Digyalipopeptide A, an antiparasitic cyclic peptide from the Ghanaian Bacillus sp. strain DE2B.

Adwoa P Nartey* (Corresponding Author), Aboagye K Dofuor, Kofi B A Owusu, Anil S Camas, Hai Deng, Marcel Jaspars, Kwaku Kyeremeh* (Corresponding Author)

*Corresponding author for this work

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Abstract

During the continued isolation of different bacteria from highly diverse, low human activity environments in Ghana and the subsequent characterization and biological activity studies of their secondary metabolites, we found both Gram-positive and Gram-negative Bacillus strains to be ubiquitous and widespread. One of such strains, the Ghanaian novel Bacillus sp. strain DE2B was isolated from rhizosphere soils collected from the Digya National Park in Ghana. Chromatographic purifications of the fermented culture extract of the strain DE2B, led to the isolation of a cyclic lipopeptide, digyalipopeptide A ( 1). Using 1D and 2D NMR data, mass spectrometry sequence tagging, advanced Marfey's analysis, and the GNPS molecular networking we solved the full structure of digyalipopeptide A ( 1). We found that compound 1 is a member of a somewhat homologous series of peptides produced as a mixture by the strain containing the same amino acid sequence in the cyclic peptide backbone but differing only by the length of aliphatic fatty acid side chains. When tested against Trypanosoma brucei subsp. brucei strain GUTat 3.1 and Leishmania donovani (Laveran and Mesnil) Ross (D10), digyalipopeptide A ( 1) gave IC 50 values of 12.89 µM (suramin IC 50 0.96 µM) and 4.85 µM (amphotericin B IC 50 4.87 µM), respectively. Furthermore, digyalipopeptide A ( 1) produced IC 50 values of 10.07 µM (ampicillin IC 50 0.18 µM) and 10.01 µM (ampicillin IC 50 1.53 µM) for Staphylococcus aureus and Shigella sonnei, respectively. The selectivity and toxicity profile of compound 1 was investigated using normal cell lines, macrophages RAW 264.7. When tested against normal macrophages, compound 1 gave an IC 50 value of 71.32 μM. Selectivity indices (SI) were obtained by calculating the ratio of the IC 50 in RAW 264.7 to the IC 50 in the respective microbe and neglected parasite. In the presence of RAW 264.7 cell lines, compound 1 was particularly selective towards Leishmania donovani (Laveran and Mesnil) Ross (D10) with an SI value of 14.71. The bioactivity studies conducted confirm the role of these cyclic lipopeptides as defense chemicals in their natural environment and their ability to be biologically active across different species.

Original languageEnglish
Pages (from-to)1763-1771
Number of pages9
JournalBeilstein journal of organic chemistry
Volume18
Early online date28 Dec 2022
DOIs
Publication statusPublished - 28 Dec 2022

Bibliographical note

Acknowledgements
We acknowledge the mass spectrometry data received from the laboratory of Professor Pieter C. Dorrestein and Andrés Mauricio Caraballo Rodrígueze.

Funding
K.K., H.D and M.J. are grateful for the financial support of Leverhulme Trust-Royal Society Africa award (AA090088) and the jointly funded UK Medical Research Council–UK Department for International Development (MRC/DFID) Concordat Agreement African Research Leaders Award (MR/S00520X/1). A.P.N. is thankful for the award of a Ph.D. scholarship by the Organization for Women in Science for the Developing World (OWSD), the Swedish International Development Cooperation Agency (SIDA) and the Carnegie BANGA-Africa Project Award for a Ph.D. scholarship.

Data Availability Statement

Supporting Information
Experimental protocols, phylogenetic data, compound characterization data (1D, 2D NMR), stereochemistry determination, tables, and figures.[https://www.beilstein-journals.org/bjoc/content/
supplementary/1860-5397-18-185-S1.pdf].

Keywords

  • Leishmania
  • lipopeptides
  • molecular networking
  • sequence tagging
  • trypanosomes

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