Bacteriocin production and technological properties of Enterococcus mundtii and Enterococcus faecium strains isolated from sheep and goat colostrum

• Published in: Veterinary research communications Vol. 47; no. 3; pp. 1321 - 1345
• Main Authors: Öztürk, Hüseyin, Geniş, Burak, Özden Tuncer, Banu, Tuncer, Yasin
• Format: Journal Article
• Language: English
• Published: Dordrecht Springer Netherlands 01.09.2023; Springer Nature B.V
• Subjects: Acid phosphatase; Acid production; Aroma; Bacteriocins; Biomedical and Life Sciences; Colostrum; Dairy products; Detergents; Enterococcus faecium; Enterococcus mundtii; Esterase; Fermented food; Lactic acid bacteria; Life Sciences; Nucleotide sequence; Phosphohydrolase; Phylogeny; Proteolysis; Proteolytic enzymes; rRNA 16S; Sensory evaluation; Sheep; Shelf life; Starter cultures; Strains (organisms); Veterinary Medicine/Veterinary Science; Zoology; α-Amylase; Technological properties; Colostrum; Tricine-SDS-PAGE; PCR; Bacteriocin; Enterococcus
• ISSN: 0165-7380; 1573-7446
• DOI: 10.1007/s11259-023-10080-7

Enterococci are lactic acid bacteria (LAB) that play a role in the aroma formation, maturation, and sensory development of fermented foods such as meat and dairy products. They also contribute to the improvement of the extended shelf life of fermented foods by producing bacteriocin. The aim of this study was to isolate bacteriocin-producing LAB from sheep and goat colostrum, to characterize the bacteriocin-producing strains, and determine the technological properties of the strains. A total of 13 bacteriocin-producing LAB was isolated and identified as 11 Enterococcus mundtii and two Enterococcus faecium . The strains were found to be genetically different from each other by phylogenetic analysis of 16S rRNA gene sequences and random amplified polymorphic-DNA (RAPD-PCR). It has been determined that bacteriocins show activity in a wide pH range and are resistant to heat, lose their activity with proteolytic enzymes and α-amylase, but are resistant to detergents. While the presence of the munKS gene was detected in all of the strains, it was determined that E. faecium HC121.4, HC161.1, E. mundtii HC147.1, HC166.5, and HC166.8 strains contained multiple enterocin genes. Trisin-SDS-PAGE analysis revealed two active protein bands of approximately 5.1 and 5.5 kDa in E. faecium HC121.4 and one active protein band with a weight of approximately 4.96 kDa in other strains. E. mundtii strains and E. faecium HC161.1 were identified as mundticin KS producers, and E. faecium HC121.4 was defined as an enterocin A and B producer. Except for E. mundtii HC166.8, acid production of strains was found to be slow at 6 h and moderate at 24 h. None of them showed extracellular proteolytic and lipolytic activities. It was found that the strains had esterase, esterase lipase, leucine arylamidase, acid phosphatase, and naphthol-AS-Bl-phosphohydrolase activities, while protease activities were low and peptidase activities were high. In conclusion, bacteriocin producer 13 Enterococcus strains isolated from sheep and goat colostrum were found to have the potential to be included in starter culture combinations.