42 research outputs found

    Effect of environmental and nutritional factors on the production of bacteriocin-like inhibitory substances (BLIS) by Enterococcus faecium strains

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    Five bacteriocin-like inhibitory substances (BLIS)-producer Enterococcus faecium strains (WGW7.2, WGJ17.2, WGJ21.2, WGJ28.1 and WGW33.2) were characterized for their antimicrobial compound production under several growth conditions, at different concentrations and with different sources of nutritional factors and in the presence of ethanol and NaCl. The strains showed different behaviours. MRS and SDB were found to be the optimal media for BLIS expression. A higher BLIS production was observed at 30° and 37°C and at a pH in the neutral range. Low or no BLIS activity was detected after growth in the absence of nitrogen sources, carbohydrates, MgSO4 and MnSO4. Ethanol did not generally play a negative role, while NaCl determined a consistent decrease in BLIS activity that was proportional to its concentration. Due to the absence of plasmids, BLIS production by all strains was chromosomally encoded. This study is part of a more comprehensive study aimed at characterizing lactic acid bacteria (LAB) associated with the raw materials used to prepare sourdough

    “Application of a novel polyphasic approach to study the lactobacilli composition of sourdoughs from the Abruzzo region (central Italy)”

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    Aims: To characterize the lactobacilli community of 20 sourdoughs using a novel polyphasic approach. Methods and Results: A polyphasic approach, consisting of a two-step multiplex polymerase chain reaction (PCR) system, 16S rRNA gene sequence analysis and physiological features, was applied to identify 127 isolates, representing about 37% of the presumptive lactobacilli collected from sourdough samples. Multiplex PCR successfully identified 111 isolates, while 16S rRNA gene sequencing was applied for the other 16 isolates, two of which could not be associated with any previously described lactic acid bacteria (LAB) species. Strain diversity was evaluated by phenotypic and random amplified polymorphic DNA-PCR analysis. Molecular detection of Lactobacillus group species was also performed on total DNA extracted from the doughs. Conclusions: Abruzzo region sourdough lactobacilli biodiversity, reflected in both Lactobacillus species composition and strain polymorphism, is similar to that of other Italian regions and is a source of novel LAB species. Significance and Impact of the Study: Within culture-independent methods, multiplex PCR is a rapid tool to study the lactobacilli population of sourdoughs

    Identification of subdominant lactic acid bacteria and their evolution during laboratory-scale fermentations

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    Presumptive lactic acid bacterial cocci were found in six sourdoughs (out of 20) from the Abruzzo region (central Italy) and subjected to phenotypic and genotypic characterization. A total of 21 isolates, recognized as seven strains by randomly amplified polymorphic DNA (RAPD)–polymerase chain reaction (PCR) typing, were identified by a polyphasic approach, consisting of 16S rRNA gene sequencing, multiplex PCR assays and physiological features, as Enterococcus faecium and Pediococcus pentosaceus. Four strains belonging to those species and previously isolated from wheat kernels were inoculated in sterile flour to verify their capacity to grow in sourdough environment. Doughs with several dual bacterial combinations, including Lactobacillus sanfranciscensis, were propagated for 11 days and pH measurements and bacterial counts were carried ou
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