EFSA Panel on Food Enzymes (FEZ), Holger Zorn, José Manuel Barat Baviera, Claudia Bolognesi, Francesco Catania, Gabriele Gadermaier, Ralf Greiner, Baltasar Mayo, Alicja Mortensen, Yrjö Henrik Roos, Marize L. M. Solano, Monika Sramkova, Henk Van Loveren, Laurence Vernis, Andrew Chesson, Lieve Herman, Natália Kovalkovičová, Magdalena Andryszkiewicz, Daniele Cavanna, Simone Lunardi, Roos Anna de Nijs, Yi Liu
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Since residual amounts of food enzyme-total organic solids (TOS) are removed in two processes, dietary exposure was calculated only for the remaining eight food manufacturing processes. It was estimated to be up to 0.568 mg TOS/kg body weight (bw) per day in European populations. Genotoxicity tests did not indicate a safety concern. The systemic toxicity was assessed by means of a repeated dose 90-day oral toxicity study in rats. The Panel identified a no observed adverse effect level of 1962 mg TOS/kg bw per day, the highest dose tested, which when compared with the estimated dietary exposure, resulted in a margin of exposure of at least 3454. A search for the homology of the amino acid sequence of the cellulose 1,4-β-cellobiosidase (non-reducing end) to known allergens was made and no match was found. The Panel considered that a risk of allergic reactions upon dietary exposure to the food enzyme cannot be excluded, but the likelihood is low. 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引用次数: 0
摘要
食用酶纤维素1,4-β-纤维素生物苷酶(非还原端)(EC 3.2.1.91)是由Shin Nihon Chemical Co., Ltd.用非转基因的citriinoviride木霉C1-5-2菌株生产的。食品酶被认为不受生产生物的活细胞的影响。它旨在用于十种食品生产过程。由于食品酶-总有机固体(TOS)的残留量在两个过程中被去除,因此仅计算了其余八个食品制造过程的膳食暴露量。据估计,欧洲人群每天每公斤体重(bw)可摄入0.568 mg TOS。基因毒性测试没有显示安全问题。通过90天重复给药的大鼠口服毒性研究来评估全身毒性。小组确定了每日1962毫克TOS/公斤体重的未观察到的不良影响水平,这是测试的最高剂量,与估计的饮食暴露量相比,其暴露幅度至少为3454。对纤维素1,4-β-纤维素生物苷酶(非还原端)的氨基酸序列与已知过敏原的同源性进行了搜索,未发现匹配。专家小组认为,不能排除通过饮食接触这种食物酶而产生过敏反应的风险,但这种可能性很低。根据所提供的数据,小组得出结论,在预期的使用条件下,这种食品酶不会引起安全问题。
Safety evaluation of the food enzyme cellulose 1,4-β-cellobiosidase (non-reducing end) from the non-genetically modified Trichoderma citrinoviride strain C1-5-2
The food enzyme cellulose 1,4-β-cellobiosidase (non-reducing end) (EC 3.2.1.91) is produced with the non-genetically modified Trichoderma citrinoviride strain C1-5-2 by Shin Nihon Chemical Co., Ltd. The food enzyme was considered free from viable cells of the production organism. It is intended to be used in ten food manufacturing processes. Since residual amounts of food enzyme-total organic solids (TOS) are removed in two processes, dietary exposure was calculated only for the remaining eight food manufacturing processes. It was estimated to be up to 0.568 mg TOS/kg body weight (bw) per day in European populations. Genotoxicity tests did not indicate a safety concern. The systemic toxicity was assessed by means of a repeated dose 90-day oral toxicity study in rats. The Panel identified a no observed adverse effect level of 1962 mg TOS/kg bw per day, the highest dose tested, which when compared with the estimated dietary exposure, resulted in a margin of exposure of at least 3454. A search for the homology of the amino acid sequence of the cellulose 1,4-β-cellobiosidase (non-reducing end) to known allergens was made and no match was found. The Panel considered that a risk of allergic reactions upon dietary exposure to the food enzyme cannot be excluded, but the likelihood is low. Based on the data provided, the Panel concluded that this food enzyme does not give rise to safety concerns, under the intended conditions of use.
期刊介绍:
The EFSA Journal covers methods of risk assessment, reports on data collected, and risk assessments in the individual areas of plant health, plant protection products and their residues, genetically modified organisms, additives and products or substances used in animal feed, animal health and welfare, biological hazards including BSE/TSE, contaminants in the food chain, food contact materials, enzymes, flavourings and processing aids, food additives and nutrient sources added to food, dietetic products, nutrition and allergies.