GC-MS screening of the phytochemical composition of Ziziphus honey: ADME properties and in vitro/in silico study of its antimicrobial activity

被引:9
|
作者
Bouali, Nouha [1 ]
Ahmad, Iqrar [2 ]
Patel, Harun [2 ]
Alhejaili, Elham Bader [1 ]
Hamadou, Walid Sabri [1 ,3 ]
Badraoui, Riadh [1 ,4 ,5 ]
Hadj Lajimi, Ramzi [6 ,7 ]
Alreshidi, Mousa [1 ,8 ]
Siddiqui, Arif Jamal [1 ]
Adnan, Mohd [1 ]
Abdulhakeem, Mohammad A. [1 ]
Bazaid, Abdulrahman S. [8 ]
Patel, Mitesh [9 ,10 ]
Saeed, Mohd [1 ]
Snoussi, Mejdi [1 ,11 ,12 ]
Noumi, Emira [1 ,11 ,12 ]
机构
[1] Univ Hail, Coll Sci, Dept Biol, Hail, Saudi Arabia
[2] Prof Ravindra Nikam Coll Pharm, Dept Pharmaceut Chem, Dhule, Maharashtra, India
[3] Univ Medecine Sousse, Dept Biochem, Res Unit Mol Biol Leukemia & Lymphoma, Sousse, Tunisia
[4] Univ Tunis El Manar, Univ Med Tunis, Sect Histol Cytol, Tunis, Tunisia
[5] Univ Sfax, Med Fac Sfax, Dept Histo Embryol & Cytogenet, Sfax, Tunisia
[6] Univ Hail, Coll Sci, Dept Chem, Hail, Saudi Arabia
[7] Ctr Res & Water Technol, Lab Water Membranes & Environm Biotechnol, Soliman, Tunisia
[8] Univ Hail, Coll Appl Med Sci, Dept Med Lab Sci, Hail, Saudi Arabia
[9] Parul Univ, Parul Inst Appl Sci, Dept Biotechnol, Vadodara, India
[10] Parul Univ, Ctr Res Dev, Vadodara, India
[11] High Inst Biotechnol Univ Monastir, Lab Genet Biodivers & Valorisat Bioressources, Monastir, Tunisia
[12] Univ Hail, Coll Sci, Dept Biol, POB 2440, Hail 2440, Saudi Arabia
来源
关键词
Antimicrobial activity; molecular docking; molecular dynamic; Ziziphus honey; chemical composition; INDUCED FIT DOCKING; MICROBIAL RESISTANCE; DRUG DISCOVERY; INHIBITION;
D O I
10.1080/07391102.2023.2205945
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
A revival interest has been given to natural products as sources of phytocompounds to be used as alternative treatment against infectious diseases. In this context, we aimed to investigate the antimicrobial potential of Ziziphus honey (ZH) against twelve clinical bacterial strains and several yeasts and molds using in vitro and computational approaches. The well-diffusion assay revealed that ZH was able to induce growth inhibition of most Gram-positive and Gram-negative bacteria. The high mean growth inhibition zone (mGIZ) was recorded in E. coli (Clinical strain, 217), S. aureus followed by E. coli ATCC 10536 (mGIZ values: 41.00 +/- 1 mm, 40.67 +/- 0.57 mm, and 34.67 +/- 0.57 mm, respectively). The minimal bactericidal concentrations (MBCs) and minimal fungicidal concentration values (MFCs) from approximately 266.33 mg/mL to over 532.65 mg/mL. Molecular docking results revealed that the identified compounds maltose, 2-furoic acid, isopropyl ester, 2,4-imidazolidinedione, 5-(2-methylpropyl)-(S)- and 3,4,5-trihydroxytoluene, S-Methyl-L-Cysteine, 2-Furancarboxylic acid, L-Valine-N-ethoxycarbonyl, Hexanoic acid, 3,5,5-trimethyl-, Methyl-beta-D-thiogalactoside, gamma-Sitosterol, d-Mannose, 4-O-Methylmannose, 2,4-Imidazolidinedione, 5-(2-methylpropyl)- (S) were found to have good affinity for targeted receptor, respectively. Through a 100-ns dynamic simulation research, binding interactions and stability between promising phytochemicals and the active residues of the studied enzymes were confirmed. The ADMET profiling of all identified compounds revealed that most of them could be qualified as biologically active with good absorption and permeation. Overall, the results highlighted the efficiency of ZH against the tested clinical pathogenic strains. The antimicrobial potential and the potency displayed by the identified compounds could imply their further pharmacological applications.Communicated by Ramaswamy H. Sarma
引用
收藏
页码:1368 / 1380
页数:13
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