# Exploring the Potential of Plant Cytokinins Against Common Human Pathogens: In Vitro Assessment and In Silico Insights

**Authors:** Jelena Lazarević, Aleksandar Veselinović, Marija Stojiljković, Miloš Petrović, Pierangela Ciuffreda, Enzo Santaniello

PMC · DOI: 10.3390/plants14121749 · Plants · 2025-06-07

## TL;DR

This study explores how plant hormones called cytokinins can inhibit the growth of certain bacteria and fungi, particularly showing strong antifungal effects against Candida albicans.

## Contribution

The first report linking natural cytokinins to direct antifungal action against C. albicans supported by in silico evidence.

## Key findings

- Kinetin (K) and kinetin riboside (KR) showed strong antifungal activity against Candida albicans with MIC values comparable to nystatin.
- Molecular docking studies revealed favorable interactions of K and KR with SAP3 and DHFR in C. albicans.
- Cytokinins exhibited bacteriostatic activity against Bacillus subtilis and Enterococcus faecalis but not against Gram-negative bacteria.

## Abstract

Cytokinins, plant hormones derived from adenine, are best known for regulating growth and stress responses in plants. Recent findings suggest they may also influence microbial viability, yet their direct antimicrobial potential remains underexplored. This study evaluates the antimicrobial activities of four natural cytokinins (iPA, B, K, and p-T) and their N9-ribosides (iPAR, BR, KR, and p-TR) against selected human pathogens. Using the broth microdilution method, we assessed their effects on Gram-positive and Gram-negative bacteria, as well as fungal strains. While Gram-negative species showed no susceptibility, all tested compounds exhibited bacteriostatic activity against Bacillus subtilis and Enterococcus faecalis. Most notably, kinetin (K) and kinetin riboside (KR) displayed strong antifungal activity against Candida albicans, with MIC values comparable to the reference drug nystatin. Molecular docking studies supported these findings by showing that K and KR form favorable interactions with two validated antifungal targets in Candida albicans: secreted aspartic proteinase 3 (SAP3) and dihydrofolate reductase (DHFR). This is, to our knowledge, the first report linking natural cytokinins to direct antifungal action against C. albicans supported by in silico evidence. These findings highlight the potential of K and KR as promising leads for the development of cytokinin-based antifungal agents.

## Linked entities

- **Chemicals:** B (PubChem CID 5462311), K (PubChem CID 813), p-T (PubChem CID 23939), BR (PubChem CID 259), KR (PubChem CID 5416), nystatin (PubChem CID 4568)
- **Species:** Bacillus subtilis (taxon 1423), Enterococcus faecalis (taxon 1351), Candida albicans (taxon 5476)

## Full-text entities

- **Genes:** DHFR (dihydrofolate reductase) [NCBI Gene 1719] {aka DHFR1, DYR}
- **Chemicals:** nystatin (MESH:D009761), BR (MESH:D001966), kinetin (MESH:D007701), Cytokinins (MESH:D003583), B (MESH:D001895), adenine (MESH:D000225), K (MESH:D011188), KR (MESH:C527965), iPAR (-), N (MESH:D009584)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Candida albicans (species) [taxon 5476], Enterococcus faecalis (species) [taxon 1351], Homo sapiens (human, species) [taxon 9606], Bacillus subtilis (species) [taxon 1423]

## Full text

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## Figures

2 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12196393/full.md

## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12196393/full.md

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Source: https://tomesphere.com/paper/PMC12196393