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首页> 外文期刊>Le Lait >Impact of broken cells of lactococci or propionibacteria on the ripeningof Saint-Paulin UF-cheeses: extent of proteolysis and GC-MS profiles
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Impact of broken cells of lactococci or propionibacteria on the ripeningof Saint-Paulin UF-cheeses: extent of proteolysis and GC-MS profiles

机译:乳球菌或丙酸杆菌破碎细胞对圣保林超滤奶酪成熟的影响:蛋白水解程度和GC-MS谱

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UF-cheeses have been successfully developed in many countries. However, proteolysis and the general extent of ripening were shown to be far slower compared to traditional varieties. The absence of starter lysis has been cited as a plausible explanation. In this work, propionibacteria and lactococci cells were disrupted using a new pilot homogenizer. Crude broken suspension (CBS), or cell-free extract (CFE), obtained after centrifugation, were added to UF-St Paulin retentate (concentration factor 6) made with a usual lactic starter. RO water was added to the control. Proteolysis was estimated by NCN, NPN and free amino acids. Neutral volatile compounds were determined by GC-MS. A low extent of ripening was noted in the control and the absence of starter lysis was effectively proved using immunodetection of lactococci cytoplasmic proteins. The addition of lactococci CBS or CFE increased free amino acid content (1.5 to 3 times) whereas propionibacteria CBS or CFE exhibited no significant increase, even when cheeses were ripened at 20 degreesC instead of 12 degreesC. By contrast, addition of propionibacteria CBS generated a significant increase in several volatile compounds like alcohols and ketones, whereas CFE did not, showing that the presence of live cells was required to form these compounds. CBS or CFE of lactococci did not significantly change the volatile compound profile. In conclusion, it was possible to influence the ripening of UF-cheese by the addition of crude broken bacterial cell suspensions. Other strains and species should now be investigated.
机译:UF奶酪已经在许多国家成功开发。然而,与传统品种相比,蛋白水解和成熟的一般程度要慢得多。缺乏起始剂裂解被认为是合理的解释。在这项工作中,使用新型先导匀浆器破坏了丙酸杆菌和乳球菌细胞。将离心后获得的粗碎悬浮液(CBS)或无细胞提取物(CFE)添加到用常规乳酸发酵剂制成的UF-St Paulin渗余液中(浓缩系数6)。将RO水添加至对照。通过NCN,NPN和游离氨基酸评估蛋白水解。通过GC-MS测定中性挥发性化合物。在对照组中注意到成熟程度低,并且通过乳球菌胞质蛋白的免疫检测有效地证实了发酵剂不存在。乳球菌CBS或CFE的添加增加了游离氨基酸含量(1.5到3倍),而丙酸杆菌CBS或CFE则没有显示出明显的增加,即使奶酪在20摄氏度而不是12摄氏度下熟化也是如此。相比之下,丙酸杆菌CBS的添加显着增加了几种挥发性化合物(如醇和酮)的含量,而CFE却没有,表明形成这些化合物需要存在活细胞。乳球菌的CBS或CFE并未显着改变挥发性化合物的特性。总之,有可能通过添加粗碎细菌细胞悬浮液来影响超滤奶酪的成熟。现在应调查其他菌株和物种。

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