http://dx.doi.org/10.4314/tjpr.v11i5.5
Abstract
Purpose: To isolate and identify an
antibiotic produced by a soil bacterium, Intrasporangium
strain N8, with antibacterial activity against both
Gram-positive and Gram-negative bacteria.
Methods: Fermentation followed by extraction
using a three-solvent system (petroleum ether, acetone
and ethyl acetate) and pH precipitation, successfully
separated the antibiotic complex from the culture broth.
Purification was carried out using flash column
chromatography (FCC), thin-layer chromatography (TLC)
and reverse phase high performance liquid chromatography
(HPLC). The identities of the molecules were elucidated
by gas chromatography-mass spectrometry (GC-MS)
analysis.
Results: Three main components of the
antibiotic were isolated and identified as
4-methyl-3-penten-2-one, 4-hydroxy-4-methyl-2-pentanone
and N-acetyltryptamine. Bioassay results showed activity
against both mammalian and plant pathogenic bacteria
including Pseudomonas fluorescens, Xanthomonas
campestris pv campestris, Escherichia coli and Serratia
marcescens. Pseudomonas fluorescens (MIC = 0.0625 μg/ml)
and Xanthomonas campestris pv campestris (MIC = 0.0026
μg/ml) represent the two plant pathogenic genera that
are notoriously difficult to contain in the field.
Conclusions: Since the antibiotic isolated during
this study showed activity against both mammalian and
plant pathogenic bacteria, it is hoped that this work
will encourage further investigation in this field. This
antibiotic could become very useful as an agricultural
bacteriocide against some resistant plant pathogens.
Keywords: Intrasporangium N8, Tryptamine,
Antibiotic, Purification, Pathogenic bacteria.