1Laboratory for Animal Nutrition and Animal Product Quality,Department of Animal Production,Ghent University,Coupure Links 653,Block F,9000 Ghent,Belgium.
2Particle and Interfacial Technology Group, Faculty of Bioscience Engineering,Ghent University,Coupure Links 653,Block B,9000 Ghent,Belgium.
Animal. 2018 Dec;12(12):2539-2550. doi: 10.1017/S1751731118000423. Epub 2018 Mar 16.
Previously, polyunsaturated fatty acids (PUFA) from linseed oil were effectively protected (>80%) against biohydrogenation through polyphenol-oxidase-mediated protein crosslinking of an emulsion, prepared with polyphenol oxidase (PPO) extract from potato tuber peelings. However, until now, emulsions of only 2 wt% oil have been successfully protected, which implies serious limitations both from a research perspective (e.g. in vivo trials) as well as for further upscaling toward practical applications. Therefore, the aim of this study was to increase the oil/PPO ratio. In the original protocol, the PPO extract served both an emulsifying function as well as a crosslinking function. Here, it was first evaluated whether alternative protein sources could replace the emulsifying function of the PPO extract, with addition of PPO extract and 4-methylcatechol (4MC) to induce crosslinking after emulsion preparation. This approach was then further used to evaluate protection of emulsions with higher oil content. Five candidate emulsifiers (soy glycinin, gelatin, whey protein isolate (WPI), bovine serum albumin and sodium caseinate) were used to prepare 10 wt% oil emulsions, which were diluted five times (w/w) with PPO extract (experiment 1). As a positive control, 2 wt% oil emulsions were prepared directly with PPO extract according to the original protocol. Further, emulsions of 2, 4, 6, 8 and 10 wt% oil were prepared, with 80 wt% PPO extract (experiment 2), or with 90, 80, 70, 60 and 50 wt% PPO extract, respectively (experiment 3) starting from WPI-stabilized emulsions. Enzymatic crosslinking was induced by 24-h incubation with 4MC. Ruminal protection efficiency was evaluated by 24-h in vitro batch simulation of the rumen metabolism. In experiment 1, protection efficiencies were equal or higher than the control (85.5% to 92.5% v. 81.3%). In both experiments 2 and 3, high protection efficiencies (>80%) were achieved, except for emulsions containing 10 wt% oil emulsions (<50% protection), which showed oiling-off after enzymatic crosslinking. This study demonstrated that alternative emulsifier proteins can be used in combination with PPO extract to protect emulsified PUFA-rich oils against ruminal biohydrogenation. By applying the new protocol, 6.5 times less PPO extract was required.
先前,通过多酚氧化酶介导的乳液蛋白质交联作用,亚麻籽油中的多不饱和脂肪酸(PUFA)可以得到有效保护(>80%),该交联作用是用马铃薯皮多酚氧化酶(PPO)提取物制备乳液时发生的。然而,直到现在,只有 2wt%的油乳液才成功得到了保护,这意味着从研究角度(例如体内试验)以及进一步扩大到实际应用方面都存在严重的局限性。因此,本研究的目的是增加油/PPO 比例。在原始方案中,PPO 提取物既具有乳化功能,也具有交联功能。在这里,首先评估了替代蛋白质来源是否可以替代 PPO 提取物的乳化功能,方法是在制备乳液后添加 PPO 提取物和 4-甲基儿茶酚(4MC)以诱导交联。然后,采用该方法进一步评估了具有更高油含量的乳液的保护效果。使用五种候选乳化剂(大豆分离蛋白、明胶、乳清蛋白分离物(WPI)、牛血清白蛋白和酪蛋白酸钠)制备 10wt%油乳液,然后将其与 PPO 提取物以五倍重量比(w/w)稀释(实验 1)。作为阳性对照,直接根据原始方案用 PPO 提取物制备 2wt%油乳液。此外,还分别用 80wt%PPO 提取物(实验 2)或 90wt%、80wt%、70wt%、60wt%和 50wt%PPO 提取物(实验 3)制备了 2wt%、4wt%、6wt%、8wt%和 10wt%油的乳液,从 WPI 稳定的乳液开始。通过 24 小时孵育 4MC 诱导酶促交联。通过 24 小时体外模拟瘤胃代谢来评估瘤胃保护效率。在实验 1 中,保护效率与对照组相等或更高(85.5%至 92.5%v.81.3%)。在实验 2 和 3 中,除了含有 10wt%油乳液(<50%保护)在酶促交联后出现油分离外,均实现了>80%的高保护效率。本研究表明,替代乳化蛋白可以与 PPO 提取物结合使用,以保护乳化富含多不饱和脂肪酸的油免受瘤胃生物氢化作用的影响。应用新方案后,PPO 提取物的用量减少了 6.5 倍。