Hop products with isomerized or reduced iso α-acids intended for use in beer brewing or elsewhere in the food industry
Hop products with isomerized or reduced iso α-acids are dissolved with methanol. The bitter acids are separated through reverse phase high-pressure liquid chromatography (RP-HPLC) and isocratic elution. They are then measured at a wavelength of 270 nm.
This method describes how to determine the β-glucan in laboratory wort by means of a fluorimetric method using microtiter plates (MTP).
Applicable for all (laboratory) worts
The cations in beer and wort are determined with this analysis.
This method is suitable for both wort and beer.
Inductively coupled plasma optical emission spectroscopy (ICP-OES) is a fast and reliable method for the laboratory analysis of metals. Inductively coupled plasma (ICP), a high frequency field of ionized gas, serves as a medium for atomizing and exciting the substances found in samples. Liquid, dissolved or aerosol samples are injected into the ionized gas stream. In emission spectroscopy, ICP can be used in conjunction with a number of optical and electronic systems either simultaneously or sequentially in multi-element spectrometers. In the plasma, the atoms and ions are excited to a higher energy state bringing about the emission of electromagnetic radiation (light), primarily in the ultraviolet and visible region of the spectrum. Metals ordinarily occur as ions in the temperature range typical for ICP of 6000 to 10000 K; however, non-metals and metalloids are only partially ionized.
ICP-OES operates within a very wide range. This usually encompasses six orders of magnitude in concentrations smaller than μg/l up to g/l, depending upon the element and the concentrations used for the set of analysis data. With ICP-OES, beer and wort can also be analyzed without prior processing of the samples, in contrast to AAS. Methods for determining the following in beer and wort will be described below: Al, B, Ba, Ca, Co, Cu, Fe, K, Mg, Mn, Mo, Na, P, Si, Sr, Sn and Zn.
This analysis is suitable for determining the sulfate content of beer, wort, water, NAB and fruit juice.
Sulfate ions are precipitated with barium ions in the form of barium sulfate and determined gravimetrically.
Determination of D-isocitric acid by enzymatic means
This analysis is suitable for non-alcoholic and beer-based beverages.
Fruit juices:
The acid spectrum typical of certain types of fruit are used, along with other criteria, as a basis for recognizing unadulterated fruit juices. Tartaric acid, citric acid and L-malic acid are recorded here, which, with a few exceptions, determine the total acidity of the fruit.
Citric acid occurs as the primary acid in citrus juices and other juices. Orange juice usually contains 3–17 g/l citric acid (AIJN).
In citrus juices, an addition of citric acid can be detected via the citric acid/D-isocitric acid ratio, as this lies within relatively narrow limits. In orange juice, values below 130 are found.
D-isocitric acid is partly present in fruit products as a lactone. The lactone must first be saponified prior to enzymatic determination in order to detect the total D-isocitric acid content.
D-Isocitrate in the sample is isolated as a barium salt through precipitation. The concentration of D-isocitrate is determined enzymatically. The enzyme isocitrate dehydrogenase (ICDH) catalyzes the oxidative decarboxylation of D-isocitrate to α-ketoglutarate with nicotinamide adenine dinucleotide phosphate (NADP):
D-Isocitrate + NADP+ \(^{\underrightarrow{ICDH}}\)α-ketoglutarate + NADPH + CO2 + H+
The amount of NADPH formed is proportional to the amount of D-isocitrate and is measured photometrically through the increase in absorbance.
Determination of the amount of cold break material in the pitching wort
Cast-out wort, wort from the midpoint of chilling/pitching wort (without yeast)
The hot break material (trub) and any hop particles which may be present in the wort, must first be removed. After the wort has been cooled to 2 °C, it is filtered through a glass fiber filter. The residue remaining on the filter is dried and then weighed.
Cold break material or cold trub refers to all material that settles out in the process of chilling wort after separation of the hot trub or hot break material. Cold trub can be filtered out of the wort and primarily consists of proteins (48–57 %), tannins (11–26 %) and carbohydrates (20–36 %). The amount of cold break material in wort depends on the quality and composition of the raw materials, brewhouse equipment and wort handling. In academic and professional circles, opinions regarding the significance of cold break material for downstream processes and for the quality of the finished beer are strongly divided [1, 2, 5]. Under certain circumstances, the quantity of cold break material in wort may exceed 250 mg/l, especially where accelerated fermentation is practiced. Ultimately, this can detract from the flavor of the finished beer [3]. Breweries, where removal of the cold break material has been practiced successfully, determine the quantity of cold break in their pitching wort at regular intervals, in order to evaluate the efficacy of their separation equipment.