuracea as eco-friendly agents to control algal proliferation, specifically targeting the cyanobacterium Microcystis aeruginosa and the green microalga Chlorella sorokiniana. Both extracts exhibited potent anti-microalgal activity against the two species with a minimum inhibitory concentration (MIC) ranging from 375 to 750 µg/mL. Furthermore, both extracts reduced cell density by more than 98% after eight days of treatment. Chlorophyll a and protein levels decreased significantly (>80%) in both species, indicating suppression of pigment synthesis. However, their physiological responses were distinct: M. aeruginosa underwent early acute oxidative stress and severe membrane damage, while C. sorokiniana exhibited delayed oxidative activation and a negative growth rate, suggesting non-lytic metabolic inhibition. An in silico study by molecular docking of the most abundant compounds identified in these volatile extracts, such as terpenoids (abietatriene, δ-cadinene) and a phenolic compound (atraric acid), showed that these compounds interact with vital cellular targets in M. aeruginosa and C. sorokiniana and likely contribute to the effects observed in these two species. Predictive toxicity by applying the ADMET framework confirmed the favorable bioavailability and low acute toxicity of these volatile compounds. Therefore, P. furfuracea volatiles are promising, species-specific, and environmentally safe candidates for mitigating aquatic algal proliferation through targeted oxidative and metabolic interference.
