Food research international (Ottawa, Ont.)最新文献

Ya'an Tibetan tea, a dark tea with a rich historical heritage, is typically processed using two primary piling fermentation methods: wet piling with rolled leaves (moisture content around 60%) and dry piling with sun-dried or baked green tea leaves (moisture content below 30%). This study employed sensory evaluation, targeted and non-targeted metabolomics, and fungal Internal Transcribed Spacer (ITS) sequencing to investigate changes in quality components and fungal composition in Tibetan tea processed by both wet and dry-piling methods. The results revealed that 3,7-Dimethyl-1,5,7-octatriene-3-ol and D-limonene were identified as key volatile metabolites contributing to the aroma variations between the dry and wet-piled teas. More pronounced differences were observed in non-volatile components, with 407 differential metabolites identified between the wet- and dry-piled teas. Linear discriminant analysis effect size (LEfSe) identified Rhizomucor, Aspergillus, Thermomyces, Setophoma, and Debaryomyces as the key fungal genera with significant differences between the two piling methods, also dominating in abundance and playing a crucial role in the fermentation process of Tibetan tea. Correlation analysis between microbial communities and differential metabolites showed that Debaryomyces, Thermomyces, and Setophoma were significant contributors to the aroma differences between the teas produced by the two piling methods, while Rhizomucor and Aspergillus had a greater influence on non-volatile metabolites. Since Rhizomucor and Aspergillus were the most dominant fungi in the wet (63.05%) and dry-piled (68.70%) samples, respectively, and showed opposite correlations with major non-volatile differential metabolites, they may underlie the flavor differences between the two piled teas, such as mellowness, thickness, and sweet aftertaste. This study sheds light on the chemical and fungal mechanisms underlying the quality formation of Ya'an Tibetan tea processed by wet and dry piling methods, providing theoretical guidance for the improvement, standardization, and potential enhancement of production efficiency of Ya'an Tibetan tea production.

Consumption of healthy diets with low environmental impact is crucial for improving global health. Legumes, like chickpeas, serve as valuable meat alternatives due to their nutritional profile, which may be improved through fermentation. This study aimed to develop innovative fermented chickpea flours using lactic acid bacteria (LAB) strains from diverse ecosystems and evaluate their nutritional and functional properties in vitro. Fourteen batches of 20% chickpea-based puree were produced and fermented with 14 LAB isolated from different ecosystems. After fermentation, flours were obtained by freeze-drying. Most LAB grew well and reduced the pH of chickpea purees below 5 within 48 h. The flours were characterized for the content of polyphenols, bioactive peptides (BAPs), free amino groups (FAG), and phytic acid along with the total antioxidant capacity (TAC). Results showed that flours fermented by four LAB strains, including Enterococcus hirae and Enterococcus faecium had higher FAG and BAPs, including inhibitors of Dipeptidyl peptidase-IV and Angiotensin-converting enzyme. Flours fermented by Leuconostoc mesenteroides OM94, Lactiplantibacillus plantarum 299v, Lactiplantibacillus plantarum E75, Lactiplantibacillus plantarum LPPB, and Lacticaseibacillus casei LBC491 contained higher amounts of polyphenols, had soluble TAC that was 10-fold and direct TAC 3-fold higher, and lower phytic acid content than the control flour. Pyrogallol was detected in fermented products for the first time, and protocatechuic 4-O-glucoside increased three times in chickpea flours fermented by Leuconostoc mesenteroides OM94 compared to the control. In conclusion, fermentation improved the nutritional and functional qualities of chickpea flour, identifying promising LAB strains to enhance antioxidant capacity and polyphenols availability.

This study explored how setting conditions affect the gel properties of shrimp surimi from Solenocera crassicornis using a two-step heating process with varying temperatures (30, 40, 50 °C) and durations (0-120 min). At 30 °C, increased hydrogen bonds and cross-linking promoted macromolecular polymer formation, with optimal elasticity achieved at 15-30 min, but longer times led to gel aggregation and uneven structure. At 40 °C, macromolecular polymer decreased, while sulfhydryl groups increased, leading to disulfide bond formation, which disrupted hydrogen bonds and increased hydrophobic groups. Gel strength decreased over setting time, with a soft and smooth texture observed after 15-30 min. Setting at 50 °C disrupted chemical bonds, exposed hydrophobic groups, and resulted in less significant changes in storage modulus and loss modulus. After high-temperature gelation at 90 °C, disulfide bonds were further disrupted, reducing the stability of gel properties. Moreover, an increase in the setting temperature affected the internal water distribution within the shrimp surimi gel. A shorter setting time promoted the absorption of water molecules by starch in the gel, thereby reducing the free water content. However, when the setting time exceeded 60 min, the proportions of bound water and immobile water decreased, gradually transforming into free water. This transformation increased the drip loss and softened the texture of gel. In summary, setting conditions significantly influenced moisture distribution, viscoelasticity, and chemical forces in shrimp surimi gels.

