Evidence map›Paper›PMID 41673880›Full record

ArticleMicrobial cell factories2026

Antibacterial potential, DNA binding and molecular docking investigations of newly green synthesized zinc oxide/chitosan/vancomycin nanocomposite using Bacillus licheniformis ATCC 4527 against some drug-resistant bacteria.

Shimaa M El-Salamony, Zakaria A M Baka, Mohamed I Abou-Dobara, Hanaa M Salama, Mohamed M El-Zahed

Abstract read
In one paragraph

Article in Microbial cell factories, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

5 authors.

Shimaa M El-SalamonyBotany and Microbiology Department, Faculty of Science, Damietta University, New Damietta, Egypt.
Zakaria A M BakaBotany and Microbiology Department, Faculty of Science, Damietta University, New Damietta, Egypt.
Mohamed I Abou-DobaraBotany and Microbiology Department, Faculty of Science, Damietta University, New Damietta, Egypt.
Hanaa M SalamaChemistry Department, Faculty of Science, Port Said University, Port Said, Egypt.
Mohamed M El-ZahedBotany and Microbiology Department, Faculty of Science, Damietta University, New Damietta, Egypt. mohamed.marzouq91@du.edu.eg.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe increasing crisis of multidrug-resistant (MDR) bacteria requires the creation of new, highly effective, and safe antibacterial agents. This study introduces a simple and cost-effective green synthesis method for a novel zinc oxide/chitosan/vancomycin (ZnO/CS/VA) nanocomposite to improve antibacterial activity against priority MDR strains. Zinc oxide nanoparticles (ZnO NPs) were biosynthesized using Bacillus licheniformis ATCC 4527 and then combined with vancomycin (VA) and chitosan (CS) in an environmentally friendly process. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), ultraviolet-visible spectroscopy (UV-Vis), and zeta potential studies were conducted to validate and characterize the production of ZnO/CS/VA. The antibacterial activity of the nanoparticles was tested against several multidrug-resistant (MDR) strains, including Bacillus cereus HES3, methicillin-resistant S. aureus (MRSA), Escherichia coli D8, Pseudomonas aeruginosa, and Klebsiella pneumoniae H4. Further assessment included molecular docking interactions with E. coli (PDB: 3T88) and MRSA (PDB: 4DKI) targets, CT-DNA binding, and cytotoxicity testing on the Vero cell line. Characterization confirmed the successful formation of the nanocomposite, revealing ZnO nanoparticles ranging from 33.24 to 69.11 nm and high stability (zeta potential: -17.78 mV). The ZnO/CS/VA nanocomposite exhibited superior dose-dependent antibacterial activity compared to ZnO nanoparticles or VA alone against all tested MDR strains, including MRSA and E. coli D8. Molecular docking demonstrated strong binding, with scores ranging from -0.7 to -10.85 kcal/mol. The nanocomposite exhibited a hypochromism when interacting with CT-DNA, suggesting intercalation. Importantly, the CC50 values of ZnO NPs and ZnO/CS/VA against Vero cells were 146.62±1.03 and 162.86±1.07 μg/mL, respectively, indicating their high level of safety.

conclusionsThe green-synthesized ZnO/CS/VA nanocomposite is a promising alternative candidate for treating various MDR bacterial infections. It offers utility in biomedical and pharmaceutical applications due to its high efficacy and low cytotoxicity.

Indexed as

Anti-Bacterial AgentsBacillus licheniformisChitosanNanocompositesVancomycinZinc OxideAnimalsDrug Resistance, Multiple, BacterialEscherichia coliGreen Chemistry TechnologyMethicillin-Resistant Staphylococcus aureusMicrobial Sensitivity TestsMolecular Docking SimulationPseudomonas aeruginosaVero CellsAnti-Bacterial AgentsChitosanVancomycinZinc OxideAntibacterialBacillus licheniformisGreen synthesisMultidrug resistanceNanocompositeZnO

Identifiers

PMID41673880
PMCPMC12930810

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.