Antimicrobial Potential of Fagopyrum esculentum Monech Stem Extract: Phytochemical Characterization and Efficacy Against Drug-Resistant Pathogens

Authors

  • Prasant Kumar Dubey
  • Gaurav Tiwari
  • Naveen Gupta
  • Dharmendra Singh Rajput
  • Yogesh Pounikar

Keywords:

Fagopyrum esculentum, Antimicrobial activity, Phytochemical screening, Phenolic compounds, Flavonoids, Agar diffusion assay, Drug-resistant pathogens

Abstract

The escalating crisis of antimicrobial resistance (AMR) demands novel sources of antimicrobial agents. This study investigates the antimicrobial potential of Fagopyrum esculentum (common buckwheat) stem, integrating phytochemical analyses with in vitro antimicrobial assays against a panel of pathogenic microbes. Comprehensive phytochemical screening of the buckwheat stem revealed abundant flavonoids and phenolics; quantitative assays showed high total phenolic (1.52 mg GAE/g) as well as flavonoid (0.14 mg QE/g) contents in extract that is methanolic. Pharmacognostic fluorescence analysis further corroborated the presence of these phytochemicals. Antimicrobial efficacy was evaluated via agar diffusion assays against Staphylococcus aureus, Enterococcus faecalis, Mycobacterium tuberculosis, and a representative Enterobacteriaceae strain (E. coli/Klebsiella). The buckwheat stem extract exhibited dose-dependent inhibition of all tested microbes. Notably, at the highest concentration (3 mg/disc), it produced substantial zones of inhibition against S. aureus (~15–16 mm) and M. tuberculosis (~15–18 mm), indicating significant activity comparable to standard antibiotics’ susceptibility thresholds. Moderate activity was observed against Enterococcus (12–15 mm zone at 3 mg) and weaker effects against Gram-negative Enterobacteriaceae (8–12 mm at 3 mg). The extract’s broad-spectrum antibacterial action, especially towards Gram-positive and acid-fast organisms, is attributed to its high polyphenolic content. Potential mechanisms, such as membrane disruption and enzyme inhibition by flavonoids, are discussed. These findings highlight F. esculentum stem as a promising natural source of antimicrobial compounds, meriting further investigation for development into plant-based antimicrobials in the fight against resistant infections.

Downloads

Download data is not yet available.

References

Ventola CL. The antibiotic resistance crisis. Pharm Ther. 2015;40(4):277-83.

World Health Organization. Global action plan on antimicrobial resistance. 2015.

Laxminarayan R, Chaudhury RR. Antibiotic resistance in India: drivers and opportunities for action. PLoS Med. 2016;13(3):e1001974.

Chokshi A, Sifri Z, Cennimo D, Horng H. Global contributors to antibiotic resistance. J Glob Infect Dis. 2019;11(1):36.

Nathan C, Cars O. Antibiotic resistance—problems, progress, and prospects. N Engl J Med. 2014;371(19):1761-1763.

Cushnie TP, Lamb AJ. Antimicrobial activity of flavonoids. Int J Antimicrob Agents. 2005;26(5):343-56.

Cowan MM. Plant products as antimicrobial agents. Clin Microbiol Rev. 1999;12(4):564-582.

Sun Y, et al. Phytochemical profile and pharmacological activities of Fagopyrum esculentum. Food Chem. 2021;350:129234.

Tomotake H, et al. Nutritional characteristics and antioxidant activity of buckwheat seeds and sprouts. Food Chem. 2020;325:126808.

Kreft S, Fabjan N, Yasumoto K. Rutin content in buckwheat (Fagopyrum esculentum Moench) food materials and products. Food Chem. 2006;98(3):508-512.

Zhang Z, Zhou L, Li S, et al. Comparison of phenolics and antioxidant properties among different parts of buckwheat plant. Food Res Int. 2022;160:111700.

Ren G, Sun J, He X, et al. Flavonoid composition and antibacterial activity of buckwheat (Fagopyrum esculentum) hulls. J Food Biochem. 2019;43(7):e12891.

Wen P, Hu TG, Linhardt RJ, et al. Structure and bioactivity of polysaccharides from buckwheat: A review. Trends Food Sci Technol. 2023;133:258-268.

