4.7 Article

Multivariate correlation of infrared fingerprints and molecular weight distributions with bioactivity of poultry by-product protein hydrolysates

期刊

JOURNAL OF FUNCTIONAL FOODS
卷 95, 期 -, 页码 -

出版社

ELSEVIER
DOI: 10.1016/j.jff.2022.105170

关键词

Angiotensin-1-converting enzyme inhibition; Antioxidant; Fourier -transform infrared spectroscopy; Multivariate statistics; Protein hydrolysate; Size exclusion chromatography

资金

  1. Nofima through the PEPTEK-project
  2. Norwegian Research Council [320086]
  3. Norwegian Fund for Research Fees for Agricultural Products (FFL) [314599, 314111]

向作者/读者索取更多资源

This study investigated the correlation between chemical fingerprints and bioactivity of poultry by-product protein hydrolysates. Chemical fingerprints were obtained using Fourier-transform infrared spectroscopy and size exclusion chromatography, and the bioactivities were measured in vitro. Regression models based on the fingerprints showed good prediction performance for bioactivity, providing promising tools for quality control in the production of bioactive peptides.
Characterization of protein hydrolysates is a vital step in developing peptide-based bioactive ingredients. Multivariate correlation of chemical fingerprints and bioactivity of poultry by-product protein hydrolysates is explored as a potential analytical strategy for characterization and quality control. Chemical fingerprints of sixty hydrolysates were acquired using Fourier-transform infrared spectroscopy (FTIR) and size exclusion chromatography (SEC). Bioactivities (2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging and angiotensin-1converting enzyme (ACE-1) inhibition) were measured in vitro. Partial least squares regression models based on FTIR fingerprints or SEC chromatograms showed a better prediction performance for ACE-1 inhibition (coefficients of determination (R2) = 0.91, root mean square error of prediction (RMSECV) = 2.8; R2 = 0.85, RMSECV = 3.5, respectively) than for DPPH radical scavenging (R2 = 0.74, RMSECV = 0.3; R2 = 0.75, RMSECV = 0.3, respectively). Such models are promising tools for rapid prediction of bioactivities and as a quality control technology in production of bioactive peptides.

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