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Roasting of mustard seeds prior to oil extraction is a well-documented unit operation essential to produce canolol and other lipophilic sinapates. This study investigated the effectiveness of air frying as a seed roasting treatment operation for enhancing the recovery of lipophilic sinapates from various mustard samples and fractions/products. Air frying of seeds, powder, cake, bran, and flour from different mustard varieties was carried out at temperature-time combinations of 160, 170, and 180°C for 5, 10, 15, and 20 min, respectively. Oil was extracted using the Soxtec method. Lipophilic sinapates were extracted from the oil using equal volumes of hexane to methanol 70% (v/v) and quantified by high performance liquid chromatography-diode array detection (HPLC-DAD). The total phenolic content (TPC) and antioxidant activity of the oils were also evaluated. The results showed a time-temperature dependency for the recovery of major oil-soluble sinapates in all mustard samples and fractions. The optimum air frying condition 180°C for 15 min produced the maximum yield of canolol as well as other unidentified oil-soluble sinapates (retention time (RT)-7.7, RT-11.50, RT-14.95, and RT-16.24 min). The oil from lower grade yellow mustard seeds (LGYMS) roasted at 180°C for 20 mins specifically had the highest TPC (3402.22 ± 58.79 mg GAE/g oil), while LGYMS oils generally showed better antioxidant activities (2,2-diphenyl-1-picrylhydrazyl (DPPH), ferric ion reducing antioxidant power (FRAP), and inhibition of linoleic acid oxidation) but were lower in metal ion chelating capacity. This information would be beneficial to the oil industry because air frying generated valuable canolol and other antioxidant lipophilic sinapates from mustard varieties and their fractions. PRACTICAL APPLICATION: A major limitation in the application of natural extracts in vegetable oils is the poor lipophilic nature of phenolic compounds. This study employed a new thermal treatment (air frying) in the recovery of canolol and other lipophilic antioxidants. Such treatments can enrich mustard-based ingredients with canolol and other lipophilic antioxidants for domestic and industrial applications.

Phosphorus, an essential nutrient, performs vital functions in skeletal and non-skeletal tissues and is pivotal for energy production. The last two decades of research on the physiological importance of phosphorus have provided several novel insights about its dynamic nature as a nutrient performing functions as a phosphate ion. Phosphorous also acts as a signaling molecule and induces complex physiological responses. It is recognized that phosphorus homeostasis is critical for health. The intake of phosphorus by the general population world-wide is almost double the amount required to maintain health. This increase is attributed to the incorporation of phosphate containing food additives in processed foods purchased by consumers. Research findings assessed the impact of excessive phosphorus intake on cells' and organs' responses, and highlighted the potential pathogenic consequences. Research also identified a new class of bioactive phosphates composed of polymers of phosphate molecules varying in chain length. These polymers are involved in metabolic responses including hemostasis, brain and bone health, via complex mechanism(s) with positive or negative health effects, depending on their chain length. It is amazing, that phosphorus, a simple element, is capable of exerting multiple and powerful effects. The role of phosphorus and its polymers in the renal and cardiovascular system as well as on brain health appear to be important and promising future research directions.

Adequate thiamin levels are crucial for optimal health through maintenance of homeostasis and viability of metabolic enzymes, which require thiamine as a co-factor. Thiamin deficiency occurs during pregnancy when the dietary intake is inadequate or excessive alcohol is consumed. Thiamin deficiency leads to brain dysfunction because thiamin is involved in the synthesis of myelin and neurotransmitters (e.g., acetylcholine, γ-aminobutyric acid, glutamate), and its deficiency increases oxidative stress by decreasing the production of reducing agents. Thiamin deficiency also leads to neural membrane dysfunction, because thiamin is a structural component of mitochondrial and synaptosomal membranes. Similarly, in-utero exposure to alcohol leads to fetal brain dysfunction, resulting in negative effects such as fetal alcohol spectrum disorder (FASD). Thiamin deficiency and prenatal exposure to alcohol could act synergistically to produce negative effects on fetal development; however, this area of research is currently under-studied. This minireview summarizes the evidence for the potential role of thiamin deficiency in fetal brain development, with or without prenatal exposure to alcohol. Such evidence may influence the development of new nutritional strategies for preventing or mitigating the symptoms of FASD.

