Deacylation Kinetics Analysis of Streptococcus pneumoniae Penicillin-Binding Protein 2x Mutants Resistant to β-Lactam Antibiotics Using Electrospray Ionization– Mass Spectrometry

2000 ◽  
Vol 284 (2) ◽  
pp. 240-246 ◽  
Author(s):  
Anne Marie Di Guilmi ◽  
Nicolas Mouz ◽  
Yves Pétillot ◽  
Eric Forest ◽  
Otto Dideberg ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
Streptococcus Pneumoniae ◽  
Electrospray Ionization ◽  
Electrospray Ionization Mass Spectrometry ◽  
Binding Protein ◽  
Ionization Mass Spectrometry ◽  
Ionization Mass ◽  
Penicillin Binding Protein ◽  
Kinetics Analysis

scholarly journals Dinoxin B Withanolide from Datura inoxia Mill as an Effective Phytocompound Against Urinary Tract Infection causing Staphylococcus aureus

2021 ◽  
Vol 14 (3) ◽  
pp. 1707-1720
Author(s):  
Ruby George ◽  
Priti Mathur ◽  
Chandni Tandon
Keyword(s):  
Mass Spectrometry ◽  
Staphylococcus Aureus ◽  
Electrospray Ionization ◽  
Electrospray Ionization Mass Spectrometry ◽  
Binding Protein ◽  
Ionization Mass Spectrometry ◽  
Ionization Mass ◽  
Penicillin Binding Protein ◽  
Time Kill ◽  
Datura Inoxia

Background: Dinoxin B Withanolide was isolated from Datura inoxia and identified with its cytotoxic activity. But its antibacterial properties are not yet evaluated. We have previously reported the broad-spectrum antibacterial property of Dinoxin B Withanolide extracted from D.inoxia on standard strains. Objective: This research has focused to evaluate the efficacy of Dinoxin B Withanolide against infectious Staphylococcus aureus, including resistant strains. Methods: Electrospray Ionization-Mass Spectrometry is used to depict the presence of Dinoxin B withanolide from the chromatographic ethanolic leaf fraction. Antibacterial activity of different concentrations of Dinoxin B(12500-100000 μg/ml) was assessed using the agar diffusion, macro broth dilution, and time-kill assay methods. Docking studies and Drug likeness properties were analyzed. Result: Electrospray Ionization-Mass Spectrometry depicted the presence of Dinoxin B. All the isolates were susceptible to Dinoxin B within the range of 15±0.5mm to 24±0.5mm, and the bacteria were susceptible at a concentration rate of ≤12.5mg/ml. Time-kill assay showed that 25mg/ml of Dinoxin B displayed the highest inhibitory activity after four hours. The MBC values were compatible with the cidal concentration as seen in the time-kill study's growth curve. Computer-aided techniques resulted in a good Docking score towards Quorum-signaling Sar A protein (-7.82)and Penicillin Binding Protein(-6.9). Conclusion: Dinoxin B with its bactericidal properties and significant affinity towards Quorum-signaling Sar A protein and Penicillin Binding Protein can be considered as an effective bioactive compound against Methicillin Resistance Staphylococcus aureus.

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