dc.description.abstract |
The aim of this study was to investigate the major chemical compositions of the chloroform extract of
lichen Parmelia erumpens from Western Ghats, Kerala, India and its antimicrobial and anticancer
activities. Chloroform extract was purified by silica gel column chromatography to obtain three major
compounds and their chemical structures were characterized by
1H-NMR,
13
C-NMR, UV and HR-MS
spectroscopic methods as atranorin (1), (+)-usnic acid (2) and 2-hydroxy-4-methoxy-3,6-dimethylbenzoic acid (3). The minimal inhibitory concentration (MIC) by the broth micro dilution and
agar disc diffusion methods was used to record the antimicrobial activity. Out of three compounds
tested, 2-hydroxy-4-methoxy-3,6-dimethylbenzoic acid recorded excellent antimicrobial activity
especially against medically important bacteria and fungi and the MIC values ranged from 0.06 to 4mg
ml 1
against test bacteria and 0.12 to 16mgml 1
against test fungi. The best MIC of 0.06mgml 1
by 2-hydroxy-4-methoxy-3,6-dimethylbenzoic acid was recorded againstVibrio cholera, a human pathogenic
bacterium responsible for causing life threatening diseases like profuse watery diarrhea. Anti cancer
activity was initially screened by MTT assay in A549, B16F10, Caski and HepG2 cell lines. MTT assay
results showed that the growth of cancer cells was suppressed by 2-hydroxy-4-methoxy-3,6-dimethylbenzoic acid in both dose- and time-dependent manners. A549, B16F10 and Caski cells treated
with 2-hydroxy-4-methoxy-3,6-dimethylbenzoic acid showed typical apoptotic morphology when
stained with acridine orange–ethidium bromide and hoechst staining. Cell cycle analysis clearly indicated
that cell death was due to apoptosis. Enhancement in the proliferation of lymphocytes suggested
immunomodulatory activity of this compound. To our best knowledge anticancer activity of 2-hydroxy-4-methoxy-3,6-dimethylbenzoic acid was reported here for thefirst time. Thus the results of the present
study suggest that 2-hydroxy-4-methoxy-3,6-dimethylbenzoic acid has a strong potential to be
developed as an antimicrobial and anticancer drug target after further clinical evaluation.
1. Introduction
Multi-drug resistance is a world-wide problem, attributed to the
extensive use of antibiotics, selection pressure on bacterial
strains and lack of new drugs, vaccines and diagnostic aids.
These shortcomings lead to an urgent global call for new antimicrobial drugs, particularly from natural resources.1
Meanwhile, the emergence of severe resistance to antibiotics in
microbial pathogens, such as Gram-positive methicillin-resistant
Staphylococcus aureus(MRSA) and vancomycin-res |
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