Abstract

Tamarind has bioactive compounds that can exhibit antimicrobial activities but further information about its specific compounds and the antibacterial activity changes between crude extract and isolate had not been repoted yet. Crude extract of tamarind pulp in this experiment was tested for phytochemical compounds and antibacterial activity (MIC and MBC). In order to isolate and identify antibacterial compounds, column chromatography, thin layer chromatography (TLC), and gas chromatography (GC-MS) were applied. Mobile phase for column chromatography was ethyl acetate:ethanol in 100:0 until 0:100 ratio. The maximum wavelengths for all fractions were scanned and all concentrated fractions used for antibacterial activity test. The result showed the best inhibition zone came from FD-2 fraction (2 nd fraction of ethyl acetate:ethanol = 70:30 ratio). FD-2 fraction had MIC 1.18% and MBC 4.70% for Pseudomonas sp. , MIC 0.54% and MBC 2.16% for Listeria monocytogenes . Its activity was smaller than the crude extract that had MIC 0.65% and MBC 2.61% for Pseudomonas sp. , MIC 0.46% and MBC 1.85% for Listeria monocytogenes . For the next step, FD-2 fraction was separated using thin layer chromatography. The best single spot was given by ethyl acetate:ethanol = 0:1 with the maximum wavelength 368 nm; 458.5 nm; and 550 nm. Fraction was identified with GC-MS resulted antibacterial compounds such as hexadecanoic acid methyl ester, 11-octadecenoic acid methyl ester, 9-octadecenoic acid, eicosanioc acid, stigmasterol, and gamma-sitosterol.

Highlights

  • Tamarind has bioactive compounds that can exhibit antimicrobial activities but further information about its specific compounds and the antibacterial activity changes between crude extract and isolate had not been repoted yet

  • Crude extract of tamarind pulp in this experiment was tested for phytochemical compounds

  • all concentrated fractions used for antibacterial activity test

Read more

Summary

METODE PENELITIAN

Bahan yang diteliti adalah buah asam jawa dan kultur bakteri. Kultur yang digunakan adalah Listeria monocytogenes dan Pseudomonas sp. Metode penelitian ini adalah metode deskriptif yang akan mendeskripsikan komponen antibakteri pada asam jawa dan aktivitasnya. Mula-mula daging buah asam jawa dikeringkan pada suhu 50oC dengan cabinet dryer dan ukurannya dikecilkan dengan food processor sehingga diperoleh dried pulp asam jawa. Pemisahan senyawa antibakteri dilakukan menggunakan kromatografi kolom dengan fase diam silica gel 70-230 mesh dan fase gerak etil asetat:etanol dengan rasio 100:0, 90:10, 80:20, 70:30, 60:40, 50:50, 40:60, 30:70, 20:80, 10:90, dan 0:100. Kemudian ditambahkan lagi pelarut etil asetat (1:1), diaduk dengan batang pengaduk hingga terbentuk slurry yang siap diisikan ke dalam kolom sedikit demi sedikit, diamkan selama 15 menit, dan pealrut yang tersisa dibuang melalui katup sehingga kolom siap digunakan. Kombinasi pelarut untuk pemisahan senyawa antibakteri dengan kromatografi lapis tipis

Etil asetat:etanol:air
HASIL DAN PEMBAHASAN
Berdasarkan hasil identifikasi dengan Mass
Coklat tua FI
No peak
Asam lemak jenuh dengan
Mechanisms of Action of Chemical
Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call