Abstract
A perfusion reversed-phase (RP) HPLC method was developed for the rapid separation of the main bovine whey proteins: α-lactalbumin (α-LA), serum albumin (BSA) and the genetic variants of β-lactoglobulin (A and B) (β-LG A and β-LG B). For the method development, the influence of factors favouring structural changes of proteins (temperature and organic acid concentration in the mobile phase), gradient and other chromatographic conditions and the mass of protein injected was examined. The optimized method allowed the separation of proteins in about 1.5 min (cycle time 3.5 min) with resolution around 1.0 for the β-lactoglobulins. The method was applied to the determination of proteins in a whey from raw bovine milk. The precision of the determinations was ≤ 3.75 mg per 100 ml (S.D.). With respect to the accuracy, errors ≤ 7.0% in the determination on α-LA, β-LG A and β-LG B were obtained, compared with an RP-HPLC reference method. However, higher errors in the quantification of BSA were found owing to the lack of purity of the peak assigned. In addition, the proposed method has proved to be very useful in the detection of homologous whey proteins from different species (cow, sheep and goat) in milk mixtures.
Original language | English |
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Pages (from-to) | 99-111 |
Number of pages | 13 |
Journal | Journal of Chromatography A |
Volume | 729 |
Issue number | 1-2 |
DOIs | |
State | Published - Apr 5 1996 |
Externally published | Yes |
Funding
This work was supported by CYCIT (project ALI94-0737). The authors thank Professor M. Ramos for donating some of the samples used in this work and Dr. M. de Frutos for useful discussions.
Funders | Funder number |
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CYCIT | ALI94-0737 |
Keywords
- Albumin
- Perfusion chromatography
- Proteins
- Whey proteins
- α-Lactalbumin
- β-Lactoglobulin