Effect of ultra high temperature (UHT) treatment on coffee brew stability

In this work, the influence of an Ultra High Temperature (UHT) treatment on chemical and sensory composition of Arabica coffee brews for a longer shelf-life has been studied. A temperature of 120 °C for 2 s allows to obtain a microbiologically safe coffee brew, good valued from the sensory point of view. The behavior of the UHT vs non UHT treated coffee brew was followed throughout 120 days of storage at 4 °C. The UHT treatment keeps the typical acidity of the brews longer, delaying and softening the pH decrease and the development of sourness, which is one of the main causes for the rejection of stored coffee brews. The UHT treatment hardly affects the concentrations of caffeine and trigonelline, and of some phenolic compounds such as 5-caffeoylquinic (5-CQA), caffeic or ferulic acids. Sixteen key odorants and staling volatiles were analyzed by HS–GC–MS and lower changes were observed in the UHT treated coffee brew throughout storage. Higher DPPH scavenging activity was observed in the UHT treated coffee brew from days 60 to 120. In conclusion, the application of an UHT treatment is proposed to extend the shelf-life (up to 60 days) of stored coffee brews.     

Peroxidase (POD) and polyphenol oxidase (PPO) photo-inactivation in a coconut water model solution using ultraviolet (UV)

The interest in coconut water as a beverage is increasing due, not only to its sensory properties, but also to its nutritional characteristics. Even so, several challenges limit its processing, the inactivation of the polyphenol oxidase (PPO) and peroxidase (POD) enzymes being the most important. Although the inactivation of these enzymes has been extensively studied in coconut water, both by conventional and emerging technologies, the technologies evaluated so far are either not effective in the inactivation of these enzymes and/or result in undesirable changes. This work evaluated the photo-inactivation of POD and PPO in a coconut water model solution using ultraviolet radiation (UV). Both enzymes showed continuous inactivation behaviour in relation to the processing time, this being described by a two-portion inactivation kinetics. A possible mechanism for the observed photo-inactivation was proposed, involving steps of molecular unfolding and aggregation. The POD activity after 15 min of processing was ~ 5% of its original value, and reduced to ~ 1% after 30 min of UV processing. After 15 min of processing, PPO activity was ~ 8% of its original value, falling to ~ 2% after 30 min of UV processing. The results obtained highlight the potential use of the ultraviolet radiation to inactivate both enzymes in coconut water.     

Occurrence of furan in coffee from Spanish market: Contribution of brewing and roasting

In this work, we evaluated the occurrence of furan in brews obtained from regular, decaffeinated, and instant coffee and commercial packed capsules. For this purpose, a previously developed automated headspace solid-phase microextraction method coupled to gas chromatography–mass spectrometry (HS-SPME-GC–MS) was used. Initially, the influence of HS-SPME conditions on furan formation was evaluated. In addition, the effect of roasting conditions (temperature and time) used for coffee beans on furan formation was also studied. We found that low temperature and long roasting time (140 °C and 20 min) decreases the final furan content. Furan concentrations in regular ground coffee brews from an espresso coffee machine were higher (43–146 ng/ml) than those obtained from a home drip coffee maker (20 and 78 ng/ml), while decaffeinated coffee brews from a home drip coffee maker (14–65 ng/ml) showed a furan concentration similar to that obtained from regular coffee. Relatively low concentrations of this compound (12–35 ng/ml) were found in instant coffee brews, while commercial packed coffee capsules showed the highest concentrations (117–244 ng/ml). Finally, the daily intake of furan through coffee consumption in Barcelona (Spain) (0.03–0.38 μg/kg of body weight) was estimated.     

Pleasantness,emotions and perceptions induced by coffee beverage experience depend on the consumption motivation (hedonic or utilitarian)

Motivations to consume a given food or drink differ across consumers. For instance, coffee drinking can be motivated by sensory enjoyment (hedonic motivation) or by stimulation (functional motivation). Today it remains unknown how hedonic vs. utilitarian motivations impact consumer–product interaction. The objective of the present research was to study the impact of both motivations on consumer responses (i.e. pleasantness, emotions, and importance and satisfaction for each of the five senses) during the entire experience of a coffee beverage. Sixty participants drinking coffee beverage either for sensory enjoyment (SENS, n = 30) or to be stimulated (STIM, n = 30) were recruited. Four moments of the product experience were considered: water heating, jar handling, cup preparation and cup drinking. Self-ratings were repeatedly performed by the participants after each moment. SENS participants depicted higher positive emotions than STIM participants and even if similar levels of pleasantness were reached after cup drinking by both groups, levels of pleasantness at water heating and jar handling moments differed. The importance and satisfaction for the different senses also changed according to the participant motivation to drink the coffee beverage. Marketing implications are discussed in terms of communication materials development to more strongly engage consumers with the product.     

