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根据欧盟理事会条例(EC)No 258/97,脯氨酸特异性寡肽酶作为新型食品的安全性。

Safety of proline-specific oligopeptidase as a novel food pursuant to Regulation (EC) No 258/97.

作者信息

Turck Dominique, Bresson Jean-Louis, Burlingame Barbara, Dean Tara, Fairweather-Tait Susan, Heinonen Marina, Hirsch-Ernst Karen-Ildico, Mangelsdorf Inge, McArdle Harry J, Naska Androniki, Neuhäuser-Berthold Monika, Nowicka Grażyna, Pentieva Kristina, Sanz Yolanda, Siani Alfonso, Sjödin Anders, Stern Martin, Tomé Daniel, Vinceti Marco, Willatts Peter, Engel Karl-Heinz, Marchelli Rosangela, Pöting Annette, Poulsen Morten, Schlatter Josef, Gelbmann Wolfgang, Van Loveren Henk

出版信息

EFSA J. 2017 Feb 15;15(2):e04681. doi: 10.2903/j.efsa.2017.4681. eCollection 2017 Feb.

Abstract

Following a request from the European Commission, the EFSA Panel on Dietetic Products, Nutrition and Allergies (NDA) was asked to deliver an opinion on proline-specific oligopeptidase (Tolerase G) as a novel food ingredient submitted pursuant to Regulation (EC) No 258/97 of the European Parliament and of the Council, taking into account the comments and objections of a scientific nature raised by Member States. The novel food is an enzyme preparation of prolyl-oligopeptidase produced with a genetically modified self clone strain. The target population is the general adult population. The results from a bacterial reverse mutation test and of an chromosome aberration test did not indicate genotoxicity. The Panel considers that the reported effects observed in a 90-day rat study are treatment-related effects and can be attributed to the higher energy consumption by these animals. Taking into account the intended maximum use level for Tolerase G, its daily consumption would correspond to 2,746 mg TOS/person or to 39.2 mg TOS/kg body weight (bw) per day, when considering a default body weight of 70 kg for an adult person. The margin between this value and the dose in the rats, which caused effects attributable to the excess energy intake, is approximately 45. Noting this margin, the Panel considers that it is unlikely that such effects would occur in human at the intended use levels. The Panel concludes that the NF, Tolerase G, is safe for the intended use at the intended use level.

摘要

应欧盟委员会的要求,欧洲食品安全局(EFSA)的营养产品、营养与过敏专家组(NDA)被要求就脯氨酸特异性寡肽酶(Tolerase G)作为一种根据欧洲议会和理事会第258/97号条例提交的新型食品成分发表意见,同时考虑到成员国提出的具有科学性质的评论和反对意见。该新型食品是一种用基因改造的自我克隆菌株生产的脯氨酰寡肽酶的酶制剂。目标人群为一般成年人群。细菌回复突变试验和染色体畸变试验的结果均未表明其具有遗传毒性。专家组认为,在一项为期90天的大鼠研究中观察到的报告效应是与治疗相关的效应,可归因于这些动物较高的能量消耗。考虑到Tolerase G的预期最大使用水平,按照成人默认体重70kg计算,其每日摄入量相当于每人2746mg TOS,或每天39.2mg TOS/kg体重(bw)。该数值与大鼠中导致因能量摄入过多而产生效应的剂量之间的差距约为45。考虑到这一差距,专家组认为在预期使用水平下,人类不太可能出现此类效应。专家组得出结论,新型食品Tolerase G在预期使用水平下按预期用途使用是安全的。

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