Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 2016 Aug 12;16(1):284.
doi: 10.1186/s12906-016-1266-y.

Triterpenoids from Acacia ataxacantha DC: antimicrobial and antioxidant activities

Affiliations

Triterpenoids from Acacia ataxacantha DC: antimicrobial and antioxidant activities

Abdou Madjid O Amoussa et al. BMC Complement Altern Med. .

Abstract

Background: Acacia ataxacantha is a medicinal specie used extensively in traditional medicine of Benin republic to treat infectious diseases. Our previous study showed interesting antibacterial and antifungal activities against six strains of bacteria and six strains of fungi. The aim of this study was to investigate the antimicrobial and antioxidant activities of compounds isolated from A. ataxacantha.

Methods: Chromatographic and spectroscopic methods were used to isolate and identify three compounds (1-3) from the bark of A. ataxacantha. Phytochemical investigation of A. ataxacantha (Fabaceae) led to the isolation of three triterpenoids (1-3). The structure of isolated compounds was established by differents spectroscopic methods such as UV, (1)H NMR, (13)C NMR, 2D NMR and Mass. All isolated compounds were tested for antimicrobial activity using agar disc-diffusion and microdilution methods. The radical scavenging activity of isolated compounds was assessed using 2,2-diphenyl-1-picrylhydrazyl (DPPH) method.

Results: Phytochemical investigation led to the isolation and identification of lupeol (1), betulinic acid (2) and betulinic acid-3-trans-caffeate (3). Moderate antimicrobial activity was obtained with compound 3 against methicillin-resitant Staphylococcus aureus, Enterococcus feacalis and Pseudomonas aeruginosa with MIC value of 25 μg/ml and Staphylococcus aureus (MIC of 50 μg/ml). Compounds 3 was more active against Staphylococcus epidermidis and Candida albicans with a MIC value of 12.5 μg/ml in boths cases. Compounds 3 had also interesting antioxidant activity with an IC50 of 3.57 μg/ml compared to quercetin (1.04 μg/ml).

Conclusion: The overall results of this study provide evidence that the compound 3, isolated from A. ataxacantha, exhibit antimicrobial activity against Gram-positive and Gram-negative bacteria and yeast, especially against C. albicans.

Keywords: Acacia ataxacantha; Antibacterial; Antifungal; Antioxidant; Betulinic acid-3-trans-caffeate; Triterpene.

PubMed Disclaimer

Figures

Fig. 1
Fig. 1
Isolated triterpenes from Acacia ataxacantha. (1): lupeol; (2): Betulinic acid; (3): Betulinic acid-3-trans-caffeate
Fig. 2
Fig. 2
Bioautography of A. ataxacantha extracts. DCM: dichloromethane; AcoEt: Ethyle acetate; S.aureus: Staphylococcus aureus; S.am.r: Staphylococcus aureus meticilline resistent; S. epidermidis: Staphylococcus epidermidis; E. feacalis: Enterococcus feacalis; P. aeruginosa: Pseudomonas aeruginosa. White areas indicate where reduction of INT to the coloured formazan did not take place due to the presence of compounds that inhibited the bacterial growth
Fig. 3
Fig. 3
Bioautography of A. ataxacantha extracts sprayed with Candida albicans inoculum. DCM: dichloromethane; AcoEt: Ethyle acetate. White areas indicate where reduction of INT to the coloured formazan did not take place due to the presence of compounds that inhibited the bacterial growth

Similar articles

Cited by

References

    1. Lalitha P, Sripathi SK, Jayanthi P. Acute toxicity study of extracts of Eichhornia Crassipes (Mart.) Solms. Asian J Pharm Clin Res. 2012;5(4):59–61.
    1. Adamu M, Naidoo V, Eloff JN. Some southern African plant species used to treat helminth infections in ethnoveterinary medicine have excellent antifungal activities. BMC Complement Altern Med. 2012;12:213. doi: 10.1186/1472-6882-12-213. - DOI - PMC - PubMed
    1. Singh BN, Singh BR, Singh RI, Prakesh D, Dhakarey R, Upadhyay G, et al. Oxidative DNA Damage protective activity, antioxidant and antiquorum sensing potentiels of Moringa oleifera. Food Chem Toxicol. 2009;47:1109–1116. doi: 10.1016/j.fct.2009.01.034. - DOI - PubMed
    1. Adjanohoun I, Ahyi M, Aké A, Akouegninou A, Dalmeida J, Akpovo F, Bouke FK, et al. Contribution aux études ethnobotaniques et floristiques en République Populaire du Bénin. Paris: ACCA; 1989. p. 852.
    1. MacDonald I, Joseph OE, Harriet ME. Documentation of medicinal plants sold in markets in Abeokuta, Nigeria. Trop J Pharm Res. 2010;9(2):110–118.

MeSH terms