Improving the rheological and thermal properties of wheat dough by the addition of γ-polyglutamic acid

The rheological and thermal properties of wheat dough with the addition of γ-polyglutamic acid (PGA) (0.5, 1.0, 5.0 g kg⁻¹, w/w) was evaluated by the measurements of farinography, rapid visco analysis and differential scanning calorimetry. Adding 5.0 g kg⁻¹ PGA in wheat dough increased the mixing stability and raised the pasting temperature from 75.8 to 84.4 °C, but decreased the peak viscosity and breakdown. The water holding capacity of wheat dough increased with the addition of 5.0 g kg⁻¹ of PGA. At 5.0 g kg⁻¹ level, PGA caused significant declines in the enthalpy, onset and peak temperatures of ice-melting transition of wheat dough. Scanning electron microscopy showed that wheat bread with the addition of 1.0 and 5.0 g kg⁻¹ PGA exhibited microstructures with smoother surfaces. During storage, PGA retarded the staling process of wheat bread.     

Nitrogen extractability and buffer capacity of defatted linseed (Linum usitatissimum L.) flour

Defatted linseed flour was prepared from cold-pressed seed meal via hexane extraction of the residual oil, followed by removal of the major portion of the hulls through grinding and sieving (sieve size 0.25 mm). The resulting flour had 50% protein on a dry basis compared with 40% contained by the whole seed on an oil-free dry basis. Nitrogen extractability of the defatted flour in water was not influenced by the length of the extraction period but an increased extraction was observed at higher solid:liquid ratios up to the studied limit of 1:40. The smallest amount of nitrogen (20%) was extracted in the pH range 4.0–4.6 and the greatest (80%) at pH 12.0. Addition of NaCl (0.1–1.0 M) broadened the pH range of minimum nitrogen extractability and shifted it towards lower pH region. At higher concentrations (0.6 and 1.0 M) NaCl markedly increased nitrogen extractability in the pH range of 4.0 to 8.0. Precipitation of protein from an extract at pH 10.0 was maximum (77%) at pH 4.1. A higher buffer capacity of the flour was observed in the acidic medium (0.204 mmol HCl g^?1 flour) than in the alkaline medium (0.096 mmol NaOH g^?1 flour).     

Comparison of the cell wall composition for flesh and skin from five different plums

Cell walls were isolated from flesh and skin of five plum varieties corresponding to three species (Prunus domestica L., Prunus salicina Lindl. and Prunus insititia Lindl.) using the alcohol-insoluble solids (AIS) procedure. Yields varied from 83 to 114 g kg⁻¹ dry weight in the flesh and from 192 to 361 g kg⁻¹ dry weight in the skins. Their main sugars were uronic acid (224–322 mg g⁻¹ AIS), cellulosic glucose (139–170 mg g⁻¹ AIS), galactose and arabinose. Galactose and arabinose ratio were variable between the varieties. The degrees of methylation were high (62–84).     

Composition of rosemary essential oil (Rosmarinus officinalis) as affected by drying method

The influence of the drying method on volatile compounds of Rosmarinus officinalis was evaluated. The drying methods tested were convective (CD) and vacuum-microwave (VMD), as well as a combination of convective pre-drying and VM finish-drying (CPD–VMFD). Rosemary drying kinetics was described by a simple exponential model for CD and VMD, while VMFD kinetics consisted of two periods: linear until a critical point and exponential beyond that point. Volatile compounds of rosemary samples were extracted by steam-hydrodistillation and analyzed by GC–MS. Thirty-four compounds were tentatively identified, with α-pinene, bornyl acetate, camphene and 1,8-cineole being the major components. The total volatiles concentration of fresh rosemary (135 g kg⁻¹) decreased considerably during both CD (87.2 g kg⁻¹) and VMD (61.9 g kg⁻¹). CPD–VMFD was the best option for drying rosemary because the time required was relatively short (30 min), and the aroma quality was good according to both instrumental (100 g kg⁻¹) and sensory analyses.     

