Journal: Antibiotics
Article Title: Biochanin A, a Plant Isoflavone, Disrupts Peptidoglycan Biosynthesis by Downregulating femA and femB , and Impairs Cell Wall Integrity in Multidrug-Resistant Staphylococcus aureus
doi: 10.3390/antibiotics15020195
Figure Lengend Snippet: Evaluation of S. aureus ATCC BAA-44 viability and morphology following treatment. ( A – C ) Flow cytometry analysis of bacterial populations stained with Calcein-AM (CA) and propidium iodide (PI). ( A ) Treatment with 64 µg/mL Biochanin A demonstrates a shift towards R1 and R2, indicating significant membrane disruption and partial loss of viability. ( B ) Treatment with 70% Ethanol ( v / v ) as a positive control result in a predominant clustering in R1 (strong PI signal), indicating a high proportion of dead cells. ( C ) Treatment with DMSO as a negative control primarily shows clustering in R3 (strong CA signal), representing viable cells with intact. ( D – F ) Fluorescence microscopy visualization of stained cells. ( D ) 64 µg/mL Biochanin A -treated cells show a combination of red and green fluorescence, reflecting partial membrane disruption and loss of cell viability. ( E ) 70% Ethanol ( v / v )-treated cells exhibit red fluorescence due to PI uptake, signifying extensive membrane damage and cell death. ( F ) DMSO-treated cells display green fluorescence from CA, indicative of intact membranes and metabolic activity. ( G – I ) Scanning electron microscopy (SEM) imaging of bacterial morphology. ( G ) Biochanin A-treated cells at 64 µg/mL reveal surface disruptions and altered shapes (red arrows), confirming the compound’s effect on cell morphology. ( H ) Cells treated with 70% Ethanol ( v / v ) exhibit collapsed structures and irregular shapes, indicating severe structural damage. ( I ) DMSO-treated cells have smooth surfaces and normal morphology, consistent with unaffected bacterial integrity.
Article Snippet: The results indicated that Biochanin A displayed antibacterial activity against S. aureus ATCC BAA-44 and S. aureus ATCC 25923, with both showing an MIC80 of 64 μg/mL ( ).
Techniques: Flow Cytometry, Staining, Membrane, Disruption, Positive Control, Negative Control, Fluorescence, Microscopy, Activity Assay, Electron Microscopy, Imaging