Abstract

BackgroundLactococcus lactis is a lactic acid bacterium that has been used for centuries in the production of a variety of cheeses, as these bacteria rapidly acidify milk and greatly contribute to the flavour of the fermentation end-products. After a short growth phase during cheese ripening L. lactis enters an extended non-growing state whilst still strongly contributing to amino acid-derived flavour formation. Here, a research approach is presented that allows investigation of strain- and amino acid-specific flavour formation during the non-growing state.ResultsNon-growing cells of five selected L. lactis strains were demonstrated to degrade amino acids into flavour compounds that are relevant in food fermentations and differs greatly from production of flavour compounds using growing cells. As observed earlier in other research set-ups and with other microorganisms, addition of NADH, α-ketoglutarate and pyridoxal-5-phosphate was demonstrated to be essential for optimal flavour formation, suggesting that intracellular pools of these substrates are too low for the significant production of the flavour compounds. Production of flavours during the non-growing phase strongly depends on the individual amino acids that were supplied, on the presence of other amino acids (mixtures versus single compounds), and on the strain used. Moreover, we observed that the plasmid-free model strains L. lactis MG1363 and IL1403 produce relatively low amounts of flavour components under the various conditions tested.ConclusionsBy using this simplified and rapid approach to study flavour formation by non-growing lactic acid bacteria, lengthy ripening periods are no longer required to assess the capacity of strains to produce flavours in the long, non-growing state of dairy fermentation. In addition, this method also provides insight into the conversion of single amino acids versus the conversion of a mixture of amino acids as produced during protein degradation. The generated results are complementary to earlier generated datasets using growing cells, allowing assessment of the full flavour forming potential of strains used as starter cultures in industrial food fermentation processes.

Highlights

  • Lactococcus lactis is a lactic acid bacterium that has been used for centuries in the production of a variety of cheeses, as these bacteria rapidly acidify milk and greatly contribute to the flavour of the fermentation end-products

  • Our cell incubation system was validated using L. lactis strain 1157, well-known for its production of 3-methylbutanal and 3-methylbutanol. This strain was incubated in sodium phosphate buffer containing leucine and NADH for 24 h at 30°C followed by Gas Chromatography in combination with Mass Spectrometry (GCMS) analysis of the volatile metabolites (Table 1)

  • We have chosen to use and further develop an existing experimental method to study the role of Lactococcus lactis in cheese flavour production

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Summary

Introduction

Lactococcus lactis is a lactic acid bacterium that has been used for centuries in the production of a variety of cheeses, as these bacteria rapidly acidify milk and greatly contribute to the flavour of the fermentation end-products. In actual cheese the formation of compounds can only be followed cumulatively from beginning to the end of the ripening period and direct extraction of active microorganisms or microbial enzymes from cheese has proven to be quite difficult if not impossible [16,17] For this reason, various approaches, often with different objectives, have been designed to study cheese flavour development. Mass spectrometry metabolic fingerprinting is reported to be a comprehensive and sensitive approach to study flavour formation in a model cheese made with ultra-filtrated milk concentrate [35] For all these models it can be argued that the experimental set-up does not represent actual cheese conditions and that the models do not allow direct in situ analysis or that the models involve growing cells, whereas the major part of the cheese ripening process involves non-growing cells. There is a clear need for alternative, improved, approaches

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