Abstract

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.

Highlights

  • Cheese is a complex physiochemical and microbial system containing many interacting components

  • It is evident that the cheese pHs vary depending on the cheese manufacture treatments but all are within the range 4.99–5.31 and are typical of the pH of many natural cheese types what this method does not measure is the degree and pattern of variability in pH within each cheese matrix

  • We have confirmed that the C-SNARF-4 fluorescent pH probe may be used as a reliable ratiometric pH indicator at pH 5.5 and above (Figure 3)

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Summary

Introduction

Cheese is a complex physiochemical and microbial system containing many interacting components. It may be defined as a protein matrix entrapping fat, moisture, minerals and other solutes as well as dispersed bacterial colonies. Each inoculated bacterial cell is assumed to grow, generating colonies which are dispersed within the cheese curd. Bacterial colonies within the cheese matrix have been shown to be located on or within milk fat globular membrane material (MFGM) and at fat-protein interfaces with the curd (Laloy et al, 1996; Lopez et al, 2006) and are considered to interact with the cheese matrix during ripening (Feeney et al, 2002; McSweeney, 2004a). 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 (McSweeney, 2004a)

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