Biodiversitas Journal of Biological Diversity
Vol. 23 No. 1 (2022)

An antibacterial compound purified from a tropical coastal plant, Diospyros maritima

ALIM ISNANSETYO (Department of Fisheries, Faculty of Agriculture, Universitas Gadjah Mada. Jl. Flora, Bulaksumur, Sleman 55281, Yogyakarta, Indonesia)
DESY PUTRI HANDAYANI (Department of Fisheries, Faculty of Agriculture, Universitas Gadjah Mada. Jl. Flora, Bulaksumur, Sleman 55281, Yogyakarta, Indonesia)
INDAH ISTIQOMAH (Department of Fisheries, Faculty of Agriculture, Universitas Gadjah Mada. Jl. Flora, Bulaksumur, Sleman 55281, Yogyakarta, Indonesia)
ADITYA ARIF (Department of Fisheries, Faculty of Agriculture, Universitas Gadjah Mada. Jl. Flora, Bulaksumur, Sleman 55281, Yogyakarta, Indonesia)
TAKUSHI KANEKO (Global Alliance for TB Drug Development, Research and Development. 40 Wall Street, 24th Floor, New York, NY, USA)



Article Info

Publish Date
01 Jan 2022

Abstract

Abstract. Isnansetyo A, Handayani DP, Istiqomah I, Arif A, Kaneko T. 2021. An antibacterial compound purified from a tropical coastal plant, Diospyros maritima. Biodiversitas 23: 135-142. This study aimed to isolate, purify, and characterize an antibacterial compound from Diospyros maritima and evaluate its antibacterial activity. Diospyros maritima bark was collected from Kei Kecil Island, extracted with ethanol, separated with hexane and chloroform, and purified by column chromatography. The isolated compound was tested for antibacterial activity by paper disk diffusion on the double-layer agar medium. The minimum inhibitory concentration (MIC) was determined by the microdilution method in a 96-well microplate. The pure compound inhibited Staphylococcus aureus and Aeromonas hydrophila at MICs of 0.625 and 5 µg/mL, respectively. The molecular weight of the compound was 188 m/z based on GC-MS analysis. The 1H-NMR spectrum indicated two protons which appeared as a multiplet at 7,687.59 ppm, one proton appeared as a singlet at 6.87 ppm and one proton appeared as a doublet at 7.26 ppm. The 13C-NMR spectrum showed eleven carbon signals, eight signals for the aromatic ring (186.06, 162.38, 151.17, 137.41, 134.49, 133.76, 17.75, and 16.51 ppm) and two signals at 191.91 and 191.05 ppm. The spectrometric data showed that the isolated compound was plumbagin (1,4-naphthalenedione-5-hydroxy-2-methyl). This finding opens up a new perspective for D. maritima as a source of lead compounds for the development of antibacterial substances.

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Journal Info

Abbrev

biodiv

Publisher

Subject

Agriculture, Biological Sciences & Forestry Biochemistry, Genetics & Molecular Biology

Description

The Biodiversitas Journal was first published in 2000 by the Department of Biology, FMNS, Universitas Sebelas Maret, Surakarta, Indonesia, then in 2006 it was co-published by the Society for Indonesian Biodiversity and that department; since 2017 it was also hosted by Smujo. From 2003-2012 it was ...