Screening for potential novel probiotic Lactobacillus strains based on high dipeptidyl peptidase IV and α-glucosidase inhibitory activity
•Lactobacillus strains displayed DPP-IV inhibitory activity in vitro.•DPP-IV inhibition was concentration-dependent and stable to temperature and pH.•Trypsin treatment significantly enhanced DPP-IV inhibitory property.•Some strains showed both DPP-IV and α-glucosidase inhibitory property in vitro. L...
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Veröffentlicht in: | Journal of functional foods 2016-01, Vol.20, p.486-495 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | •Lactobacillus strains displayed DPP-IV inhibitory activity in vitro.•DPP-IV inhibition was concentration-dependent and stable to temperature and pH.•Trypsin treatment significantly enhanced DPP-IV inhibitory property.•Some strains showed both DPP-IV and α-glucosidase inhibitory property in vitro.
Lactobacillus strains were screened for inhibition of dipeptidyl peptidase IV (DPP-IV) and α-glucosidase. Cell-free excretory supernatants (CFS) and cell-free extracts (CFE) of 21 strains were prepared, and most of them showed DPP-IV inhibition in a concentration-dependent manner, which started at the exponential phase and peaked at the stationary phase of the Lactobacillus. The CFS bioactivity was heat-resistant, stable to acid–alkali and glucosidase treatment. Trypsin treatment specifically elevated CFS's DPP-IV inhibition. Lactobacillus plantarum strains CFS displayed different protein patterns and trypsin sensitive bands on SDS-PAGE, demonstrating specific peptide-cleavage contributes to higher inhibition. Seven strains with highest DPP-IV inhibition also displayed α-glucosidase inhibitory activity, of which, three strains of L. plantarum and one of Lactobacillus brevis showed tolerance to simulated gastrointestinal tract conditions and high HT-29 cell adhesion. This initial report of lactobacilli secreting strong DPP-IV and α-glucosidase inhibition components will be beneficial for selection and application of anti-diabetic probiotics. |
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ISSN: | 1756-4646 2214-9414 |
DOI: | 10.1016/j.jff.2015.11.030 |