Silano Vittorio, Barat Baviera José Manuel, Bolognesi Claudia, Cocconcelli Pier Sandro, Crebelli Riccardo, Gott David Michael, Grob Konrad, Lambré Claude, Lampi Evgenia, Mengelers Marcel, Mortensen Alicja, Rivière Gilles, Steffensen Inger-Lise, Tlustos Christina, Van Loveren Henk, Vernis Laurence, Zorn Holger, Glandorf Boet, Herman Lieve, Aguilera Jaime, Andryszkiewicz Magdalena, Liu Yi, Ranieri Sandra, Chesson Andrew
EFSA J. 2021 Mar 1;19(3):e06433. doi: 10.2903/j.efsa.2021.6433. eCollection 2021 Mar.
The food enzyme α-amylase (4-α-d-glucan glucanohydrolase; EC 3.2.1.1) is produced with the genetically modified strain NZYM-KE by Novozymes A/S. 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. The α-amylase is intended to be used in starch processing for the production of glucose syrups and other starch hydrolysates, and distilled alcohol production. Since residual amounts of the food enzyme are removed by the purification steps applied during the production of glucose syrups and distillation, no dietary exposure was calculated. 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 at the highest dose of 1,100 mg TOS/kg body weight (bw) per day. A search for similarity of the amino acid sequence of the food enzyme to known allergens was made and one match was found. The Panel considered that, under the intended conditions of use, the risk of allergic sensitisation and elicitation reactions by dietary exposure cannot be excluded, but the likelihood is considered to be 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α-淀粉酶(4-α-D-葡聚糖葡聚糖水解酶;EC 3.2.1.1)由诺维信公司(Novozymes A/S)的转基因菌株NZYM-KE生产。基因改造不存在安全问题。该食品酶不含生产生物体的活细胞及其DNA。α-淀粉酶旨在用于淀粉加工,以生产葡萄糖浆和其他淀粉水解产物,以及蒸馏酒精生产。由于在葡萄糖浆生产和蒸馏过程中应用的纯化步骤会去除食品酶的残留量,因此未计算膳食暴露量。遗传毒性试验未表明存在安全问题。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,在最高剂量为每天1100毫克总有机固体/千克体重(bw)时未观察到不良影响水平。对该食品酶的氨基酸序列与已知过敏原进行了相似性搜索,发现了一个匹配项。专家小组认为,在预期的使用条件下,不能排除因膳食暴露引起过敏致敏和激发反应的风险,但认为可能性较低。根据提供的数据,专家小组得出结论,该食品酶在预期的使用条件下不存在安全问题。