Noutsopoulos Dimitrios, Kakouri Athanasia, Kartezini Eleftheria, Pappas Dimitrios, Hatziloukas Efstathios, Samelis John
1 Dairy Research Institute, General Directorate of Agricultural Research, Hellenic Agricultural Organization DEMETER, Ethnikis Antistaseos 3, Katsikas, 45221 Ioannina, Greece.
2 Department of Biological Applications and Technology, University of Ioannina, 45110 Ioannina, Greece; and.
J Food Prot. 2017 Dec;80(12):2137-2146. doi: 10.4315/0362-028X.JFP-17-245.
This study evaluated in situ expression of the nisA gene by an indigenous, nisin A-producing (NisA+) Lactococcus lactis subsp. cremoris raw milk genotype, represented by strain M78, in traditional Greek Graviera cheeses under real factory-scale manufacturing and ripening conditions. Cheeses were produced with added a mixed thermophilic and mesophilic commercial starter culture (CSC) or with the CSC plus strain M78 (CSC+M78). Cheeses were sampled after curd cooking (day 0), fermentation of the unsalted molds for 24 h (day 1), brining (day 7), and ripening of the brined molds (14 to 15 kg each) for 30 days in a fully controlled industrial room (16.5°C; 91% relative humidity; day 37). Total RNA was directly extracted from the cheese samples, and the expression of nisA gene was evaluated by real-time reverse transcription PCR (qRT-PCR). Agar overlay and well diffusion bioassays were correspondingly used for in situ detection of the M78 NisA+ colonies in the cheese agar plates and antilisterial activity in whole-cheese slurry samples, respectively. Agar overlay assays showed good growth (>8 log CFU/g of cheese) of the NisA+ strain M78 in coculture with the CSC and vice versa. The nisA expression was detected in CSC+M78 cheese samples only, with its expression levels being the highest (16-fold increase compared with those of the control gene) on day 1, followed by significant reduction on day 7 and almost negligible expression on day 37. Based on the results, certain intrinsic and mainly implicit hurdle factors appeared to reduce growth prevalence rates and decrease nisA gene expression, as well as the nisin A-mediated antilisterial activities of the NisA+ strain M78 postfermentation. To our knowledge, this is the first report on quantitative expression of the nisA gene in a Greek cooked hard cheese during commercial manufacturing and ripening conditions by using a novel, rarely isolated, indigenous NisA+ L. lactis subsp. cremoris genotype as costarter culture.
本研究评估了由本土产乳酸链球菌亚种乳酸乳球菌(NisA+)的nisA基因在实际工厂规模的生产和成熟条件下,于传统希腊格拉维拉奶酪中的原位表达。该菌株以M78菌株为代表,属于生乳基因型。奶酪制作时添加了嗜热和嗜温混合商业发酵剂(CSC),或添加了CSC加M78菌株(CSC+M78)。在凝乳煮制后(第0天)、未加盐模具发酵24小时(第1天)、腌制(第7天)以及腌制模具(每个14至15千克)在完全受控的工业房间(16.5°C;相对湿度91%;第37天)中成熟30天后对奶酪进行采样。直接从奶酪样品中提取总RNA,并通过实时逆转录PCR(qRT-PCR)评估nisA基因的表达。琼脂覆盖法和打孔扩散生物测定法分别相应地用于在奶酪琼脂平板中原位检测M78 NisA+菌落以及在全奶酪浆液样品中检测抗李斯特菌活性。琼脂覆盖试验表明,NisA+菌株M78与CSC共培养时生长良好(>8 log CFU/克奶酪),反之亦然。仅在CSC+M78奶酪样品中检测到nisA表达,其表达水平在第1天最高(与对照基因相比增加了16倍),随后在第7天显著降低,在第37天几乎检测不到表达。基于这些结果,某些内在且主要是隐含的障碍因素似乎降低了生长流行率,降低了nisA基因表达以及NisA+菌株M78发酵后乳链菌肽A介导的抗李斯特菌活性。据我们所知,这是关于在商业生产和成熟条件下,使用一种新型、罕见分离的本土NisA+乳酸乳球菌亚种乳酸乳球菌基因型作为辅助发酵剂培养物,在希腊硬质熟奶酪中nisA基因定量表达的首次报告。