Official Journal Publication

Journal of PhytoPharmaceutical and Advanced Chemistry

Short Name: JPPAC• ISSN: 3139-9266• Peer-Reviewed Open Access

2026Volume 1 Issue 03, Pages 153-167• Published: September 28, 2026

Evaluation of Antibacterial Activity of Essential Oil Extracted from the Peels of Citrus limetta Against the Enteric Fever Pathogen Salmonella enterica serovar Typhi

Contributing Authors
MADAN Kumar DNithiya Soundari M
Digital Object Identifier (DOI):https://doi.org/10.66220/92b6a621

Abstract

Horticultural waste, though historically overlooked, serves as a valuable reservoir of bioactive compounds. Addressing the valorization of citrus byproducts, this study investigates the extraction and antimicrobial properties of essential oils derived from sweet lime (Citrus limetta) peels. Essential oils were extracted via hydrodistillation, isolated, and initially characterized using thin-layer chromatography (TLC). Subsequent qualitative profiling was conducted using Gas Chromatography-Mass Spectrometry (GC-MS), which revealed a diverse array of bioactive compounds, with limonene identified as a predominant constituent. The antimicrobial efficacy of the extracted oil was evaluated against clinical isolates of Salmonella typhi, the causative agent of enteric fever, utilizing the agar well diffusion method to assess zones of inhibition. Given the significant antimicrobial properties of limonene, the extract demonstrated strong inhibitory effects. To our knowledge, this is the first study to establish the in vitro antibacterial activity of sweet lime essential oil against Salmonella typhi, highlighting its potential therapeutic application as a natural treatment alternative for typhoid fever.

Export Citation

Generate ready-to-use citations in standard scientific formats

D, M. K. & M, N. S. (2026). Evaluation of Antibacterial Activity of Essential Oil Extracted from the Peels of Citrus limetta Against the Enteric Fever Pathogen Salmonella enterica serovar Typhi. Journal of PhytoPharmaceutical and Advanced Chemistry, Vol. 1(No. 03), pp. 153-167. https://doi.org/10.66220/92b6a621

Cited References

15 References
  1. 01.

    1. Kaza S, Yao LC, Bhada-Tata P, Van Woerden F, Levine D. What a Waste 2.0: A Global Snapshot of Solid Waste Management to 2050. Washington, DC: World Bank; 2018. doi: 10.1596/978-1-4648-1329-0.

  2. 02.

    2. UNEP. Food Waste Index Report 2024. Think Eat Save Tracking Progress to Halve Global Food Waste.2024.

  3. 03.

    3. Martins R, Sales H, Pontes R, Nunes J, Gouveia I. Food Wastes and Microalgae as Sources of Bioactive Compounds and Pigments in a Modern Biorefinery: A Review. Antioxidants. 2023 Jan 31;12(2):328. doi: 10.3390/antiox12020328.

  4. 04.

    4. Turner T, Burri B. Potential Nutritional Benefits of Current Citrus Consumption. Agriculture. 2013 Mar 19;3(1):170–87. doi: 10.3390/agriculture3010170.

  5. 05.

    5. Liu G, Zhang X, Cao Q, Chen T, Hu B, Shi H. The global burden of typhoid and paratyphoid fever from 1990 to 2021 and the impact on prevention and control. BMC Infect Dis. 2025 Jul 15;25(1):919. doi: 10.1186/s12879-025-11223-8.

  6. 06.

    6. Piovani D, Figlioli G, Nikolopoulos GK, Bonovas S. The global burden of enteric fever, 2017–2021: a systematic analysis from the global burden of disease study 2021. EClinicalMedicine. 2024 Nov;77:102883. doi: 10.1016/j.eclinm.2024.102883.

  7. 07.

    7. Wagner H, Bladt S. Plant Drug Analysis. Berlin, Heidelberg: Springer Berlin Heidelberg; 1996. doi: 10.1007/978-3-642-00574-9.

  8. 08.

    8. Pascual ME, Carretero ME, Slowing KV, Villar A. Simplified Screening by TLC of Plant Drugs. Pharm Biol. 2002 Jan 29;40(2):139–43. doi: 10.1076/phbi.40.2.139.5849.

  9. 09.

    9. de los Angeles Fernandez M, Assof M, Jofre V, Silva MF. Volatile Profile Characterization of Extra Virgin Olive Oils from Argentina by HS-SPME/GC-MS and Multivariate Pattern Recognition Tools. Food Anal Methods. 2014 Nov 17;7(10):2122–36. doi: 10.1007/s12161-014-9854-2.

  10. 10.

    10. Rocha AC, Palma C, Bettencourt da Silva RJN. Development and validation of statistically sound criteria for the match of unweathered GC-MS fingerprints in oil spill forensics. Chemosphere. 2022 Feb;289:133085. doi: 10.1016/j.chemosphere.2021.133085.

  11. 11.

    11. Verghese R, Mathew S, David A. Antimicrobial activity of Vitamin C demonstrated on uropathogenic Escherichia coli and Klebsiella pneumoniae. Journal of Current Research in Scientific Medicine. 2017;3(2):88. doi: 10.4103/jcrsm.jcrsm_35_17.

  12. 12.

    12. Tasdemir D, Dönmez A, Çalıs I, Rüedi P. Evaluation of Biological Activity of Turkish Plants. Rapid Screening for the Antimicrobial, Antioxidant, and Acetylcholinesterase Inhibitory Potential by TLC Bioautographic Methods. Pharm Biol. 2004 Jan 29;42(4–5):374–83. doi: 10.1080/13880200490519695.

  13. 13.