An investigation on the appropriateness of chocolate to match tea and coffee

The aim of this study was to provide some recommendations for selecting a befitting tea and coffee to match chocolate with different cocoa contents. Three coffee samples (chocolate flavored, vanilla flavored and unflavored coffee), four tea samples (black tea, green tea, vanilla flavored tea and citrus flavored tea) and three chocolates (30%, 70%, and 99% cocoa) were hedonically rated by eighty regular chocolate consumers. The beverages were then paired with each chocolate, and the consumers were asked to indicate the hedonic liking of the resulting pairings, and to indicate whether the chocolate or beverage flavor dominated the pairing flavor. This study showed that liking of chocolate and coffee pairings and chocolate and tea pairings significantly varied (p < 0.001) across samples. Consumers preferred pairings with 30% cocoa and 70% cocoa chocolate to pairings with 99% cocoa chocolate. Overall, coffee is significantly (p < 0.001) preferred to tea as a chocolate partner.Chocolate and beverage pairing liking was biased by the liking of the beverage tasted alone, the liking of chocolate tasted alone, beverage type, chocolate type and the level of flavor match between chocolate and tea or coffee in a given pairing. When chocolate and beverage flavor balanced out in a given pairing, chocolate and coffee/tea pairings were significantly preferred by the consumers. A significant decrease in acceptance was observed when beverage or chocolate flavor dominated the flavor of the pairing, much more so when the chocolate flavor dominated the pairing flavor. However consumers don't enjoy any preferred chocolate with any preferred tea or coffee because some flavors match better than do others. Indeed, consumers formulate their hedonic responses taking into consideration what flavors go well together more than they rely exclusively on their hedonic judgments of the chocolates, the teas, and the coffees tasted alone.     

Improvement of coffee beverage quality by using selected yeasts strains during the fermentation in dry process

Coffee is an important commercial product to Brazil with its consumption distributed globally. The aim of this work was to evaluate the potential of yeast strains as starter cultures for dry fermentation of washed and non-washed coffee beans. Four yeast strains (Saccharomyces cerevisiae UFLA YCN727, S. cerevisiae UFLA YCN724, Candida parapsilosis UFLA YCN448 and Pichia guilliermondii UFLA YCN731) were inoculated separately in washed and non washed coffee cherries and in the control was not added any of the starter cultures. The fruits inoculated were spread on trays and placed on a terrace until the coffee beans reached 11% of moisture. Samples were collected for evaluation of the persistence of the inoculum by PCR-DGGE, and for chemical composition by HPLC and GC-FID. Sensory analysis was performed using the Temporal Dominance of Sensations (TDS) methodology. In all tests the yeasts persisted until the end of fermentation. There was no propionic and butyric acid production in concentrations that could compromise the final quality of the beverage. Forty-eight volatile compounds were identified, some were similar for green and roasted coffee. The most abundant class of compounds was alcohols (11–27%) followed by furan in roasted grains (~ 27%), and aldehydes (~ 13%) in green grains. The coffee inoculated with yeast showed sensations of flavors higher than the control coffee indicating increased sensory quality. The treatment with C. parapsilosis UFLA YCN448 showed dominance rate higher (near 1) for the sensation of caramel. In non-washed coffee those sensations were not pleasant in relation to the washed coffee, except when P. guilliermondii UFLA YCN731 was inoculated, suggesting that washing the fruit before the fermentation process positively influenced the final product quality. A coffee with special aroma of caramel, herbs and fruits could be produced using the starter cultures C. parapsilosis UFLA YCN448 and S. cerevisiae UFLA YCN727 in coffee processed by the dry method.     

