Safety Evaluation of Soy Leghemoglobin Protein Preparation Derived From Pichia pastoris, Intended for Use as a Flavor Catalyst in Plant-Based Meat
The leghemoglobin protein (LegH) from soy (Glycine max) expressed in Pichia pastoris (LegH preparation, LegH Prep) imparts a meat-like flavor profile onto plant-based food products. The safety of LegH Prep was evaluated through a series of in vitro and in vivo tests. The genotoxic potential of LegH...
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Veröffentlicht in: | International journal of toxicology 2018-05, Vol.37 (3), p.241-262 |
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description | The leghemoglobin protein (LegH) from soy (Glycine max) expressed in Pichia pastoris (LegH preparation, LegH Prep) imparts a meat-like flavor profile onto plant-based food products. The safety of LegH Prep was evaluated through a series of in vitro and in vivo tests. The genotoxic potential of LegH Prep was assessed using the bacterial reverse mutation assay (Ames test) and the in vitro chromosome aberration test. LegH Prep was nonmutagenic and nonclastogenic in each test, respectively. Systemic toxicity was assessed in a 28-day dietary study in male and female Sprague Dawley rats. There were no mortalities associated with the administration of LegH Prep. There were no clinical observations, body weight, ophthalmological, clinical pathology, or histopathological changes attributable to LegH Prep administration. There were no observed effects on male reproduction in this study, but the suggestion of a potential estrous cycle distribution effect in female rats prompted a second comprehensive 28-day dietary study in female Sprague Dawley rats. This study demonstrated that female reproductive parameters were comparable between rats treated with LegH Prep and concurrent control rats. These studies establish a no observed adverse effect level of 750 mg/kg/d LegH, which is over 100 times greater than the 90th percentile estimated daily intake. Collectively, the results of the studies presented raise no issues of toxicological concern with regard to LegH Prep under the conditions tested. |
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The safety of LegH Prep was evaluated through a series of in vitro and in vivo tests. The genotoxic potential of LegH Prep was assessed using the bacterial reverse mutation assay (Ames test) and the in vitro chromosome aberration test. LegH Prep was nonmutagenic and nonclastogenic in each test, respectively. Systemic toxicity was assessed in a 28-day dietary study in male and female Sprague Dawley rats. There were no mortalities associated with the administration of LegH Prep. There were no clinical observations, body weight, ophthalmological, clinical pathology, or histopathological changes attributable to LegH Prep administration. There were no observed effects on male reproduction in this study, but the suggestion of a potential estrous cycle distribution effect in female rats prompted a second comprehensive 28-day dietary study in female Sprague Dawley rats. This study demonstrated that female reproductive parameters were comparable between rats treated with LegH Prep and concurrent control rats. These studies establish a no observed adverse effect level of 750 mg/kg/d LegH, which is over 100 times greater than the 90th percentile estimated daily intake. Collectively, the results of the studies presented raise no issues of toxicological concern with regard to LegH Prep under the conditions tested.