New chromatographic method for separation and determination of denatured αs1-, αs2-, β- and κ-caseins by hydrophobic interaction chromatography

被引:15
作者
Bramanti, E [1 ]
Sortino, C [1 ]
Raspi, G [1 ]
机构
[1] CNR, Ist Proc Chim Fis, Lab Instrumental Analyt Chem, I-56124 Pisa, Italy
关键词
hydrophobic interaction chromatography; milk; cheese; food analysis; caseins; proteins;
D O I
10.1016/S0021-9673(02)00325-4
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Separation and determination of denatured alpha-, beta- and kappa-caseins by hydrophobic interaction chromatography (HIC) was improved by using a TSK-Gel Ether-5PW column (Tosoh Biosep). The method, already proposed and performed by a TSK-Gel Phenyl-5PW column (Tosoh Biosep), is based on fast and easy solubilization of commercial and real samples by 4.0 M guanidine thiocyanate and HIC analysis in the presence of 8.0 M urea in the mobile phase. Employment of the less hydrophobic ether phase had the main advantage of separating casein fractions in less than 22 min and. additionally. of separating alpha-casein in alpha(s1)- and alpha(s2)-casein fractions. The method has been validated by the analysis of reference skim milk powder (BCR-063R) certified for total nitrogen content. A linear relationship between the concentration of casein and peak area (UV absorbance detector at 280 nm) has been obtained over the concentration range of 0.5-40 muM. The detection limit for alpha-, beta- and kappa-caseins ranged between 0.33 and 0.65 muM. The precision of the method was evaluated, the RSDs for alpha(s1)-, alpha(s2)-, beta- and kappa-casein determination ranging between 2.3 and 5.5% for standard solutions and between 4.4 and 6.2% for real sample solutions. The mean value of casein content found in eight aliquots of BCR-063R calculated with respect to the total protein content (estimated on the basis of certified total nitrogen content) was 78.3+/-6.1%. Results of linear fitting of standard additions data of alpha(s1)-, alpha(s2)-, beta- and kappa-caseins to BCR-063R were compared with linear fitting of alpha(s1)-, alpha(s2)-, beta- and kappa-casein calibration data. The method was applied to commercial caseins and to 30 real, raw samples. A statistical comparison was performed between results on quantitation of alpha-, beta- and kappa-caseins obtained by TSK-Gel Ether-5PW and TSK-Gel Phenyl-5PW HIC columns, showing more accurate results for chromatographic analysis performed by the ether column. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:157 / 166
页数:10
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