Zorn Holger, Barat Baviera José Manuel, Bolognesi Claudia, Catania Francesco, Gadermaier Gabriele, Greiner Ralf, Mayo Baltasar, Mortensen Alicja, Roos Yrjö Henrik, Solano Marize L M, Sramkova Monika, Van Loveren Henk, Vernis Laurence, Lunardi Simone, Andryszkiewicz Magdalena, Criado Ana, Liu Yi
EFSA J. 2024 Oct 16;22(10):e9038. doi: 10.2903/j.efsa.2024.9038. eCollection 2024 Oct.
The food enzyme carboxypeptidase C (EC 3.4.16.5) is produced with the genetically modified strain PEG by DSM Food Specialties B.V. The genetic modifications do not give rise to safety concerns. The food enzyme is free from viable cells of the production organism and its DNA. It is intended to be used in nine food manufacturing processes. Dietary exposure to the food enzyme-total organic solids (TOS) was estimated to be up to 2.053 mg TOS/kg body weight (bw) per day in European populations. The toxicity studies were carried out with a xylanase obtained from strain XEA. The Panel considered this food enzyme as a suitable substitute for the carboxypeptidase to be used in the toxicological studies, because both strains were derived from the same recipient strain, the location of the inserts was comparable, no partial inserts were present and the production methods were essentially the same. Genotoxicity tests did not raise 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 1850 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 901. A homology search for the amino acid sequence of the food enzyme to known allergens was made and one match with a wheat allergen was found. The Panel considered that the risk of allergic reactions by dietary exposure cannot be excluded, especially in wheat-allergic individuals, 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.
食品酶羧肽酶C(EC 3.4.16.5)由帝斯曼食品特种产品公司使用转基因菌株PEG生产。基因改造不会引发安全问题。该食品酶不含生产生物体的活细胞及其DNA。它拟用于九种食品制造工艺。据估计,欧洲人群通过膳食接触该食品酶的总有机固体(TOS)最高可达每天2.053毫克TOS/千克体重(bw)。毒性研究是使用从菌株XEA获得的木聚糖酶进行的。专家小组认为,这种食品酶可作为毒理学研究中羧肽酶的合适替代品,因为这两种菌株均源自同一受体菌株,插入片段的位置相当,不存在部分插入情况,且生产方法基本相同。遗传毒性试验未引发安全问题。通过对大鼠进行为期90天的重复剂量口服毒性研究来评估全身毒性。专家小组确定未观察到有害作用水平为每天1850毫克TOS/千克bw,这是所测试的最高剂量,与估计的膳食接触量相比,得出的接触界限至少为901。对该食品酶的氨基酸序列与已知过敏原进行了同源性搜索,发现与一种小麦过敏原匹配。专家小组认为,不能排除通过膳食接触引发过敏反应的风险,尤其是在对小麦过敏的个体中,但可能性较低。根据所提供的数据,专家小组得出结论,在预期的使用条件下,这种食品酶不会引发安全问题。