    13. DH G, R J, S S, N S. GC-MS Analysis of essential oil from Corchorus olitorius L. J Pharmacogn Phytochem. 2024 Jan 1;13(4):318–22. doi: 10.22271/phyto.2024.v13.i4d.15024.

  14. 14.

    14. Frassinetti S, Caltavuturo L, Cini M, Della Croce CM, Maserti BE. Antibacterial and Antioxidant Activity of Essential Oils from Citrus spp. Journal of Essential Oil Research. 2011 Jan;23(1):27–31. doi: 10.1080/10412905.2011.9700427.

  15. 15.

    15. Olatunya AM, Olatunya OS, Hassan GF, Adeyemi LA, Oyelami OA, Akintayo ET. Antimicrobial activities of essential oils from three species of citrus fruits against six infectious tropical bacteria: implications for the care and control of common bacterial tropical diseases in developing countries. Discover Applied Sciences. 2024 Apr 9;6(4):209. doi: 10.1007/s42452-024-05813-5.

Suggested & Related Publications

Articles in related pharmaceutical, biomedical, and life sciences research on PharmSciGate

Explore Directory →
JPPAC2026 • pp. 01-02

Launching the Journal of PhytoPharmaceutical and Advanced Chemistry

Siddiqui, Falak Arjumand; Khan, Sharuk L.

Inaugural Message from the Editor It is with great pleasure and a strong sense of responsibility that we welcome readers, authors, reviewers, and members of the scientific community to the Journal of PhytoPharmaceutical and Advanced Chemistry (JPPAC). The launch of this journal marks an important milestone in our collective effort to promote rigorous, ethical, and impactful scientific research at the intersection of phytopharmaceutical sciences and advanced chemical research.

JPPAC2026 • pp. 18-29

Computational Study of Alkaloids Targeting O-GlcNAc Transferase as Antidiabetic Agents

Pardaev Jamshid; Umida Sadikova

O-GlcNAc Transferase (OGT) plays a pivotal role in glucose metabolism and insulin signaling, making it an attractive therapeutic target for the management of diabetes mellitus. In the present study, a comprehensive in silico approach was employed to investigate the inhibitory potential of selected alkaloids against human OGT, with an emphasis on their binding affinity and pharmacokinetic suitability. Molecular docking analysis was performed using AutoDock Vina to elucidate the interaction patterns between the selected compounds and the active site of OGT. The docking results revealed that berberine exhibited the strongest binding affinity (−7.8 kcal/mol), slightly surpassing that of the native ligand (−7.7 kcal/mol), and formed stable hydrogen bonding and hydrophobic interactions with key catalytic residues such as LYS898, ASN838, and PRO559. In contrast, castanospermine and swainsonine showed comparatively weaker binding affinities, attributed to limited interaction networks within the binding pocket. To further assess the drug development potential of the studied compounds, in silico ADMET analysis was carried out using SwissADME and ADMETlab 3.0. Berberine demonstrated favorable physicochemical properties, superior drug-likeness (highest QED score), and acceptable absorption and toxicity profiles compared to the native ligand and other alkaloids. Although potential cytochrome P450 interactions and moderate bioaccumulation were predicted for berberine, its overall pharmacokinetic profile was well balanced. Collectively, the integrated docking and ADMET results highlight berberine as a promising lead alkaloid targeting OGT, warranting further in vitro and in vivo validation for its potential development as an antidiabetic agent.

JPPAC2026 • pp. 30-44

Drug repurposing of some US FDA-approved drugs using Binding strength Studies for the Treatment of Methicillin-resistant Staphylococcus aureus Infection

Roy, Dibakar

Methicillin-resistant Staphylococcus aureus (MRSA) is a major multidrug-resistant bacterial pathogen responsible for severe infections worldwide. The increasing resistance of MRSA to conventional antibiotics has created an urgent need for new therapeutic strategies. Drug repurposing of US FDA-approved drugs offers a promising approach to identify alternative anti-MRSA agents while reducing the time and cost associated with traditional drug discovery. In this study, computational Binding strength analysis was performed to evaluate the inhibitory potential of selected compounds against important MRSA target enzymes, including thioredoxin reductase 1, proton motive force protein, and penicillin-binding protein 2a (PBP2a). Molecular docking results demonstrated strong interactions between the ligands and the active sites of the selected enzymes. The native ligand NL_3QFB showed the strongest Binding strength toward thioredoxin reductase 1 with a docking score of −12.2 kcal/mol, while the reference drug Auranofin exhibited −7.8 kcal/mol. For the proton motive force protein, NL_9U6O displayed a docking score of −7.4 kcal/mol, comparable to Niclosamide (−7.5 kcal/mol). Similarly, NL_6Q9N showed strong interaction with PBP2a with a docking score of −8.6 kcal/mol, whereas Afamelanotide showed weaker binding (−1.9 kcal/mol). ADMET analysis indicated acceptable physicochemical and pharmacokinetic properties for several compounds. Overall, the findings suggest that the investigated ligands demonstrate promising Binding capability and favorable drug-like properties against MRSA target enzymes. However, further experimental validation is required to confirm their therapeutic potential.

Full-Text Access

Access Type: Open Access
License:CC BY-NC 4.0
Language:en
Publishing Journal

Journal of PhytoPharmaceutical and Advanced Chemistry

An international, peer-reviewed journal integrating phytopharmaceutical sciences, natural products, and advanced pharmaceutical chemistry.

ISSN:3139-9266
DOI Prefix:10.5530/jppac
Visit Journal Portal
Indexed on PharmSciGate by SPBSRF

This peer-reviewed publication is indexed directly from the publisher repository adhering to Open Archives Initiative (OAI-PMH) metadata standards, Crossref DOI schema, and Google Scholar Highwire Press protocols.