A 4-week consumption of medium roast and dark roast coffees affects parameters of energy status in healthy subjects

ScopeThis study intended to clarify whether two coffee brews, a market blend (MB) and a study blend (SB), containing equal amounts of caffeine, but differing in their contents of N-methylpyridinium, trigonelline and chlorogenic acids, differentially affect blood lipid profiles and glucose concentrations as well as blood platelet phosphodiesterase and lymphocyte energy charge potential in healthy volunteers.Methods and resultsIn this double-blinded, randomized, controlled cross-over intervention study, 84 healthy normal-weight female and male volunteers consumed 750 mL of medium roast MB and dark roast SB coffee per day for 4 weeks. Following MB and SB coffee intervention, plasma free fatty acid concentrations equally increased (p < 0.001) by 140 ± 187 μM and 178 ± 160 μM, respectively. Plasma glucose remained largely unchanged. Lymphocyte adenosine nucleotide analysis revealed a comparable rise in the energy charge potential, as calculated from ADP/ATP concentrations, adjusted to total adenosine nucleotides. Blood platelet phosphodiesterase activity was found decreased to about the same extent (p < 0.001). Levels of HDL-cholesterol, adiponectin, leptin, insulin and osteopontin were found to some extent differentially influenced by MB, respectively SB coffee.ConclusionThe results of this intervention study indicate that MB and SB coffees, although differing in contents of N-methylpyridinium, trigonelline and chlorogenic acids, largely exert similar biological effects as monitored by the biomarkers tested.     

Determination of 5-hydroxymethyl-2-furfural and 2-furfural in oils as indicators of heat pre-treatment

This study describes a method for the determination of 5-hydroxymethyl-2-furfural (HMF) and 2-furfural (F) in oils. The method entails liquid–liquid extraction and reversed-phase liquid chromatography. Spiked hazelnut oil was used to test the accuracy and reliability of the method. Furan compounds were extracted from oil using 70% methanol. Mean recoveries were 97 ± 2% and 99 ± 1% for HMF and F, respectively. To investigate the presence of HMF and F in oils, seven oily nuts and seeds were roasted at 180 °C for 30 min. Different oils were found to contain HMF and F ranging from 0.8 to 13.8 and 1.4 to 8.7 mg/kg, respectively. Increasing solvent polarity also increased the rate of HMF transferred to the oil. Spectral analyses of the 70% methanol extracts indicated that absorbance at 285 nm may be used to monitor the accumulation of furan compounds in oil phase during the roasting process of nuts.     

Phenolic composition,caffeine content and antioxidant capacity of coffee silverskin

Coffea arabica silverskin (CSS), the inner fruit layer surrounding coffee beans, was analyzed for its (poly)phenolic and caffeine content by means of liquid chromatography–tandem mass spectrometry and evaluated for its antioxidant properties by means of the Folin–Ciocalteu and FRAP methods. The most abundant quantified phenolics were caffeoylquinic acids, with the 5- and 3-isomers being the most relevant (199 mg/100 g and 148 mg/100 g, respectively). The three caffeoylquinic acid isomers reached a total concentration of 432 mg/100 g, corresponding to 74% of the total chlorogenic acids detected in CSS. The level of the three feruloylquinic acids detected was 143 mg/100 g, corresponding to 23%, and the two identified coumaroylquinic acids plus the two caffeoylquinic acid lactones were only marginally contributing to the final figure (only 3% of total hydroxycinnamates). No unconjugated phenolic acid was detected. Caffeine content in CSS was equal to 10 mg/g of product, 3.5 times lower than most coffee brews. The total antioxidant capacity (TAC) of CSS was 139 mmol Fe^2 +/kg, a value similar to those of valuable sources of food antioxidants like dark chocolate, herbs and spices. Besides its potential as a food supplement, CSS may represent an innovative functional ingredient exploitable to increase the TAC of a wide range of food products.     

