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欧盟评估一种食品酶复合物的安全性

   2022-04-29 食品伙伴网泽夕919
核心提示:2022年4月22日,欧盟食品安全局就一种食品酶复合物的安全性评价发布意见。……(世界食品网-www.shijieshipin.com)
     2022年4月22日,欧盟食品安全局就一种食品酶复合物的安全性评价发布意见。 
  据了解,该食品酶复合物含有来自猪胰腺的胰蛋白酶(trypsin)、胰凝乳蛋白酶(chymotrypsin)、α-淀粉酶(α-amylase)和三酰甘油脂肪酶(triacylglycerol lipase),旨在用于水解特殊医学用途食品或营养膳食管理食品中的乳蛋白。
 
  经过评估,专家小组认为该食品酶复合物不符合欧盟关于溶剂残留量的现有要求。部分原文报道如下:
 
  The food enzyme complex, containing trypsin (EC 3.4.21.4), chymotrypsin (EC 3.4.21.1), α-amylase (1,4-α-d-glucan glucanohydrolase, EC 3.2.1.1) and triacylglycerol lipase (triacylglycerol acylhydrolase, EC 3.1.1.3), is obtained from porcine pancreas by American Laboratories, Inc., USA. The food enzyme is intended primarily for the hydrolysis of milk proteins to be used in foods for special medical or nutritional dietary management. ■■■■■ is extensively used in the manufacturing process, and residual amounts of the solvent remain in the food enzyme. The applicant estimates a typical range of ■■■■■ in the food enzyme to be 10,000–13,000 mg/kg. Directive 2009/32/EC sets a maximum residue level of 10 mg/kg for foods and food ingredients produced in the EU or imported into the EU. The use of ■■■■■ for the production of a food enzyme falls within the scope of Directive 2009/32/EC. Consequently, the food enzyme does not comply with the existing requirements within the EU governing residual amount of solvent.
 
 
地区: 欧盟
行业: 进出口
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