This study aimed to generate new functional ingredients from microalgae and wine pomace through starter-assisted fermentation. Five lactic acid bacteria (LAB) and five yeasts were variously chosen for their species diversity, origin, and metabolic potential. During fermentation, the combination of Chlorella vulgaris and wine pomace overcame the limited growth observed in pomace substrate, with all LAB and yeasts effectively utilizing sugars and synthesizing microbial metabolites. Additionally, the synergistic interplay between the substrates, alongside the enzyme specificity of the starter cultures, improved the bioavailability of phenolic compounds, particularly flavanols, flavonols, and procyanidins, while simultaneously generating unique peptides in the formulated ingredients. In some cases, these metabolic changes were associated with enhanced antioxidant activity, improved protein digestibility, and overall protein quality. Our findings highlighted the potential of fermented mixed substrates as new functional ingredients, with promising health-promoting benefits and significant potential for applications in the food industry.

Lactiplantibacillus plantarum and Staphylococcus xylosus are common starters for fermented sausages. Several studies have demonstrated the impact of these two strains on the quality of fermented sausages. However, the mechanism underlying the effects of these two microorganisms on co-cultivation in sausages remains unclear. This study aimed to investigate the effects of inoculation with various combinations of starters on the microbial communities and metabolic profiles of fermented sausages. High-throughput sequencing revealed that, during sausage fermentation, Firmicutes was the dominant bacterial phylum, and the primary microorganisms were Lactococcus, Staphylococcus, Lactobacillus, and Pseudomonas. On the last day of fermentation, the highest abundance of Staphylococcus was observed in the co-inoculation group. Furthermore, inoculated fermentation effectively inhibited the growth of pathogenic and spoilage bacteria. Metabolomic analysis of the four groups of samples identified 208 metabolites in positive ion mode and 109 in negative ion mode. A total of 31 differential metabolites were identified (P < 0.05, variable importance in the projection >1.5), primarily benzene and substituted derivatives, carboxylic acids and derivatives, and fatty acyls. Five crucial differential metabolites (subaphylline, naringenin, 1-hexadecanol, beta-alanyl-L-lysine, and 3'-AMP) were identified as potential biomarkers for fermented sausages. Key differential metabolite metabolic pathways indicated that L. plantarum YR07 dominated in metabolite regulation during sausage fermentation, and S. xylosus Y-18 downregulated the fatty acid degradation pathway, which also affected the metabolism of fermented sausages. Co-cultivation of the two bacteria exhibited a synergistic effect on the metabolism of the fermented sausages. This study offers further insights into improving the quality of fermented sausages, thereby establishing a theoretical foundation for the production of excellent fermenters.

Drying is the step that is to be used to adjust and control the formation of flavour and quality in black tea processing. In the present work, the comprehensive two-dimensional gas chromatography with mass spectrometry (GC × GC-MS) and gas chromatography olfactometry with mass (GC-O-MS) were used to determine the dynamic change of the volatile compounds in black tea during drying at 90, 120, 150 °C for 1 h. Results showed that the ratio of esters and aldehydes largely declined when temperature was elevated from 90 °C to 150 °C, while the ratio of heterocycles was increased to 22.4 % from 16.5 %. A total of 15 key aroma activity volatiles were screened out in three temperature dried samples, therein 11 volatiles were connected with the Maillard reaction, meaning these volatiles were highly relevant to the degradation of amino acids during the drying process. We detected that 21 amino acids were decreased with enhanced temperature and extended the drying time, which promoted the Maillard-derived volatiles formation. Therefore, it was suggested that to control the degradation of amino acids adjust the flavour profiles of black tea by changing the drying temperature and time.

Galactomannan comes from a wide range of plant resources and has some biological activities, but its bioavailability is limited due to its large molecular weight and complex structure. In this study, three degradation methods (H₂O₂, ultrasound, and β-mannanase) combined with ethanol fractional precipitation (25 %, 50 %, and 75 %) were used to degrade and separate Gleditsia sinensis galactomannans (GSG), and the physicochemical properties and biological activities of GSG after degradation were analyzed. Comprehensive comparison indicates that H₂O₂ exhibits had a better degradation effect. After 4 h of degradation using 4 % H₂O₂, the yield of GSG precipitated with 50 % ethanol was 37.06 % (the yield of undigested GSG is 1.80 %). Simultaneously, the molecular weight (reduced from 225.25 to 36.87 kDa) and viscosity were significantly reduced under this condition, while the solubility was increased. In addition, the low-molecular-weight GSG (LGSG) obtained by 4 % H₂O₂/50 % ethanol showed the strongest free radical scavenging activity in vitro. Furthermore, the results of in vivo antioxidant assays showed that LGSG inhibited Aflatoxin B1-induced developmental toxicity by regulating gene expression in the Keap1/Nrf2 pathway. LGSG also promoted Nrf2-mediated expression of the lipid metabolism genes ppar-α and cpt1, while suppressing expression of the fatty acid synthesis genes fas and scd-1. Therefore, the liver recovered from lipid peroxidation induced nonalcoholic fatty liver disease (NAFLD). The present study introduces a method for green and efficient preparation of LGSG, indicates its potential as a nutritional product.