Four-week coffee consumption affects energy intake,satiety regulation,body fat,and protects DNA integrity

Recent epidemiological studies suggest that coffee, one of the most widely consumed beverages worldwide, may reduce risks of degenerative diseases such as diabetes type 2, cardiovascular disease and certain types of cancer. These effects have partly been ascribed to coffee's antioxidant and body weight-reducing capacities. To explore the mechanisms involved, effects of coffee consumption on body weight/composition, food intake, satiety markers (serotonin and ghrelin) and DNA integrity were monitored in a four-week double-blind randomized crossover intervention study with 84 healthy subjects. Subjects consumed two different coffee blends (study blend, SB, and market blend, MB), with similar caffeine contents but substantially differing contents of chlorogenic acids and N-methylpyridinium. The consumption of both coffees (3 × 250 mL per day) was associated with a decrease in body fat over the whole study period (p < 0.001), which was more pronounced with SB. During intervention with MB, plasma serotonin levels increased (p < 0.001) whereas plasma ghrelin levels decreased (p < 0.001) relative to levels recorded during the preceding washout period. Consumption of both coffee blends was associated with DNA-protective effects (p < 0.001). These findings suggest that regular coffee consumption may provide health benefits in terms of reducing energy intake and body fat, regulating satiety and protecting DNA integrity.     

Fat contributes to the buffering capacity of chicken skin and meat but enhances the vulnerability of attached Salmonella cells to acetic acid treatment

Chicken skin and chicken meat display different buffering effects which may impact the survival of Salmonella attached to them when treated with acids. This study investigated the role that differences in fat composition of chicken skin and meat play in their buffering capacity. The survival of Salmonella attached to chicken skin and meat in the presence of fat, and treated with acetic acid was also investigated. Fat was extracted from chicken skin and meat and the buffering capacities of chicken skin, meat, extracted fat and their respective remnants were determined. Two strains of Salmonella Typhimurium and two strains of S. Enteritidis were attached independently to each of the chicken component listed above and enumerated before and after treatment with 0.3 M acetic acid. Chicken skin has a higher fat content as compared to chicken meat. Skin (13 mmol H⁺/(pH1 kg)) had a stronger buffering capacity (p < 0.05) than the extracted fat alone and skin remnants alone (7.0 mmol H⁺/(pH 1 kg) and 6.9 mmol H⁺/(pH 1 kg) respectively). From an initial inoculum (~ 9 log CFU/g), Salmonella cells attached better (p < 0.05) to chicken meat (~ 8 log CFU/g) and chicken skin (~ 7 log CFU/g) than extracted fat (~ 1.5 log CFU/g). Skin remnants without fat were better (p < 0.05) at protecting attached Salmonella than other chicken components. For example S. Typhimurium ATCC 33062 decreased ~ 1 log CFU/g (p < 0.05) on skin remnants after acetic acid treatment while its viable counts on other components decreased from ~ 1.5 to 7 log CFU/g (p < 0.05). We suggest that the fat content present in the skin may enhance the vulnerability of attached cells to acetic acid.     

The effect of pH on the gelling behaviour of canola and soy protein isolates

The present study investigates the gelation mechanisms of a canola protein isolate (CPI) as a function of a pH (3.0–9.0), and compares it to that of a commercial soy protein isolate (SPI). A rheological investigation found that CPI was non-gelling at pH 3.0, and then formed a gel with increasing strength as pH was raised from pH 5.0 to 9.0. In contrast, the commercial SPI ingredient was found to be non-gelling at pH 9.0, but formed the strongest networks at pH 5.0 near its isoelectric point (pI = 4.6). Denaturation temperature as determined by differential scanning calorimetry were found to occur at ~ 78 °C for CPI at pH 5.0, then shifted to higher temperatures (~ 87 °C) at pH 7.0/9.0, whereas detection of SPI denaturation could not be obtained due to instrument sensitivity. Gelling temperatures were similar for both CPI and SPI (~ 82–86 °C) at all pHs, with the exception of SPI at pH 5.0 (~ 46 °C). Overall CPI networks were stronger than SPI, since the latter had weaker inter- and intramolecular junction zones. Confocal laser scanning microscopy images indicated that CPI gels became denser with lower lacunarity values as pH increased from 3.0 to 9.0. Moreover, the fractal dimension of CPI gels was found to increase from ~ 1.5-1.6 to ~ 1.8 as pH increased from 5.0/7.0 to 9.0, respectively suggesting diffusion-limited cluster-cluster aggregation. Images of SPI networks were not concurrent with fractal analysis under the conditions examined. Despite CPI having excellent gelling properties that are comparable to SPI, its need for alkaline pH conditions will limit its applicability in foods.     

