Skip to main content
Log in

Exploring the in silico studies of the endophyte fungus Phoma herbarum against mur enzymes of Staphylococcus aureus – a computational approach

  • Research Articles
  • Published:
Vegetos Aims and scope Submit manuscript

Abstract

Endophyte fungus Phoma herbarum (NFCCI 4035) was previously isolated and identified from healthy leaf tissue of Meriandra bengalensis Benth plant from Manipur. We recently established the antibacterial activity of ethyl acetate extracts of endophyte fungus P. herbarum in vitro and identified some potentially active components using GC-MS. The current study aims to perform molecular docking of the discovered P. herbarum compounds against Mur enzymes (Mur A, Mur C, Mur D, and Mur F) of Staphylococcus aureus using Auto Dock Tools 1.5.6. SwissADME online tool was used to calculate the drug-likeness characteristics. According to the findings, only 14 of 23 bioactive compounds evaluated from P. herbarum extract adhered to Lipinski’s Rule of Five (LRo5) and had binding affinity ranged between − 3.5 to -6.5 (kcal/mol) with at least one of the four targeted Mur enzymes. When compared to all other bioactive compounds that interact with target Mur enzymes, 2-Palmitoylglycerol molecule demonstrated highest binding affinity (-6.5 kcal/mol) with Mur F ligase. However, (1R,2R,3R,5 S)-2,6,6-Trimethylbicyclo[3.1.1]heptan-3-amine has shown excellent binding affinity for all selected target (Mur A, Mur C, Mur D, and Mur F) enzymes. Also, this study confirmed that the bioactive compounds can be developed into more potent inhibitors targeting S. aureus-related infections.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4

Similar content being viewed by others

References

  • Adetutu A, Olaniyi TD, Owoade OA (2021) GC-MS analysis and in silico assessment of constituents of Psidium guajava leaf extract against DNA gyrase of Salmonella enterica serovar Typhi. Inf Med Unlocked 26:100722. https://doi.org/10.1016/j.imu.2021.100722

    Article  Google Scholar 

  • Adnan M, Nazim Uddin Chy M, Mostafa Kamal AT, Azad MO, Paul A, Uddin SB, Barlow JW, Faruque MO, Park CH, Cho DH (2019) Investigation of the biological activities and characterization of bioactive constituents of Ophiorrhiza rugosa var. prostrata (D. Don) & Mondal leaves through in vivo, in vitro, and in silico approaches. Molecules. 24(7):1367

  • Chakravarthi V, Karthikeyan M, Lakshmanan L, Murugesan S, Arivuchelvan A, Sukumar K, Arulmozhi A, Jagadeeswaran A (2023) Computational study of Piper betle L. phytocompounds by in silico and ADMET analysis for prediction of potential xanthine oxidase inhibitory activity. BioRxiv. https://doi.org/10.1101/2023.01.13.523909

    Article  PubMed  PubMed Central  Google Scholar 

  • Daina A, Michielin O, Zoete V (2017) SwissADME: a free web tool to evaluate pharmacokinetics, drug-likeness and medicinal chemistry friendliness of small molecules. Sci Rep 7:42717

    Article  PubMed  PubMed Central  Google Scholar 

  • Devi WS, Surendirakumar K, Singh MS (2022) Distribution of endophytic fungi associated with Meriandra bengalensis Benth. And assessment of their bioactive potential in vitro. Vegetos 35:995–1006

    Article  Google Scholar 

  • Engel H, Gutiérrez-Fernández J, Flückiger C, Martínez-Ripoll M, Mühlemann K, Hermoso JA, Hilty M, Hathaway LJ (2013) Heteroresistance to fosfomycin is predominant in Streptococcus pneumoniae and depends on the murA1 gene. Antimicrob Agents Chemother 57(6):2801–2808. https://doi.org/10.1128/AAC.00223-13

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Freiberg C, Pohlmann J, Nell PG, Endermann R, Schuhmacher J, Newton B, Otteneder M, Lampe T, Häbich D, Ziegelbauer K (2006) Novel bacterial acetyl coenzyme a carboxylase inhibitors with antibiotic efficacy in vivo. Antimicrob Agents Chemother 50(8):2707–2712

