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Dietary fibre analyser

Manufactured by ANKOM Technology

The Dietary Fibre Analyser is a laboratory instrument designed to determine the dietary fibre content in various food and feed samples. It operates by enzymatic-gravimetric analysis to quantify the insoluble and soluble dietary fibre fractions.

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2 protocols using dietary fibre analyser

1

Comprehensive Nutritional Analysis of Bread

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Moisture content was determined by drying the samples at 105 °C to a constant weight (ICC 109/01). The ash content was determined gravimetrically as residue after combustion in a muffle furnace to 550 °C following AACC 08-01. Amino acid composition of wheat flour, microalgae and bread was estimated after hydrolysis in 6 M HCl for 22 h at 110 °C and analysed using HPLC and fluorescence detection [23 (link)]. The protein content of wheat flour, microalgae and bread are reported as the sum of all protein-bound amino acids. For protein digestibility determination [24 (link)] the protein content of the bread and digests was determined by combustion [25 (link)] using a Vario EL elemental analyser (Elementar, Langenselbold, Germany) with a nitrogen to protein conversion factor of 5.7 [26 (link)]. Free amino acids were determined by homogenizing the sample in an internal standard solution, derivatization with phenyl isothiocyanate, separation with reverse HPLC and detection by UV [27 ]. Crude fat content was estimated by a gravimetric method using solvent extraction [28 (link)]. The total dietary fibre (TDF) was measured gravimetrically following AOAC method 985.29 using an Ankom dietary fibre analyser. At least duplicate analyses were performed for all measurements.
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2

Comprehensive Microalgae Nutrient Analysis

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Moisture content was measured by drying at 105 • C to constant weight (ICC 109/01). The ash content was determined gravimetrically as residue after combustion in a muffle furnace (AACC 08-01). Protein content was determined by combustion (Kirsten, 1979) (link) using a Vario EL elemental analyser (Elementar, Langenselbold, Germany) . A nitrogen to protein conversion factor of 4.78 was used for microalgae (Tibbetts et al., 2015) (link). Total amino acids (AA) were analysed using HPLC with fluorescence detection (Cohen & Michaud, 1993) (link), after the samples were hydrolysed in 6 N HCl for 22 h at 110 • C. Free amino acids (FAA) were determined by homogenizing the sample in an internal standard solution, derivatization with phenyl isothiocyanate, separation with reverse-phase HPLC and UV detection (Brekken, 1989) . Crude fat content was estimated by a gravimetric method using solvent extraction (Bligh & Dyer, 1959) (link). The total dietary fibre (TDF) was measured gravimetrically (AOAC 985.29) using an Ankom dietary fibre analyser. Total starch content was measured according AOAC 996.11.
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