Composition of oregano essential oil (Origanum vulgare) as affected by drying method

The influence of the drying method on volatile compounds of Origanum vulgare was evaluated. The drying methods tested were convective (CD) at 60 °C and vacuum-microwave (VMD), as well as a combination of convective pre-drying and VM finish-drying (CPD–VMFD). The volatile compounds of fresh and dried oregano were extracted by steam-hydrodistillation and analyzed by GC–MS. Oregano drying kinetics was described by a simple exponential model for CD and CPD–VMFD, while VMD kinetics consisted of two periods: linear until a critical point and exponential beyond that point. Thirty-four compounds were tentatively identified, with carvacrol, thymol, and γ-terpinene, being the major components. The total volatiles concentration of fresh oregano (33.0 g kg⁻¹) decreased significantly during drying, independently of the method used (CD: 10.2 g kg⁻¹, CPD–VMFD: 13.1 g kg⁻¹, and VMD: 27.9 g kg⁻¹). The final conclusion was that VM dehydrated Polish oregano was of better aromatic quality than that dried using hot air.     

Tempeh flour from chickpea (Cicer arietinum L.) nutritional and physicochemical properties

The effects of solid state fermentation (SSF) on physicochemical and nutritional properties of chickpea flour were studied. Fermented (tempeh) flour showed higher particle size index, gelatinization temperature, dispersability and resistant starch content, and lower gelatinization enthalpy and water solubility than unfermented flour. SSF increased the content of the essential amino acids (EAA) Ile, total sulphur (Met + Cys), total aromatic (Phe + Tyr), and Thr in 37, 41, 107, and 39 g kg⁻¹ protein, respectively; Trp content decreased 8 g kg⁻¹ protein. Total sulphur (EAA score = 0.87) was limiting in unfermented flour and Trp (0.93) in tempeh flour. SSP improved the in vitro and true protein digestibility (72.2–83.2% and 83.7–88.8%, respectively), protein efficiency ratio (PER, 1.59–2.31), cPER (1.54–2.21), and corrected protein digestibility (0.73–0.89). Chickpea tempeh flour may be considered for the fortification of widely consumed legume-based food products.     

Comparison of sterol composition between Tuber fermentation mycelia and natural fruiting bodies

Truffle, belonging to Tuber genera, is a nutritious and sterol-rich edible fungus, and sterol is a potential health beneficial compound. A comparison of Tuber sterol composition indicates that the total sterol contents in the fermentation mycelia (i.e., 10.5 mg g⁻¹) (n = 3) were approximately 3.2-5.6 times higher than that of the fruiting bodies (p < 0.05) with the addition of soybean flour into the basal fermentation media. Moreover, the phytosterol profile of fermentation mycelia could be significantly improved by adding soybean flour into the fermentation media. After the addition of soybean flour, stigmasterol and β-sitosterol appeared in the fermentation mycelia and the contents of total phytosterols (2279 μg g⁻¹) (n = 3), brassicasterol (943 μg g⁻¹) (n = 3), and campesterol (418 μg g⁻¹) (n = 3) were all increased significantly (p < 0.05). Moreover, the total contents of sterols and phytosterols in the fermentation mycelia cultured in the soybean media were much higher than those in the fruiting bodies (i.e., 1883-3240 and 479-1832 μg g⁻¹, respectively) (n = 3, p < 0.05). This work confirms the potentiality of Tuber fermentation mycelia as the alternative resource for its fruiting bodies from the viewpoint of sterols production.     

Chemical composition of cultivated seaweed Ulva clathrata (Roth) C. Agardh

Samples of cultivated Ulva clathrata were collected from a medium scale system (MSS, 1.5 × 1.5 m tank), or from a large scale system (LSS, 0.8 ha earthen pond). MSS samples were dried directly while the LSS sample was washed in freshwater and pressed before drying. Crude protein content ranged 20–26%, essential amino acids accounting for 32–36% of crude protein. The main analysed monosaccharides were rhamnose (36–40%), uronic acids (27–29%), xylose (10–13%) and glucose (10–16%). Some notable variations between MSS and LSS samples were observed for total dietary fibre (26% vs 41%), saturated fatty acids (31% vs 51%), PUFAS (33% vs 13%), carotenoids (358 vs 169 mg kg⁻¹ dw) and for Ca (9 vs 19 g kg⁻¹), Fe (0.6 vs 4.2 g kg⁻¹), Cu (44 vs 14 mg kg⁻¹), Zn (93 vs 17 mg kg⁻¹) and As (2 vs 9 mg kg⁻¹). The chemical composition of U. clathrata indicates that it has a good potential for its use in human and animal food.     