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Frisvad JC, Houbraken J, Popma S, Samson RA (2013) Two new Penicillium species Penicillium buchwaldii and Penicillium spathulatum, producing the anticancer compound asperphenamate. FEMS Microbiol Lett 339:77–92

    Article  CAS  PubMed  Google Scholar 

  • Funes Chabán M, Hrast M, Frlan R, Graikioti DG, Athanassopoulos CM, Carpinella MC (2021) Inhibition of Mur a enzyme from Escherichia coli and Staphylococcus aureus by Diterpenes from Lepechinia Meyenii and their synthetic analogs. Antibiotics 10(12):1535. https://doi.org/10.3390/antibiotics10121535

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Gaur V, Bera S (2022) Recent developments on UDP-N-acetylmuramoyl-L-alanine-D-gutamate ligase (mur D) enzyme for antimicrobial drug development: an emphasis on in-silico approaches. Curr Res Pharmacol Drug Disc 3:100137. https://doi.org/10.1016/j.crphar.2022.100137

    Article  Google Scholar 

  • Hashmi AA, Naz S, Hashmi SK, Irfan M, Hussain ZF, Khan EY, Asif H, Faridi N (2019) Epidermal growth factor receptor (EGFR) overexpression in triple-negative breast cancer: association with clinicopathologic features and prognostic parameters. Surg Exp Pathol 2(6):1–7

    Google Scholar 

  • Hrast M, Sosič I, Šink R, Gobec S (2014) Inhibitors of the peptidoglycan biosynthesis enzymes MurA-F. Bioorg Chem 55:2–15

    Article  CAS  PubMed  Google Scholar 

  • Jha RK, Khan RJ, Amera GM, Singh E, Pathak A, Jain M, Muthukumaran J, Singh AK (2020) Identification of promising molecules against MurD ligase from Acinetobacter baumannii: insights from comparative protein modelling, virtual screening, molecular dynamics simulations and MM/PBSA analysis. J Mol Model 26:1–7

    Article  Google Scholar 

  • Kotnik M, Humljan J, Contreras-Martel C, Oblak M, Kristan K, Hervé M, Blanot D, Urleb U, Gobec S, Dessen A, Solmajer T (2007) Structural and functional characterization of enantiomeric glutamic acid derivatives as potential transition state analogue inhibitors of MurD ligase. J Mol Biol 370(1):107–115

    Article  CAS  PubMed  Google Scholar 

  • Kouidmi I, Levesque RC, Paradis-Bleau C (2014) The biology of Mur ligases as an antibacterial target. Mol Microbiol 94(2):242–253

    Article  CAS  PubMed  Google Scholar 

  • Laddomada F, Miyachiro MM, Dessen A (2016) Structural insights into protein-protein interactions involved in bacterial cell wall biogenesis. Antibiotics 5(2):14. https://doi.org/10.3390/antibiotics5020014

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Lipinski CA, Lombardo F, Dominy BW, Feeney PJ (2001) Experimental and computational approaches to estimate solubility and permeability in drug discovery and development settings. Adv Drug Deliv Rev 46:3–26

    Article  CAS  PubMed  Google Scholar 

  • Liu Y, Breukink E (2016) The membrane steps of bacterial cell wall synthesis as antibiotic targets. Antibiotics 5(3):28. https://doi.org/10.3390/antibiotics5030028

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mehjabeen H, Dil USC, Jacy Farhana, Mohammed TA, Ananya C, Shamima I, Adnan M (2013) Identification of potential targets in Staphylococcus aureus N315 using computer aided protein data analysis. Bioinformation 9(4):187–192

    Article  Google Scholar 

  • Mihalovits LM, Ferenczy GG, Keseru GM (2019) Catalytic mechanism and covalent inhibition of UDP-N-acetylglucosamine enolpyruvyl transferase (MurA): implications to the design of novel antibacterials. J Chem Inf Model 59:5161–5173

