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Surfactant exopolysaccharide of Ochrobactrum pseudintermedium C1 has antibacterial potential: Its bio-medical applications in vitro

机译:Ochrobactrum伪模拟C1的表面活性剂脱果具有抗菌潜力:其生物医学应用在体外

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Since the advent of biologics in human welfare various bio-molecules have been explored. Different bacterial exopolysaccharides have proved their worth in many industrial and commercial applications. In this perspective, while exploring a surfactant exopolysaccharide of Ochrobactrum pseudintermedium C1, it is strikingly observed that it possesses a potent antibacterial property which encourages its bio-medical applications. Following isolation and purification of the said exopolysaccharide, its structural configuration and functional attributes are studied by several analytical procedures involving FTIR, C-13-NMR, CHN-analysis, estimation of zeta potential, XRD-study and digital tensiometry. When treated with pathological samples in vitro, it distinctly elicits its antibacterial property by exhibiting a characteristic zone of inhibition. Combined with a standard antibiotic (like ciprofloxacin), it enhances the action of antibiotic also. Mechanism of its antibacterial action is evaluated by crystal violet entrapment assay with UV-vis spectrophotometry, bacterial cell viability assay by trypan blue staining and SEM study. Results show that its basic surfactant property, anionic character, crystalline nature and scaffolding architecture are supposed to facilitate its antibacterial property which is manifested by its capability of disrupting bacterial cell envelope causing eventual cell death. In the current global scenario, an increasing threat of antibiotic resistance is prevailing due to their indiscriminate use. If used as an adjuvant with a judicious dose of antibiotic, this bio-molecule might play a significant role in bio-medicine to combat such threat.
机译:自从人类福利的生物学出现以来,已经探索了各种生物分子。在许多工业和商业应用中证明了不同的细菌脱寡糖。在这种观点中,在探索Ochrobactrum伪模拟C1的表面活性剂泛糖,令人惊讶地观察到它具有促进其生物医学应用的有效抗菌性能。通过涉及FTIR,C-13-NMR,CHN分析,Zeta潜力估计,XRD研究和数字张力学研究其结构构型和功能属性,研究其结构构型和功能属性。当用体外进行病理样品处理时,它通过表现出抑制特征区域而明显引起其抗菌性。结合标准抗生素(如环丙沙星),它还增强了抗生素的作用。通过用UV-Vis分光光度法测定含有UV-Vis分光光度法的晶体紫色熵测定来评估其抗菌作用的机制,通过台盼蓝染色和SEM研究进行细菌细胞活力测定。结果表明,其基本表面活性剂特性,阴离子特征,晶体性质和脚手架结构应促进其抗菌性,其表现出其破坏细菌细胞包膜的能力,从而导致最终的细胞死亡。在目前的全局情景中,由于其滥用使用,抗生素抗性的越来越大的威胁。如果用作明智剂量的抗生素的佐剂,这种生物分子可能在生物医学中发挥重要作用,以打击这种威胁。

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