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利用小角中子散射、中子自旋回波和动态光散射测量研究β-乳球蛋白的酒精诱导胶凝。

A study of alcohol-induced gelation of beta-lactoglobulin with small-angle neutron scattering, neutron spin echo, and dynamic light scattering measurements.

机构信息

Advanced Materials Institute, and Department of Chemistry, Faculty of Science, Fukuoka University, 8-19-1 Nanakuma, Jonan-ku, Fukuoka 814-0180, Japan.

出版信息

Phys Chem Chem Phys. 2010 Apr 7;12(13):3260-9. doi: 10.1039/b920187d. Epub 2010 Feb 11.

Abstract

Gelation of beta-lactoglobulin (beta-Lg) in various alcohol-water mixtures with 0.1 M (M = mol L(-1)) hydrochloric acid was investigated with small-angle neutron scattering (SANS), neutron spin echo (NSE), and time-resolved dynamic light scattering (TRDLS) measurements. The beta-Lg in alcohol-water solutions undergoes gelation at specific alcohol concentrations where the alcohol-induced alpha-helical structure of beta-Lg is stabilized. The SANS profiles showed that beta-Lg exists as a single molecule at a low alcohol concentration. With increasing alcohol concentration, the profiles indicate a power law behavior of approximately 1.7 when the samples gelate. These behaviors were observed in all alcohol-water mixtures used, but the alcohol concentrations where the SANS profiles change shift to a lower alcohol concentration region with an increase in the size of the hydrophobic group of the alcohols. Apparent diffusion constants, obtained from the intermediate scattering function (ISF) of NSE and the intensity time correlation function (ITCF) of TRDLS, mainly depend on the viscosity of alcohol-water mixtures before gelation. After gelation, on the other hand, the ISFs of gels do not change appreciably in the range of the NSE time scale, indicating the microscopically rigid structure of beta-Lg gel. The ITCF functions obtained from TRDLS follow a double exponential decay type before gelation, but a logarithmic one (exponent alpha = 0.7) after gelation. It is most likely that the alcohol-induced gelation undergoes a similar mechanism to that for the heat-induced one at pH = 7 where beta-Lg aggregates stick together to form a fractal network, although the gelation time is faster in the former than in the latter.

摘要

β-乳球蛋白(β-Lg)在 0.1 M(M = mol L(-1))盐酸存在下在不同醇-水混合物中的胶凝作用,通过小角中子散射(SANS)、中子自旋回波(NSE)和时间分辨动态光散射(TRDLS)测量进行了研究。β-Lg 在醇-水溶液中在特定的醇浓度下发生胶凝作用,在该醇浓度下,β-Lg 的醇诱导的α-螺旋结构得到稳定。SANS 图谱表明,β-Lg 在低醇浓度下以单分子形式存在。随着醇浓度的增加,当样品胶凝时,图谱显示出约 1.7 的幂律行为。这些行为在所有使用的醇-水混合物中都观察到,但 SANS 图谱变化的醇浓度区域随着醇的疏水区基团的增大而向较低的醇浓度区域转移。从中子自旋回波的中间散射函数(ISF)和时间分辨动态光散射的强度时间相关函数(ITCF)获得的表观扩散常数主要取决于胶凝前醇-水混合物的粘度。另一方面,胶凝后,凝胶的 ISF 在 NSE 时间尺度范围内没有明显变化,表明β-Lg 凝胶具有微观刚性结构。从 TRDLS 获得的 ITCF 函数在胶凝前遵循双指数衰减类型,但在胶凝后遵循对数类型(指数α=0.7)。很可能,醇诱导的胶凝作用经历了与 pH = 7 下热诱导胶凝作用类似的机制,其中β-Lg 聚集体粘在一起形成分形网络,尽管前者的胶凝时间比后者快。

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