    Article  CAS  PubMed  Google Scholar 

  • Mol CD, Brooun A, Dougan DR, Hilgers MT, Tari LW, Wijnands RA, Knuth MW, McRee DE, Swanson RV (2003) Crystal structures of active fully assembled substrate-and product-bound complexes of UDP-N-acetylmuramic acid: L-alanine ligase (MurC) from Haemophilus influenzae. J Bacteriol 185(14):4152–4162

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Mousa WK, Raizada MN (2013) The diversity of anti-microbial secondary metabolites produced by fungal endophytes: an interdisciplinary perspective. Front Microbiol 4:65. https://doi.org/10.3389/fmicb.2013.00065

    Article  PubMed  PubMed Central  Google Scholar 

  • Ononamadu CJ, Ibrahim A (2021) Molecular docking and prediction of ADME/drug-likeness properties of potentially active antidiabetic compounds isolated from aqueous-methanol extracts of Gymnema sylvestre and Combretum micranthum. Biotechnologia 102(1):85–99

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  • Rani N, Kumar C, Arunachalam A, Lakshmi PTV (2018) Rutin as a potential inhibitor to target peptidoglycan pathway of Staphylococcus aureus cell wall synthesis. Clin Microbiol Infect Dis 3:15761. https://doi.org/10.15761/CMID.1000142

    Article  Google Scholar 

  • Rath S, Jagadeb M, Bhuyan R (2021) Molecular docking of bioactive compounds derived from Moringa oleifera with p53 protein in the apoptosis pathway of oral squamous cell carcinoma. Genomics Inf 19(4):e46. https://doi.org/10.5808/gi.21062

    Article  Google Scholar 

  • Srinivasan K, Altemimi AB, Narayanaswamy R, Vasantha Srinivasan P, Najm MA, Mahna N (2023) GC-MS, alpha‐amylase, and alpha‐glucosidase inhibition and molecular docking analysis of selected phytoconstituents of small wild date palm fruit (Phoenix pusilla). Food Sci Nutr 1–14. https://doi.org/10.1002/fsn3.3489

  • Staniek A, Woerdenbag J, Kayser O (2008) Endophytes exploiting biodiversity for the improvement of natural product-based drug discovery. J Plant Interact 3:75–98

    Article  CAS  Google Scholar 

  • Suresh E, Sureshkumar P (2019) Antimicrofouling activity of Calotropis gigantea (L). R. Br. Indian J Geo-Mar Sci 48(12):1843–1848

    Google Scholar 

  • Tiwari P, Srivastava Y, Bae H (2021) Endophytes: Trend of pharmaceutical design of endophytes as anti-infective. Curr Top Med Chem 21:1572–1586

    Article  CAS  PubMed  Google Scholar 

  • Umamaheswari A, Pradhan D, Hemanthkumar M (2010) Virtual screening for potential inhibitors of homology modeled Leptospira interrogans MurD ligase. J Chem Biol 3:175–187

    Article  PubMed  PubMed Central  Google Scholar 

  • Vollmer W, Blanot D, De Pedro MA (2008) Peptidoglycan structure and architecture. FEMS Microbiol Rev 32:149–167

    Article  CAS  PubMed  Google Scholar 

  • Yashodeep S, Iqrar Ahmad, Sanjay S, Harun P (2021) The mur enzymes chink in the armour of Mycobacterium tuberculosis cell wall. Eur J Med Chem 222(23–24):113568

    Google Scholar 

Download references

Acknowledgements

The author (WSD) wishes to express her gratitude to the Head of the Department of Life Sciences (Botany), Manipur University, for providing lab space for her Ph.D. research.

Author information

Authors and Affiliations

Authors

Corresponding author

Correspondence to Kannaiah Surendirakumar.

Ethics declarations

Conflict of interest

The authors have declared no conflicts of interest.

Additional information

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Electronic supplementary material

Below is the link to the electronic supplementary material.

Supplementary Material 1

Rights and permissions

Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Surendirakumar, K., Devi, W.S. & Vaithilingam, S. Exploring the in silico studies of the endophyte fungus Phoma herbarum against mur enzymes of Staphylococcus aureus – a computational approach. Vegetos (2023). https://doi.org/10.1007/s42535-023-00738-7

Download citation

  • Received:

  • Revised:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1007/s42535-023-00738-7

Keywords

Navigation