Effects of skin and grilling method on formation of heterocyclic amines in chicken pectoralis superficialis muscle

Mutagenic heterocyclic amines (HAs) originate in processed proteinaceous foods. The effects of the presence of skin (with vs. without) and of grilling method (two plate vs. infrared) on the content of HAs in grilled chicken pectoralis superficialis muscle (temperature, 220 °C) were investigated. HA precursors (creatine, creatinine, free amino acids and carbohydrates) and HAs of these raw and grilled breast muscles were determined. The muscles originated from 24 birds of either sex (provenance Ross; aged 40-45 days). The HA content was determined in homogenates of the upper and lower surface slices of the grilled muscles (T_i = 82 °C). A higher content of total free amino acids was seen for the muscle (27.1 mmol kg⁻¹ raw meat) than for the skin (21.7 mmol kg⁻¹ raw meat). The creatine, creatinine and carbohydrate levels in the skin were below the limits of detection. The contents of creatine (31.8-38.7 mmol kg⁻¹) and creatinine (0.24-0.33 mmol kg⁻¹) in the breast muscle were determined. Relatively high levels were seen for glucose (23 mmol kg⁻¹ raw meat) and fructose (10 mmol kg⁻¹ raw meat) in the muscle, with other sugars present at low levels (<2 mmol kg⁻¹ raw meat). For the chicken muscle grilled on a two-plate grill, the contents of total HAs (PhIP, MeIQx, DiMeIQx, Harman and Norharman) were lower with the skin in place than in the muscle grilled without the skin (3.5 μg kg⁻¹vs. 4.8 μg kg⁻¹). Also, during infrared grilling with the skin, lower amounts of HAs were formed than with grilling on the two-plate grill (2.4 μg kg⁻¹vs. 3.5 μg kg⁻¹). On average, the infrared-grilled samples with skin contained 3-fold more total HAs than similar samples without the skin (2.4 μg kg⁻¹vs. 0.8 μg kg⁻¹), with the highest levels seen for PhIP and MeIQx.     

Extraction optimisation,purification and major antioxidant component of red pigments extracted from Camellia japonica

The optimised extraction conditions of red pigments (RP) from Camellia japonica obtained with an orthogonal design L₉(3⁴) were solid/liquid ratio, temperature, pH and extraction time as 1/10, 60 °C, 1.5 and 4 h, respectively. The RP were then purified by the macroporous resin method, which showed the resin LX-68 was appropriate for purifying the pigments from C. japonica. The antioxidant activities of these pigments were also investigated using 1,1-diphenyl-2-picrylhydrazyl (DPPH) and hydroxyl radical in vitro model systems. The DPPH scavenging activity of pigment extract was comparable to that of standard butylated hydroxyanisole (BHA). The IC₅₀ values of the RP and BHA were 4.55 and 4.17 μg ml⁻¹, respectively. The pigments showed higher hydroxyl radical-scavenging activities than that of mannitol at the same concentration. Following activity-oriented separation, (−)-epicatechin was isolated as an active principle, which exhibited excellent DPPH free radical scavenging activities with IC₅₀ 5.08 μg ml⁻¹.     

Effect of a commercial adjunct culture on organic acid contents of low-fat Feta-type cheese

The effect of a commercial adjunct culture (CR-213, containing Lactococcus lactis subsp. cremoris and Lactococcus lactis susp. lactis and added at the level of 0.6 g kg⁻¹ or 0.9 g kg⁻¹ cheese milk) on the organic acid (OA) content of low-fat Feta-type cheese was studied. Full-fat (∼220 g kg⁻¹) and a low-fat (∼70 g kg⁻¹) cheeses were used as controls. The main OA of all cheeses throughout ripening were lactic, citric and acetic acids. The effect of ripening time was significant (P < 0.05) for all OA but treatments did not affect acetic, succinic and uric acids. Cheeses with lower fat content were found to contain significantly (P < 0.05) more lactic and citric but less butyric acid than the full-fat control. The addition of the adjunct culture had a positive effect on butyric acid, propionic acid and acetoin content. The use of the adjunct culture could enhance the production of OA in low-fat Feta-type cheeses with eventual positive effect on their sensory properties.     

