Literature DB >> 22491990

Growth and survival of lactic acid bacteria in lucerne silage.

Eva Vlková1, Vojtěch Rada, Věra Bunešová, Sárka Ročková.   

Abstract

A rifampicin-resistant variant of two strains of Lactobacillus plantarum, one strain of Pediococcus acidilactici, and one strain of Enterococcus faecium were used for the experimental production of lucerne silage. Laboratory silage without inoculants served as a control. Counts of total anaerobes, total lactic acid bacteria (LAB), lactobacilli, pediococci, and enterococci were determined on days 14, 21, 30, 49, and 60 of lucerne fermentation. LAB dominated in silage microflora, reaching a percentage between 59 and 95 % of total anaerobes. Lactobacilli were found as a predominant group of LAB during the whole study. Lactobacilli reached numbers 8.74 log CFU/g in treated silage and 8.89 log CFU/g in the control at the first observation. Their counts decreased to 4.23 and 4.92 log CFU/g in treated silage and the control, respectively, on day 63 of fermentation. Similar decreases were observed in all bacterial groups. The treated silage samples possessed lower pH (4.2 vs. 4.5 in control samples) and contained more lactic acid compared to control silage. The identity of re-isolated rifampicin-resistant bacteria with those inoculated to the lucerne was evaluated by fingerprinting techniques. The fingerprint profiles of re-isolated bacteria corresponded to the profiles of strains used for the treatment. It could be concluded that supplemented LAB dominated in laboratory silage and overgrew naturally occurring LAB.

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Year:  2012        PMID: 22491990     DOI: 10.1007/s12223-012-0142-5

Source DB:  PubMed          Journal:  Folia Microbiol (Praha)        ISSN: 0015-5632            Impact factor:   2.099


  8 in total

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Authors:  J Walter; G W Tannock; A Tilsala-Timisjarvi; S Rodtong; D M Loach; K Munro; T Alatossava
Journal:  Appl Environ Microbiol       Date:  2000-01       Impact factor: 4.792

2.  Applicability of rep-PCR fingerprinting for identification of Lactobacillus species.

Authors:  D Gevers; G Huys; J Swings
Journal:  FEMS Microbiol Lett       Date:  2001-11-27       Impact factor: 2.742

3.  Detection of glycopeptide resistance genotypes and identification to the species level of clinically relevant enterococci by PCR.

Authors:  S Dutka-Malen; S Evers; P Courvalin
Journal:  J Clin Microbiol       Date:  1995-01       Impact factor: 5.948

4.  Bacterial and fungal communities of wilted Italian ryegrass silage inoculated with and without Lactobacillus rhamnosus or Lactobacillus buchneri.

Authors:  Y Li; N Nishino
Journal:  Lett Appl Microbiol       Date:  2011-01-17       Impact factor: 2.858

5.  A meta-analysis of the effects of Lactobacillus buchneri on the fermentation and aerobic stability of corn and grass and small-grain silages.

Authors:  D H Kleinschmit; L Kung
Journal:  J Dairy Sci       Date:  2006-10       Impact factor: 4.034

6.  Genetic heterogeneity and functional properties of intestinal bifidobacteria.

Authors:  J Mättö; E Malinen; M-L Suihko; M Alander; A Palva; M Saarela
Journal:  J Appl Microbiol       Date:  2004       Impact factor: 3.772

7.  Lactic acid bacteria used in inoculants for silage as probiotics for ruminants.

Authors:  Zwi G Weinberg; Richard E Muck; Paul J Weimer; Yaira Chen; Mira Gamburg
Journal:  Appl Biochem Biotechnol       Date:  2004 Jul-Sep       Impact factor: 2.926

8.  Characterization and identification of Pediococcus species isolated from forage crops and their application for silage preparation.

Authors:  Y Cai; S Kumai; M Ogawa; Y Benno; T Nakase
Journal:  Appl Environ Microbiol       Date:  1999-07       Impact factor: 4.792

  8 in total

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