AI Article Synopsis

  • Acacia modesta is a valuable medicinal plant known for its antibacterial and antioxidant properties, but it grows slowly, posing challenges for sustainable use.
  • The study successfully induced callus from A. modesta using specific growth mediums, resulting in significantly higher levels of beneficial secondary metabolites compared to regular leaf extracts.
  • The research concludes that in vitro callus culture can boost the production of important compounds like phenolics and flavonoids, enhancing the plant's medicinal benefits.

Article Abstract

Background: Acacia species are economically significant as medicinal plants that have been utilized since ancient times. Acacia modesta has been reported to possess potent antibacterial and antioxidant properties, but its growth rate is slow. In this study, we hypothesized that inducing callus in vitro from A. modesta could enhance the production of antibacterial and antioxidant secondary metabolites, thereby circumventing the issues of slow growth and excessive harvesting of the plant.

Results: The callus was induced from axillary buds on MS medium supplemented with 1 mg/L of 2,4-D and 1 mg/L of BAP. The secondary metabolites, volatile compounds, antibacterial activity, and antioxidant activity of the callus and parent plant leaf extracts were evaluated. The results revealed that the content of phenolics and flavonoids, the number of volatile compounds, and the antibacterial and antioxidant activities of the callus extract were significantly enhanced (P ≤ 0.05) compared to the leaf extract. The antibacterial and antioxidant effects were strongly correlated with the total phenolic and flavonoid content in the extracts.

Conclusions: Our findings suggest that in vitro callus culture increases the production of phenolics, flavonoids, and volatile compounds. This subsequently enhances the antibacterial and antioxidant properties of A. modesta.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10848437PMC
http://dx.doi.org/10.1186/s12870-024-04747-9DOI Listing

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