# Safety evaluation of an extension of use of the food enzyme pullulanase from the non‐genetically modified Pullulanibacillus naganoensis strain AE‐PL

**Authors:** 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, Monika Sramkova, Henk Van Loveren, Laurence Vernis, Daniele Cavanna, Ana Criado, Rita Sofia Ferreira de Sousa, Yi Liu, Roos Anna de Nijs

PMC · DOI: 10.2903/j.efsa.2024.8947 · 2024-07-31

## TL;DR

This study confirms the safety of using the food enzyme pullulanase in eight food manufacturing processes, including new uses and revised levels.

## Contribution

The study provides an updated safety evaluation for extended use of a food enzyme in multiple manufacturing processes.

## Key findings

- Dietary exposure was estimated at up to 0.004 mg TOS/kg body weight per day in European populations.
- A no observed adverse effect level of 643 mg TOS/kg bw per day was identified in a 90-day rat toxicity study.
- The margin of exposure was at least 160,750, indicating no safety concerns under the revised conditions.

## Abstract

The food enzyme pullulanase (pullulan 6‐α‐glucanohydrolase; EC 3.2.1.41) is produced with the non‐genetically modified Pullulanibacillus naganoensis strain AE‐PL by Amano Enzyme Inc. A safety evaluation of this food enzyme was made previously, in which EFSA concluded that this food enzyme did not give rise to safety concerns when used in one food manufacturing process. Subsequently, the applicant has requested to extend its use to include seven additional processes and to revise the previous use level. In this assessment, EFSA updated the safety evaluation of this food enzyme when used in a total of eight food manufacturing processes. As the food enzyme‐total organic solids (TOS) are not carried into the final foods in two food manufacturing processes, the dietary exposure was estimated only for the remaining six processes. The dietary exposure was calculated to be up to 0.004 mg TOS/kg body weight (bw) per day in European populations. The Panel evaluated the repeated dose 90‐day oral toxicity study in rats submitted in the previous application and identified a no observed adverse effect level of 643 mg TOS/kg bw per day, the highest dose tested. When compared with the calculated dietary exposure, this resulted in a margin of exposure of at least 160,750. Based on the data provided for the previous evaluation and the revised margin of exposure in the present evaluation, the Panel concluded that this food enzyme does not give rise to safety concerns under the revised intended conditions of use.

## Linked entities

- **Proteins:** LDA (limit dextrinase)
- **Species:** Rattus norvegicus (taxon 10116)

## Full-text entities

- **Diseases:** toxicity (MESH:D064420)
- **Species:** Rattus norvegicus (brown rat, species) [taxon 10116]

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Source: https://tomesphere.com/paper/PMC11289615