Evidence map›Paper›PMID 41922614›Full record

ArticleScientific reports2026

Comparative evaluation of antimicrobial activities and molecular docking of selected medicinal plants used in arab countries using zamzam water and conventional solvents.

Momeer Fathi Mohamed Dawod, Siddig Ibrahim Abdelwahab, Heyam Sidahmed, Manal Mohamed Elhassan Taha, Ali Ibrahim Elamin, Adel S Al-Zubairi

Abstract readComparative Study
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Momeer Fathi Mohamed DawodDepartment of Microbiology and Immunology, Faculty of Medicine, National University, Khartoum, Sudan.
Siddig Ibrahim AbdelwahabHealth Research Centre, Jazan University, Jazan, Saudi Arabia. Siddigroa@yahoo.com.
Heyam SidahmedDepartment of Pharmaceutical Chemistry, Faculty of Pharmacy, Al-Neelain University, Khartoum, Sudan.
Manal Mohamed Elhassan TahaDepartment of Microbiology and Immunology, Faculty of Medicine, National University, Khartoum, Sudan.
Ali Ibrahim ElaminDepartment of Public Health, College of Nursing and Health Sciences, Jazan University, Jazan, Saudi Arabia.
Adel S Al-ZubairiDepartment of Laboratory Medicine, Faculty of Applied Medical Sciences, Al-Baha University, Al-Baha, Saudi Arabia. adelalzubairi@hotmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing prevalence of antimicrobial resistance has renewed interest in plant-derived bioactive compounds as alternative therapeutic agents. Although medicinal plants are widely studied, limited research has examined the comparative efficacy of Zamzam water as an extraction solvent or integrated in vitro antimicrobial findings with molecular docking analysis to explore potential mechanisms of action. This study aimed to evaluate the antimicrobial activity of ethanol, methanol, petroleum ether, aqueous, and Zamzam water extracts of Origanum majorana, Costus speciosus, Lepidium sativum, and Linum usitatissimum, and to investigate potential molecular interactions of selected phytocompounds with key bacterial targets. Antimicrobial activity was assessed using agar well diffusion and microbroth dilution methods against five standard microorganisms: Bacillus subtilis (ATCC 11774), Staphylococcus aureus (ATCC 25923), Proteus vulgaris (ATCC 33420), Klebsiella pneumoniae (ATCC 10031), and Candida albicans (ATCC 10231). Molecular docking was performed using FLARE software to evaluate selected plant-derived compounds against DNA gyrase (Gram-negative target) and dihydrofolate reductase (DHFR, Gram-positive target). Ethanol, methanol, and Zamzam water extracts produced larger inhibition zones than aqueous extracts, with greater activity observed at higher concentrations. L. usitatissimum seed extracts demonstrated strong activity against P. vulgaris and K. pneumoniae. Docking analysis revealed that β-caryophyllene from O. majorana exhibited high predicted binding affinities to DNA gyrase (− 11.549 kcal/mol) and DHFR (− 13.169 kcal/mol). Flavonoids, including quercetin and kaempferol, also showed favorable binding interactions. These in silico results provide supportive mechanistic insight into the observed antimicrobial effects. The findings indicate that selected medicinal plant extracts, particularly those obtained using alcohol-based and Zamzam water solvents, demonstrate notable antimicrobial activity. The combined experimental and computational approach suggests that specific phytocompounds merit further investigation for the development of novel antibacterial agents.

Indexed as

Anti-Infective AgentsMolecular Docking SimulationPlant ExtractsPlants, MedicinalSolventsAnti-Bacterial AgentsCandida albicansMicrobial Sensitivity TestsStaphylococcus aureusWaterAnti-Bacterial AgentsAnti-Infective AgentsPlant ExtractsSolventsWaterAntimicrobial activityMedicinal plantsMolecular dockingZamzam waterβ-Caryophyllene

Identifiers

PMID41922614
PMCPMC13183934

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