The foaming properties of proteins isolated from barley

Albumin and hordein protein fractions have been isolated from barley by extraction with salt and aqueous ethanol respectively. Both produce stable foams as assessed by a shaking procedure, and in each case foaming was enhanced by denaturation of the proteins. Foam power was increased rather more for albumin than for hordein, especially by heat, and this was accompanied by an increase in hydrophobic character as assessed by the fluorochrome 1‐anilino‐8‐napthalenesulphonic acid. Iso‐α‐acids and reduced iso‐α‐acids increased the foam stability of both albumin and hordein, with there being a proportionately greater increase for the undenatured proteins. Albumin is resistant to hydrolysis by the cysteine proteinases ficin and papain but is hydrolysed by the serine proteinase trypsin. In the latter instance, hydrolysis is accompanied by a loss of foam stability. By contrast, hordein is resistant to digestion by trypsin but is susceptible to the action of ficin and papain. In these instances, limited proteolysis leads to a substantial enhancement of foam stability from hordein, though prolonged proteolysis is detrimental. Proteinase A from yeast hydrolyses both protein classes and lowers their ability to give stable foams. It is concluded that polypeptides derived from both albumin and hordein could make a contribution to the foam potential of beer. © 2002 Society of Chemical Industry     

The foaming of mixtures of albumin and hordein protein hydrolysates in model systems

Although hydrolysed albumin and hydrolysed hordein derived from barley are independently capable of stabilising foams in model beer solutions, when both are present together, the net foam stability is less than anticipated. In particular, it seems that hordein, even in an unhydrolysed state, interferes with the ability of albumin‐derived polypeptides to stabilise foam. It appears, therefore, that the observed foam stability of a product such as beer is not only dependent on the absolute level of individual foam‐stabilising polypeptides but also on the relative proportions of polypeptides derived from the albumin and hordein protein subsets. Copyright © 2004 Society of Chemical Industry     

Inhibition of Aldose Reductase Activity by Extracts from Hops

The inhibitory effect of beer on aldose reductase was investigated. Components present in beer strongly inhibited aldose reductase. Inhibition activity was observed primarily in the methanol‐soluble fraction of the beer and active components were identified to be of hop origin. Further, a component was identified as iso‐α‐acids, which are well known as main bitter components of beer. The inhibition rate of iso‐α‐acids was similar to quercetin, which is known to be a strong inhibitor of aldose reductase activity.     

Relationships of Sensory Bitterness in Lager Beers to Iso‐α‐Acid Contents

Iso‐α‐acids and their chemically modified variants play a large role in evoking the bitter sensory attributes of lager character, but individual consumers may vary in their perception of bitterness. Sixteen lagers were scored in rank‐rating for bitterness by 14 trained assessors and the concentrations of the six bitter components in these beers were determined by high performance liquid chromatography. Relationships between bitterness intensity and the bitter components were modelled well using partial least square regression with a correlation value of 0.92. When 8 assessors carried out time‐intensity scoring of bitterness, profiles for single products were very different. However, single assessor profiles for multiple products showed qualitative similarities but quantitative differences. That individual assessors perceived bitter characters differently in relation to time has implications for new product development.     

The Significance of Iso‐α‐Acids for Beer Quality Cambridge Prize Paper

The iso‐α‐acids and their chemically‐modified variants play a disproportionately large role in the final quality of beer. Here, fundamental aspects of two of these quality issues — foam and bitterness — are discussed. A common feature of both issues is the dependence on the hydrophobic character of the hop compounds on both bitterness potency and ability to stabilise foams. Thus the isocohumulones appear significantly less bitter than the other, more hydrophobic hop compounds. Also apparent were the differences in bitterness between the cis‐ and the trans‐isomers, with the former being the more potent. Also described are the differences in the partitioning of the cis‐ and trans‐iso‐α‐acids into beer foam. The trans‐isomers are enriched in foam relative to their cis‐counterparts and may account for the observed enrichment of cis‐isomers in the final beer relative to the common ratios observed upstream.     