With an ever-increasing global population and dwindling natural resources, a shift towards more sustainable food systems is required. Important aspects to aid in this transition are the reduction of food waste, and a movement towards non-animal protein sources. Brewers spent yeast (BSY) is an abundant by-product of the brewing industry, which is generally regarded as waste, despite its high nutritional value. Previous work has shown that fermentation of BSY with Lactobacillus amylovorus FST 2.11 resulted in changes in composition, functionality, and improved palatability of the processed raw material (PBSY). In this study, in vitro protein digestibility, amino acid bioaccessability, and protein quality of PBSY was explored using the static INFOGEST in vitro model. In vitro protein digestibility of PBSY (73.0 %) was almost two-fold higher than that of CBSY (40.0 %), while PBSY also displayed significantly higher in vitro bioaccessability values for all essential amino acids, except for tryptophan. Investigation of protein quality using the digestible indispensable amino acid score (DIAAS) values and the FAO recommended amino acid scoring pattern for individuals >3 years old showed that the protein quality for CBSY was low (DIAAS of 17.0 %), while PBSY was considered to be of "good" protein quality (DIAAS of 98.2 %). Investigation of the modulation potential of PBSY on the gut microbiome using an in vitro colon model system showed an increase in gut microbiome α-diversity indices and an abundance of beneficial Mediterranean diet-responsive taxa after 24 h. Overall, this study highlights the potential of BSY as raw material for the production of a high-quality food ingredient with potential prebiotic effects, aiding in the reduction food waste and supporting global food systems.

Fermented foods of the Indian Himalaya are unexplored functional resources with high nutritional potential. Chhurpi cheese, fermented by defined native proteolytic lactic acid bacteria of Sikkim was assessed for ACE inhibitory, HOCl reducing, and MPO inhibitory, activity across varying stages of gastrointestinal (GI) digestion. The enhanced bioactivity of Lactobacillus delbrueckii WS4 chhurpi was associated with the generation of bioactive and multifunctional peptides during fermentation and GI digestion. Qualitative and quantitative in silico tools were employed for prediction of ACE inhibitory activity of novel chhurpi peptides. Selected peptides, with highest predictive ACE inhibitory potential were synthesized and in vitro validation revealed the ACE inhibitory potential of peptides HPHPHLSFM and LKPTPEGDL. LKPTPEGDL showed the most potent ACE inhibitory activity (IC₅₀ of 25.82 ± 0.26 µmol) which slightly decreased upon GI digestion. The peptides demonstrated a non-competitive type mixed ACE inhibition modality. Furthermore, the two peptides exerted observable HOCl reducing and MPO inhibitory activity, demonstrating their antioxidative potential. HPHPHLSFM exhibited superior HOCl reduction (EC₅₀ of 0.29 ± 0.01 mmol), while LKPTPEGDL demonstrated higher MPO (IC₅₀ of 0.29 ± 0.01 mmol) inhibition. Molecular docking of the two peptides with MPO revealed proline and aspartate near peptidyl C-terminus to bind with enzyme catalytic residues. This study presents the first peptidome analysis of chhurpi produced through controlled fermentation and identifies novel peptides with MPO and ACE inhibitory activity. Furthermore, it marks the first synthesis and in vitro bioactivity validation of bioactive peptides from chhurpi cheese, highlighting its multifunctional potential.

Maillard reaction products (MRPs) were prepared at high temperatures using soybean protein hydrolysates (SPH) and reducing pentose (xylose and arabinose), hexose (galactose and glucose), and disaccharide (maltose), and their potential as flavoring in plant protein foods was evaluated. The results indicated that, after sugar was involved in the reaction, the unfolding of proteins enabled aromatic amino acid residues to enter a more hydrophobic environment, contributing to the reduction of bitterness in MRPs and formation of caramelization. This effect was partially attributed to the interaction forces, hydrogen bonds and van der Waals forces, that existed between the sugars and SPH involved in Maillard reaction. More basic amino acid residues interacted with pentose during the reaction, which exhibited faster reaction rate and promoted the formation of pyrazines and oxygen containing compounds, thereby contributing to meaty, roasted and caramelized flavors. Trimethyl pyrazine, 3-ethyl-2,5-dimethylpyrazine, 2-methylpyrazine, and 2-heptanone were the most abundant in pentose MRPs, and these volatile compounds were positively correlated with umami and richness. Overall, MRPs prepared with arabinose may serve as a potential meaty flavoring with notable umami, and hexose contributed to the enrichment of nutty flavor profiles, while the MRPs formed by disaccharide exhibited the characteristics of superior fruity aromas. MRPs from different reducing sugar may be used to develop different food ingredients.