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通过PGSE高分辨魔角旋转核磁共振探测溶胶-凝胶基质微环境。

Probing sol-gel matrices microenvironments by PGSE HR-MAS NMR.

作者信息

Ferreira Ana S D, Barreiros Susana, Cabrita Eurico J

机构信息

UCIBIO, REQUIMTE, Departamento de Química, Faculdade de Ciências e Tecnologia, Universidade Nova de Lisboa, Caparica, Portugal.

Centro de Química Estrutural, Instituto Superior Técnico, Lisboa, Portugal.

出版信息

Magn Reson Chem. 2017 May;55(5):452-463. doi: 10.1002/mrc.4427. Epub 2016 Mar 14.

DOI:10.1002/mrc.4427
PMID:26987451
Abstract

We applied Pulsed Gradient Spin Echo diffusion with high-resolution magic angle spinning NMR to study sol-gel matrices used to encapsulate enzymes for biocatalysis (TMOS/MTMS and TMOS/BTMS) to gain insight into the local chemical microenvironment. Transport properties of solvents with different polarities (1-pentanol, acetonitrile and n-hexane) were studied through their apparent self-diffusion coefficients. The spin echo attenuation of the solvents shows two distinct diffusion domains, one with fast diffusion (D ) associated with interparticle diffusion and another with slow diffusion (D ) corresponding to the displacement inside the pores within the sol-gel particles. The analysis of the root mean square displacements at different diffusion times showed that the D domain has a free diffusion regime in both matrices (the root mean square displacement is linearly dependent of the diffusion time), while the D domain shows a different regime that depends on the matrix. We investigated the exchange regime between the two diffusion sites. In both matrices, n-hexane was in intermediate exchange between diffusion domains, while the polar solvents were in slow exchange in TMOS/BTMS and in intermediate exchange in TMOS/MTMS. Data were fitted for TMOS/BTMS with the Kärger model, and the physical parameters were obtained. The results add to the evidence that the pores are a hydrophobic environment but that the presence of some free hydrophilic groups inside the pore, as observed in the TMOS/BTMS, has a key role in slowing down the exchange of polar solvents and that this is relevant to explain previously reported enzyme activity in these materials. Copyright © 2016 John Wiley & Sons, Ltd.

摘要

我们应用脉冲梯度自旋回波扩散结合高分辨率魔角旋转核磁共振技术,研究用于生物催化中封装酶的溶胶 - 凝胶基质(TMOS/MTMS和TMOS/BTMS),以深入了解局部化学微环境。通过不同极性溶剂(1 - 戊醇、乙腈和正己烷)的表观自扩散系数研究其传输性质。溶剂的自旋回波衰减显示出两个不同的扩散域,一个具有与颗粒间扩散相关的快速扩散(D ),另一个具有对应于溶胶 - 凝胶颗粒内孔内位移的慢速扩散(D )。对不同扩散时间的均方根位移分析表明,D 域在两种基质中都具有自由扩散机制(均方根位移与扩散时间呈线性相关),而D 域表现出依赖于基质的不同机制。我们研究了两个扩散位点之间的交换机制。在两种基质中,正己烷处于扩散域之间的中间交换状态,而极性溶剂在TMOS/BTMS中处于慢速交换,在TMOS/MTMS中处于中间交换。用卡尔格模型对TMOS/BTMS的数据进行拟合,并获得了物理参数。结果进一步证明,孔是疏水环境,但如在TMOS/BTMS中观察到的,孔内存在一些游离亲水基团在减缓极性溶剂的交换方面起关键作用,这与解释先前报道的这些材料中的酶活性相关。版权所有© 2016约翰威立父子有限公司。

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