Free α-amino nitrogen production in sorghum beer mashing

Free α-amino nitrogen (FAN) is an essential nutrient for yeast growth during fermentation. Under normal conditions of sorghum beer mashing, 60°C at pH 4.0, production of FAN by proteolysis accounts for approximately 30% of wort FAN, the remaining 70% being preformed in the malt and adjunct. The quality of the FAN in sorghum beer worts is good as it does not contain a high percentage of proline. Optimum conditions for FAN production during mashing are 51°C and pH 4.6. Wort FAN was increased proportionally by raising the ratio of sorghum malt to adjunct and conversely decreased by raising the ratio of adjunct to malt. FAN was also increased by the addition to the mash of a microbial proteolytic enzyme. Wort FAN is directly proportional to malt FAN.     

Changes in β-glucan and other carbohydrate components of barley during malting

Changes in total (1→3), (1→4)-β-glucan content were followed during the micro-malting of nine varieties of barley with a wide range of malting qualities. These changes were related to estimates of endosperm modification based upon staining with Calcofluor. β-Glucan content declined from an average of 3.54% in the barley to 0.75% in the malt. Pentosan and total starch (including starch-derived oligosaccharides) levels showed comparatively little change during malting. β-Glucan composition of the barley was a poor indicator of malting performance. However, the β-glucan, starch and xylose contents of the malt all showed significant correlations with malt extract. Estimation of malt β-glucan content gave the best indication of malt quality. Direct determination of β-glucan may be of more value in assessing malt quality than indirect techniques based upon assessing modification of stained grains.     

Enzyme activities,dietary fibre components and rheological properties of wholemeal flours from rye cultivars grown in Finland

Total and soluble dietary fibre, total and soluble pentosan and β‐glucan contents, activities of α‐amylase (EC 3.2.1.1) and endo‐β‐xylanase (EC 3.2.1.8) and viscous properties of aqueous suspensions of wholemeal flours during heating were determined in nine winter rye cultivars (Secale cereale L) grown in Finland in 1998–2001. There was marked annual and varietal differences in grain quality. In the rainy summer 1998 the yield was low, grains were small and dietary fibre content of the grains was high. Xylanase activity of the grains was high, which corresponded to the high content of soluble pentosans. In the dry summer of 1999, the pentosan content of the grains was low and β‐glucan content high. The effect of weather conditions and cultivar were also apparent in the differences in falling numbers, amylogram and swelling curve results. The two hybrid rye cultivars Esprit and Picasso had consistently highest falling numbers and amylogram peak viscosities. The activities of α‐amylase and xylanase had a moderate positive correlation with total pentosan content and the content of soluble pentosan. Xylanase activity had better correlation with the viscous properties of flour–water suspensions than α‐amylase. Surprisingly, α‐amylase activity had only a moderate negative correlation with falling number. Copyright © 2005 Society of Chemical Industry     

Enhanced Quantitative Extraction and HPLC Determination of Hop and Beer Bitter Acids

A pleasant and consistent bitterness is an essential flavour attribute of beer. Hop‐derived iso‐α‐acids are largely responsible for beer bitterness and accurate determination of these primary flavour compounds is very important in relation to quality control. The most widely used way to determine beer bitterness is based on spectrophotometry, measuring the absorbance of an iso‐octane extract of acidified beer. However, this approach is far from specific as it measures all of the extracted compounds, including non‐bittering principles. For that particular reason, High Performance Liquid Chromatography (HPLC) is increasingly applied for the quantitative determination of hop‐derived iso‐α‐acids and, if present, reduced iso‐α‐acids. However, to obtain accurate data on beer bitterness profiles, both quantitative sample preparation and state‐of‐the‐art HPLC are essential. In this paper, several extraction procedures based on solid phase extraction (SPE) and liquid‐liquid extraction (LLE), respectively, were evaluated and an optimised extraction methodology using H₃PO₄ for sample acidification prior to extraction is presented. The proposed extraction/HPLC methodology allows for the quantitative recovery and analysis of hop‐derived beer bitterness.     

