Isolation and Plasmid Characterization of a Lactobacillus Species Involved in the Manufacture of Fermented Sausage1

1985 ◽  
Vol 48 (12) ◽  
pp. 1028-1035 ◽  
Author(s):  
DENNIS A. ROMERO ◽  
LARRY L. McKAY

Isolation and characterization of a Lactobacillus species capable of proper acid production in a sausage environment is described. The isolate from sausage, categorized as a lactobacillus in the subgenus Streptobacterium, was designated Lactobacillus sp. DR1. Growth occurred at 5 and 42°C but not at 45°C. Fructose, galactose, glucose, mannose, melibiose, N-acetylglucosamine, ribose, sucrose and trehalose were fermented. Gas production from glucose was not observed. In MRS glucose broth, D(−) and L(+) lactic acid were produced. Lactobacillus sp. DR1 contained a single cryptic plasmid of approximately 30 megadaltons (Mdal). In sausage fermentation trials, both Lactobacillus sp. DR1 and plasmid-free derivative DR1C lowered the pH to below 5.3 after 8 h in the smokehouse. Conjugation was demonstrated through the transfer of plasmid pAMβ1, which encodes erythromycin resistance, from Streptococcus lactis 2301β to Lactobacillus sp. DR1. Mutanolysin-generated protoplasts could be regenerated using 0.5 M ammonium chloride, lactose, maltose or sucrose as osmotic stabilizers. Regeneration frequencies ranged from less than 1.0% up to 35%; however, transformation of Lactobacillus sp. DR1 protoplasts by plasmid DNA in the presence of polyethylene glycol (PEG) was unsuccessful.

2018 ◽  
Vol 6 (2) ◽  
pp. 500-508
Author(s):  
Julie Ann A. Arcales ◽  
Garner Algo L.Alolod

Isolation and characterization of bacteria in food products are important to determine and distinguish the beneficial or harmful effects of microbiota in certain samples. Lactic acid bacteria in food products had long been associated to good factors as food preservatives and with added fermentation metabolites. This study isolated and characterized lactic acid bacteria from burong bangus. The culture and purification process of bacteria isolation resulted to 4 strains of lactic acid bacteria namely Enterococcus faecalis, Tetragenococcus muriaticus, Lactobacillus delbrueckii subp. delbrueckii and Carnobacterium divergens. High enzymatic activity were observed with E. faecalis particularly on lipase and protease assay. While C. divergens have no enzymatic activity against lipase, protease, amylase and cellulase. The antimicrobial property of L. delbrueckii is only susceptible to amoxicillin unlike the other three bacteria isolates. No antagonistic activity were observed with the four bacterial strains against Bacillus subtilis, Staphylococcus aureus and Escherichia coli. The result of this study showed promising benefits to the industry especially in developing countries like the Philippines because population are not yet so aware of this organisms and the benefits that can be derived through their consumption.


2012 ◽  
Vol 63 (2) ◽  
pp. 607-614 ◽  
Author(s):  
Yi-sheng Chen ◽  
Hui-chung Wu ◽  
Shwu-fen Pan ◽  
Bo-guang Lin ◽  
Yen-hung Lin ◽  
...  

2014 ◽  
Vol 50 (2) ◽  
pp. 321-327 ◽  
Author(s):  
Krischina Singer Aplevicz ◽  
Jaciara Zarpellon Mazo ◽  
Eunice Cassanego Ilha ◽  
Andréia Zilio Dinon ◽  
Ernani Sebastião Sant´Anna

Sourdough is a mixture of flour and water fermented by lactic acid bacteria and yeast, with a large use in bakery products. This study was developed with Brazilian grape (Niagara rosada) sourdough obtained from spontaneous fermentation. The aim of this work was to characterize genotypic and phenotypically lactic acid bacteria and yeasts isolated from sourdough. The phenotypic identification for bacteria and yeasts was performed by using the kit API50CHL and 20CAUX and the genotypic characterization was performed by sequencing method. A total of four isolated strains were analyzed in this study. Two of these strains were phenotypically and genotypic identified as Lactobacillus paracasei and one as Saccharomyces cerevisiae. Another sample phenotypically identified as Candida pelliculosa did not show the same identity by sequencing. It shows the need to use phenotypic and genotypic characterization associated for the correct microorganism identification.


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