Emerging antimicrobial resistance has highlighted the need to design more effective antibiotics to treat deadly bacterial infections. Acinetobacter baumannii's outer membrane protein A (OmpA) is a critical virulence component involved in biofilm formation, immunomodulation, and antibiotic resistance, which characterizes it as a potential therapeutic target. The present study aimed to screen the natural product database (>1,00,000) to identify the potential inhibitor against OmpA. Molecular docking studies revealed that 10 compounds had good docking scores (≤ -7 kcal/mol) compared to the reported inhibitor epiestriol (-3.079). Further, these 10 compounds were subjected to ADME analysis and MMGBSA analysis. Based on MMGBSA results, we selected 5 compounds [NP-1 (MolPort-039-337-117), NP-5(MolPort-019-932-973), NP-6 (MolPort-005-948-336), NP-8(MolPort-042-673-978) and NP-9(MolPort-042-673-766)] with high binding affinity. Molecular dynamics simulation found that NP-5, NP-8, and NP-9 were stable after analysing their RMSD, RMSF, the radius of gyration, and hydrogen interactions of complexes. Our study revealed that NP-5, NP-8, and NP-9 bind perfectly with OmpA and can act as its potential inhibitors. The results of this study imply that the identified inhibitors have the potential for further investigation.Communicated by Ramaswamy H. Sarma.

2023-03-13·Antibiotics (Basel, Switzerland)

Myco-Nanofabrication of Silver Nanoparticles by Penicillium brasilianum NP5 and Their Antimicrobial, Photoprotective and Anticancer Effect on MDA-MB-231 Breast Cancer Cell Line.

Article

作者: Kumar, Raju Suresh ; Nayaka, Sreenivasa ; Gunagambhire, Pooja Vidyasagar ; Perumal, Karthikeyan ; Nagaraja, Shashiraj Kareyellappa ; Hiremath, Halaswamy ; Almansour, Abdulrahman I. ; Rudrappa, Muthuraj

Currently, the exploration of fungal organisms for novel metabolite production and its pharmacological applications is much appreciated in the biomedical field. In the present study, the fungal strains were isolated from soil of unexplored Yellapura regions. The potent isolate NP5 was selected based on preliminary screening and identified as Penicillium brasilianum NP5 through morphological, microscopic, and molecular characterizations. Synthesis of silver nanoparticles from P. brasilianum was confirmed by the color change of the reaction mixture and UV-visible surface plasmon resonance (SPR) spectra of 420 nm. Fourier transform infrared (FTIR) analysis revealed the functional groups involved in synthesis. Atomic force microscopy (AFM) and transmission electron microscope (TEM) analysis showed aggregation of the NPs, with sizes ranged from 10 to 60 nm, an average particle size of 25.32 nm, and a polydispersity index (PDI) of 0.40. The crystalline nature and silver as the major element in NP5-AgNPs was confirmed by X-ray diffraction (XRD) and energy dispersive X-ray (EDX) analysis. The negative value -15.3 mV in Zeta potential exhibited good stability, and thermostability was recorded by thermogravimetric analysis (TGA). NP5-AgNPs showed good antimicrobial activity on selected human pathogens in a concentration-dependent manner. The MTT assay showed concentration-dependent anticancer activity with an IC₅₀ of 41.93 µg/mL on the MDA-MB-231 cell line. Further, apoptotic study was carried out by flow cytometry to observe the rate of apoptosis. The calculated sun protection factor (SPF) value confirms good photoprotection capacity. From the results obtained, NP5-AgNPs can be used in the pharmaceutical field after successful in vitro clinical studies.

2013-04-01·Journal of Colloid and Interface Science2区 · 化学

Influence of surfactant polydispersity on the structure of polyoxyethylene (5) nonylphenyl ether/cyclohexane/water reverse microemulsions

2区 · 化学

Article

作者: Sergey A. Tovstun ; Vladimir F. Razumov ; Anastasia V. Ivanchikhina

The distribution of the number of oxyethylene groups in molecules of polyoxyethylene (5) nonylphenyl ether (NP5) is shown to significantly affect the structure of NP5/cyclohexane/water reverse microemulsions. The effect is caused by the difference in solubility of NP5 components. This difference leads to fractionation: surfactant molecules dissolved in the intermicellar nonpolar medium have, on average, shorter polyoxyethylene chains than surfactant molecules forming reverse micelles. A model is proposed which takes into account the influence of this fractionation on reverse micelle size and free surfactant concentration. The validity of this model for NP5/cyclohexane/water reverse microemulsions is experimentally confirmed by dynamic light scattering. It is found that changing the degree of surfactant fractionation in the above mentioned microemulsions can result in the formation of non-spherical reverse micelles.

100 项与 NP-5 相关的药物交易

登录后查看更多信息