Mechanism of gushing induction by carbon dioxide transfer activator

The article deals with the activation of carbon dioxide transfer from carbonated beverages. As a model compounds agents produced by Trichoderma reesei and harzianum and degraded hop iso‐extract were selected. These substances were added to the carbonated water or beer and their effect was compared. The method of pressure growth in the bottle headspace after rapid piercing and re‐closing the bottle was used. Some carbon dioxide transfer activators accelerated CO₂ escape even at rest; others required shaking for different periods. The pressure growth measurement allowed the prediction of gushing before its occurrence. Copyright © 2017 The Institute of Brewing & Distilling     

Dextrin as the main turbidity components in wort produced from major malting barley cultivars of Jiangsu province in China

As wort is the sweet starter liquid for beer, its quality needs to be strictly controlled. It is generally accepted that wort turbidity is of importance in terms of the brewing process and the resulting beer quality. This study investigated the major ingredients of wort turbidity using the malting barley cultivar Dan'er, grown in Jiangsu province, China. It was found that dextrins of low molecular weight constituted the vast majority of the polysaccharides causing wort turbidity. To solve the turbidity problem with the Dan'er malt, the present study supplemented 80 U g^?1 of β‐amylase, and as an activator, an extra 50 mg  L^?1 of Ca²⁺ to the malting process of Dan'er barley. The turbidity of the resulting congress wort of the Dan'er malt declined to <5.0 EBC units, which then met the quality guidelines of the brewery. The results of the present study may also help in developing new turbidity detection methods and yield breeding clues for quality improvement of the barley cultivars in the Jiangsu province of China. Copyright © 2016 The Institute of Brewing & Distilling     

Alterations of the Profiles of Iso‐α‐Acids During Beer Ageing,Marked Instability of Trans‐Iso‐α‐Acids and Implications for Beer Bitterness Consistency in Relation to Tetrahydroiso‐α‐Acids

Age‐induced decomposition of iso‐α‐acids, the main bittering principles of beer, determines the consistency of the beer bitter taste. In this study, the profiles of iso‐α‐acids in selected high‐quality top‐fermented and lager beers were monitored by quantitative high‐performance liquid chromatography at various time intervals during ageing. The degradation of the iso‐α‐acids as a function of time is represented by the ratio, in percentage, of the sum of the concentrations of trans‐isocohumulone and trans‐isohumulone to the sum of the concentrations of cis‐isocohumulone and cis‐isohumulone. This parameter is relevant with respect to the evaluation of bitterness deterioration in aged beers. Trans‐iso‐α‐acids having a shelf half‐life of less than one year proved to be significantly less stable than cis‐iso‐α‐acids, but it appears feasible to counteract degradation if a suitable beer matrix is available. The fate of the trans‐iso‐α‐acids in particular adversely affects beer bitterness consistency. In addition to using hop products containing low amounts of trans‐iso‐α‐acids, brewers may profit of the remarkable stability of tetrahydroiso‐α‐acids, even on prolonged storage, for the production of consistently bitter beers.     

Relationship between Kolbach index and other quality parameters of wheat malt

In order to determine suitable Kolbach indices in wheat malting, the relationships between the Kolbach index and other quality parameters in wheat malt were studied. Eight white wheat malts with different Kolbach indices (31.4, 33.1, 37.0, 37.6, 39.5, 40.7, 42.8 and 45.5%) from the same wheat variety were prepared. The increase ratio of the ALSP (albumins and other soluble proteins) and the decrease ratio of the glutenins were found to have a significant positive correlation with the Kolbach index, and the corresponding r‐values were 0.883 and 0.975 (p < 0.01). The ALSP of the wheat malts had a positive correlation with chromaticity, extract, free amino nitrogen (FAN), viscosity, acidity, xylan glycosidase activity, endo‐β‐1,4‐xylanase activity and malting loss (p < 0.05). When the Kolbach indices were 31.4, 33.1, 37.0, 37.6 and 39.5%, there was a positive correlation between the soluble xylan and the viscosity, and the r‐value was 0.888 (p < 0.05). Comparing the malts, it could be concluded that, for this particular wheat variety, when the Kolbach index was 39.5%, the wheat malts exhibited the best characteristics; the extract was 81.98%, the FAN content was 166.03 mg per 100 mg, the saccharifying power was 496.72 WK, the viscosity was 1.61 cP, and the saccharification time was 6 min. Copyright © 2012 The Institute of Brewing & Distilling     

An improved HPLC method for single‐run analysis of the spectrum of hop bittering compounds usually encountered in beers

