Veselovsky Vladimir A, Boldyreva Daria I, Olekhnovich Evgenii I, Klimina Ksenia M, Babenko Vladislav V, Zakharevich Natalia V, Larin Andrey K, Morozov Maxim D, Zoruk Polina Y, Sergiev Petr V, Dontsova Olga A, Maev Igor V, Novik Tamara S, Kotlobay Anatoly A, Lazarev Vassili N, Lagarkova Maria A
Lopukhin Federal Research and Clinical Centre of Physical-Chemical Medicine, Moscow, Russia.
A.N. Belozersky Institute of Physico-Chemical Biology, Lomonosov Moscow State University, Moscow, Russia.
Front Nutr. 2024 Mar 21;11:1362529. doi: 10.3389/fnut.2024.1362529. eCollection 2024.
Sweet-tasting proteins (SPs) are proteins of plant origin initially isolated from tropical fruits. They are thousands of times sweeter than sucrose and most artificial sweeteners. SPs are a class of proteins capable of causing a sweet taste sensation in humans when interacting with the T1R2/T1R3 receptor. SP thaumatin has already been introduced in the food industry in some countries. Other SPs, such as monellin and brazzein, are promising products. An important stage in researching SPs, in addition to confirming the absence of toxicity, mutagenicity, oncogenicity, and allergenic effects, is studying their influence on gut microbiota. In this paper we describe changes in the composition of rat gut microbiota after six months of consuming one of two recombinant SPs-brazzein or monellin. A full length 16S gene sequencing method was used for DNA library barcoding. The MaAsLin2 analysis results showed noticeable fluctuations in the relative abundances of in brazzein-fed rat microbiota, and of in monellin-fed rat microbiota, which, however, did not exceed the standard deviation. The sucrose-fed group was associated with an increase in the relative abundance of , which may contribute to obesity. Overall, prolonged consumption of the sweet proteins brazzein and monellin did not significantly change rat microbiota and did not result in the appearance of opportunistic microbiota. This provides additional evidence for the safety of these potential sweeteners.
甜味蛋白(SPs)是最初从热带水果中分离出来的植物源蛋白质。它们比蔗糖和大多数人工甜味剂甜数千倍。SPs是一类在与T1R2/T1R3受体相互作用时能在人类中引起甜味感觉的蛋白质。索马甜蛋白已在一些国家的食品工业中得到应用。其他SPs,如莫内林和布拉齐因,都是很有前景的产品。研究SPs的一个重要阶段,除了确认其无毒性、致突变性、致癌性和过敏作用外,还包括研究它们对肠道微生物群的影响。在本文中,我们描述了大鼠食用两种重组SPs之一——布拉齐因或莫内林六个月后肠道微生物群组成的变化。采用全长16S基因测序方法进行DNA文库条形码分析。MaAsLin2分析结果显示,食用布拉齐因的大鼠微生物群中,[此处原文缺失具体内容]的相对丰度有明显波动,食用莫内林的大鼠微生物群中,[此处原文缺失具体内容]的相对丰度也有明显波动,但均未超过标准差。喂食蔗糖的组与[此处原文缺失具体内容]相对丰度的增加有关,这可能导致肥胖。总体而言,长期食用甜味蛋白布拉齐因和莫内林并没有显著改变大鼠的微生物群,也没有导致机会性微生物群的出现。这为这些潜在甜味剂的安全性提供了额外的证据。