Xie Y, Yang W, Tang F, Chen X, Ren L. Antibacterial activities of flavonoids: structure-activity relationship and mechanism. Curr Med Chem. 2015;22(1):132-49.

Hosaka A, et al. Wound healing properties of buckwheat extracts. Phytother Res. 2019;33(8):2063-2071.

Zhang L, et al. Phenolic profiles and antioxidant activity of buckwheat hulls, leaves and stems. J Funct Foods. 2021;86:104693.

Clinical and Laboratory Standards Institute (CLSI). Performance standards for antimicrobial susceptibility testing. 2022.

Kumarasamy KK, et al. Emergence of a new antibiotic resistance mechanism in India, Pakistan, and the UK: a molecular, biological, and epidemiological study. Lancet Infect Dis. 2010;10(9):597-602.

Dahiya N, et al. Recent advancements in antimicrobial resistance of Gram-negative bacteria: a review. Microorganisms. 2023;11(2):427.

Hernando-Amado S, Coque TM, Baquero F, Martínez JL. Defining and combating antibiotic resistance from One Health and Global Health perspectives. Nat Microbiol. 2019;4(9):1432-1442.

Indian Pharmacopoeia Commission. Indian Pharmacopoeia. Ghaziabad: IPC; 2018.

WHO. Quality control methods for medicinal plant materials. Geneva: World Health Organization; 2011.

Chase CR, Pratt RS. Fluorescence of powdered vegetable drugs with particular reference to development of a system of identification. J Am Pharm Assoc. 1949;38:324–331.

Sasidharan S, et al. Extraction, isolation and characterization of bioactive compounds from plants’ extracts. Afr J Tradit Complement Altern Med. 2011;8(1):1-10.

Harborne JB. Phytochemical methods: a guide to modern techniques of plant analysis. 3rd ed. Springer; 1998.

Singleton VL, Rossi JA Jr. Colorimetry of total phenolics with phosphomolybdic-phosphotungstic acid reagents. Am J Enol Vitic. 1965;16(3):144-158.

Chang CC, Yang MH, Wen HM, Chern JC. Estimation of total flavonoid content in propolis by two complementary colorimetric methods. J Food Drug Anal. 2002;10(3):178-182.

Wagner H, Bladt S. Plant Drug Analysis: A Thin Layer Chromatography Atlas. 2nd ed. Springer; 1996.

Esau K. Anatomy of Seed Plants. 2nd ed. John Wiley & Sons; 1977.

Zhang R, et al. Extraction and evaluation of the antioxidant and antimicrobial activities of polyphenols from buckwheat (Fagopyrum esculentum) hull. Food Sci Nutr. 2020;8(6):2853-2860.

Dziedzic K, Górecka D, Szwengiel A, et al. Influence of buckwheat hull and flour on functional and antioxidant properties of bread. LWT. 2019;102:497-502.

Lin LZ, Harnly JM. Phenolic component profiles of buckwheat (Fagopyrum esculentum Moench) and related species. J Agric Food Chem. 2008;56(18):8891-8898.

Krol W, et al. The influence of flavonoid fractions from buckwheat (Fagopyrum esculentum) on antibiotic activity and cell membranes. Acta Pol Pharm. 2021;78(4):641-647.

Pandey A, et al. Antimicrobial activities of buckwheat (Fagopyrum esculentum Moench) extracts against drug-resistant pathogens. Indian J Exp Biol. 2016;54:150-156.

Sagdic O, et al. Antimicrobial activity of flavonoids and phenolics from buckwheat. J Sci Food Agric. 2003;83(1):39-47...

-.

Downloads

Published

2024-12-02

How to Cite

1.
Dubey PK, Tiwari G, Gupta N, Rajput DS, Pounikar Y. Antimicrobial Potential of Fagopyrum esculentum Monech Stem Extract: Phytochemical Characterization and Efficacy Against Drug-Resistant Pathogens. J Neonatal Surg [Internet]. 2024Dec.2 [cited 2025Dec.8];13(1):1775-87. Available from: https://jneonatalsurg.com/index.php/jns/article/view/9627

Issue

Section

Original Article

Most read articles by the same author(s)