A single‐run reverse phase‐high performance liquid chromatography method for the quantification of humulinones, α‐acids, iso‐α‐acids and reduced iso‐α‐acids (where present) in commercial beer samples is presented. The method utilizes a binary solvent system consisting of (A) 1% v/v acetic acid and (B) 0.1% v/v orthophosphoric acid in acetonitrile. Separation was achieved on a Purospher® star RP‐18 column (250 × 46 mm, 3 µm) with a flow rate of 0.5 mL/min. The compounds of interest eluted within 32 min. The method was fully validated according to International Conference on Harmonization guidelines and subsequently applied to monitor degradation of hop acids in a storage trial where four lager beers were aged at 28 and 38 °C for 70 and 60 days, respectively. Results confirmed the widely reported degradation through storage of trans‐iso‐α‐acids whilst demonstrating that the HLPC method was sufficiently sensitive to monitor and model this degradation. One beer exhibited a significantly lower (P < 0.05) rate of trans‐iso‐α‐acid degradation than the other conventionally hopped beers in the study, which might have been linked to its higher pH (4.71 vs 4.36). The relative stability of reduced iso‐α‐acids during ageing was also confirmed.     

The enrichment of Asian noodles with fiber‐rich fractions derived from roller milling of hull‐less barley

Fiber‐rich fractions (FRF) derived from roller milling of waxy (W) and high amylose (HA) starch hull‐less barley genotypes were evaluated for suitability as functional ingredients in fresh and dried white salted (WSN) and fresh yellow alkaline (YAN) noodles. FRF‐W and FRF‐HA both contained over 300 g kg⁻¹ dietary fiber, and over 200 g kg⁻¹ of β‐glucans. Replacement of 250 g kg⁻¹ Canada Prairie Spring White (cv AC Vista) wheat patent flour with the FRF posed no problems in noodle processing, although water absorption had to be substantially increased. All three noodle types enriched with the FRF were significantly darker and contained more brown specks than the wheat flour control noodles. The presence of the FRF reduced cooking time of fresh YAN and WSN by ∼50%. The addition of FRF improved cooked YAN texture, as evidenced by increased firmness and resistance to compression. FRF‐enriched fresh WSN were comparable to the wheat flour control noodles for those parameters, whereas enrichment of dry WSN by FRF imparted less firmness and less chewiness. FRF‐enriched fresh YAN and WSN offer consumer convenience due to shorter cooking time, improved nutritional quality and acceptable cooking quality. These features might make FRF‐enriched noodles sufficiently attractive to health‐conscious consumers to overcome the negative effects of color and appearance Copyright © 2005 Society of Chemical Industry     

Extraction,optimisation and characterisation of phenolics from Thymus vulgaris L.: phenolic content and profiles in relation to antioxidant,antidiabetic and antihypertensive properties

The objectives of this study were to examine varying extraction conditions of Thymus vulgaris L. as related to phenolic content and profiles of the extracts and their antioxidant, antihypertensive and antidiabetic properties. Phenolics were extracted under various conditions pertaining to free and bound phenolics, solvent type and combination of extraction time and temperature, and these extracts were evaluated in terms of their antioxidant activities and inhibitory activities of angiotensin‐converting enzyme (ACE), α‐glucosidase and α‐amylase. The acetone–water solvent mixture (1:1; v/v) produced the extract with the greatest phenolic content, antioxidant activity and inhibitory activities of ACE and α‐glucosidase. The optimal extraction temperature for maximum phenolic content and antioxidant activity associated with methanol extraction was 60 °C, whereas a lower temperature at 40 °C was required to maximise inhibitory activities for ACE, α‐glucosidase and α‐amylase. An inverse relationship was seen between antioxidant and glucosidase inhibitory activities vs. the ACE and α‐amylase inhibitory activities, which suggests the need for extractions to be directed to specific bioactivities of thyme extracts. Generally, the results indicate major differences in phenolic profiles among the tested extraction conditions with thymol as the predominant phenolic seen in most extractions, while gallic acid, rosmarinic acid or diosmin also predominated in other extracts. Extracts with the same predominant phenolic compound and similar phenolic content showed major disparities in their ACE, glucosidase and α‐amylase inhibitory activities, indicating that the major phenolic profiles of thyme extracts may not be necessarily related to the degree of inhibition of ACE, glucosidase and α‐amylase enzymes.