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Commiphora leptophloeos Phytochemical and Antimicrobial Characterization.

Authors :
de Souza Pereira JJ
Pereira AP
Jandú JJ
da Paz JA
Crovella S
Dos Santos Correia MT
de Azevêdo Silva J
Source :
Frontiers in microbiology [Front Microbiol] 2017 Jan 24; Vol. 8, pp. 52. Date of Electronic Publication: 2017 Jan 24 (Print Publication: 2017).
Publication Year :
2017

Abstract

Commiphora leptophloeos is a plant specie usually known for its medicinal purposes in local communities in Northeast Brazil. In order to evaluate its therapeutic potential, we aimed to determine the phytochemical and antimicrobial properties of C. leptophloeos extracts. Thin Layer Chromatography (TLC) was able to detect the presence of phenolic compounds, flavonoids and reducing sugars. Three phenolic compounds were identified by HPLC and described as Gallic, Chlorogenic and Protocatechuic acids. On the other hand, H <superscript>1</superscript> NMR analysis revealed the presence of hinokinin, a bioactive lignan further characterized in the present work. The minimum inhibitory concentration (MIC) values for hinokinin ranged from 0.0485 to 3.125 mg/mL in different S. aureus clinical isolates and showed a bactericidal activity against MRSA isolated from blood (MMC 0.40 mg/mL) and postoperative secretion (MMC = 3.125 mg/mL). C. leptophloeos extracts also showed antimicrobial activity against Mycobacterium species such as M. smegmatis (MIC = 12.5 mg/mL) and M. tuberculosis (MIC = 52 mg/mL). Additionally, we determined the toxicity of C. leptophloeos by in vitro HC <subscript>50</subscript> tests with hemolytic activity detected of 313 ± 0.5 μg/mL. Our results showed that C. leptophloeos possesses inhibitory properties against MRSA as well as several other clinically important microorganisms. Furthermore, the present work is the first report of the presence of hinokinin in Commiphora genus.

Details

Language :
English
ISSN :
1664-302X
Volume :
8
Database :
MEDLINE
Journal :
Frontiers in microbiology
Publication Type :
Academic Journal
Accession number :
28174564
Full Text :
https://doi.org/10.3389/fmicb.2017.00052