Jianjun Yang , Zhi Zhao , Liang Zhao , Yue Sang , Yongxiang Zhang , Jing Zhan , Baochao Hou , Yangyang Yu , Pengjie Wang , Xiaoxia Li , Ran Wang
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Abstract
Post-acidification remains a persistent quality defect in yogurt production. Enzymatic intervention can modulate it by regulating microbial metabolism. This study evaluated 0.00–0.12 U/mL protein glutaminase (PG) effects on post-acidification through fermentation kinetics and organic acid analysis. Notably, 0.06 U/mL PG controlled acidification, showing a Δ7 °T acidity increase and 9.06 mg/g lactic acid over 14-day storage, enhancing water holding capacity, viscosity, texture, and casein matrix compactness. Metabolomic and peptidomic analyses showed PG at this dose increased peptide concentration to 24.31 μg/μL, modifying 26 amino acids/small peptides (54.54 % tripeptides). After 14 days, enriched amino acids were linked to amino acid and fatty acid biosynthesis pathways. Gene-level investigations revealed upregulated arginine (argJ –H , 1.1–17.5-fold) and fatty acid synthesis genes (accA –fabK , 1.0–6.0-fold) in starter cultures, increasing membrane UFA/SFA ratios. Collectively, 0.06 U/mL PG treatment enhanced polypeptide levels, activated pathways for arginine, polyamines, and fatty acids, improved membrane fluidity, reduced post-acidification, and enhanced yogurt quality.
蛋白质-谷氨酰胺酶衍生的小肽通过激活精氨酸-脂肪酸代谢途径减轻酸奶中的后酸化
后酸化是酸奶生产中一个持续存在的质量缺陷。酶的干预可以通过调节微生物代谢来调节它。本研究通过发酵动力学和有机酸分析,评价了0.00-0.12 U/mL谷氨酰胺酶(PG)对后酸化的影响。值得注意的是,0.06 U/mL PG控制酸化,在14天的储存中显示出Δ7°T的酸度增加和9.06 mg/g的乳酸,增强了保水能力、粘度、质地和酪蛋白基质致密性。代谢组学和肽组学分析表明,PG使肽浓度增加到24.31 μg/μL,修饰了26个氨基酸/小肽(54.54%的三肽)。14天后,富集的氨基酸与氨基酸和脂肪酸的生物合成途径相连。基因水平研究显示,发酵剂中精氨酸(argJ-H, 1.1 - 17.5倍)和脂肪酸合成基因(accA-fabK, 1.0 - 6.0倍)上调,增加了膜UFA/SFA比率。总的来说,0.06 U/mL PG处理提高了多肽水平,激活了精氨酸、多胺和脂肪酸的途径,改善了膜流动性,减少了后酸化,提高了酸奶质量。
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