2019
DOI: 10.1134/s0003683819060048
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Lactic and Propionic Acid Bacteria: the Formation of a Community for the Production of Functional Products with Bifidogenic and Hypotensitive Properties

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Cited by 11 publications
(5 citation statements)
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“…Further, the pathogens were able to grow beyond the point of inoculation at the edges of Petri plate where the Propionibacterium freudenreichii influence would be less. The results are in accordance with data stating that P. freudenreichii possess higher biocontrol towards pathogenic S. arureus than E. coli [29]. Propionicin is a major bacteriocin known to be produced by majority of propionibacteria [30][31][32] that is responsible for inhibition of growth of various Gram-positive bacteria, Gram-negative bacteria and some molds.…”
Section: Surfacesupporting
confidence: 88%
“…Further, the pathogens were able to grow beyond the point of inoculation at the edges of Petri plate where the Propionibacterium freudenreichii influence would be less. The results are in accordance with data stating that P. freudenreichii possess higher biocontrol towards pathogenic S. arureus than E. coli [29]. Propionicin is a major bacteriocin known to be produced by majority of propionibacteria [30][31][32] that is responsible for inhibition of growth of various Gram-positive bacteria, Gram-negative bacteria and some molds.…”
Section: Surfacesupporting
confidence: 88%
“…In our previous work, we demonstrated that Lactobacillus helveticus NK1, Lactobacillus rhamnosus F and Lactobacillus reuteri LR1 strains exhibit good safety and technological performance, as well as provide good probiotic properties to the final products [ 11 , 12 ]. In this article, the proteolytic activity of these LABs and their ability to release bioactive peptides with antioxidant and angiotensin I-converting enzyme inhibitory (ACE-I) properties were investigated.…”
Section: Introductionmentioning
confidence: 99%
“…An antagonistic activity of isolates of microorganisms against microscopic fungi was determined using a plate method (double culture method) [22]. To obtain an isolate sample, individual bacterial isolate was cultivated in a Petri dish on a Luria-Bertani (LB) agar medium at 37±1°C for 48 h to the moment of a continuous microorganism mycelium cover formation.…”
Section: Experiments Location Conditions and Layoutmentioning
confidence: 99%