Canola meal, a by-product of oil pressing, is a rich source of phenolic antioxidants. However, its use in the food and feed sector is still limited by the need for greener, sustainable, and more cost-effective extraction methods. This study used accelerated solvent extraction (ASE) to enhance the extraction efficiency of the phenolic antioxidants. The high selectivity and short extraction time associated with ASE were ideal for obtaining high yields of these antioxidants. The structure-based activity of phenolic compounds may be influenced by the high pressure and temperature of the greener ASE process. The present study evaluated the effect of temperature (140, 160, and 180 °C) and pressure (1,500 psi) on the extraction and yield of phenolic compounds from canola meal as well as the solvent type (ethanol and methanol) and concentration (30%, 40%, 60%, and 70% v/v). Antioxidant activity was determined by 2,2-diphenyl-1-picrylhydrazyl, ferric reducing/antioxidant power assay, and ion-chelating activity. The highest yield of phenolic compounds was obtained with 70% methanol (20.72 ± 1.47 mg SAE/g DM [milligrams of sinapic acid equivalents per gram of dry matter]) and 70% ethanol (24.71 ± 2.77 mg SAE/g DM) at 180 °C temperature. A similar trend was observed for the antioxidant activity of the extracts and their total flavonoid content. The structure-based antioxidant activity of the extracts examined increased with the increase in the percentage of the extracting solvent (P > 0.05). This study established ASE as an efficient green method for extracting phenolic compounds from canola meal, with potential application for the production of natural bioactive compounds from underutilized agricultural by-products. PRACTICAL APPLICATION: ASE is an efficient eco-friendly method for extracting phenolic compounds from agricultural by-products such canola meal. Under the conditions of high pressure and temperature, ASE significantly improved the yields of phenolic compounds, sinapine, sinapic acid, and canolol. Under these conditions, water, as an extractant, was not effective in extracting sianpine. Moreover, it was much less effective than both 70% ethanol and 70% methanol in extracting sinapine or canolol. These phenolic compounds are of great interest as natural antioxidants for enhancing the shelf life of food products. They also represent new sources of neutraceuticals for improving human health.

Phenolic compounds in beer are derived from grains and hops during processing and production. Thus, the total phenolic content (TPC) of beer extracts, from selected Canadian and foreign commercial, and laboratory produced beers were examined and ranged from 3.72 ± 0.23 to 13.73 ± 0.49 mg GAE/100 mL beer. The total flavonoid content (TFC) of the same beer extracts varied from 0.82 ± 0.02 to 5.28 ± 0.04 mg CE/100 mL beer. Of particular interest were the hydroxycinnamic acids (HCAs) and derivatives in beer extracts because of their antioxidant properties. Main HCAs and a key derivative of ferulic acid, 4-vinylguaiacol (4-VG), were identified in beer extracts by high performance liquid chromatography (HPLC). Significant variations in TPC, TFC, HCAs and 4-VG content were observed among the beer extracts. Antioxidant activities of beer extracts, determined by radical scavenging and ferric-reducing assays, were positively correlated (p 0.05). The positive correlation of 4-VG with ABTS radical cation scavenging and reducing power assays is reported first time. These findings suggest that phenolic compounds and a key derivative of the hydroxycinnamic acid, 4-VG, may have the protective role in the beer as an antioxidant.

The effects of yellow mustard mucilage (YMM) on the functional and rheological properties of buckwheat and pea starch were studied. Addition of YMM resulted in a marked increase of peak viscosity for both buckwheat and pea starches. Dynamic oscillation measurements showed that the storage modulus ( G ′), loss modulus ( G ″) and dynamic viscosity ( η *) of buckwheat and pea starches were increased but tangent δ was decreased by addition of YMM. The gel textures of both starches were markedly changed by the presence of YMM, which resulted in an increase of hardness, adhesiveness and chewiness but a decrease of resilience. Differential scanning calorimetry showed that the presence of YMM slightly increased melting enthalpy (Δ H ) and the phase transition temperature range ( T c – T o ) of buckwheat starch but these did not change much for pea starch. Addition of YMM–locust bean gum mixture (9:1) similarly increased the viscosity of buckwheat and pea starches but decreased gel hardness. The swelling powers of both starches and solubility of buckwheat starch were slightly decreased in the presence of YMM. Addition of YMM slowed the syneresis of buckwheat and pea starch gels.

