Domingos-Lopes M F P, Stanton C, Ross P R, Dapkevicius M L E, Silva C C G
Centro de Investigação e Tecnologia Agrária e do Ambiente dos Açores (CITA-A), Universidade dos Açores, Angra do Heroísmo, Portugal.
Teagasc Moorepark Food Research Centre, Fermoy, Cork, Ireland.
Food Microbiol. 2017 May;63:178-190. doi: 10.1016/j.fm.2016.11.014. Epub 2016 Nov 23.
A total of 114 lactic acid bacteria were isolated at one and 21 days of ripening from a traditional raw cow's milk cheese without the addition of starter culture, produced by three artisanal cheese-makers in Azores Island (Pico, Portugal). Identification to species and strain level was accomplished by16S rRNA gene and PFGE analysis. Carbohydrate utilization profiles were obtained with the relevant API kits. Isolates were evaluated according to safety and technological criteria. The most frequently observed genus identified by 16S rRNA sequencing analysis was Enterococcus, whereas API system mostly identified Lactobacillus. The highest percentages of antibiotic resistance were to nalidixic acid (95%), and aminoglycosides (64-87%). All isolates were sensitive to several beta-lactam antibiotics and negative for histamine and DNase production. Gelatinase activity was detected in 49.1% of isolates, 43% were able to degrade casein and 93% were α-hemolytic. Most enterococci presented virulence genes, such as gelE, asaI, ace. Diacetyl production was found to be species dependent and one strain (Leu. citreum) produced exopolysaccharides. Selected strains were further studied for technological application and were found to be slow acid producers in milk and experimental cheeses, a desirable trait for adjunct cultures. Two strains were selected on the basis of technological and safety application as adjunct cultures in cheese production and presented the best cheese aroma and flavor in consumer preference tests. This is the first effort to characterize Pico cheese LAB isolates for potential application as adjunct cultures; the results suggest the potential of two strains to improve the quality of this traditional raw milk product.
从亚速尔群岛(葡萄牙皮科岛)的三位手工奶酪制造商生产的未添加发酵剂的传统生牛乳奶酪中,在成熟1天和21天时共分离出114株乳酸菌。通过16S rRNA基因和脉冲场凝胶电泳(PFGE)分析完成了对菌株的种属鉴定。使用相关的API试剂盒获得碳水化合物利用图谱。根据安全性和技术标准对分离株进行评估。16S rRNA测序分析鉴定出最常见的属是肠球菌,而API系统大多鉴定为乳杆菌。抗生素耐药性最高的是萘啶酸(95%)和氨基糖苷类(64 - 87%)。所有分离株对几种β-内酰胺类抗生素敏感,组胺和DNA酶产生检测为阴性。49.1%的分离株检测到明胶酶活性,43%能够降解酪蛋白,93%为α-溶血。大多数肠球菌呈现毒力基因,如gelE、asaI、ace。发现双乙酰生成具有种属依赖性,一株(柠檬明串珠菌)产生胞外多糖。对选定的菌株进行了进一步的技术应用研究,发现它们在牛奶和实验奶酪中是缓慢产酸菌,这是辅助发酵剂的一个理想特性。根据技术和安全应用选择了两株作为奶酪生产的辅助发酵剂,在消费者偏好测试中呈现出最佳的奶酪香气和风味。这是首次对皮科奶酪乳酸菌分离株进行潜在应用为辅助发酵剂的特性研究;结果表明两株菌株具有改善这种传统生鲜乳产品质量的潜力。