</description><identifier>ISSN: 1091-5818</identifier><identifier>EISSN: 1092-874X</identifier><identifier>DOI: 10.1177/1091581818766318</identifier><identifier>PMID: 29642729</identifier><language>eng</language><publisher>Los Angeles, CA: SAGE Publications</publisher><subject>Animals ; Chromosome Aberrations - chemically induced ; Female ; Flavoring Agents - adverse effects ; Glycine max ; Leghemoglobin - adverse effects ; Male ; Meat ; Mutagenicity Tests ; Pichia - metabolism ; Plant Preparations - adverse effects ; Plants, Genetically Modified ; Rats ; Rats, Sprague-Dawley ; Regular ; Reproduction - drug effects</subject><ispartof>International journal of toxicology, 2018-05, Vol.37 (3), p.241-262</ispartof><rights>The Author(s) 2018</rights><rights>The Author(s) 2018 2018 American College of Toxicology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c434t-8ead5e2e2b7f599d7f282bbe3355302e2733cd05f23903d4ba159acee92763e3</citedby><cites>FETCH-LOGICAL-c434t-8ead5e2e2b7f599d7f282bbe3355302e2733cd05f23903d4ba159acee92763e3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://journals.sagepub.com/doi/pdf/10.1177/1091581818766318$$EPDF$$P50$$Gsage$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://journals.sagepub.com/doi/10.1177/1091581818766318$$EHTML$$P50$$Gsage$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,21798,27901,27902,43597,43598</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29642729$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fraser, Rachel Z.</creatorcontrib><creatorcontrib>Shitut, Mithila</creatorcontrib><creatorcontrib>Agrawal, Puja</creatorcontrib><creatorcontrib>Mendes, Odete</creatorcontrib><creatorcontrib>Klapholz, Sue</creatorcontrib><title>Safety Evaluation of Soy Leghemoglobin Protein Preparation Derived From Pichia pastoris, Intended for Use as a Flavor Catalyst in Plant-Based Meat</title><title>International journal of toxicology</title><addtitle>Int J Toxicol</addtitle><description>The leghemoglobin protein (LegH) from soy (Glycine max) expressed in Pichia pastoris (LegH preparation, LegH Prep) imparts a meat-like flavor profile onto plant-based food products. The safety of LegH Prep was evaluated through a series of in vitro and in vivo tests. The genotoxic potential of LegH Prep was assessed using the bacterial reverse mutation assay (Ames test) and the in vitro chromosome aberration test. LegH Prep was nonmutagenic and nonclastogenic in each test, respectively. Systemic toxicity was assessed in a 28-day dietary study in male and female Sprague Dawley rats. There were no mortalities associated with the administration of LegH Prep. There were no clinical observations, body weight, ophthalmological, clinical pathology, or histopathological changes attributable to LegH Prep administration. There were no observed effects on male reproduction in this study, but the suggestion of a potential estrous cycle distribution effect in female rats prompted a second comprehensive 28-day dietary study in female Sprague Dawley rats. This study demonstrated that female reproductive parameters were comparable between rats treated with LegH Prep and concurrent control rats. These studies establish a no observed adverse effect level of 750 mg/kg/d LegH, which is over 100 times greater than the 90th percentile estimated daily intake. Collectively, the results of the studies presented raise no issues of toxicological concern with regard to LegH Prep under the conditions tested.</description><subject>Animals</subject><subject>Chromosome Aberrations - chemically induced</subject><subject>Female</subject><subject>Flavoring Agents - adverse effects</subject><subject>Glycine max</subject><subject>Leghemoglobin - adverse effects</subject><subject>Male</subject><subject>Meat</subject><subject>Mutagenicity Tests</subject><subject>Pichia - metabolism</subject><subject>Plant Preparations - adverse effects</subject><subject>Plants, Genetically Modified</subject><subject>Rats</subject><subject>Rats, Sprague-Dawley</subject><subject>Regular</subject><subject>Reproduction - drug effects</subject><issn>1091-5818</issn><issn>1092-874X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>AFRWT</sourceid><sourceid>EIF</sourceid><recordid>eNp1UVtr2zAUFqNjvWzveyr6AXOri2VZL4UtTdpCSgPpYG_m2D5OVBwrSEogf6O_uEqzlW1QzsO5fBeBPkK-cnbBudaXnBmuSp5KF4Xk5Qdykk4iK3X-6-h15tkePyanITwxxgqt-CdyLEyRCy3MCXmeQ4dxR8db6DcQrRuo6-jc7egUF0tcuUXvajvQmXcRXzuuwR-I1-jtFls68W5FZ7ZZWqBrCNF5G77RuyHi0Ca4c57-DEghUKCTHrZpH0GEfhci3Vv2MMTsB4TEvUeIn8nHDvqAX373M_I4GT-ObrPpw83d6Ps0a3KZx6xEaBUKFLXulDGt7kQp6hqlVEqydNdSNi1TnZCGyTavgSsDDaIRupAoz8jVwXa9qVfYNjhED3219nYFflc5sNW_yGCX1cJtK2VUoYoyGbCDQeNdCB67Ny1n1T6e6v94kuT87zffBH_ySITsQAiwwOrJbfyQvuB9wxdZM5rs</recordid><startdate>20180501</startdate><enddate>20180501</enddate><creator>Fraser, Rachel Z.