Effects of vacuum level and microwave power on rosemary volatile composition during vacuum-microwave drying

The influence of the vacuum level and the microwave power on aroma compounds and sensory quality of Rosmarinus officinalis dehydrated by vacuum-microwave (VM) method was evaluated. VM drying kinetics consisted of two periods: linear until a critical point and exponential beyond that point. The time needed to dry rosemary was shorter for high values of microwave power and vacuum intensity. Volatile compounds of rosemary samples were extracted by steam-hydrodistillation and analyzed by GC-MS. Thirty-one compounds were identified, with α-pinene, verbenone and 1,8-cineole being the major components; monoterpenoids were the predominant chemical family. The total quantity of volatiles of fresh rosemary (27.2 g kg⁻¹) decreased during drying, independently of treatments, to a mean of 14.8 g kg⁻¹. Soft conditions of VM drying (low vacuum level and microwave power) are recommended to get the highest concentrations of volatiles and the best sensory quality (e.g. 72-74 kPa and 360 W).     

Supramolecular solvent-based microextraction of Sudan dyes in chilli-containing foodstuffs prior to their liquid chromatography-photodiode array determination

A supramolecular solvent made up of reverse micelles of decanoic acid was proposed for the simple and rapid extraction of Sudan I, II, III and IV from chilli-containing foodstuffs. The procedure involved the extraction of minute quantities (0.5–1 g) of homogenised food sample with an aqueous solution containing 10% THF and 200 mg of decanoic acid, conditions under which the supramolecular solvent (around 330 μL) formed in situ and instantaneously. The overall sample treatment took about 30 min and several samples could be simultaneously treated using conventional lab equipment. No clean-up or solvent evaporation were required before determination of Sudan dyes by liquid chromatography and photometric detection. Extractions were independent of salt addition (up to 1 M), the temperature (up to 60 °C) and the pH (below 4) rendering the method robust. The detection limits of the method were 4.2, 2.7, 6.5 and 7.4 μg kg⁻¹ for Sudan I, II, III and IV, respectively. Recoveries obtained by applying this approach to the analysis of six chilli-containing sauces fortified with Sudan dyes at the μg kg⁻¹ level were in the interval 86–108% with relative standard deviations between 2% and 7%.     

Determination of diquat and paraquat in olive oil by ion-pair liquid chromatography–electrospray ionization mass spectrometry (MRM)

For the first time a method for determination of herbicides diquat (DQ) and paraquat (PQ) in olive oil was developed utilising liquid chromatography–electrospray ionization mass spectrometry (MRM). n-Hexane/10 mM HFBA aqueous solution partitioning was used as the extraction method. Separation was carried out in an Xterra C8 column (100 × 21 mm, 3 μm), using the gradient mode. Solvent A was a HFBA aqueous solution (5 mM, pH 2) and solvent B acetonitrile/methanol 75/25 (v/v). Peaks used for quantification were m/z = 157 (diquat) and m/z = 158 (paraquat). Detection limit found for both diquat and paraquat was 4 μg kg⁻¹. The method can also be applied for determination of chlormequat (CQ, quantification peak m/z = 58), the detection limit being 0.3 μg kg⁻¹. Such limits are clearly lower than the MCLs commonly applied to olive oil as reference criteria (5 times MCLs in olives). Good reproducibilities (day to day and run to run) were obtained.     

