Bayburt Aysegul Aybuke, Yuksekdag Zehranur, Cinar-Acar Berat
Graduate School of Natural and Applied Science, Department of Biology, Gazi University, Ankara, Turkey.
Faculty of Science, Department of Biology, Gazi University, Ankara, Turkey.
Folia Microbiol (Praha). 2025 Sep 12. doi: 10.1007/s12223-025-01330-z.
Two lactic acid bacteria strains, Ligilactobacillus salivarius KC27L and Limosilactobacillus reuteri KC21L, were investigated for their ability to produce exopolysaccharides (EPS). The study evaluated the influence of different physical and nutritional factors, including carbon and nitrogen sources, pH, incubation time, temperature, and CO concentration, to identify optimal conditions for EPS production. Under optimized conditions, L. salivarius KC27L reached 464 mg/L and L. reuteri KC21L achieved 433 mg/L, representing substantial increases compared to standard medium. A combined culture strategy, integrating sucrose as the primary carbon source and strain-specific nitrogen supplements, further enhanced yields and demonstrated the importance of tailored optimization. To gain molecular insight, expression levels of key EPS biosynthesis genes were examined under control versus optimized conditions. In L. salivarius KC27L, upregulation of the epsC gene was observed, suggesting its central role in enhanced EPS production, while other genes showed reduced expression. In L. reuteri KC21L, most analyzed genes were downregulated, indicating strain-specific regulatory mechanisms. Overall, the findings highlight the potential of optimization strategies to significantly enhance EPS yields in LAB strains. Moreover, the observed link between growth conditions and epsC expression provides a promising molecular target for improving EPS biosynthesis, supporting the industrial and biotechnological application of these strains.
对唾液乳杆菌KC27L和罗伊氏乳杆菌KC21L这两种乳酸菌菌株产生胞外多糖(EPS)的能力进行了研究。该研究评估了不同物理和营养因素的影响,包括碳源、氮源、pH值、培养时间、温度和二氧化碳浓度,以确定EPS产生的最佳条件。在优化条件下,唾液乳杆菌KC27L达到464毫克/升,罗伊氏乳杆菌KC21L达到433毫克/升,与标准培养基相比有显著增加。一种将蔗糖作为主要碳源和特定菌株氮补充剂相结合的混合培养策略进一步提高了产量,并证明了定制优化的重要性。为了深入了解分子机制,在对照条件和优化条件下检测了关键EPS生物合成基因的表达水平。在唾液乳杆菌KC27L中,观察到epsC基因上调,表明其在增强EPS产生中起核心作用,而其他基因表达降低。在罗伊氏乳杆菌KC21L中,大多数分析基因下调,表明存在菌株特异性调控机制。总体而言,研究结果突出了优化策略在显著提高LAB菌株EPS产量方面的潜力。此外,观察到的生长条件与epsC表达之间的联系为改善EPS生物合成提供了一个有前景的分子靶点,支持了这些菌株在工业和生物技术中的应用。