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Gouda Cheese with Modified Content of β-Casein as a Source of Peptides with ACE- and DPP-IV-Inhibiting Bioactivity: A Study Based on In Silico and In Vitro Protocol

机译:Gouda乳酪具有β-酪蛋白的改性含量作为肽和DPP-IV抑制生物活性的肽来源:基于硅和体外方案的研究

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摘要

In silico and in vitro methods were used to analyze ACE- and DPP-IV-inhibiting potential of Gouda cheese with a modified content of β-casein. Firstly, the BIOPEP-UWM database was used to predict the presence of ACE and DPP-IV inhibitors in casein sequences. Then, the following Gouda cheeses were produced: with decreased, increased, and normative content of β-casein after 1 and 60 days of ripening each (six variants in total). Finally, determination of the ACE/DPP-IV-inhibitory activity and the identification of peptides in respective Gouda-derived water-soluble extracts were carried out. The identification analyses were supported with in silico calculations, i.e., heatmaps and quantitative parameters. All Gouda variants exhibited comparable ACE inhibition, whereas DPP-IV inhibition was more diversified among the samples. The samples derived from Gouda with the increased content of β-casein (both stages of ripening) had the highest DPP-IV-inhibiting potency compared to the same samples measured for ACE inhibition. Regardless of the results concerning ACE and DPP-IV inhibition among the cheese samples, the heatmap showed that the latter bioactivity was predominant in all Gouda variants, presumably because it was based on the qualitative approach (i.e., peptide presence in the sample). Our heatmap did not include the bioactivity of a single peptide as well as its quantity in the sample. In turn, the quantitative parameters showed that the best sources of ACE/DPP-IV inhibitors were all Gouda-derived extracts obtained after 60 days of the ripening. Although our protocol was efficient in showing some regularities among Gouda cheese variants, in vivo studies are recommended for more extensive investigations of this subject.
机译:在硅和体外方法中,用于分析Gouda Cheese的Ace-and DPP-IV抑制潜力,其具有β-酪蛋白的改性含量。首先,BioPep-UWM数据库用于预测酪蛋白序列中ACE和DPP-IV抑制剂的存在。然后,产生以下牙龈奶酪:在每次成熟的1和60天后,β-酪蛋白的减少,增加和规范性含量(总共六种变体)。最后,进行了ACE / DPP-IV抑制活性的测定和各种荷衍生的水溶性提取物中的肽鉴定。在硅计算中支持鉴定分析,即加热线和定量参数。所有Gouda变体都表现出相当的ACE抑制,而DPP-IV抑制在样品中更多样化。与β-酪蛋白(成熟阶段)的增加的荷达含量衍生的样品具有最高的DPP-IV抑制效力,与用于ACE抑制的相同样品相比。无论奶酪样品中的ACE和DPP-IV抑制的结果如何,Heatmap都显示出后一种生物活性在所有Gouda变体中占主导地位,可能是因为它基于定性方法(即,样品中的肽存在)。我们的热爱图不包括单一肽的生物活性以及样品中的量。反过来,定量参数表明,ACE / DPP-IV抑制剂的最佳来源是在成熟的60天后获得的所有Gouda衍生的提取物。虽然我们的协议在展示了Gouda奶酪变体中的一些规律方面,但在体内研究中建议进行更广泛的调查。

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