2021
DOI: 10.2139/ssrn.3955899
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An Analysis of the Regulatory Framework Applicable to Products Obtained from Mushroom and Mycelium

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Cited by 10 publications
(5 citation statements)
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“…The FDA leaves it up to manufacturers to evaluate the safety and labeling of products. The Recommended Dietary Allowance for protein intake is 46 g per day for women and 56 g for men [107]. It has been reported that edible mushroom extract containing a high amount of L-Ergothioneine, which is received in a concentration up to 30 mg/day for adults and 20 mg per day for children, has been proven not to be genotoxic [108].…”
Section: Discussionmentioning
confidence: 99%
“…The FDA leaves it up to manufacturers to evaluate the safety and labeling of products. The Recommended Dietary Allowance for protein intake is 46 g per day for women and 56 g for men [107]. It has been reported that edible mushroom extract containing a high amount of L-Ergothioneine, which is received in a concentration up to 30 mg/day for adults and 20 mg per day for children, has been proven not to be genotoxic [108].…”
Section: Discussionmentioning
confidence: 99%
“…[ 116 ] Such regulations are part of policies designed by the European Green Deal to make the Union climate‐neutral by 2050. [ 117 ] Such a regulatory framework requires the material to be subjected to specifications associated with the food industry. Amongst these requirements, we find the need to specify a) biological source and taxonomic information about the fungus, b) the origin of fungal strains, c) laboratory conditions, d) substrate information, and e) type of cultures.…”
Section: Perspectivementioning
confidence: 99%
“…Additionally, three SCP fungal strains are accepted for food use in EU countries, only one of them (the yeast Yarrowia lipolytica ) has been authorized via the Novel Food Regulation ((EU) 2017/2470), and its use is restricted to food supplements. Molitorisová et al (2021) mapped the regulatory environment that governs mushrooms and mycelium products (MMP) in EU countries—food law provisions applicable to MMP produced or marketed in the EU [ 162 ]. They found that the sector is still in the developing phase, and regulatory framework application to MMP comprises numerous legal doubts.…”
Section: Safety Of Fungal Proteinsmentioning
confidence: 99%