Value added fish by-products - Nordic Innovation
Value added fish by-products - Nordic Innovation
Value added fish by-products - Nordic Innovation
Create successful ePaper yourself
Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.
Table 3.1. Mince samples with dry addition of the gelatin powders. (CP=Collagen peptide).<br />
Group/marking Gelatin addition Gelatin concentration Storage<br />
C None 0% Freezing<br />
F1 CP 0.5% Freezing<br />
F2 CP 1.5% Freezing<br />
F3 CP 3.0% Freezing<br />
3.1.10.1 Determination of water holding capacity and transverse relaxation time T2<br />
For determination of water holding capacity and measurements of transverse relaxation times<br />
were carried out as described above, paragraphs 1.1.1.1 and 1.1.1.2, respectively.<br />
3.1.10.2 Texture<br />
Textural properties of the thawed mince samples with <strong>added</strong> gelatin were measured in respect<br />
to hardness (kg) <strong>by</strong> using TA-XT2 (TA-XT2 Texture Analyser, Stable Microsystems, Surrey,<br />
UK). The mince samples were put into a box, 3.0 cm high and 3.5 cm in diameter before<br />
measuring. The samples were pressed downwards at constant speed of 1 mm s -1 into the<br />
samples until it had reached 50% of the samples height. The data processing was done in a<br />
program called Texture Expert Exceed, version 2.64.<br />
4 Comparison between protein ingredients for injection in fillets<br />
4.1 Comparison of properties of protein solutions for injection<br />
In order to examine chemical- and physicochemical characteristics, and other properties of the<br />
protein <strong>products</strong>, specific measurements were performed on the protein <strong>products</strong>.<br />
Weight loss, viscosity, colour (whiteness) and chemical content of the protein solutions were<br />
evaluated according to methods described above, paragraphs 1.1.2.2.4, 1.1.2.2.5, 1.1.2.2.6 and<br />
1.1.2.2.3 respectively. Protein patterns of the protein <strong>products</strong> were analysed using sodium<br />
dodecyl sulphate-polyacrylamide gel electrophoresis (SDS-PAGE) according to the method of<br />
Laemmli (1970), using 10% separating gel and 4% stacking gel (Laemmli 1970), as described<br />
above in paragraph 3.1.4 on page 103.<br />
106