The effect of yellow mustard mucilage (YMM) on gelatinization and retrogradation of wheat and rice starches were studied. Considerable interactions were observed between YMM and wheat and rice starches which were accompanied by a marked increase in viscosity. DSC studies showed that the presence of YMM did not affect peak gelatinization temperature (Tp) of wheat and rice starches, but slightly increased melting enthalpy (ΔH) and the phase transition temperature range (Tc−T0). Addition of YMM markedly changed wheat and rice starch gel textures by increasing hardness, adhesiveness, chewiness and springiness. The addition of YMM–locust bean gum (LBG) mixture (9:1) similarly increased the viscosity of wheat and rice starches but decreased gel hardness. The swelling power as well as solubilized starch and amylose were decreased for both starches in the presence of YMM. Syneresis in wheat and rice starches was also decreased by the presence of YMM.

Copyright: © 2012 Eskin NAM. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Oxidative stress is involved in the development of many chronic diseases including cancer. It has been defined as an imbalance between the level of pro-oxidants (reactive oxygen species, ROS) produced during normal metabolism and the organism’s endogenous antioxidant defence system. The role of various natural antioxidant defence systems to minimize oxidative damage caused by these free radicals was established using animal models in which these defence systems were knocked out [1]. This resulted in the promotion of cancer which was attributed to DNA damage by the formation of 8-hydroxy2-deoxyguanosine (8OHdg). Consequently, a concerted effort has been made to establish the efficacy of such traditional antioxidants as vitamins A, E and C, as well as a search for new antioxidants to minimize such damage. Over 200 epidemiological studies strongly associated low consumption of fruits and vegetables with the incidence of cancer suggesting that antioxidants might be a solution [2]. Consequently, should cancer patients be encouraged to take multivitamin supplements as part of their therapy?

This chapter provides an in-depth review of the biochemical changes involved in the conversion of muscle into edible meat and fish. Major advances in our understanding of the nature and structure of muscle over the past two decades have been incorporated into this chapter. The latest information on the mechanisms of postmortem tenderization is included, focusing on the involvement of lysosomal cathepsin, calpains, and proteasomes. The chapter concludes with a comprehensive discussion of meat and fish pigments, including a detailed review of the structure of myoglobins and effective methods of preservation.

The effects of haze composition variation on sedimentation phenomenon in canola oil were studied. Comparisons were made of the physical properties between an oil sediment (S5) and the high- and low-melting fractions obtained by step crystallisation at 32 and 5 °C (F32 and F5). The phase transition behaviour and crystalline characteristics of the sediments were examined by differential scanning calorimetry (DSC), hot-stage microscopy, spectrophotometry, and X-ray diffraction (XRD). The compositions of the sediments were determined by GC-MS. The melting behaviour of S5 resembled that of F5, whereas S5 behaved more like F32 in crystallisation. Oils containing F32 clouded much faster than oils containing F5. The interfacial surface free energies and the XRD patterns were similar for the two fractions, suggesting identical crystalline structures. The molecular origin of the varied phase transition behaviour of the sediments was attributed to the composition variation in waxes, particularly the acid component in the materials.

Volatiles obtained from distillation of Dwarf quince (Chaenomeles japanica) were analyzed by gas chromatography-mass spectrometry. Twenty-one compounds including 7 esters, 7 alcohols, 4 terpenes and 3 miscellaneous were identified. In addition, 2 nonvolatile sugar alcohols, mannitol (16.4% of the total) and sorbitol (30% of the total), were also identified. Aromagrams indicated that esters and alcohols contributed to the fruity flavor of Dwarf quince.