Bioassay Guided Fractionation of Marine Streptomyces sp. GMY01 and Antiplasmodial Assay using Microscopic and Flow Cytometry Method

Genome mining study showed that marine-derived Streptomyces sp. GMY01 is a potential actinobacteria with abundant of secondary metabolite and anticancer activity. The study aimed to evaluate bioassay guided fractionation for antiplasmodial screening of GMY01 extract and to predict compound on active...

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Autores principales: Ema Damayanti, Jaka Widada, Puspa Dewi N. Lotulung, Achmad Dinoto, Mustofa Mustofa
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Lenguaje:EN
Publicado: Universitas Gadjah Mada 2020
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Acceso en línea:https://doaj.org/article/06f54a8cb4134c538460cc8007f577fa
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spelling oai:doaj.org-article:06f54a8cb4134c538460cc8007f577fa2021-11-15T06:08:47ZBioassay Guided Fractionation of Marine Streptomyces sp. GMY01 and Antiplasmodial Assay using Microscopic and Flow Cytometry Method2338-94272338-948610.22146/ijp.809https://doaj.org/article/06f54a8cb4134c538460cc8007f577fa2020-12-01T00:00:00Zhttps://jurnal.ugm.ac.id/v3/IJP/article/view/809https://doaj.org/toc/2338-9427https://doaj.org/toc/2338-9486Genome mining study showed that marine-derived Streptomyces sp. GMY01 is a potential actinobacteria with abundant of secondary metabolite and anticancer activity. The study aimed to evaluate bioassay guided fractionation for antiplasmodial screening of GMY01 extract and to predict compound on active fractions. Ethyl acetate fraction was obtained from 11 days fermentation product of GMY01 and then it was fractionated using n-hexane and methanol solvent. Refractionated was applied using flash chromatography and column chromatography. Antiplasmodial assay was performed on Plasmodium falciparum FCR3 by microscopic method using thin blood smear + Giemsa stain, and flow cytometry method using SYBR Green I stain. Toxicity assay was performed on Vero cells line. Main constituent of active fraction was analyzed using LCMS/MS. The result of the study showed that ethyl acetate-methanol fraction has high antiplasmodial activity (IC50=3.96 µg/mL) with very low toxicity on Vero cells (IC50=30,072 µg/mL). Bioassay guided fractionation resulted F4.7 as highest Plasmodium inhibition (94.3% at 5 µg/mL) and was confirmed by microscopic and flow cytometry assay. Main constituent analysis showed C10H13NO (163.09971 Da) as mayor compound and predicted as nonribosomal polyketide synthetase (NRPS) secondary metabolite.Ema DamayantiJaka WidadaPuspa Dewi N. LotulungAchmad DinotoMustofa MustofaUniversitas Gadjah Madaarticledrug discoverymalariaantiplasmodial assayactinomycetesPharmacy and materia medicaRS1-441ENIndonesian Journal of Pharmacy, Pp 281–289-281–289 (2020)
institution DOAJ
collection DOAJ
language EN
topic drug discovery
malaria
antiplasmodial assay
actinomycetes
Pharmacy and materia medica
RS1-441
spellingShingle drug discovery
malaria
antiplasmodial assay
actinomycetes
Pharmacy and materia medica
RS1-441
Ema Damayanti
Jaka Widada
Puspa Dewi N. Lotulung
Achmad Dinoto
Mustofa Mustofa
Bioassay Guided Fractionation of Marine Streptomyces sp. GMY01 and Antiplasmodial Assay using Microscopic and Flow Cytometry Method
description Genome mining study showed that marine-derived Streptomyces sp. GMY01 is a potential actinobacteria with abundant of secondary metabolite and anticancer activity. The study aimed to evaluate bioassay guided fractionation for antiplasmodial screening of GMY01 extract and to predict compound on active fractions. Ethyl acetate fraction was obtained from 11 days fermentation product of GMY01 and then it was fractionated using n-hexane and methanol solvent. Refractionated was applied using flash chromatography and column chromatography. Antiplasmodial assay was performed on Plasmodium falciparum FCR3 by microscopic method using thin blood smear + Giemsa stain, and flow cytometry method using SYBR Green I stain. Toxicity assay was performed on Vero cells line. Main constituent of active fraction was analyzed using LCMS/MS. The result of the study showed that ethyl acetate-methanol fraction has high antiplasmodial activity (IC50=3.96 µg/mL) with very low toxicity on Vero cells (IC50=30,072 µg/mL). Bioassay guided fractionation resulted F4.7 as highest Plasmodium inhibition (94.3% at 5 µg/mL) and was confirmed by microscopic and flow cytometry assay. Main constituent analysis showed C10H13NO (163.09971 Da) as mayor compound and predicted as nonribosomal polyketide synthetase (NRPS) secondary metabolite.
format article
author Ema Damayanti
Jaka Widada
Puspa Dewi N. Lotulung
Achmad Dinoto
Mustofa Mustofa
author_facet Ema Damayanti
Jaka Widada
Puspa Dewi N. Lotulung
Achmad Dinoto
Mustofa Mustofa
author_sort Ema Damayanti
title Bioassay Guided Fractionation of Marine Streptomyces sp. GMY01 and Antiplasmodial Assay using Microscopic and Flow Cytometry Method
title_short Bioassay Guided Fractionation of Marine Streptomyces sp. GMY01 and Antiplasmodial Assay using Microscopic and Flow Cytometry Method
title_full Bioassay Guided Fractionation of Marine Streptomyces sp. GMY01 and Antiplasmodial Assay using Microscopic and Flow Cytometry Method
title_fullStr Bioassay Guided Fractionation of Marine Streptomyces sp. GMY01 and Antiplasmodial Assay using Microscopic and Flow Cytometry Method
title_full_unstemmed Bioassay Guided Fractionation of Marine Streptomyces sp. GMY01 and Antiplasmodial Assay using Microscopic and Flow Cytometry Method
title_sort bioassay guided fractionation of marine streptomyces sp. gmy01 and antiplasmodial assay using microscopic and flow cytometry method
publisher Universitas Gadjah Mada
publishDate 2020
url https://doaj.org/article/06f54a8cb4134c538460cc8007f577fa
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