Abstract

Kombucha is a fermented beverage containing organic acids by yeast and acetic acid bacteria. In this study, microbial community analysis of kombucha produced in Korea was performed, and changes in components during kombucha fermentation were analyzed using commercial kombucha pellicle and culture broth as starter. The major phylum-level strains of commercial kom-1 and kom-2 showed differences in proteobacteria of 35.60% and 78.1%, and Firmicutes of 64.06% and 15.57%, respectively. During fermentation with pellicle (Kom-P) and broth (Kom-F), the level of reducing sugar during fermentation tended to decrease rapidly. The production of acetic acid and D-saccharic acid-1,4-lactone (DSL) in Kom-P and -F tended to increase with increasing fermentation time. In Kom-P, lactic acid and glucuronic acid production increased until 7 days of fermentation and then decreased, whereas in Kom-F, it continued to increase with fermentation time. ABTS radical scavenging activity tended to decrease with increasing fermentation time. However, DPPH radical scavenging activity increased within 7 days of fermentation and then decreased slightly (Kom-P) or remained constant (Kom-F). It has been found that the use of culture broth rather than the use of pellicle as a starter is advantageous to increase the active compound content and DPPH radical scavenging ability.

Highlights

  • Fermentation is one of the oldest methods to improve food value and preservation via a low-cost energy conservation system

  • Despite the various physiological effects of kombucha, its application and utilization in the industry are remarkably low. This is mainly due to insufficient analysis of microbial species, distribution, and metabolites produced during the fermentation of kombucha, which occurs through symbiosis of microorganisms

  • Among the microorganisms belonging to the phylum Proteobacteria, Komagataeibacter hansenii and Gluconobacter oxydans were the main species (Figure 1)

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Summary

Introduction

Fermentation is one of the oldest methods to improve food value and preservation via a low-cost energy conservation system. Kombucha is a beverage produced by Saccharomyces and Brettanomyces, which are yeasts that use sugar to produce alcohol, and Acetobacter that use alcohol to produce various organic acids including acetic acid and gluconic acid. It is characterized by the formation of a pellicle, a gel-like membrane of cellulose produced by a symbiotic strain on the surface of the kombucha culture (Jayabalan et al, 2014). Despite the various physiological effects of kombucha, its application and utilization in the industry are remarkably low This is mainly due to insufficient analysis of microbial species, distribution, and metabolites produced during the fermentation of kombucha, which occurs through symbiosis of microorganisms. We intend to provide data that must be secured for the mass production and industrialization of kombucha

Materials and methods
DNA extraction and metagenomic sequencing of 16S rRNA
Analytical method
Assay of radical scavenging activity
Statistical analysis
Results and discussion
Conclusion
Full Text
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