Laboratory of Food Chemistry, Wageningen University, P.O. Box 8129, 6700 EV Wageningen, The Netherlands.
Biomacromolecules. 2010 Dec 13;11(12):3578-83. doi: 10.1021/bm1010432. Epub 2010 Nov 11.
The complex formation between β-lactoglobulin and pectins of varying overall charge and local charge density were investigated. Isothermal titration calorimetry experiments were carried out to determine the enthalpic contribution to the complex formation at pH 4.25 and various ionic strengths. Complex formation was found to be an exothermic process for all conditions. Combination with previously published binding constants by Sperber et al. (Sperber, B. L. H. M.; Cohen Stuart, M. A.; Schols, H. A.; Voragen, A. G. J.; Norde, W. Biomacromolecules 2009, 10, 3246-3252) allows for the determination of the changes in the Gibbs energy and the change in entropy of the system upon complex formation between β-lactoglobulin and pectin. The local charge density of pectin is found to determine the balance between enthalpic and entropic contributions. For a high local charge density pectin, the main contribution to the Gibbs energy is of an enthalpic nature, supported by a favorable entropy effect due to the release of small counterions. A pectin with a low local charge density has a more even distribution of the enthalpic and entropic part to the change of the Gibbs energy. The enthalpic part is reduced due to the lower charge density, while the relative increase of the entropic contribution is thought to be caused by a change in the location of the binding place for pectin on the β-lactoglobulin molecule. The association of the hydrophobic methyl esters on pectin with an exposed hydrophobic region on β-lg results in the release of water molecules from the hydrophobic region and surrounding the methyl esters of the pectin molecule. An increase in the ionic strength decreases the enthalpic contribution due to the shielding of electrostatic attraction in favor of the entropic contribution, supporting the idea that the release of water molecules from hydrophobic areas plays a part in the complex formation.
研究了不同总电荷和局部电荷密度的果胶与β-乳球蛋白之间的复合物形成。在 pH 4.25 和不同离子强度下进行等温滴定微量热实验,以确定复合物形成的焓贡献。对于所有条件,复合物形成都是放热过程。与 Sperber 等人之前发表的结合常数相结合(Sperber,B. L. H. M.;Cohen Stuart,M. A.;Schols,H. A.;Voragen,A. G. J.;Norde,W. Biomacromolecules 2009,10,3246-3252),可以确定β-乳球蛋白和果胶之间复合物形成时系统的吉布斯自由能变化和熵变。果胶的局部电荷密度决定了焓和熵贡献之间的平衡。对于局部电荷密度高的果胶,吉布斯自由能的主要贡献是焓性质,由于释放小的抗衡离子,有利的熵效应支持这一点。局部电荷密度低的果胶对吉布斯自由能的焓和熵部分的分布更为均匀。由于电荷密度较低,焓部分减少,而熵贡献的相对增加被认为是由于果胶在β-乳球蛋白分子上的结合位置发生变化所致。果胶的疏水性甲酯与β-lg 上暴露的疏水区的缔合导致水分子从疏水区释放出来并包围果胶分子的甲酯。离子强度的增加会由于静电吸引的屏蔽而降低焓贡献,有利于熵贡献,这支持了水分子从疏水区释放出来在复合物形成中起作用的观点。