Protein composition of pulses and their protein isolates from different sources and in different isolation pH values using a reverse phase high performance liquid chromatography method
•A RP-HPLC method was used to evaluate protein composition of different pulses.•Chromatography peaks were identified as albumin, legumin and vicilin fractions.•Lentil showed the highest vicilin content and vicilin/legumin ratio among pulses.•Albumin content significantly reduced during the isoelectr...
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Veröffentlicht in: | Food chemistry 2023-05, Vol.409, p.135278-135278, Article 135278 |
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Sprache: | eng |
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Zusammenfassung: | •A RP-HPLC method was used to evaluate protein composition of different pulses.•Chromatography peaks were identified as albumin, legumin and vicilin fractions.•Lentil showed the highest vicilin content and vicilin/legumin ratio among pulses.•Albumin content significantly reduced during the isoelectric isolation process.•Higher isolation pH increases protein yield while reduces water solubility.
The objective of this study was to compare the composition of pulse proteins isolated from lentils and green and yellow peas at two isolation pH values (9 and 11) and determine the effect of this variability on protein functionality. Chromatogram peaks obtained from reverse-phase high performance liquid chromatography were identified by isolation of albumin-, vicilin- and legumin-rich fractions for the three pulses. Protein composition was obtained for each isolate and compared against that of the originating pulse flour. Lentil flour showed the highest level of vicilin with a vicilin/legumin ratio of ∼ 2.5, while this ratio was 1.3 and 1.2 for green and yellow pea flour, respectively. Albumin content of yellow pea flour was high (∼36.1 %), which reduced to ∼ 15–19 % in isolated proteins showing a loss in albumins during the isolation. Higher extraction pH increased pea protein yield but led to lower protein solubility with no changes in foaming properties and in-vitro digestibility. |
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ISSN: | 0308-8146 1873-7072 |
DOI: | 10.1016/j.foodchem.2022.135278 |