Consumption of highly processed foods: Effects on bioavailability and status of zinc and copper in adolescents

The effects of consuming diets with different Maillard reaction products (MRP) content on zinc and copper bioavailability and status were examined. In a 2-week randomised 2-period crossover trial, 18 male adolescents consumed two diets, named white diet (WD) and brown diet (BD), which were poor and rich in MRP, respectively. A 3-day balance was performed at the end of each period and fasting blood samples were collected. Zinc bioavailability did not vary significantly between the diets (%WD: 21.0 ± 5.0, %BD: 15.1 ± 5.1), but BD consumption increased copper faecal excretion (~ 1.8-fold) and significantly decreased its bioavailability (~ 3.0-fold). Biochemical parameters related to zinc metabolism remained unaltered whereas copper in serum and erythrocytes significantly decreased after consumption of the BD (72.47 ± 2.42 μg/dl and 0.93 ± 0.01 μg/ml in serum and erythrocytes with WD compared to 65.87 ± 3.11 μg/dl and 0.84 ±0.02 μg/ml with BD). The present results suggest that the high presence of MRP in the diet does not affect zinc but negatively affects copper bioavailability. As both minerals are essential trace elements involved in adolescents' growth and development, possible long-term effects of excessive MRP intake during adolescence warrant attention.     

Caffeine metabolism rate influences coffee perception,preferences and intake

Several factors – genetic, demographic and environmental – contribute to individual differences in sensitivity to the pharmacological effects of caffeine. Caffeine metabolism influences coffee consumption, but its effect on bitterness perception in, and preference for, coffee is unknown.This study explores the possible relationship between caffeine metabolism rate and coffee preferences and consumption habits. In addition, the extent to which caffeine metabolism interacted with variations in bitterness perception was investigated. Caffeine metabolism rate was assayed by competitive immuno-enzymatic assay in one-hundred thirty-five coffee consumers who provided saliva samples after 12 h caffeine abstinence and at 30 and 90 min after ingestion of caffeine (100 mg). A caffeine metabolism index (CmI) was computed as the ratio between the amount of residual caffeine in saliva 60 min after the adsorption peak and the amount of caffeine at the adsorption peak corrected with the baseline. Ninety-one subjects were selected to investigate the relationships between inter-individual variation in caffeine metabolism, bitterness perception and coffee preference. Subjects rated liking for, and sourness, bitterness and astringency of, six unsweetened and freely sweetened coffee samples varying in roasting degree, caffeine content and bitterness. They also rated the bitterness of six caffeine and six quinine (equi-intense) solutions. Finally, subjects choose coffee to drink on the basis of a label (strong vs balanced flavor) both after caffeine abstinence and after no restrictions on caffeine intake. The CmI was strongly associated with the frequency of daily coffee consumption. Subjects with lower CmI gave higher bitterness ratings than other subjects for both coffee and caffeine solutions, but not for quinine solutions. They also added more sugar to the coffee samples. Following caffeine abstinence, all subjects chose the “strong flavor” coffee, while without caffeine restrictions, subjects with lower CmI preferentially tended to choose the “balanced flavor” coffee. These results provide the first link between caffeine metabolism and bitterness perception, and to the use of sugar to modify coffee bitterness.     

The effect of the duration of infusion,temperature, and water volume on the rutin content in the preparation of mate tea beverages: An optimization study

The consumption of tea beverages has increased 30% over the last decade, mainly due to the presence of bioactive compounds. Mate tea, produced by infusing the leaves and stems of Ilex paraguariensis, is the most widely consumed beverage in Brazil. The present study employed a central composite experimental design to optimize the transfer of rutin from the leaves and stems to the beverage during the infusion process. The optimum condition was applied to three batches of mate tea beverages from five commercial samples. Analysis of the rutin content was performed by high performance liquid chromatography coupled to a photo diodo array detector. The maximum rutin content in the beverage was obtained when the infusion was performed using 2 g of mate tea added to 100 mL of water at 72 °C and infused for 9 min. The commercial tea beverages prepared under these conditions contained from 0.16 to 1.1 mg of rutin in the ready-to-drink product.     