Effect of dehydration on the quality and storage stability of immature dates (Pheonix dactylifera)

Dates (Pheonix dactylifera) harvested from Kutch district of Gujarat, India were processed for the development of dehydrated dates. Dates grown in the Kutch region of Gujarat are harvested before maturation, i.e. Khalal stage to prevent spoilage caused due to rains. The processing and dehydration conditions for the preparation of dehydrated dates from immature date fruits were evaluated. Processing of dates by blanching in water at 96±1 °C and subsequent dehydration at 60±2 °C for 18-20 h resulted in good quality dehydrated dates as compared to the dates dried without heat treatment. The dehydrated dates were found to be acceptable with respect to colour, flavour, taste and overall quality. The dehydrated dates contained a total sugars of 520 g kg⁻¹, reducing sugars of 415.1 g kg⁻¹, tannins 13.5 g kg⁻¹ and ascorbic acid 33.7 mg kg⁻¹. Equilibrium relative humidity (ERH) of the dehydrated dates was found to be 75.9% with an initial moisture content of 159 g kg⁻¹. The dehydrated dates packed in 75 μ low-density polyethylene packaging material were shelf stable for 6 months at room temperature. The dehydrated dates remained acceptable during the storage period.     

Chemical characterization of a traditional honey-based Sardinian product: Abbamele

The first chemical characterization of abbamele, a traditional honey decoction from Sardinia (Italy) is hereby reported. Water content (from 17.7% to 27.7%), electrical conductivity (from 0.19 to 0.81 mS cm⁻¹), pH (from 3.21 to 3.92), free acidity (from 26.1 to 87.6 meq kg⁻¹), invertase activity (from 0 to 1.02 U kg⁻¹), 5-(hydroxymethyl)-2-furaldehyde, HMF (from 881 to 4776 mg kg⁻¹), total polyphenols (from 188 to 984 mg kg⁻¹) and free amino acid contents of thirteen abbamele samples, from industrial and traditional producers, were obtained in an attempt to compare this traditional product with honey and to study the relationship between its main features and the production procedures. The long thermal treatment involved in the production of abbamele has been identified as the main cause of very low (or absent) invertase activity and free amino acid content as well as the very high content of HMF.     

Physical properties and microstructure of pidan yolk as affected by different divalent and monovalent cations

Changes in physical property and microstructure of pidan yolk were monitored during pickling in the presence of different divalent (CaCl₂, MgCl₂) and monovalent (KCl) cations at different levels (2 and 5 g kg⁻¹) up to 3 weeks, followed by ageing for another 3 weeks. Pidan prepared following the commercial process, in which PbO₂ or ZnCl₂ at a level of 2 g kg⁻¹ was incorporated, was also tested. Hardness, hardening ratio, NaCl content and pH of yolk gradually increased, whereas moisture content, cohesiveness and adhesiveness decreased as the pickling/ageing time increased up to 6 weeks, regardless of cations used. During pickling/ageing, L* and b* values of interior yolk and a* of exterior yolk decreased, while L* and b* values of exterior yolk and a* value of interior yolk increased (P < 0.05). Yolk of pidan treated with PbO₂ at a level of 2 g kg⁻¹ was semisolid with lower hardening ratio, hardness, cohesiveness and adhesiveness, compared with those from other treatments. Those treated with ZnCl₂ or CaCl₂ at a level of 2 g kg⁻¹ yielded higher hardening ratio, hardness and cohesiveness but lower adhesiveness than others. Confocal laser scanning microscope indicated that the greater dehydration and release of lipids took place in pidan yolk during pickling/ageing of 6 weeks.     

Trace element levels in honeys from different regions of Turkey

A survey of 25 honey samples from different botanical origin, collected all over the Turkey was conducted to assess their trace element contents. The aim of this study was to determine the levels of cadmium (Cd), lead (Pb), iron (Fe), manganese (Mn), copper (Cu), nickel (Ni), chromium (Cr), zinc (Zn), aluminium (Al) and selenium (Se) in honey samples from different regions of Turkey. Trace element contents were determined by a flame and graphite furnace atomic absorption spectrometry technique after dry-ashing, microwave digestion and wet-digestion. The accuracy of the method was corrected by the standard reference material, NIST-SRM 1515 Apple leaves. The contents of trace elements in honey samples were in the range of 0.23–2.41 μg g⁻¹, 0.32–4.56 μg g⁻¹, 1.1–12.7 μg g⁻¹, 1.8–10.2 μg g⁻¹, 8.4–105.8 μg kg⁻¹, 2.6–29.9 μg kg⁻¹, 2.4–37.9 μg kg⁻¹, 0.9–17.9 μg kg⁻¹, 83–325 μg kg⁻¹ and 38–113 μg kg⁻¹ for Cu, Mn, Zn, Fe, Pb, Ni, Cr, Cd, Al and Se, respectively. Iron was the most abundant element while cadmium was the lowest element in the Turkish honeys surveyed. The results showed that trace element concentrations in the honeys from different regions were generally correlated with the degree of trace element contamination of the environment.     

