Oyster-Derived Zinc-Binding Peptide Modified by Plastein Reaction via Zinc Chelation Promotes the Intestinal Absorption of Zinc

Marine Drugs - Tập 17 Số 6 - Trang 341
Chonghe Li1, Huili Gong1, Wang1, Gao2, Ren Ren3, Aimin Zhou4, Wang4, Xu5, Xiao Xiao6, Mingwu Shen1, Zhao1
1College of Food Science and Engineering, Ocean University of China, Qingdao 266003, China
2School of Food and Bioengineering, Jiangsu University, Zhenjiang 212013, China
3School of Food Sciences and Engineering, South China University of Technology, Guangzhou 510641, China
4Hisense (Shandong) Refrigerator Co., Ltd., Qingdao 266100, China
5Jiangsu Baoyuan Biotechnology Co. Ltd., Lianyungang 222100, China
6College of Food and Bioengineering, Henan University of Science and Technology, Luoyang 471023, China

Tóm tắt

Zinc-binding peptides from oyster (Crassostrea gigas) have potential effects on zinc supplementation. The aim of this study was to prepare efficient zinc-binding peptides from oyster-modified hydrolysates by adding exogenous glutamate according to the plastein reaction and to further explore the zinc absorption mechanism of the peptide-zinc complex (MZ). The optimum conditions for the plastein reaction were as follows: pH 5.0, 40 °C, substrate concentration of 40%, pepsin dosage of 500 U/g, reaction time of 3 h and l-[1-13C]glutamate concentration of 10 mg/mL. The results of 13C isotope labelling suggested that the addition of l-[1-13C]glutamate contributed to the increase in the zinc-binding capacity of the peptide. The hydrophobic interaction was the main mechanism of action of the plastein reaction. Ultraviolet spectra and scanning electronic microscopy (SEM) revealed that the zinc-binding peptide could bind with zinc and form MZ. Furthermore, MZ could significantly enhance zinc bioavailability in the presence of phytic acid, compared to the commonly used ZnSO4. Additionally, MZ significantly promoted the intestinal absorption of zinc mainly through two pathways, the zinc ion channel and the small peptide transport pathway. Our work attempted to increase the understanding of the zinc absorption mechanism of MZ and to support the potential application of MZ as a supplementary medicine.

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Tài liệu tham khảo

Prasad, 2014, Zinc: An antioxidant and anti-inflammatory agent: Role of zinc in degenerative disorders of aging, J. Trace Elem. Med. Biol., 28, 364, 10.1016/j.jtemb.2014.07.019

Trame, 2018, A short 18 items food frequency questionnaire biochemically validated to estimate zinc status in humans, J. Trace Elem. Med. Biol., 49, 285, 10.1016/j.jtemb.2018.02.020

Spenser, 2015, Chronic zinc deficiency alters chick gut microbiota composition and function, Nutrients, 7, 9768, 10.3390/nu7125497

Choi, 2018, Zinc deficiency and cellular oxidative stress: Prognostic implications in cardiovascular diseases, Acta Pharmacol. Sin., 39, 1120, 10.1038/aps.2018.25

Udechukwu, 2016, Prospects of enhancing dietary zinc bioavailability with food-derived zinc-chelating peptides, Food Funct., 7, 4137, 10.1039/C6FO00706F

Dostal, 2011, Iron depletion and repletion with ferrous sulfate or electrolytic iron modifies the composition and metabolic activity of the gut microbiota in rats, J. Nutr., 142, 271, 10.3945/jn.111.148643

Puckett, 2012, Oyster demographics in a network of no-take reserves: Recruitment, growth, survival, and density dependence, Mar. Coast. Fish., 4, 605, 10.1080/19425120.2012.713892

Liu, 2008, Production of cysteine-rich antimicrobial peptide by digestion of oyster (Crassostrea gigas) with alcalase and bromelin, Food Control, 19, 231, 10.1016/j.foodcont.2007.03.004

Qian, 2008, Protective effect of an antioxidative peptide purified from gastrointestinal digests of oyster, Crassostrea gigas against free radical induced DNA damage, Bioresour. Technol., 99, 3365, 10.1016/j.biortech.2007.08.018

