Hüfner Eric, Markieton Tobias, Chaillou Stéphane, Crutz-Le Coq Anne-Marie, Zagorec Monique, Hertel Christian
Institute of Food Science and Biotechnology, Section Food Microbiology, University of Hohenheim, Garbenstr. 28, Stuttgart, Germany.
Appl Environ Microbiol. 2007 Apr;73(8):2522-31. doi: 10.1128/AEM.02396-06. Epub 2007 Feb 16.
Lactobacillus sakei is a lactic acid bacterium that is ubiquitous in the food environment and is one of the most important constituents of commercial meat starter cultures. In this study, in vivo expression technology (IVET) was applied to investigate gene expression of L. sakei 23K during meat fermentation. The IVET vector used (pEH100) contained promoterless and transcriptionally fused reporter genes mediating beta-glucuronidase activity and erythromycin resistance. A genomic library of L. sakei 23K was established, and the clones were subjected to fermentation in a raw-sausage model. Fifteen in carne-induced fusions were identified. Several genes encoded proteins which are likely to contribute to stress-related functions. One of these genes was involved in acquisition of ammonia from amino acids, and the remaining either were part of functionally unrelated pathways or encoded hypothetical proteins. The construction and use of isogenic mutants in the sausage model suggested that four genes have an impact on the performance of L. sakei during raw-sausage fermentation. Inactivation of the heat shock regulator gene ctsR resulted in increased growth, whereas knockout of the genes asnA2, LSA1065, and LSA1194 resulted in attenuated performance compared to the wild-type strain. The results of our study are the first to provide an insight into the transcriptional response of L. sakei when growing in the meat environment. In addition, this study establishes a molecular basis which allows investigation of bacterial properties that are likely to contribute to the ecological performance of the organism and to influence the final outcome of sausage fermentation.
清酒乳杆菌是一种在食品环境中普遍存在的乳酸菌,是商业肉类发酵剂培养物的最重要成分之一。在本研究中,采用体内表达技术(IVET)来研究清酒乳杆菌23K在肉类发酵过程中的基因表达。所使用的IVET载体(pEH100)包含无启动子且转录融合的报告基因,介导β-葡萄糖醛酸酶活性和红霉素抗性。构建了清酒乳杆菌23K的基因组文库,并将克隆在生香肠模型中进行发酵。鉴定出15个肉诱导融合体。几个基因编码的蛋白质可能有助于与应激相关的功能。其中一个基因参与从氨基酸获取氨,其余基因要么是功能无关途径的一部分,要么编码假定蛋白质。在香肠模型中构建和使用同基因突变体表明,四个基因对清酒乳杆菌在生香肠发酵过程中的性能有影响。热休克调节基因ctsR的失活导致生长增加,而与野生型菌株相比,asnA2、LSA1065和LSA1194基因的敲除导致性能减弱。我们的研究结果首次深入了解了清酒乳杆菌在肉类环境中生长时的转录反应。此外,本研究建立了一个分子基础,可用于研究可能有助于该生物体生态性能并影响香肠发酵最终结果的细菌特性。