Determination of tetracyclines in multi-specie animal tissues by pressurized liquid extraction and liquid chromatography–tandem mass spectrometry

A specific, sensitive and robust pressurized liquid extraction (PLE) and liquid chromatography tandem mass spectrometry (LC–MS/MS) method for determining tetracycline, chlortetracycline, oxytetracycline and doxycycline in bovine, swine, poultry and lamb muscle tissues is presented. PLE was performed using an ASE^® 200 from Dionex and water as extractant, followed by solid-phase extraction (SPE) using an Oasis HLB cartridge. The method was validated for beef, chicken, pork and lamb meat in compliance with the requirements set by Commission Decision, 2002/657/EC [Commission Decision 2002/657/EC (2002). Implementing Council Directive 96/23/EC concerning the performance of analytical methods and interpretation of results. Official Journal of European Communities, L239, 66–98. (Available at: <http://europe.eu.int>)]. The average recoveries of the different meat samples, spiked with the four tetracyclines at three levels (1, 100 and 200 μg kg⁻¹ of each tetracycline), were always higher than 89% with intraday and interday precision lower than 15% and 17%, respectively. A good linearity was established for the four tetracyclines in the range from 5 to 10,000 μg kg⁻¹ with r > 0.995. The limits of quantification (LOQs) were between 0.5 and 1 μg kg⁻¹, which are well below the tolerance levels set by the European Union. The decision limit (CCα) and the decision capability (CCβ) were in the range 101–116 and 112–130 μg kg⁻¹, respectively. Compared with previous methods, sample preparation time required for the analysis and LOQs, are reduced. The method demonstrated its successful application for the analysis of 100 meat samples. Two samples of beef and one sample of chicken out of 25 of each type tested positive while none of 25 samples of either, lamb or pork, tested positive.     

Nutrient contents of kale (Brassica oleraceae L. var. acephala DC.)

Fructose, glucose and sucrose, as the major soluble sugars and citric and malic acids, as the major organic acids, were identified and determined in kale (Brassica oleraceae L. var. acephala DC., black cabbage) leaves. Fructose was the predominant sugar (2011 mg 100 g⁻¹ dry wt) identified, followed by glucose (1056 mg 100 g⁻¹ dry wt) and sucrose (894 mg 100 g⁻¹ dry wt). The contents of citric and malic acids were at 2213 and 151 mg 100 g⁻¹ dry wt in the leaves. The 16:0, 18:2n − 6 and 18:3n − 3 fatty acids were the most abundant fatty acids in the leaves. Considering the level of these fatty acids, 18:3n − 3 was found to be the highest (85.3 μg g⁻¹ dry wt), contributing 54.0% of the total fatty acid content. Linoleic acid (18:2n − 6), being the second most abundant fatty acid was present at 18.6 μg g⁻¹ dry wt, contributing 11.8% of the total fatty acid content. In the seed oil of kale, 22:1n − 9 was the most abundant fatty acid (4198 μg g⁻¹ dry wt, 45.7%), with 18:2n − 6 (1199 μg g⁻¹ dry wt, 12.3%) and 18:1n − 9 (1408 μg g⁻¹ dry wt, 14.8%) being the second next most abundant fatty acids. The most abundant amino acid was glutamic acid (Glu) which was present at 33.2 mg g⁻¹ dry wt. Aspartic acid, which was the second most abundant amino acid, was present at 27.6 mg g⁻¹ dry wt and accounted for 10.2% of the total amino acid content of kale leaf. The amino acid content was assessed by comparing the percentages of the essential amino acids in kale leaf versus those of a World Health Organization (WHO) standard protein. The protein of kale leaf compares well with that of the WHO standard. Only one amino acid, lysine, had a score that fell below 100%; the lysine score of kale leaf was 95%. This study attempts to contribute to knowledge of the nutritional properties of the plant. These results may be useful for the evaluation of dietary information.