利用发酵乳酸杆菌制备具有抗炎特性的发酵奶酪乳清抗糖尿病和抗氧化肽及其分子动力学研究。

IF 2.6 4区 医学 Q2 PHARMACOLOGY & PHARMACY
Bhagyashree Das, Bethsheba Basaiawmoit, Amar Ashok Sakure, Ruchika Maurya, Mahendra Bishnoi, Kanthi Kiran Kondepudi, Bipransh Kumar Tiwary, Pooja Mounil Mankad, Ashish Patel, Subrota Hati
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引用次数: 0

摘要

本研究旨在通过将奶酪乳清废物转化为具有多种健康益处的生物活性肽来实现其价值,这可能导致营养药品和功能食品的开发,并用于制药工业。方法:研究了发酵乳杆菌(M4)发酵奶酪乳清的抗糖尿病、抗氧化和抗炎特性,以及抗氧化和抗糖尿病肽的产生。SDS PAGE和2D PAGE通过分子量和等电点对蛋白质进行鉴定,RP-HPLC对肽段进行鉴定。利用RPLC/MS对2D凝胶点的肽段序列进行鉴定,利用RP-HPLC对3 kDa和10 kDa的渗透物进行分析。Peakview软件表征了LC/MS结果,FTIR分析测量了生物活性肽的结构变化。结果:用M4发酵的奶酪乳清的抗氧化和抗糖尿病特性随着发酵时间的延长而逐渐增强,发酵48小时后效果更好。对α-葡萄糖苷酶、α-淀粉酶和脂肪酶的抑制活性分别为65.39%、66.09%和56.74%。ABTS法测定抗氧化活性(63.39%),2.5%接种48 h时水解蛋白活性最高(7.62 mg/ml)。在SDS-PAGE中,可以观察到10 ~ 30 kDa之间的蛋白带,而在2D PAGE上也可以看到10 ~ 70 kDa范围内的肽点。采用反相高效液相色谱法对多肽的不同组分进行了区分。采用反相高效液相色谱法和液相色谱/质谱法对2D凝胶点的肽序列进行鉴定。利用Peakview软件对LC/MS结果进行表征。从BIOPEP数据库中检索α-乳清蛋白和β-乳球蛋白产生的肽序列,验证发酵奶酪乳清肽的抗糖尿病和抗氧化活性。0.50 mg/mL发酵奶酪乳清显著LPS抑制RAW 264.7细胞中促炎细胞因子及其调控介质包括IL-6、IL-1β、NO和TNF-α的产生。FTIR分析了蛋白质的二级结构和构象变化。结论:本研究旨在利用乳制品废弃物和奶酪乳清生产抗糖尿病和抗氧化肽。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Production, Characterization, and Molecular Dynamic Study of Antidiabetic and Antioxidative Peptides of Fermented Cheese Whey with Anti-inflammatory Properties using Limosilactobacillus fermentum.

Introduction: This study aims to valorise cheese whey waste by converting it into bioactive peptides that have several health benefits, potentially leading to the development of nutraceuticals and functional foods and also used in pharmaceutical industry.

Methods: The study evaluates the antidiabetic, antioxidative, and anti-inflammatory properties of fermented cheese whey with Limosilactobacillus fermentum (M4), along with the production of antioxidative and antidiabetic peptides. SDS PAGE and 2D PAGE were also performed to identify proteins by molecular weight and isoelectric point, while RP-HPLC distinguished peptide fractions. Peptide sequences from 2D gel spots were identified using RPLC/MS, and RP-HPLC analyzed 3 kDa and 10 kDa permeates. Peakview software characterized the LC/MS results, and FTIR analysis measured structural changes in bioactive peptides.

Results: The antioxidative and antidiabetic properties in cheese whey fermented with M4 showed a progressive growth over extended incubation periods, higher effects were observed after fermentation for 48 hours. Inhibitory activities in α-glucosidase, α-amylase & lipase were found to be 65.39%, 66.09%, and 56.74% respectively. ABTS assay was performed to measure antioxidant activity (63.39%) and the highest proteolytic activity (7.62 mg/ml) was measured at 2.5% inoculation rate for 48 hours. In SDS-PAGE, protein bands between 10 & 30 kDa were observed, whereas peptide spots within the range of 10 to 70 kDa were also visualized on the 2D PAGE. RP-HPLC was used to distinguish different fractions of a peptide. Peptide sequences from 2D gel spots were identified using RP-HPLC & RPLC/MS. Peakview software was utilized to characterize the LC/MS results. Sequences of peptides generated from α-lactalbumin and β-lactoglobulin were searched in the BIOPEP database to validate the antidiabetic and antioxidative activities of fermented cheese whey peptides. 0.50 mg/mL of fermented cheese whey significantly LPS suppressed the production of proinflammatory cytokines as well as the mediators that govern them including IL-6, IL-1β, NO, and TNF-α in RAW 264.7 cells. FTIR was used to analysis of protein secondary structure and conformational changes.

Conclusion: This study aims to the production of antidiabetic and antioxidative peptides from dairy waste, and cheese whey.

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来源期刊
CiteScore
6.30
自引率
0.00%
发文量
302
审稿时长
2 months
期刊介绍: Current Pharmaceutical Design publishes timely in-depth reviews and research articles from leading pharmaceutical researchers in the field, covering all aspects of current research in rational drug design. Each issue is devoted to a single major therapeutic area guest edited by an acknowledged authority in the field. Each thematic issue of Current Pharmaceutical Design covers all subject areas of major importance to modern drug design including: medicinal chemistry, pharmacology, drug targets and disease mechanism.
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