Safety evaluation of the food enzyme aspergillopepsin I from the non‐genetically modified Aspergillus sp. strain AE‐PRHF
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, Henk Van Loveren, Laurence Vernis, Natália Kovalkovičová, Daniele Cavanna

TL;DR
This study evaluates the safety of aspergillopepsin I, a food enzyme produced by a non-genetically modified Aspergillus strain, for use in food manufacturing.
Contribution
The study provides a comprehensive safety assessment of aspergillopepsin I, including toxicity and allergenicity evaluations.
Findings
Dietary exposure to the enzyme was estimated at up to 2.172 mg TOS/kg body weight per day in European populations.
Genotoxicity tests showed no safety concerns, and the no observed adverse effect level was 2003 mg TOS/kg bw per day.
A risk of allergic reactions cannot be excluded, but the likelihood is considered low.
Abstract
The food enzyme aspergillopepsin I (EC 3.4.23.18) is produced with the non‐genetically modified Aspergillus sp. strain AE‐PRHF by AMANO ENZYME INC. The food enzyme was free from viable cells of the production organism. It is intended to be used in 15 food manufacturing processes. Since residual amounts of food enzyme–total organic solids (TOS) are removed in two processes, dietary exposure was calculated for the remaining 13 food manufacturing processes. It was estimated to be up to 2.172 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 2003 mg TOS/kg bw per day, the highest dose tested, which when compared with the estimated dietary exposure, resulted in a margin of…
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Taxonomy
TopicsOccupational exposure and asthma · Agricultural safety and regulations · Contact Dermatitis and Allergies
