Biogenic Amine Formation in Artisan Galotyri PDO Acid-Curd Cheeses Fermented with Greek Indigenous Starter and Adjunct Lactic Acid Bacteria Strain Combinations: Effects of Cold (4 °C) Ripening and Biotic Factors Compromising Cheese Safety

Charikleia Tsanasidou, L. Bosnea, A. Kakouri, J. Samelis
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Abstract

The formation of biogenic amines (BAs) in artisan Galotyri PDO cheeses fermented with Sterptococcus thermophilus ST1 and the Greek indigenous nisin A-producing Lactococcus lactis spp. cremoris M78 (A1cheese), or with the A1 starter supplemented with either the enterocin A-B-P-producing Enterococcus faecium KE82 (A2cheese) or the multi-functional Lactiplantibacillus plantarum H25 (A4cheese) adjunct strains was evaluated. Three pilot-scale cheese trials, GL1, GL2, and GL3, made from boiled ewes’ milk, were analyzed for their BA contents before and after cold ripening at 4 °C for 30 days. Total BAs of the fresh GL1 and GL3 cheeses (pH 4.3–4.5) were below 50 mg/kg, except for the A1/GL1 and A1/GL3 cheeses, which contained ca. 300 mg/kg (81.2% histamine) and 1250 mg/kg (45.6% putrescine) BAs, respectively. Whereas due to an outgrowth (>7 log cfu/g) of post-thermal Gram-negative bacteria contaminants during fermentation, most fresh GL2 cheeses (pH 4.7–5.0) accumulated more than 1500 mg/kg of total BAs, which exceeded 3800 mg/kg in all GL2 cold-ripened cheeses due to major increases in cadaverine and putrescine. Tyramine and histamine exceeded 500 mg/kg in the fresh A1/GL2cheeses. Conversely, total BAs remained or declined below 50 mg/kg in all cold-ripened GL3 cheeses. None of the starter or adjunct cultures could be correlated with a specific BA increase, despite E. faecium KE82, which increased at 7.6–9.2 log cfu/g in the A2 cheeses is a strong tyramine producer in culture BA broth with 1% tyrosine in vitro. The adoption of strict hygienic measures during artisan Galotyri PDO cheese production (trial GL3) enabled the best performance of all starter LAB strain combinations and reduced BA formation, whereas the high presence of Gram-negative decarboxylating bacteria contaminants compromised cheese (trial GL2) safety.
使用希腊本土起始菌和辅助乳酸菌株组合发酵的手工制作的 Galotyri PDO 酸凝乳干酪中生物胺的形成:低温(4 °C)熟化和影响奶酪安全的生物因素的影响
用嗜热链球菌 ST1 和希腊本土产尼生素 A 的乳球菌 cremoris M78(A1cheese)发酵,或用 A1 发酵剂辅以产肠球菌 A-B-P 的粪肠球菌 KE82(A2cheese)发酵,手工制作的 Galotyri PDO 奶酪中生物胺(BAs)的形成情况。在对 A1 发酵剂与嗜热链球菌 ST1 和希腊本土产尼生素 A 的乳球菌 cremoris M78(A1 奶酪)进行发酵,或在 A1 发酵剂中添加产肠球菌毒素 A-B-P 的粪肠球菌 KE82(A2 奶酪)或多功能植物乳杆菌 H25(A4 奶酪)辅助菌株进行发酵的结果进行了评估。在 4 °C 冷熟化 30 天之前和之后,对用煮沸的母羊奶制成的三种试验性奶酪 GL1、GL2 和 GL3 的 BA 含量进行了分析。新鲜的 GL1 和 GL3 奶酪(pH 值为 4.3-4.5)的 BA 总含量低于 50 毫克/千克,但 A1/GL1 和 A1/GL3 奶酪除外,它们的 BA 含量分别为约 300 毫克/千克(组胺含量为 81.2%)和 1250 毫克/千克(腐胺含量为 45.6%)。而由于发酵过程中热后革兰氏阴性菌污染物的大量繁殖(>7 log cfu/g),大多数新鲜的 GL2 奶酪(pH 值为 4.7-5.0)都积累了超过 1500 毫克/千克的 BAs 总量,由于尸胺和腐胺的大量增加,所有 GL2 冷熟化奶酪的 BAs 总量都超过了 3800 毫克/千克。在新鲜的 A1/GL2 奶酪中,酪胺和组胺的含量超过了 500 毫克/千克。相反,在所有冷熟化的 GL3 奶酪中,BA 总量保持或下降到 50 毫克/千克以下。尽管粪肠球菌 KE82 在 A2 奶酪中以 7.6-9.2 log cfu/g 的速度增长,但在体外含 1%酪氨酸的 BA 培养液中,粪肠球菌 KE82 是一种很强的酪氨酸生产者。在 Galotyri PDO 手工奶酪生产过程中采取严格的卫生措施(试验 GL3)可使所有起始 LAB 菌株组合发挥最佳性能并减少 BA 的形成,而革兰氏阴性脱羧菌污染物的大量存在则影响了奶酪(试验 GL2)的安全性。
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