INRA, UMR1253 Science et Technologie du Lait et de l'OEuf, F-35000 Rennes, France.
Appl Environ Microbiol. 2010 Feb;76(4):1181-8. doi: 10.1128/AEM.02453-09. Epub 2009 Dec 28.
Lipolysis plays an important role in the formation of cheese flavor. In Emmental cheese, the main part of lipolysis has been associated with the presence of Propionibacterium freudenreichii, a species used as a ripening culture. Our aim was to identify the most probable lipolytic esterase(s) involved in cheese lipolysis by P. freudenreichii. Since cheese lipolysis mainly occurs during P. freudenreichii growth, we hypothesized that P. freudenreichii possesses secreted lipolytic esterase(s). For 12 putative esterase genes previously identified from the genome of P. freudenreichii CIRM1, the level of expression was quantified by real-time reverse transcriptase (RT)-PCR, and the subcellular localization of esterases was predicted in silico. The esterase activity in extracellular and intracellular extracts of P. freudenreichii was characterized by zymography, and the extracellular esterases were identified by mass spectrometry. Finally, the best candidate was overexpressed in the same strain. All of the 12 genes encoding putative esterases were expressed. Esterase PF#279 was predicted to be secreted in the medium, PF#774 to be surface exposed, and the 10 remaining putative esterases to be intracellular. Zymography revealed that esterase activities in culture supernatant differed from the ones detected in intracellular extracts. PF#279 was identified as the sole esterase present in culture supernatant. Transformed P. freudenreichii CIRM1 clones overexpressing PF#279 showed 5 to 8 times more lipolytic activity on milk fat than the wild-type strain. Combining in silico, biochemical, and genetic approaches, we showed that PF#279 is the sole secreted esterase in P. freudenreichii and is active on milk fat. Therefore, it is likely a key component in cheese lipolysis by P. freudenreichii.
脂肪分解在奶酪风味的形成中起着重要作用。在埃曼塔尔奶酪中,脂肪分解的主要部分与丙酸杆菌属的存在有关,该物种被用作成熟培养物。我们的目的是通过丙酸杆菌属鉴定参与奶酪脂肪分解的最可能的脂肪酶。由于奶酪脂肪分解主要发生在丙酸杆菌属生长过程中,我们假设丙酸杆菌属具有分泌的脂肪酶。对于先前从丙酸杆菌属 CIRM1 基因组中鉴定出的 12 种假定酯酶基因,通过实时逆转录酶(RT)-PCR 定量了表达水平,并通过计算机预测了酯酶的亚细胞定位。通过凝胶电泳法对丙酸杆菌属细胞外和细胞内提取物中的酯酶活性进行了表征,并通过质谱法鉴定了细胞外酯酶。最后,在相同的菌株中过表达了最佳候选物。编码假定酯酶的 12 个基因均有表达。预测酯酶 PF#279 被分泌到培养基中,PF#774 暴露在表面,其余 10 种假定酯酶定位于细胞内。凝胶电泳显示,培养物上清液中的酯酶活性与细胞内提取物中检测到的活性不同。PF#279 被鉴定为培养物上清液中唯一存在的酯酶。过表达 PF#279 的转化丙酸杆菌属 CIRM1 克隆比野生型菌株的脂肪分解活性高 5 至 8 倍。通过计算机模拟、生物化学和遗传方法相结合,我们表明 PF#279 是丙酸杆菌属中唯一分泌的酯酶,并且对乳脂肪有活性。因此,它很可能是丙酸杆菌属奶酪脂肪分解的关键组成部分。