Please use this identifier to cite or link to this item: https://ir.swu.ac.th/jspui/handle/123456789/13114
Title: Lupinifolin from Derris reticulata possesses bactericidal activity on Staphylococcus aureus by disrupting bacterial cell membrane
Authors: Yusook K.
Weeranantanapan O.
Hua Y.
Kumkrai P.
Chudapongse N.
Keywords: ampicillin
bactericide
Derris reticulata extract
lupinifolin
plant extract
unclassified drug
antiinfective agent
flavonoid
lupinifolin
antibiotic sensitivity
Article
bacterial cell wall
bactericidal activity
carbon nuclear magnetic resonance
controlled study
Derris
Derris reticulata
drug identification
drug isolation
drug mechanism
drug potency
drug screening
flow cytometry
mass spectrometry
minimum bactericidal concentration
minimum inhibitory concentration
nonhuman
plant stem
proton nuclear magnetic resonance
scanning electron microscopy
Staphylococcus aureus
transmission electron microscopy
ultrastructure
cell membrane
chemistry
pathogenicity
Staphylococcus aureus
Anti-Bacterial Agents
Cell Membrane
Derris
Flavonoids
Plant Stems
Staphylococcus aureus
Issue Date: 2017
Abstract: In this study, lupinifolin, a prenylated flavonoid, was isolated from Derris reticulata stem, identified by NMR spectra and confirmed with mass spectrometry. Lupinifolin was freshly prepared by solubilizing in 0.1 N NaOH and immediately diluted in Müller–Hinton broth for antibacterial testing. The data showed that Gram-positive bacteria were more susceptible to lupinifolin than Gram-negative bacteria. Of four strains of Gram-positive bacteria tested, Staphylococcus aureus was the most susceptible. Using the two-fold microdilution method, it was found that lupinifolin possessed antimicrobial activity against S. aureus with minimum inhibitory concentration and minimum bactericidal concentration of 8 and 16 µg/ml, respectively, which is less potent than ampicillin. However, from the time–effect relationship, it was shown that lupinifolin had faster onset than ampicillin. The faster onset of lupinifolin was confirmed by scanning electron microscopy. To investigate the mechanism of action of lupinifolin, transmission electron microscopy (TEM) was performed to observe the ultrastructure of S. aureus. The TEM images showed that lupinifolin ruptured the bacterial cell membrane and cell wall. Due to its fast onset, it is suggested that the action of lupinifolin is likely to be the direct disruption of the cell membrane. This hypothesis was substantiated by the data from flow cytometry using DiOC2 as an indicator. The result showed that the red/green ratio which indicated bacterial membrane integrity was significantly decreased, similar to the known protonophore carbonyl cyanide 3-chlorophenylhydrazone. It is concluded that lupinifolin inhibits the growth of S. aureus by damaging the bacterial cytoplasmic membrane. © 2016, The Japanese Society of Pharmacognosy and Springer Japan.
URI: https://ir.swu.ac.th/jspui/handle/123456789/13114
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85007441143&doi=10.1007%2fs11418-016-1065-2&partnerID=40&md5=d9e82075077be35f929b4a89fbf7e08c
ISSN: 13403443
Appears in Collections:Scopus 1983-2021

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