Umayaparvathi, 2014, Antioxidant activity and anticancer effect of bioactive peptide from enzymatic hydrolysate of oyster (Saccostrea cucullata), Biomed. Prev. Nutr., 4, 343, 10.1016/j.bionut.2014.04.006

Zeng, 2008, Antiviral active peptide from oyster, Chin. J. Oceanol. Limn., 26, 307, 10.1007/s00343-008-0307-x

Shiozaki, 2010, Identification of oyster-derived hypotensive peptide acting as angiotensin-I-converting enzyme inhibitor, Fish. Sci., 76, 865, 10.1007/s12562-010-0264-0

Coombs, 1972, The distribution of zinc in the oyster Ostrea edulis and its relation to enzymic activity and to other metals, Mar. Biol., 12, 170, 10.1007/BF00350752

Chen, 2013, Purification and characterisation of a zinc-binding peptide from oyster protein hydrolysate, J. Funct. Foods, 5, 689, 10.1016/j.jff.2013.01.012

Zhang, 2018, Particulate nanocomposite from oyster (Crassostrea rivularis) hydrolysates via zinc chelation improves zinc solubility and peptide activity, Food Chem., 258, 269, 10.1016/j.foodchem.2018.03.030

Cao, 2018, Separation and identification of oyster peptide modified by plastein reaction and characterization of peptide-zinc complexes, Chem. J. Chin. Univ., 39, 470

Li, J., Liu, Z., Zhao, Y., Zhu, X., Yu, R., Dong, S., and Wu, H. (2018). Novel natural angiotensin converting enzyme (ACE)-inhibitory peptides derived from sea cucumber-modified hydrolysates by adding exogenous proline and a study of their structure–activity relationship. Mar. Drugs, 16.

Brownsell, 2001, Application of the plastein reaction to mycoprotein: II. Plastein properties, Food Chem., 72, 337, 10.1016/S0308-8146(00)00234-X

Suisui, 2018, Modification of ACE-inhibitory peptides from Acaudina molpadioidea using the plastein reaction and examination of its mechanism, Food Biosci., 26, 1, 10.1016/j.fbio.2018.08.008

Sun, S., Xu, X., Sun, X., Zhang, X., Chen, X., and Xu, N. (2019). Preparation and identification of ACE inhibitory peptides from the marine macroalga ulva intestinalis. Mar. Drugs, 17.

Piper, 1965, pH stability and activity curves of pepsin with special reference to their clinical importance, Gut, 6, 506, 10.1136/gut.6.5.506

Mauri, 2015, Amaranth protein films reinforced with maize starch nanocrystals, Food Hydrocolloid., 47, 146, 10.1016/j.foodhyd.2015.01.026

Grallert, A., and Hagan, I.M. (2017). Preparation of protein extracts from Schizosaccharomyces pombe using trichloroacetic acid precipitation. Cold Spring Harb. Protoc., 139–143.

Makhatadze, 1992, Protein interactions with urea and guanidinium chloride: A calorimetric study, J. Mol. Biol., 226, 491, 10.1016/0022-2836(92)90963-K

Sharma, 2013, The effect of Cu2+ and Zn2+ on the Aβ42 peptide aggregation and cellular toxicity, Metallomics, 5, 1529, 10.1039/c3mt00161j

Feng, 2018, Biogenic polyphosphate nanoparticles from Synechococcus sp. PCC 7002 exhibit intestinal protective potential in human intestinal epithelial cells in vitro and murine small intestine ex vivo, J. Agric. Food Chem., 66, 8026, 10.1021/acs.jafc.8b03381

Ranaldi, 2013, Intracellular zinc is required for intestinal cell survival signals triggered by the inflammatory cytokine TNFα, J. Nutr. Biochem., 24, 967, 10.1016/j.jnutbio.2012.06.020

Fukada, 2011, Zinc homeostasis and signaling in health and diseases: Zinc signaling, J. Biol. Inorg. Chem., 16, 1123, 10.1007/s00775-011-0797-4

Luo, 2018, 3-Hydroxyflavone enhances the toxicity of ZnO nanoparticles in vitro, J. Appl. Toxicol., 38, 1206, 10.1002/jat.3633

Tacnet, 1993, Mechanisms of zinc transport into pig small intestine brush-border membrane vesicles, J. Physiol., 465, 57, 10.1113/jphysiol.1993.sp019666

