Teagasc Food Research Centre Moorepark, Fermoy, Ireland.
Department of Biology, W. M. Keck Center for Cellular Imaging, University of Virginia Charlottesville, VA, USA.
Front Microbiol. 2015 Mar 6;6:183. doi: 10.3389/fmicb.2015.00183. eCollection 2015.
Cheese, a product of microbial fermentation may be defined as a protein matrix entrapping fat, moisture, minerals and solutes as well as dispersed bacterial colonies. The growth and physiology of bacterial cells in these colonies may be influenced by the microenvironment around the colony, or alternatively the cells within the colony may modify the microenvironment (e.g., pH, redox potential) due to their metabolic activity. While cheese pH may be measured at macro level there remains a significant knowledge gap relating to the degree of micro-heterogeneity of pH within the cheese matrix and its relationship with microbial, enzymatic and physiochemical parameters and ultimately with cheese quality, consistency and ripening patterns. The pH of cheese samples was monitored both at macroscopic scale and at microscopic scale, using a non-destructive microscopic technique employing C-SNARF-4 and Oregon Green 488 fluorescent probes. The objectives of this work were to evaluate the suitability of these dyes for microscale pH measurements in natural cheese matrices and to enhance the sensitivity and extend the useful pH range of these probes using fluorescence lifetime imaging (FLIM). In particular, fluorescence lifetime of Oregon Green 488 proved to be sensitive probe to map pH micro heterogeneity within cheese matrices. Good agreement was observed between macroscopic scale pH measurement by FLIM and by traditional pH methods, but in addition considerable localized microheterogeneity in pH was evident within the curd matrix with pH range between 4.0 and 5.5. This technique provides significant potential to further investigate the relationship between cheese matrix physico-chemistry and bacterial metabolism during cheese manufacture and ripening.
奶酪是微生物发酵的产物,可以定义为一种蛋白质基质,其中包含脂肪、水分、矿物质和溶质,以及分散的细菌菌落。这些菌落中的细菌细胞的生长和生理可能受到菌落周围微环境的影响,或者菌落中的细胞可能由于其代谢活动而改变微环境(例如 pH 值、氧化还原电位)。虽然奶酪的 pH 值可以在宏观水平上进行测量,但在奶酪基质内 pH 值的微观不均匀性及其与微生物、酶和物理化学参数的关系,以及最终与奶酪质量、一致性和成熟模式之间的关系方面,仍然存在着很大的知识差距。本研究采用非破坏性的微观技术,使用 C-SNARF-4 和 Oregon Green 488 荧光探针,在宏观和微观尺度上监测奶酪样品的 pH 值。本工作的目的是评估这些染料在天然奶酪基质中进行微尺度 pH 值测量的适用性,并通过荧光寿命成像(FLIM)提高这些探针的灵敏度和扩展其有用的 pH 范围。特别是,Oregon Green 488 的荧光寿命被证明是一种灵敏的探针,可以在奶酪基质内绘制 pH 微观不均匀性的图谱。通过 FLIM 和传统 pH 方法进行的宏观尺度 pH 值测量之间观察到了良好的一致性,但在凝乳基质内还存在明显的局部 pH 微观不均匀性,pH 值范围在 4.0 到 5.5 之间。这项技术为进一步研究奶酪基质物理化学性质和细菌代谢之间的关系提供了很大的潜力,这些关系存在于奶酪制造和成熟过程中。