Malt intended for use in beer brewing or elsewhere in the food industry.
This method is based upon on the fact that the β-glucan-rich cell walls of the endosperm are progressively broken down during malting. This process can be made visible by staining the cell walls that are still intact with the fluorochrome Calcofluor, which exclusively binds β-glucans starting at a molecular weight of approx. 10,000 D.
Modification is revealed by allowing the barley kernels, which have been cut in half, to react with Calcofluor (with Fast Green as a contrast medium). The kernels are subsequently examined under UV light (365 nm) in a suitable analyzer device. An intense, bright blue fluorescence occurs where unmodified endosperm cells are present, while the modified parts appear dark blue.
The β-glucan content of barley intended for use in beer production should be known.
The fluorochrome Calcofluor forms a complex with high molecular weight β-glucans (molecular weight greater than 5 kDa). Complex formation results in an increase in fluorescence; however, this fluorescence is extremely unstable due to photochemical degradation.
Through measurement in an automatic analysis system based on flow injection (flow-injection analysis, fig. 1), reproducible measurements for fluorescence and determination of β-glucan are possible. For barley analysis, it is necessary to use a short acid hydrolysis procedure to bring insoluble β-glucan into solution. The apparatus is calibrated using purified barley β-glucan standards.
This method describes the fluorimetric determination of high-molecular weight β-glucans in malt.
Malt intended for use in beer brewing or elsewhere in the food industry
Water intended for use as an ingredient in the production of beer (brewing liquor) or other foods
A specified quantity of water is evaporated, and any remaining moisture is subsequently eliminated in a drying oven. The dry residue is then weighed.
The method provides an estimate of the portion of pre-germinated barley grains at the time of harvest or prior to storage in silos.
Barley intended for the production of malt is evaluated with regard to pre-germination.
The onset of germination is accompanied by the synthesis of enzymes, which can be made visible using fluorescein dibutyrate (FDB). The reagent fluoresces in the presence of lipases.
In order to make the enzyme activity visible, the kernels are first split in half and coated with the FDB reagent after which they are examined in a suitable measuring device under UV light. An intense yellow fluorescence can be seen in the parts of the kernels where enzyme activity is present.
This method describes how to determine the extract content of malt used to produce laboratory wort.
Malt intended for use in beer brewing or elsewhere in the food industry
The extract content of malt refers to the compounds from finely ground malt (fine grind), which are brought into solution during a standardized mashing process.
The extract content is determined by the weight ratio sL 20/20 of the wort on the basis of the official sugar tables (Plato tables) at 20 °C. sL 20/20 stands for the weight ratio of a volume of wort at 20 °C to the same volume of water at the same temperature.