Two-dimensional quantitative nuclear magnetic resonance (2D qNMR)-based metabolomics was performed to understand characteristic metabolic profiles in different aging regimes (crust from dry-aged beef, inner edible flesh of dry-aged beef, and wet-aged beef striploin) over 4 weeks. Samples were extracted using 0.6 M perchlorate to acquire polar metabolites. Partial least squares-discriminant analysis showed a good cumulative explained variation (R² = 0.967) and predictive ability (Q² = 0.935). Metabolites of crust and aged beef (dry- and wet-aged beef) were separated in the first week and showed a completely different aspect in the second week via NMR-based multivariable analyses. Moreover, NMR-based multivariable analyses could be used to distinguish the method, degree, and doneness of beef aging. Among them, the crust showed more unique metabolic changes that accelerated proteolysis (total free amino acids and biogenic amines) and inosine 5′-monophosphate depletion than dry-aged beef and generated specific microbial catabolites (3-indoxyl sulfate) and γ-aminobutyric acid (GABA), while asparagine, glutamine, tryptophan, and glucose in the crust were maintained or decreased. Compared to the crust, dry-aged beef showed similar patterns of biogenic amines, as well as bioactive compounds and GABA, without a decrease in free amino acids and glucose. Based on these results, the crust allows the inner dry-aged beef to be aged similarly to wet-aged beef without microbial effects. Thus, 2D qNMR-based metabolomic techniques could provide complementary information about biochemical factors for beef aging.

The objective of this study was to investigate the effects of canola and flaxseed oils on the physicochemical properties and sensory quality of emulsion-type sausage made from spent layer meat. Three types of sausage were manufactured with different fat sources: 20% pork back fat (CON), 20% canola oil (CA) and 20% flaxseed oil (FL). The pH value of the CA was significantly higher than the others (p<0.05). The highest water holding capacity was also presented for CA; in other words, CA demonstrated a significantly lower water loss value among the treatments (p<0.05). CA had the highest lightness value (p<0.05). However, FL showed the highest yellowness value (p<0.05) because of its own high-density yellow color. The texture profile of the treatments manufactured with vegetable oils showed higher values than for the CON (p<0.05); furthermore, CA had the highest texture profile values (p<0.05) among the treatments. The replacement of pork back fat with canola and flaxseed oils in sausages significantly increased the omega-3 fatty acid content (p<0.05) over 15 to 86 times, respectively. All emulsion sausages containing vegetable oil exhibited significantly lower values for saturated fatty acid content and the omega-6 to omega-3 ratios compared to CON (p<0.05). The results show that using canola or flaxseed oils as a pork fat replacer has a high potential to produce healthier products, and notably, the use of canola oil produced characteristics of great emulsion stability and sensory quality.

In this study, we investigated the antimicrobial effects of plasma activated fine droplet (PAD) produced from arc discharge plasma on planktonic Listeria monocytogenes and Escherichia coli O157:H7. NaCl (0.9%, w/v) was used as the feeding solution for the plasma discharge. The inactivation mechanism of the PAD treatment was also investigated. PAD mainly contains H ₂ O ₂ and OCl ⁻ , which play a significant role in the inactivation process against L. monocytogenes and E. coli O157:H7. The population of L. monocytogenes and E. coli O157:H7 was significantly reduced by approximately 3 and 4 log units, respectively, within 5 min of exposure to PAD. However, the bactericidal effects of PAD against L. monocytogenes and E. coli O157:H7 showed different trends by showing 0.58 and 4.13 log reductions, respectively, after 1 min of PAD exposure time. The change of membrane integrity was evaluated using two DNA-binding fluorescence dyes, SYTO 9 and propidium iodide (PI). The breakage of the cell wall and membrane of both microorganisms was evidenced by the uptake of PI by cells after 5 min of exposure to PAD, but the effect was less in L. monocytogenes compared to E. coli O157:H7 after 1 min of PAD exposure time. The transmission electron microscopy results clearly showed morphological changes in both microorganisms, including denaturation or leakage of intracellular materials as a consequence of PAD treatment. These findings suggest that PAD-induced chemical species can eventually affect the intracellular materials of bacterial cells by passing through or attacking the cell envelope. In addition, L. monocytogenes are less susceptible to PAD compared with E. coli O157:H7.

