Thesis Open Access
Missael Mekonnen
A process for the preparation of Holetta 1 mustard protein isolate, comprising steps such as
ground the seed, removal of oil with hexane, followed by extraction at alkaline pH 10, 11 and
12. The protein was subjected to separation by centrifugation, neutralization, washing and
freeze-drying. The parameters evaluated were protein yield, purity and presence of some
antinutritional factors. The protein yield was 56-80%.The purity of the protein isolate was
73.29%, 75.40% and 68.225 at pH value of 10, 11 and 12 respectively. The antinutritional
factors levels of defatted meal was as follows, glucosinolates represents 5.1%, phytate was
3.19% and tannins was 0.35% but after processing its value was 0.013%, 0.035 and 0.65% at
pH10, 0.012%, 0.03% and 0.75% at pH11 and 0.02%, 0.215% and 1.45% at pH12
respectively. The lowest protein solubility was achieved at pH 5.some functional properties
such as water adsorption(WA), fat adsorption (FA), emulsifying activiy (EA) and foaming
capacity (FC) were evaluated.Holetta1 mustard defatted meal were compared with soybean
meal in terms of functional properties. The tested result showed a high water absorbtion and
was superior to soybean meal in FA, EA and foaming properties
The chemical composition results of mustard variety of Holleta 1 defatted meal was 38.42%
of protein, 5.03% of ash, 7.10% of moisture, 31.15% of fiber, 7.79% of crude fat and 10.53%
of carbohydrate but after processing, the mustard precipitated protein isolate contained
75.40% of protein, 2.64% of ash, 7.97% of moisture, 0.08% of fiber, 12.61% of crude fat and
1.31% of carbohydrate
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