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1.
Benef Microbes ; 10(4): 449-461, 2019 Apr 19.
Article in English | MEDLINE | ID: mdl-30957533

ABSTRACT

Anti-genotoxic or anti-mutagenic activity has been described for a number of Gram-positive probiotic bacterial species. Here we present evidence that Gram-negative Escherichia coli Nissle 1917 (EcN) also displays anti-genotoxic/anti-mutagenic activity, as assessed in vitro by the Comet Assay and the Ames Test, respectively. This activity was demonstrated by use of the mutagens 4-nitroquinoline-1-oxide (NQO), hydrogen peroxide (H2O2) and benzo(a) pyrene (B[a]P). For both assays and all three test agents the anti-genotoxic/anti-mutagenic activity of EcN was shown to be concentration dependent. By the use of extracts of bacteria that were inactivated by various procedures (heat treatment, ultrasound sonication or ultraviolet light irradiation), mechanistic explanations could be put forward. The proposed mechanisms were enforced by treating the bacterial material with proteinase K prior to testing. The mutagen H2O2 is most likely inactivated by enzymic activity, with catalase a likely candidate, while several explanations can be put forward for inactivation of B[a]P. NQO is most likely inactivated by metabolising enzymes, since the formation of the metabolite 4-aminoquinoline could be demonstrated. In conclusion, the in vitro results presented here make a strong case for antimutagenic properties of EcN.


Subject(s)
Antimutagenic Agents/metabolism , Escherichia coli/metabolism , Mutagens/metabolism , 4-Nitroquinoline-1-oxide/metabolism , 4-Nitroquinoline-1-oxide/pharmacology , Aminoquinolines/metabolism , Benzo(a)pyrene/metabolism , Benzo(a)pyrene/pharmacology , Caco-2 Cells , Culture Media, Conditioned , Endopeptidase K/pharmacology , Escherichia coli/drug effects , Humans , Hydrogen Peroxide/metabolism , Hydrogen Peroxide/pharmacology , Mutagenicity Tests , Mutagens/pharmacology
2.
Food Res Int ; 102: 748-758, 2017 12.
Article in English | MEDLINE | ID: mdl-29196008

ABSTRACT

The effect of buttermilk powder addition post-curd formation or buttermilk addition to cheese milk on total and individual phospholipid content, chemical composition, enzyme activity, microbial populations and microstructure within Cheddar-style cheese was investigated. Buttermilk or buttermilk powder addition resulted in significant increases in total phospholipid content and their distribution throughout the cheese matrix. Addition of 10% buttermilk powder resulted in higher phospholipid content, moisture, pH and salt in moisture levels, and lower fat, fat in dry matter, L. helveticus and non-starter bacteria levels in cheeses. Buttermilk powder inclusion resulted in lower pH4.6/Soluble Nitrogen (SN) levels and significantly lower free amino acid levels in 10% buttermilk powder cheeses. Buttermilk addition provided a more porous cheese microstructure with greater fat globule coalescence and increased free fat pools, while also increasing moisture and decreasing protein, fat and pH levels. Addition of buttermilk in liquid or powdered form offers potential for new cheeses with associated health benefits.


Subject(s)
Buttermilk , Cheese/analysis , Cheese/microbiology , Food Handling/methods , Microbial Viability , Phospholipids/analysis , Amino Acids/analysis , Animals , Food, Preserved , Health Promotion , Hydrogen-Ion Concentration , Milk , Sodium Chloride , Water/analysis
3.
Food Chem ; 141(2): 879-88, 2013 Nov 15.
Article in English | MEDLINE | ID: mdl-23790862

ABSTRACT

The main objective of this study was to investigate the oxidative stability and non-enzymatic browning reactions of marine PL in the presence or in the absence of primary amine group from aminophospholipids and amino acids. Marine phospholipids liposomal dispersions were prepared from two authentic standards (phosphatidylcholine and phosphatidylethanolamine) and two purified PL from marine sources with and without addition of amino acids (leucine, methionine and lysine). Samples were incubated at 60°C for 0, 2, 4 and 6days. Non-enzymatic browning reactions were investigated through measurement of (i) Strecker derived volatiles, (ii) yellowness index (YI), (iii) hydrophobic and (iv) hydrophilic pyrroles content. The oxidative stability of the samples was assessed through measurement of secondary lipid derived volatile oxidation products. The result showed that the presence of PE and amino acids caused the formation of pyrroles, generated Strecker derived volatiles, decreased the YI development and lowered lipid oxidation. The lower degree of lipid oxidation in liposomal dispersions containing amino acids might be attributed to antioxidative properties of pyrroles or amino acids.


Subject(s)
Amino Acids/chemistry , Phospholipids/chemistry , Drug Stability , Lipid Peroxidation , Lipids/chemistry , Molecular Structure
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