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Spectroscopic Characteristics and Energy Transfer of Bacterial Pigment: (Pyocyanin / Curcumin)

机译:细菌颜料的光谱特性和能量转移:(碧糖素/姜黄素)

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In this research used a new strategy in the detection of residues Pseudomonas aeruginosa (Pyocyanin), using the fluorescence spectrum alongside the absorption spectrum of the detection of metabolite in pure water. The bacterial metabolite was successfully measured, by taking the clinically relevant range into account (7-130 μM); at a concentration of [10 μm]. Were measured, the Pyocyanin solutions spectrum consist of three peaks and one shoulder, located at wavelengths (230 nm), (316nm), (370nm), (700 nm), respectively, but the concentration [1μM], its absorption spectrum doesn't appear clearly and disappears due to dilution, spectra of fluorescence have been measured As in the case of absorption, at optimal wavelength excitation (380 nm), band have appeared at wavelength (443 nm) at all concentrations. To calculate energy transfer, it must be calculated Forster's radius Ro for FRET between Pyocyanin molecule as a donor was calculated with the Curcumin molecule as an acceptor and its value was Ro=7.6235 ?A, this is the limit lower for Forester's energy transfer from molar absorptivity of concentration [100 μm] from spectral overlap by used the MatLab program. Then, calculated energy transfer values and the quenching factor, When mixing the Curcumin dissolved in water with Pyocyanin were studied at different concentrations at room temperature at ratio (1/99), (7/93), (11/89). It was found that the increase of energy transfer from the donor to the acceptor with the increasing of the donor maxing rate, the quenching factor is reduced by increasing the presence of the donor and values do depend on concentration. We have achieved great importance in this research by knowing the spectral properties of the respective bacterial dyes. Thus, the data obtained is useful enough to be relied upon as a database for Pyocyanin dye spectra.
机译:在本研究中,使用了一种在检测残留物假单胞菌铜绿假单胞菌(盐粘蛋白)的新策略,使用荧光光谱以及纯水中代谢物检测的吸收光谱。通过考虑临床相关范围(7-130μm),成功测量了细菌代谢物;以[10μm]的浓度。测量,盐素素溶液谱分别由三个峰和一个肩部组成,位于波长(230nm),(316nm),(370nm),(700nm),但浓度[1μm],其吸收光谱不会nn' T由于稀释而显然并且消失,荧光的光谱已经如在吸收的情况下,在最佳波长激发(380nm)时,在所有浓度下出现波长(443nm)。为了计算能量转移,必须计算猴蛋白分子分子在猪蛋白分子之间的褶皱的半径Ro,用姜黄素分子作为受体计算,其值为RO = 7.6235?a,这是林务员的能量转移的限制较低的摩尔通过使用MATLAB程序,浓度[100μm]的浓度[100μm]吸收率。然后,在将溶解在水中的姜黄素混合在用粘糊体的姜黄素混合在与碧糊中混合在室温(1/99),(7/93),(11/89)的不同浓度下,在将溶解在水中溶解在水中的溶解在水中的姜黄素的能量转移值和猝灭因子。(7/93),(11/89)。结果发现,随着供体的增加,从供体的能量转移到受体,通过增加供体的存在和值依赖于浓度来降低猝灭因子。通过了解各种细菌染料的光谱性能,我们在这项研究中取得了重要意义。因此,所获得的数据足以依赖于碧粘蛋白染料光谱的数据库。

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