Authors
Info
A. Lam-Guti?rrez1, T. R.
Ayora-Talavera2, E. R. Garrido-Ram?rez3, F. A.
Guti?rrez-Miceli1, J. A. Montes-Molina1,
S. Lagunas-Rivera4 and
V. M. Ru?z-Valdiviezo1* ??
1Laboratory of
Molecular Biology,
National
Technological Institute of Mexico, Institute Technological of Tuxtla
Guti?rrez, Tuxtla Guti?rrez, Chiapas, C.P. 29050, M?xico
2Research and
Assistance Center
Technology and
Design of the State of Jalisco A.C. Scientific Park and
Technological of
Yucatan, Merida, Yucatan, M?xico
3INIFAP, Experimental
Field
Ctr Chiapas, Ocozocoautla
29140, Chiapas,
Mexico
4Department of
Chemistry, University of Guanajuato, Noria Alta, 36050, Mexico
*Corresponding
Author Email :
bioqvic@hotmail.com
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Abstract
Aim: The present study
aimed to identify the phytochemicals of methanolic extract from Baccharis glutinosa
(chilca) roots (MEBg) and to evaluate its antifungal activity on two major
fungal pathogens of agricultural importance.
Methodology: The antifungal
activity was evaluated by inhibition halo, minimum inhibitory concentration
(MIC), minimum fungicidal concentration (MFC) and % sporulation against A.
ochraceus and F. moniliforme. As a preliminary test, inhibition
halo was tested using 1, 10, 100 and 270 mg ml-1 of MEBg.
Different concentrations of MEBg were applied for MIC and MFC tests.
Ketoconazole was used as positive control. The treatments were applied in
triplicate. The phytochemical compounds of MEBg were determined by GC-MS
analysis.
Results: The MEBg produced
an inhibition zone of 2 to 4 mm in the inhibition halo test, with
concentrations of 100 and 270 mg ml-1 for A. ochraceus and F.
moniliforme, respectively. Reduction in % sporulation above 50 was shown
in concentrations over 8 mg ml-1. MEBg were reported to exhibit
antifungal activities against A. ochraceus and F. moniliforme
with the MIC values ranging from 2 to 5.6 mg∙ml-1 and the
MFC from 12 to 15? mg ml-1. GC-MS analysis of Chilca extracts
revealed that the most abundant metabolites were furfural compounds and
organic acids. The most abundant furfural compounds were 5-(hydroxymethyl)
furan-2-carbaldehyde (38.59%), furan-2-carbaldehyde (4.103%) and
5-methylfuran-2-carbaldehyde (2.1%). ????????????
Interpretation: The MEBg revealed
efficient antifungal activity, likely due to the presence of bioactive
compounds, which could be used as an alternative for biological control of
pathogenic fungi in maize and coffee crops.
Key words: Antifungal activity, Aspergillus ochraceus, Baccharis
glutinosa, Furfural compounds, Fusarium moniliforme
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