Chair of Food Biochemistry, Faculty of Food Science, University of Warmia and Mazury in Olsztyn, Pl. Cieszyński 1, 10-726 Olsztyn-Kortowo, Poland.
Department of Dairy Science and Quality Management, Faculty of Food Science, University of Warmia and Mazury in Olsztyn, Oczapowskiego 7, 10-719 Olsztyn-Kortowo, Poland.
Int J Mol Sci. 2021 Mar 14;22(6):2949. doi: 10.3390/ijms22062949.
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.
采用计算机模拟和体外方法分析了β-酪蛋白含量改良的高达干酪的 ACE 和 DPP-IV 抑制潜力。首先,使用 BIOPEP-UWM 数据库预测乳清蛋白序列中 ACE 和 DPP-IV 抑制剂的存在。然后,制作了以下高达干酪:每 1 天和 60 天成熟时β-酪蛋白含量降低、增加和正常(共 6 种变体)。最后,测定各自的高达衍生水溶性提取物中的 ACE/DPP-IV 抑制活性和肽的鉴定。鉴定分析得到了计算机模拟计算的支持,即热图和定量参数。所有高达变体的 ACE 抑制活性相当,而 DPP-IV 抑制活性在样品之间则更为多样化。与相同的 ACE 抑制样品相比,来自成熟度较高的β-酪蛋白含量增加的高达(两个成熟阶段)的样品具有最高的 DPP-IV 抑制活性。无论奶酪样品的 ACE 和 DPP-IV 抑制结果如何,热图显示后者在所有高达变体中都占主导地位,可能是因为它基于定性方法(即样品中存在肽)。我们的热图没有包括单个肽的生物活性及其在样品中的数量。相反,定量参数表明,ACE/DPP-IV 抑制剂的最佳来源是经过 60 天成熟后获得的所有高达衍生提取物。尽管我们的方案能够有效地显示高达干酪变体之间的一些规律,但建议进行体内研究以更广泛地研究这一主题。