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金枪鱼心脏动脉球中的生物活性肽:制备、鉴定、抗氧化活性以及对热、pH 值和模拟胃肠道消化处理的稳定性。

Bioactive Peptides from Skipjack Tuna Cardiac Arterial Bulbs: Preparation, Identification, Antioxidant Activity, and Stability against Thermal, pH, and Simulated Gastrointestinal Digestion Treatments.

机构信息

Zhejiang Provincial Engineering Technology Research Center of Marine Biomedical Products, School of Food and Pharmacy, Zhejiang Ocean University, Zhoushan 316022, China.

National and Provincial Joint Laboratory of Exploration, Utilization of Marine Aquatic Genetic Resources, National Engineering Research Center of Marine Facilities Aquaculture, School of Marine Science and Technology, Zhejiang Ocean University, Zhoushan 316022, China.

出版信息

Mar Drugs. 2022 Sep 30;20(10):626. doi: 10.3390/md20100626.

DOI:10.3390/md20100626
PMID:36286450
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9604775/
Abstract

Cardiac arterial bulbs of Skipjack tuna () are rich in elastin, and its hydrolysates are high quality raw materials for daily cosmetics. In order to effectively utilizing Skipjack tuna processing byproducts-cardiac arterial bulbs and to prepare peptides with high antioxidant activity, pepsin was selected from six proteases for hydrolyzing proteins, and the best hydrolysis conditions of pepsin were optimized. Using ultrafiltration and chromatographic methods, eleven antioxidant peptides were purified from protein hydrolysate of tuna cardiac arterial bulbs. Four tripeptides (QGD, PKK, GPQ and GLN) were identified as well as seven pentapeptides (GEQSN, GEEGD, YEGGD, GEGER, GEGQR, GPGLM and GDRGD). Three out of them, namely the tripeptide PKK and the pentapeptides YEGGD and GPGLM exhibited the highest radical scavenging activities on 2,2-diphenyl-1-picrylhydrazyl (DPPH), hydroxyl, 2,2'-azino-bis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS) and superoxide anion assays. They also showed to protect plasmid DNA and HepG2 cells against HO-induced oxidative stress. Furthermore, they exhibited high stability under temperature ranged from 20-100 °C, pH values ranged from 3-11, and they simulated gastrointestinal digestion for 240 min. These results suggest that the prepared eleven antioxidant peptides from cardiac arterial bulbs, especially the three peptides PKK, YEGGD, and GPGLM, could serve as promising candidates in health-promoting products due to their high antioxidant activity and their stability.

摘要

大眼金枪鱼()的心脏动脉球富含弹性蛋白,其水解产物是高品质的日常化妆品原料。为了有效利用大眼金枪鱼加工副产物——心脏动脉球,并制备具有高抗氧化活性的肽,本研究从 6 种蛋白酶中选择胃蛋白酶来水解蛋白质,并对胃蛋白酶的最佳水解条件进行了优化。利用超滤和色谱方法,从金枪鱼心脏动脉球蛋白水解物中纯化出 11 种抗氧化肽。鉴定出 4 个三肽(QGD、PKK、GPQ 和 GLN)和 7 个五肽(GEQSN、GEEGD、YEGGD、GEGER、GEGQR、GPGLM 和 GDRGD)。其中 3 种,即三肽 PKK 和五肽 YEGGD 和 GPGLM,对 2,2-二苯基-1-苦基肼基(DPPH)、羟基、2,2'-联氮基-3-乙基苯并噻唑啉-6-磺酸(ABTS)和超氧阴离子自由基具有最高的清除活性。它们还能保护质粒 DNA 和 HepG2 细胞免受 HO 诱导的氧化应激。此外,它们在 20-100°C 的温度范围内、pH 值 3-11 范围内以及模拟胃肠道消化 240 分钟的条件下均表现出较高的稳定性。这些结果表明,从心脏动脉球制备的 11 种抗氧化肽,特别是 PKK、YEGGD 和 GPGLM 这 3 种肽,由于其高抗氧化活性和稳定性,可能成为促进健康产品的有前途的候选物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/a98fbf9311f4/marinedrugs-20-00626-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/4530e48eb385/marinedrugs-20-00626-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/89b4013bd383/marinedrugs-20-00626-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/0417710f3c94/marinedrugs-20-00626-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/bb1ed009578b/marinedrugs-20-00626-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/770e863f62eb/marinedrugs-20-00626-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/414f5f07ec9b/marinedrugs-20-00626-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/60fce9889de0/marinedrugs-20-00626-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/8dc4648d11df/marinedrugs-20-00626-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/c32f8da830ce/marinedrugs-20-00626-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/546c12dfa257/marinedrugs-20-00626-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/a98fbf9311f4/marinedrugs-20-00626-g014.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/4530e48eb385/marinedrugs-20-00626-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/9fc419258f27/marinedrugs-20-00626-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/b9f995a7e1b8/marinedrugs-20-00626-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/38983631d069/marinedrugs-20-00626-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/89b4013bd383/marinedrugs-20-00626-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/0417710f3c94/marinedrugs-20-00626-g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/bb1ed009578b/marinedrugs-20-00626-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/770e863f62eb/marinedrugs-20-00626-g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/414f5f07ec9b/marinedrugs-20-00626-g009.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/60fce9889de0/marinedrugs-20-00626-g010.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/8dc4648d11df/marinedrugs-20-00626-g011.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/c32f8da830ce/marinedrugs-20-00626-g012.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/546c12dfa257/marinedrugs-20-00626-g013.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cf67/9604775/a98fbf9311f4/marinedrugs-20-00626-g014.jpg

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