Autor: |
Tetevi, Gilbert Mawuli, Kwain, Samuel, Mensah, Thomas, Camas, Anil Sazak, Camas, Mustafa, Dofuor, Aboagye Kwarteng, Azerigyik, Faustus Akankperiwen, Oluwabusola, Emmanuel, Deng, Hai, Jaspars, Marcel, Kyeremeh, Kwaku |
Předmět: |
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Zdroj: |
Molbank; Dec2019, Vol. 2019 Issue 4, pM1094-M1094, 1p |
Abstrakt: |
The Ghanaian Paenibacillus sp. DE2SH (GenBank Accession Number: MH091697) is a prolific producer of potent antiparasitic alkaloids. Further detailed study of the culture broth of this strain produced the compound Paenidigyamycin G (1), which is a derivative of the known antiparasitic compound Paenidigyamycin A (2). Compound (1) was isolated on HPLC at tR ≈ 37.5 min and its structure determined by IR, UV, MS, 1D, and 2D-NMR data. Compound 1 produced weak to moderate antileishmanial and antitrypanosomal activity when tested against Leishmania donovani (Laveran and Mesnil) Ross (D10) and Trypanosoma brucei subsp. brucei strain GUTat 3.1 with IC50 = 115.41 and 28.75 μM, respectively. This result is interesting since the parent compound 2 is known to possess consistent and potent antiparasitic activity. However, 1 displayed a promising selectivity profile towards T. brucei subsp. brucei due to its relatively low toxicity against normal mouse macrophages RAW 264.7 cells (SI = 8.70). Given that compound 1 is also the main metabolite found in the hexane fraction of all extracts produced by Paenibacillus sp. DE2SH when it is co-cultured with other bacteria strains, it must possess some unique biological functions which should make it an excellent candidate for further biological activity screening in other bioassays. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
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