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钙、磷酸盐和柠檬酸根离子在酪蛋白胶束稳定中的作用。

The role of calcium, phosphate and citrate ions in the stabilization of casein micelles.

作者信息

Visser J, Schaier R W, van Gorkom M

出版信息

J Dairy Res. 1979 Apr;46(2):333-5. doi: 10.1017/s002202990001726x.

Abstract

To obtain greater insight into the interaction of Ca, citrate and phosphate ions with casein, 31PNMR measurements were performed on combinations of these ions with alphas- and kappa-caseins. It was found that addition of alphas-casein to a Ca phosphate solution in D2O at 27 degrees C and pD 6.4 resulted in a downfield shift of the 31P singlet. An almost identical shift was observed with kappa-casein, but no shift was found when only phosphate ions were present or when Ca2+ were added to phosphate ions in the absence of casein. Separate experiments with poly-L-lysine, mol. wt approx. 35,000, resulted in similar downfield 31P chemical shifts of Ca phosphate as with both caseins, whereas no shift was observed when poly-glycine was added. From these results it can be concluded that Ca and phosphate ions associate with casein in a co-operative manner, probably in the way described by ter Horst (1963) as a complex with the NH3+-groups of lysine or arginine in a structure such as: (casein--NH3+)--PO43---Ca2+. The formation of this complex may be enhanced by citrate ions, since preliminary results have shown that addition of Na citrate to a solution of alphas-casein with added Ca phosphate produces a broadening of the 31P signal as well as a chemical shift.

摘要

为了更深入地了解钙、柠檬酸盐和磷酸盐离子与酪蛋白的相互作用,对这些离子与α-和κ-酪蛋白的组合进行了³¹P NMR测量。发现在27℃、pD 6.4的重水磷酸钙溶液中加入α-酪蛋白会导致³¹P单峰向低场移动。κ-酪蛋白也观察到了几乎相同的移动,但仅存在磷酸根离子时或在无酪蛋白的情况下向磷酸根离子中加入Ca²⁺时未发现移动。用分子量约为35,000的聚-L-赖氨酸进行的单独实验,得到了与两种酪蛋白类似的磷酸钙³¹P化学位移向低场移动的结果,而加入聚甘氨酸时未观察到移动。从这些结果可以得出结论,钙和磷酸根离子以协同方式与酪蛋白结合,可能是以ter Horst(1963年)描述的方式,即与赖氨酸或精氨酸的NH₃⁺基团形成复合物,结构如下:(酪蛋白--NH₃⁺)--PO₄³⁻---Ca²⁺。柠檬酸盐离子可能会增强这种复合物的形成,因为初步结果表明,向添加了磷酸钙的α-酪蛋白溶液中加入柠檬酸钠会导致³¹P信号变宽以及化学位移。

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