The key reactive species generated by non-thermal plasma bubbles for the inactivation of Salmonella Typhimurium and the effects of organic matter on the inactivation efficacy were investigated. Plasma, which is primarily composed of ozone (O₃), was generated by dielectric barrier discharge and injected into a solution (400 mL) as a bubble. The surviving population of S. Typhimurium decreased in proportion to the treatment time, resulting in a 5.29 log reduction after 5 min of treatment. Verification tests to specify key reactive species were conducted using an O₃ destruction unit and reactive oxygen species scavengers. The results indicated that singlet oxygen (¹O₂) contributes substantially to the inactivation of S. Typhimurium, and that the presence of superoxide anion radicals (O₂^·−) from O₃ is essential for the production of ¹O₂. When a S. Typhimurium suspension containing organic matter (final concentration: 0, 0.005, 0.05, 0.1, and 0.5 g/L), consisting of beef extract and peptone, was treated with plasma bubbles for 5, 10, 15, 20, 25, and 30 min, respectively, the potential of the plasma bubbles for inactivating S. Typhimurium successfully was verified with longer contact time, despite organic matter attenuating the inactivation efficiency in a dose-dependent manner.

Objective: This study observed the effects of cooking method and final core temperature on cooking loss, lipid oxidation, aroma volatiles, nucleotide-related compounds and aroma volatiles of Hanwoo brisket (deep pectoralis). Methods: Deep pectoralis muscles (8.65% of crude fat) were obtained from three Hanwoo steer carcasses with 1(+) quality grade. Samples were either oven-roasted at 180 degrees C (dry heat) or cooked in boiling water (moist heat) to final core temperature of 70 degrees C (medium) or 77 degrees C (well-done). Results: Boiling method reduced more fat but retained more moisture than did the oven roasting method (p<0.001), thus no significant differences were found on cooking loss. However, samples lost more weight as final core temperature increased (p<0.01). Further, total saturated fatty acid increased (p = 0.02) while total monounsaturated fatty acid decreased (p = 0.03) as final core temperature increased. Regardless the method used for cooking, malondialdehyde (p<0.01) and free iron contents (p<0.001) were observed higher in samples cooked to 77 degrees C. Oven roasting retained more inosinic acid, inosine and hypoxanthine in samples than did the boiling method (p<0.001), of which the concentration decreased as final core temperature increased except for hypoxanthine. Samples cooked to 77 degrees C using oven roasting method released more intense aroma than did the others and the aroma pattern was discriminated based on the intensity. Most of aldehydes and pyrazines were more abundant in oven-roasted samples than in boiled samples. Among identified volatiles, hexanal had the highest area unit in both boiled and oven-roasted samples, of which the abundance increased as the final core temperature increased. Conclusion: The boiling method extracted inosinic acid and rendered fat from beef brisket, whereas oven roasting intensified aroma derived from aldehydes and pyrazines and prevented the extreme loss of inosinic acid.

This study investigated the optimum conditions to maximize the inactivation of biofilms using both plasma-treated solutions and post-treatment storage conditions. Chemical properties of plasma-treated solutions were also analyzed to identify their possible biofilm inactivation mechanisms. Escherichia coli O157:H7 biofilms on stainless steel were prepared and immersed in distilled water (DW), 100 ppm of sodium chloride solution (NaCl), or 100 ppm of sodium hypochlorite solution (NaOCl), followed by container-type plasma treatment for 10 min (15 kHz and 250 W). After plasma discharge was switched off, biofilms immersed in the plasma-treated solution were stored for 10 min with the plasma apparatus closed or open. The log reduction of E. coli O157:H7 was NaOCl (3.58) > NaCl (2.06) = DW (1.95) in the closed storage condition. In addition, the bactericidal effect of NaOCl was higher in the closed condition than in the open condition. Concentrations of the hydroxyl radical (OH·) and peroxynitrite (ONOO⁻) were also the highest for NaOCl in the closed condition. Consequently, plasma treatment using NaOCl solution in the closed condition was found to be the optimum method for inactivation of E. coli O157:H7 biofilms, due to high hydroxyl radical and peroxynitrite concentrations. This method also has the merit of using a lower concentration of NaOCl than that used typically in industry.