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Biotransformation of isocostic acid from Dittrichia viscosa essential oil by Saccharomyces cerevisiae : in vitro anti-tyrosinase effect, insights from molecular docking and drug-likeness prediction

化学 生物转化 体外 酿酒酵母 生物化学 立体化学 药理学 生物 酵母
作者
Faisal K. Algethami,Mayssa Ben Mustapha,Mohamed R. Elamin,Babiker Y. Abdulkhair,Hichem Ben Jannet
出处
期刊:Plant Biosystems [Informa]
卷期号:157 (6): 1132-1141
标识
DOI:10.1080/11263504.2023.2257703
摘要

AbstractThe purpose of this study was to investigate the biotransformation of the essential oil of Dittrichia viscosa leaves (LEO) by Saccharomyces cerevisiae (baker's yeast) and to evaluate its anti-tyrosinase property. The chemical analysis of the biotransformed essential oil (BEO) was determined by GC-FID and GC/MS. The results showed that isocostic acid, the predominant constituent of LEO (70.8%) was found to be totaly converted by S. cerevisiae into its isomer valerenic acid representing 78.4% of the total composition of BEO. The biotransformed essential oil (BEO) exhibited promising anti-tyrosinase activity (IC50 = 8.54 µg/mL) six times greater than that of LEO (IC50 = 53.44 µg/mL). The experimental results were reinforced by the molecular docking analysis and drug-likeness prediction carried out on the two major sesquiterpene acids detected in LEO and BEO (isocostic acid and valerenic acid, respectively). Valerenic acid showed lower binding energy (−6.3 kcal/mol) compared to isocostic acid (−5.9 kcal/mol), a correct mode and a large number of interactions in the active pocket of the enzyme which can explain the strong inhibitory effect of tyrosinase. Therefore, these results suggest that the bioconverted essential oil could be regarded as safe and effective source of skin whitening agent for cosmetic and medical applications.Keywords: Dittrichia viscosaessential oilbiotransformationSaccharomyces cerevisiaeanti-tyrosinasein silico AcknowledgmentsThe authors extend their appreciation to the Deanship of Scientific Research, Imam Mohammad Ibn Saud Islamic University (IMSIU), Saudi Arabia, for funding this research work through Grant No. (221412005).Disclosure statementNo potential conflict of interest was reported by the authors.

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