Toxicological Evaluation of the Sweet Protein Brazzein Derived From Komagataella phaffii for Use as a Sweetener in Foods and Beverages.

IF 2.7 4区 医学 Q3 TOXICOLOGY
Jwar Meetro, Labiba Nahian, Kirt R Phipps, Trung Duc Vo, Irina Dahms, Minal Lalpuria, Hadi Omrani
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Abstract

Brazzein is a promising new protein sweetener that has gained significant attention by the food and beverage industry in recent years. Brazzein has a sweetness intensity significantly greater than that of other low- and no-calorie sweeteners currently on the global market and can provide a comparable sweetness at lower use levels within food and beverage products. In this study, a safety assessment of the sweet protein brazzein, produced from the fermentation of Komagataella phaffii, was undertaken in an in vitro digestibility study, an in silico allergenicity assessment, an in vitro reverse mutation assay, an in vitro mammalian micronucleus assay, and a 90-day oral toxicity study in rats. The results of the in silico and in vitro studies indicate that brazzein is not readily digestible, does not have allergenic potential, and does not have genotoxic or mutagenic potential. In the 90-day toxicity study, brazzein was not associated with any adverse systemic effects at up to 2000 mg/kg body weight/day, the highest dose tested. The dose of 2000 mg/kg body weight/day was concluded to be the no observed adverse effect level. The findings from the current safety assessment demonstrate that brazzein is safe for use as a sweetener in foods and beverages for human consumption.

食品和饮料中甜蛋白Brazzein的毒理学评价
Brazzein是一种很有前途的新型蛋白质甜味剂,近年来受到食品和饮料行业的极大关注。Brazzein的甜味强度明显高于目前全球市场上的其他低热量和无热量甜味剂,并且可以在食品和饮料产品中提供较低使用水平的甜度。在这项研究中,通过体外消化率研究、硅致敏性评估、体外反向突变试验、体外哺乳动物微核试验和90天大鼠口服毒性研究,对由Komagataella phaffii发酵产生的甜蛋白brazzein进行了安全性评估。硅和体外研究的结果表明,铜黄蛋白不易消化,没有致敏潜力,也没有遗传毒性或致突变潜力。在为期90天的毒性研究中,当试验的最高剂量为2000mg /kg体重/天时,brazzein未与任何不良全身反应相关。结论2000mg /kg体重/天的剂量为未观察到不良反应水平。目前的安全评估结果表明,brazzein作为人类食用的食品和饮料中的甜味剂是安全的。
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来源期刊
CiteScore
7.00
自引率
6.10%
发文量
145
审稿时长
1 months
期刊介绍: Journal of Applied Toxicology publishes peer-reviewed original reviews and hypothesis-driven research articles on mechanistic, fundamental and applied research relating to the toxicity of drugs and chemicals at the molecular, cellular, tissue, target organ and whole body level in vivo (by all relevant routes of exposure) and in vitro / ex vivo. All aspects of toxicology are covered (including but not limited to nanotoxicology, genomics and proteomics, teratogenesis, carcinogenesis, mutagenesis, reproductive and endocrine toxicology, toxicopathology, target organ toxicity, systems toxicity (eg immunotoxicity), neurobehavioral toxicology, mechanistic studies, biochemical and molecular toxicology, novel biomarkers, pharmacokinetics/PBPK, risk assessment and environmental health studies) and emphasis is given to papers of clear application to human health, and/or advance mechanistic understanding and/or provide significant contributions and impact to their field.
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