Cousins, 2010, Gastrointestinal factors influencing zinc absorption and homeostasis, Int. J. Vitam. Nutr. Res., 80, 243, 10.1024/0300-9831/a000030

Ito, 2015, Preparation, solubility, and cytocompatibility of zinc-releasing calcium phosphate ceramics, J. Biomed. Mater. Res. A, 50, 178, 10.1002/(SICI)1097-4636(200005)50:2<178::AID-JBM12>3.0.CO;2-5

Hansen, 1996, The effect of casein phosphopetides on zinc and calcium absorption from high phytate infant diets assessed in rat pups and Caco-2 cells, Pediatr. Res., 40, 547, 10.1203/00006450-199610000-00006

Zhu, 2015, Isolation and characterization of zinc-chelating peptides from wheat germ protein hydrolysates, J. Funct. Foods, 12, 23, 10.1016/j.jff.2014.10.030

Deng, 2017, Effects of dietary supplementation with tribasic zinc sulfate or zinc sulfate on growth performance, zinc content and expression of zinc transporters in young pigs, Anim. Sci. J., 88, 1556, 10.1111/asj.12788

Beck, 2004, Differential expression of hZnT-4 in Human prostate tissues, Prostate, 58, 374, 10.1002/pros.10344

Jappar, 2010, Significance and regional dependency of peptide transporter (PEPT) 1 in the intestinal permeability of glycylsarcosine: In situ single-pass perfusion studies in wild-type and Pept1 knockout mice, Drug Metab. Dispos., 38, 1740, 10.1124/dmd.110.034025

Maubon, 2007, Analysis of drug transporter expression in human intestinal Caco-2 cells by real-time PCR, Fund. Clin. Pharmacol., 21, 659, 10.1111/j.1472-8206.2007.00550.x

Ledoux, 1986, Determination of proteins and sulfobetaine with the Folin-phenol reagent, Anal. Biochem., 157, 28, 10.1016/0003-2697(86)90191-0

Zhang, 2015, Stability of modified peptide using zinc binding and plastein reaction, Mod. Food Sci. Technol., 31, 150

Moro, 2001, Hydrophobicity of whey protein concentrates measured by fluorescence quenching and its relation with surface functional properties, J. Agric. Food Chem., 49, 4784, 10.1021/jf001132e

Hartnett, 2010, The formation of heat and enzyme induced (plastein) gels from pepsin-hydrolyzed soy protein isolate, J. Food Biochem., 14, 1, 10.1111/j.1745-4514.1990.tb00817.x

Zou, 2017, Characterization of key factors of anchovy (Engraulis japonicus) meat in the nanoparticle-mediated enhancement of non-heme iron absorption, J. Agric. Food Chem., 65, 11212, 10.1021/acs.jafc.7b04547

Duan, 2014, Transport characteristics of isorhamnetin across intestinal Caco-2 cell monolayers and the effects of transporters on it, Food Chem. Toxicol., 66, 313, 10.1016/j.fct.2014.02.003

Wu, 2014, Enhancement of non-heme iron absorption by anchovy (Engraulis japonicus) muscle protein hydrolysate involves a nanoparticle-mediated mechanism, J. Agric. Food Chem., 62, 8632, 10.1021/jf5018719

Makhov, 2008, Zinc chelation induces rapid depletion of the X-linked inhibitor of apoptosis and sensitizes prostate cancer cells to TRAIL-mediated apoptosis, Cell Death Differ., 15, 1745, 10.1038/cdd.2008.106

Sreenivasulu, 2008, Effect of dietary ligands and food matrices on zinc uptake in Caco-2 cells: Implications in assessing zinc bioavailability, J. Agric. Food Chem., 56, 10967, 10.1021/jf802060q

Li, 2019, Cooperation of lactic acid bacteria regulated by the AI-2/LuxS system involve in the biopreservation of refrigerated shrimp, Food Res. Int., 120, 679, 10.1016/j.foodres.2018.11.025

Gori, 2009, AI-2 signalling is induced by acidic shock in probiotic strains of Lactobacillus spp., Int. J. Food Microbiol., 135, 295, 10.1016/j.ijfoodmicro.2009.08.011