Exploring the Physicochemical Characteristics of Marine Protein Hydrolysates and the Impact of In Vitro Gastrointestinal Digestion on Their Bioactivity.

IF 4.9 2区 医学 Q1 CHEMISTRY, MEDICINAL
Marine Drugs Pub Date : 2024-10-01 DOI:10.3390/md22100452
Deepanshi Sharma, Snehal Gite, Maria G Tuohy
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引用次数: 0

Abstract

Fish protein hydrolysates (FPHs) were obtained from different fish sources using a combination of microbial enzymes. The industrially produced FPHs from blue whiting (Micromesistius poutassou) and sprat (Sprattus sprattus) were compared to freeze-dried FPHs generated in-house from hake (Merluccius merluccius) and mackerel (Scomber scombrus) in terms of their physicochemical composition and functionality. Significant differences (p < 0.05) were observed in the protein, moisture, and ash contents of the FPHs, with the majority having high levels of protein (73.24-89.31%). Fractions that were more extensively hydrolysed exhibited a high solubility index (74.05-98.99%) at different pHs. Blue whiting protein hydrolysate-B (BWPH-B) had the highest foaming capacity at pH 4 (146.98 ± 4.28%) and foam stability over 5 min (90-100%) at pH 4, 6, and 8. The emulsifying capacity ranged from 61.11-108.90 m2/g, while emulsion stability was 37.82-76.99% at 0.5% (w/v) concentration. In terms of peptide bioactivity, sprat protein hydrolysate (SPH) had the strongest overall reducing power. The highest Cu2+ chelating activity was exhibited by hake protein hydrolysate (HPH) and mackerel protein hydrolysate (MPH), with IC50 values of 0.66 and 0.78 mg protein/mL, respectively, while blue whiting protein hydrolysate-A (BWPH-A) had the highest activity against Fe2+ (IC50 = 1.89 mg protein/mL). SPH scavenged DPPH and ABTS radicals best with IC50 values of 0.73 and 2.76 mg protein/mL, respectively. All FPHs displayed noteworthy scavenging activity against hydroxyl radicals, with IC50 values ranging from 0.48-3.46 mg protein/mL. SPH and MPH showed the highest scavenging potential against superoxide radicals with IC50 values of 1.75 and 2.53 mg protein/mL and against hydrogen peroxide with 2.22 and 3.66 mg protein/mL, respectively. While inhibition of α-glucosidase was not observed, the IC50 values against α-amylase ranged from 8.81-18.42 mg protein/mL, with SPH displaying the highest activity. The stability of FPHs following simulated gastrointestinal digestion (SGID) showed an irregular trend. Overall, the findings suggest that marine-derived protein hydrolysates may serve as good sources of natural nutraceuticals with antioxidant and antidiabetic properties.

探索海洋蛋白质水解物的理化特性以及体外胃肠消化对其生物活性的影响
利用微生物酶的组合从不同鱼类来源获得了鱼蛋白水解物(FPHs)。将从蓝鳕鱼(Micromesistius poutassou)和鲱鱼(Sprattus sprattus)中工业化生产的 FPH 与从无须鳕(Merluccius merluccius)和鲭鱼(Scomber scombrus)中自行生产的冻干 FPH 在理化成分和功能方面进行了比较。观察发现,FPH 的蛋白质、水分和灰分含量存在显著差异(p < 0.05),其中大部分蛋白质含量较高(73.24%-89.31%)。水解程度较高的馏分在不同的 pH 值下表现出较高的溶解指数(74.05-98.99%)。蓝鳕鱼蛋白水解物-B(BWPH-B)在 pH 值为 4 时的发泡能力最高(146.98 ± 4.28%),在 pH 值为 4、6 和 8 时,5 分钟内的泡沫稳定性最高(90-100%)。乳化能力在 61.11-108.90 m2/g 之间,乳化稳定性在 0.5%(w/v)浓度时为 37.82-76.99%。在肽的生物活性方面,鲱鱼蛋白水解物(SPH)的总体还原力最强。无须鳕蛋白水解物(HPH)和鲭鱼蛋白水解物(MPH)的 Cu2+ 螯合活性最高,IC50 值分别为 0.66 和 0.78 毫克蛋白/毫升,而蓝鳕蛋白水解物-A(BWPH-A)对 Fe2+ 的活性最高(IC50 = 1.89 毫克蛋白/毫升)。SPH 清除 DPPH 和 ABTS 自由基的能力最强,IC50 值分别为 0.73 和 2.76 毫克蛋白质/毫升。所有 FPH 对羟自由基都有显著的清除活性,IC50 值为 0.48-3.46 毫克蛋白质/毫升。SPH 和 MPH 对超氧自由基的清除潜力最高,IC50 值分别为 1.75 和 2.53 毫克蛋白/毫升,对过氧化氢的清除潜力分别为 2.22 和 3.66 毫克蛋白/毫升。虽然未观察到对α-葡萄糖苷酶的抑制作用,但对α-淀粉酶的 IC50 值介于 8.81-18.42 毫克蛋白/毫升之间,其中 SPH 的活性最高。模拟胃肠道消化(SGID)后,FPHs 的稳定性呈不规则趋势。总之,研究结果表明,海洋衍生蛋白水解物可作为具有抗氧化和抗糖尿病特性的天然营养保健品的良好来源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Marine Drugs
Marine Drugs 医学-医药化学
CiteScore
9.60
自引率
14.80%
发文量
671
审稿时长
1 months
期刊介绍: Marine Drugs (ISSN 1660-3397) publishes reviews, regular research papers and short notes on the research, development and production of drugs from the sea. Our aim is to encourage scientists to publish their experimental and theoretical research in as much detail as possible, particularly synthetic procedures and characterization information for bioactive compounds. There is no restriction on the length of the experimental section.
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