合成乳清蛋白和牛乳清蛋白的蛋白质组和 N-聚糖比较及其对人体肠道微生物群的影响

Matthew Bolino, Hatice Duman, Izzet Avci, H Mehmet Kayili, Juli Petereit, Chandler Zundel, Bekir Salih, Sercan Karav, Steven A Frese
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摘要

食品生产系统的进步和客户的接受程度促使通过现代生物技术方法生产的膳食蛋白质作为传统农业来源的替代品投入商业市场。与此同时,对膳食成分如何与肠道微生物组相互作用的深入了解凸显了了解膳食与微生物组相互作用的细微差别的重要性。新型食品蛋白质因其各自的生产系统而具有不同的翻译后修饰,但这些蛋白质的特征尚未确定,也不知道它们与传统生产的同类产品有何不同。为了解决这个问题,我们对从市售冰淇淋中分离出来的酵母合成乳清蛋白成分的原蛋白组成和 N-糖蛋白进行了鉴定,并将这种新型成分与从牛乳中提取的分离乳清蛋白粉进行了比较。我们发现,尽管蛋白质组成非常相似,但这些蛋白质来源的 N-lycome却有很大差异,这反映了生产系统的生物合成机制。此外,尽管合成乳清蛋白和牛乳清蛋白都主要由β-乳球蛋白组成,但合成乳清蛋白的蛋白质组成和多样性都低于牛乳清蛋白。最后,为了了解这些 N-糖蛋白的差异是否会影响人体肠道微生物群,我们在体外粪便发酵模型中对这些蛋白质进行了测试。我们发现,两种乳清蛋白来源在三种不同的微生物组成中产生了显著差异,我们推测这是这些代表性微生物群落的 N-糖组成和降解差异的产物。这项工作强调了了解新型生物技术系统的差异如何影响这些原蛋白的生物活性,以及这些差异如何影响人类肠道微生物群的必要性。
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Proteomic and N-glycomic comparison of synthetic and bovine whey proteins and their effect on human gut microbiomes
Advances in food production systems and customer acceptance have led to the commercial launch of dietary proteins produced via modern biotechnological approaches as alternatives to traditional agricultural sources. At the same time, a deeper understanding of how dietary components interact with the gut microbiome has highlighted the importance of understanding the nuances underpin-ning diet-microbiome interactions. Novel food proteins with distinct post-translational modifications resulting from their respective production systems have not been characterized, nor how they may differ from their traditionally produced counterparts. To address this, we have characterized the pro-tein composition and N-glycome of a yeast-synthesized whey protein ingredient isolated from com-mercially available ice cream and compared this novel ingredient to whey protein powder isolate derived from bovine milk. We found that despite strong similarities in protein composition, the N-glycome significantly differs between these protein sources, reflecting the biosynthetic machinery of the production systems. Further, the composition profile and diversity of proteins found in the syn-thetic whey protein were lower relative to bovine whey protein, despite both being predominantly composed of β-lactoglobulin. Finally, to understand whether these differences in N-glycome profiles affected the human gut microbiome, we tested these proteins in an in vitro fecal fermentation model. We found that the two whey protein sources generated significant differences among three distinct microbial compositions, which we hypothesize is a product of differences in N-glycan composition and degradation by these representative microbial communities. This work highlights the need to understand how differences in novel biotechnological systems affect the bioactivity of these pro-teins, and how these differences impact the human gut microbiome.
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