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1.
Pol J Vet Sci ; 17(2): 321-9, 2014.
Article in English | MEDLINE | ID: mdl-24988859

ABSTRACT

The molecular-typing strategy, ERIC-PCR was used in an attempt to determine the genomic relationship of 28 P. aeruginosa strains isolated from faeces of healthy bovine, bovine mastitis and from faeces of hospital patients as well as from environment. ERIC-PCR fingerprinting revealed large molecular differentiation within this group of isolates. Twenty two out of 28 strains tested generated unique patterns of DNA bands and only three genotypes consisted of two isolates each were identified. We also tested the P. aeruginosa isolates for their ability to form a biofilm on abiotic surfaces including polyvinylchloride and polystyrene. Different biofilm-forming abilities were demonstrated among strains; however, most of them (64.3%) showed moderate-biofilm forming ability. The strains with increased swimming and twitching motility displayed elevated biofilm formation. However, a negative correlation was found between slime and initial biofilm production. On the basis of the results obtained, we suggest that there are no major differences in phenotypic properties between P. aeruginosa strains isolated from different sources.


Subject(s)
Biofilms/growth & development , Environmental Microbiology , Polymerase Chain Reaction/methods , Pseudomonas aeruginosa/genetics , Pseudomonas aeruginosa/physiology , Animals , Cattle , DNA, Bacterial/genetics , Feces , Female , Genetic Markers , Genotype , Humans , Mastitis, Bovine/microbiology , Movement , Pseudomonas Infections/microbiology
2.
Food Chem ; 161: 224-9, 2014 Oct 15.
Article in English | MEDLINE | ID: mdl-24837944

ABSTRACT

The purpose of the research was to examine the effect of the laboratory production of dried potato dice on the content of phenolic compounds in one yellow-fleshed potato variety and four blue-fleshed potatoes varieties. Coloured-flesh potato varieties were characterised by about three times higher amount of total phenolic content than traditional yellow-fleshed ones. The predominating phenolic acids in potato were chlorogenic acid and its isomers, which account about 90% of total phenolic content in tubers. The phenolic acid content decreased by 80% after peeling the blue-fleshed potatoes and by 60% after peeling the yellow variety. The dried potato dice obtained from yellow-fleshed potatoes had no content of phenolic acids but produced from colour-fleshed potatoes contained about 4% of the original phenolic content of the raw material. Chlorogenic acid amounted about 97% of total phenolic acid content, and the rest was neochlorogenic acid.


Subject(s)
Plant Tubers/chemistry , Polyphenols/chemistry , Solanum tuberosum/chemistry , Hydroxybenzoates
3.
Food Chem ; 159: 512-8, 2014 Sep 15.
Article in English | MEDLINE | ID: mdl-24767090

ABSTRACT

Protein hydrolysates of profitable properties were prepared from the fodder potato protein concentrate. The hydrolysis process was performed with the use of commercial available enzyme (Alcalase) over a 2 and 4 h incubation period. Chemical and amino acid composition as well as functional properties of resultant hydrolysates were determined. A 2 h long process occurred profitable to obtain preparations of well balanced amino acid composition as well as proved functional properties. The industrial preparation, modified within proteolytic enzyme, totally soluble (average 98%), was characterised by fivefold higher oil holding capacity (average 5.4 cm(3)/g) and much better foam capacity (more than 150%) as compared to the material underwent modification (13.00%, 2.1 cm(3)/g and 5.33%, respectively). Presented results suggested potential use of fodder potato protein not destined directly for food purposes as the suitable product for preparations characterised by high nutritive value and functional properties.


Subject(s)
Food Analysis/methods , Protein Hydrolysates/chemistry , Solanum tuberosum/chemistry , Amino Acids/chemistry , Amino Acids/metabolism , Animal Feed , Bacillus/metabolism , Colorimetry , Hydrolysis , Molecular Weight , Nutritive Value , Peptide Hydrolases/metabolism , Proteolysis , Reproducibility of Results , Solubility , Spectrophotometry , Subtilisins/metabolism
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