Ochratoxin A in commercial soluble coffee and coffee substitutes

Coffee and cereals are recognized sources of ochratoxin A (OTA) in the human diet, but data concerning its amounts in soluble coffee substitutes are scarce. This work aimed to determine the amounts of OTA in commercial soluble coffee substitutes (mixtures of barley, malt, and chicory, either with or without coffee). OTA was isolated by immunoaffinity columns and quantified by HPLC with fluorescence detection.In a total of 40 samples analyzed, including 10 of soluble coffee, 13 mixtures with coffee and 17 mixtures without coffee, all commercialized in Portugal, 35 samples were positive for OTA, with concentrations ranging from < 0.15 to 11.8 μg/kg. Overall, coffee-containing samples had significantly higher amounts of OTA (p < 0.001) than substitutes without coffee. Indeed, coffee was the main determinant for the OTA content in the substitute beverages analyzed, with a highly significant linear correlation (r = 0.559, p < 0.001) between OTA amounts and coffee percentage in the mixtures. The high variability observed between samples is influenced by the “brand” effect as well as by raw-material quality.Globally, OTA amounts in coffee substitutes are generally low and within the regulated and safety limits. Their contribution to the provisional tolerable daily intake (PTDI) is therefore reduced (from 1.0 to 2.0% on average). Nevertheless, the high incidence of OTA contamination in these products should not be disregarded.     

Investigation and kinetic evaluation of furan formation in tomato paste and pulp during heating

Due to its high ascorbic acid content and acidic environment, tomato is susceptible for furan formation during heat treatment. In this study, kinetics of furan formation was analyzed in order to have an understanding of the reactions taking place in tomato pulp during heating. Also several tomato paste samples were investigated in terms of their furan and hydroxymethylfurfural (HMF) concentrations, and the possible furan precursors. Paste samples were found to contain 3.3–13 ng/g furan and 0.9–39.4 μg/g HMF (dry weight basis). Freshly prepared tomato pulps were heated at 70, 80, and 90 °C for different times, and analyzed for ascorbic acid, dehydroascorbic acid, and furan concentrations. The formation rates of furan in the very first 5 min of heating at 70, 80, and 90 °C were 0.0071, 0.0130, and 0.0168 nmol/g·min, respectively. Rate constants related to reactions taking place during furan formation were estimated by multi-response kinetic modeling. The results revealed that ascorbic acid oxidation is the critical step in furan formation reaction mechanism during heating of tomato pulp, and prevention of oxidation during processing might help to limit furan formation.     

Effects of catechin-enriched green tea beverage on visceral fat loss in adults with a high proportion of visceral fat: A double-blind,placebo-controlled,randomized trial

The effects of catechin-enriched green tea on Chinese adults with a high proportion of abdominal visceral fat were evaluated. Subjects (118) were randomly assigned to consume daily a beverage containing 609.3 mg catechins and 68.7 mg caffeine or a control beverage for 12 weeks. Abdominal fat area, body weight and composition were measured at week 0, week 8, and week 12. One hundred and four subjects completed the trial. Average visceral fat area, body weight, and body fat were reduced significantly by catechin-enriched green tea treatment but these effects were not seen in the control group with per-protocol sets analysis. The decrease at week 12 in the visceral fat area in the catechin group was greater than that in the control group (P = 0.04). Thus, consumption of the catechin-enriched green tea beverage for 12 weeks induced visceral fat loss in Chinese adults with a high proportion of abdominal visceral fat.     

Influence of extraction process on antioxidant capacity of spent coffee

Spent coffee that is produced in tons by restaurants and cafeterias, and consumers at domestic levels, could be a good opportunity to have an important source of natural antioxidants. The main aim of this work was to study the influence of several process factors on the antioxidant capacity extraction from spent coffee. Total phenolic compounds, radical scavenging activity (ABTS and DPPH) and browned compounds (Abs 420 nm) of spent coffee extracts obtained with continuous (Soxhlet 1 h and 3 h) and discontinuous methods (solid–liquid extraction and filter coffeemaker), several solvents (water, ethanol, methanol and their mixtures), successive extractions, and water with different pHs (4.5, 7.0 and 9.5) were carried out. Spent coffee extracts with the highest antioxidant capacity were obtained after one extraction with neutral water (pH 7.0) in a filter coffeemaker (24 g spent coffee per 400 mL water). Furthermore, spent coffee defatting and extract lyophilization allowed us to obtain spent coffee extracts powder with high antioxidant capacity that can be used as an ingredient or additive in food industry with potential preservation and functional properties.