TL;DR: In this paper, the effects of lactic acid bacteria (LAB) on hydrogen fermentation of organic waste were investigated, and it was shown that the inhibitory effect of LAB on hydrogen production was caused by bacteriocins excreted from LAB which have a deleterious effect on other bacteria.
TL;DR: The applied wastewater treatment processes considerably reduced the number of fecal indicators, Nevertheless their number in the WWTP effluent was higher than 10(4) CFU per 100 ml and periodically contained 90% of bacteria with antimicrobial resistance patterns.
TL;DR: Enterococcus durans LAB18s showed resistance to acid conditions, showing ability to survive in the presence of simulated gastric juice at pH 3.5, and could be useful as a source of dietary selenium supplementation.
TL;DR: The post-electrophoretic detection of esterase activities showed that the esterolytic system of enterococci was rather complex, and E. faecalis strains were generally more active compared to E. durans strains in respect of most biochemical properties considered.
TL;DR: The aim of this study was to isolate and identify bacteriocin‐producing lactic acid bacteria (LAB) issued from Mongolian airag (traditional fermented mare's milk), and to purify and characterize bacteriOCins produced by these LAB.
Abstract: Aims: The aim of this study was to isolate and identify bacteriocin-producing lactic acid bacteria (LAB) issued from Mongolian airag (traditional fermented mare's milk), and to purify and characterize bacteriocins produced by these LAB.
Methods and Results: Identification of the bacteria (Enterococcus durans) was carried out on the basis of its morphological, biochemical characteristics and carbohydrate fermentation profile and by API50CH kit and 16S rDNA analyses. The pH-neutral cell-free supernatant of this bacterium inhibited the growth of several Lactobacillus spp. and food-borne pathogens including Escherichia coli, Staphylococcus aureus and Listeria innocua. The antimicrobial agent (enterocin A5-11) was heat stable and was not sensitive to acid and alkaline conditions (pH 2–10), but was sensitive to several proteolytic enzymes. Its inhibitory activity was completely eliminated after treatment with proteinase K and α-chymotrypsin. The activity was however not completely inactivated by other proteases including trypsin and pepsin. Three-step purification procedure with high recovery yields was developed to separate two bacteriocins. The applied procedure allowed the recovery of 16% and 64% of enterocins A5-11A and A5-11B, respectively, present in the culture supernatant with purity higher than 99%. SDS-PAGE analyses revealed that enterocin A5-11 has a molecular mass of 5000 Da and mass spectrometry analyses demonstrates molecular masses of 5206 and 5218 Da for fractions A and B, respectively. Amino acid analyses of both enterocins indicated significant quantitative difference in their contents in threonine, alanine, isoleucine and leucine. Their N-termini were blocked hampering straightforward Edman degradation.
Conclusions: Bacteriocins A5-11A and B from Ent. durans belong to the class II of bacteriocins.
Significance and Impact of the Study: Judging from molecular masses, amino acid composition and spectrum of activities, bacteriocins A5-11A and B from Ent. durans show high degree of similarity with enterocins L50A and L50B isolated from Enterococcus faecium (Cintas et al. 1998, 2000) and with enterocin I produced by Ent. faecium 6T1a, a strain originally isolated from a Spanish-style green olive fermentation (Floriano et al. 1998).