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利用荧光 CTP1L 溶菌酶细胞壁结合域研究酪丁酸梭菌在奶酪成熟过程中的进化。

Use of fluorescent CTP1L endolysin cell wall-binding domain to study the evolution of Clostridium tyrobutyricum during cheese ripening.

机构信息

Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Departamento de Tecnología de Alimentos, Carretera de La Coruña Km 7, 28040, Madrid, Spain.

Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA), Departamento de Tecnología de Alimentos, Carretera de La Coruña Km 7, 28040, Madrid, Spain.

出版信息

Food Microbiol. 2019 Apr;78:11-17. doi: 10.1016/j.fm.2018.09.018. Epub 2018 Sep 29.

DOI:10.1016/j.fm.2018.09.018
PMID:30497591
Abstract

Clostridium tyrobutyricum is a bacteria of concern in the cheese industry, capable of surviving the manufacturing process and causing butyric acid fermentation and late blowing defect of cheese. In this work, we implement a method based on the cell wall-binding domain (CBD) of endolysin CTP1L, which detects C. tyrobutyricum, to monitor its evolution in cheeses challenged with clostridial spores and in the presence or absence of reuterin, an anti-clostridial agent. For this purpose, total bacteria were extracted from cheese samples and C. tyrobutyricum cells were specifically labelled with the CBD of CTP1L attached to green fluorescent protein (GFP), and detected by fluorescence microscopy. By using this GFP-CBD, germinated spores were visualized on day 1 in all cheeses inoculated with clostridial spores. Vegetative cells of C. tyrobutyricum, responsible for butyric acid fermentation, were detected in cheeses without reuterin from 30 d onwards, when LBD symptoms also became evident. The number of fluorescent Clostridium cells increased during ripening in the blowing cheeses. However, vegetative cells of C. tyrobutyricum were not detected in cheese containing the antimicrobial reuterin, which also did not show LBD throughout ripening. This simple and fast method provides a helpful tool to study the evolution of C. tyrobutyricum during cheese ripening.

摘要

酪丁酸梭菌是奶酪工业中令人关注的细菌,能够在生产过程中存活下来,并导致丁酸发酵和奶酪后期胀包缺陷。在这项工作中,我们实施了一种基于内切溶素 CTP1L 的细胞壁结合结构域(CBD)的方法来检测 C. tyrobutyricum,以监测其在受到梭状芽孢杆菌孢子挑战的奶酪中的演变情况,以及在存在或不存在抗梭状芽孢杆菌剂雷替丁的情况下。为此,从奶酪样品中提取总细菌,并将 CTP1L 的 CBD 与绿色荧光蛋白(GFP)连接,特异性标记 C. tyrobutyricum 细胞,然后通过荧光显微镜检测。使用这种 GFP-CBD,在所有接种了梭状芽孢杆菌孢子的奶酪中,第 1 天就能观察到发芽的孢子。在不含雷替丁的奶酪中,从 30 天开始检测到 C. tyrobutyricum 的营养细胞,此时 LBD 症状也变得明显。在吹胀奶酪的成熟过程中,荧光梭菌细胞的数量增加。然而,在含有抗菌雷替丁的奶酪中没有检测到 C. tyrobutyricum 的营养细胞,整个成熟过程中也没有出现 LBD。这种简单快速的方法为研究 C. tyrobutyricum 在奶酪成熟过程中的演变提供了一个有用的工具。

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