</creator><creator>Shitut, Mithila</creator><creator>Agrawal, Puja</creator><creator>Mendes, Odete</creator><creator>Klapholz, Sue</creator><general>SAGE Publications</general><scope>AFRWT</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>5PM</scope></search><sort><creationdate>20180501</creationdate><title>Safety Evaluation of Soy Leghemoglobin Protein Preparation Derived From Pichia pastoris, Intended for Use as a Flavor Catalyst in Plant-Based Meat</title><author>Fraser, Rachel Z. ; Shitut, Mithila ; Agrawal, Puja ; Mendes, Odete ; Klapholz, Sue</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c434t-8ead5e2e2b7f599d7f282bbe3355302e2733cd05f23903d4ba159acee92763e3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Animals</topic><topic>Chromosome Aberrations - chemically induced</topic><topic>Female</topic><topic>Flavoring Agents - adverse effects</topic><topic>Glycine max</topic><topic>Leghemoglobin - adverse effects</topic><topic>Male</topic><topic>Meat</topic><topic>Mutagenicity Tests</topic><topic>Pichia - metabolism</topic><topic>Plant Preparations - adverse effects</topic><topic>Plants, Genetically Modified</topic><topic>Rats</topic><topic>Rats, Sprague-Dawley</topic><topic>Regular</topic><topic>Reproduction - drug effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fraser, Rachel Z.</creatorcontrib><creatorcontrib>Shitut, Mithila</creatorcontrib><creatorcontrib>Agrawal, Puja</creatorcontrib><creatorcontrib>Mendes, Odete</creatorcontrib><creatorcontrib>Klapholz, Sue</creatorcontrib><collection>Sage Journals GOLD Open Access 2024</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>International journal of toxicology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fraser, Rachel Z.</au><au>Shitut, Mithila</au><au>Agrawal, Puja</au><au>Mendes, Odete</au><au>Klapholz, Sue</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Safety Evaluation of Soy Leghemoglobin Protein Preparation Derived From Pichia pastoris, Intended for Use as a Flavor Catalyst in Plant-Based Meat</atitle><jtitle>International journal of toxicology</jtitle><addtitle>Int J Toxicol</addtitle><date>2018-05-01</date><risdate>2018</risdate><volume>37</volume><issue>3</issue><spage>241</spage><epage>262</epage><pages>241-262</pages><issn>1091-5818</issn><eissn>1092-874X</eissn><abstract>The leghemoglobin protein (LegH) from soy (Glycine max) expressed in Pichia pastoris (LegH preparation, LegH Prep) imparts a meat-like flavor profile onto plant-based food products. The safety of LegH Prep was evaluated through a series of in vitro and in vivo tests. The genotoxic potential of LegH Prep was assessed using the bacterial reverse mutation assay (Ames test) and the in vitro chromosome aberration test. LegH Prep was nonmutagenic and nonclastogenic in each test, respectively. Systemic toxicity was assessed in a 28-day dietary study in male and female Sprague Dawley rats. There were no mortalities associated with the administration of LegH Prep. There were no clinical observations, body weight, ophthalmological, clinical pathology, or histopathological changes attributable to LegH Prep administration. There were no observed effects on male reproduction in this study, but the suggestion of a potential estrous cycle distribution effect in female rats prompted a second comprehensive 28-day dietary study in female Sprague Dawley rats. This study demonstrated that female reproductive parameters were comparable between rats treated with LegH Prep and concurrent control rats. These studies establish a no observed adverse effect level of 750 mg/kg/d LegH, which is over 100 times greater than the 90th percentile estimated daily intake. Collectively, the results of the studies presented raise no issues of toxicological concern with regard to LegH Prep under the conditions tested.</abstract><cop>Los Angeles, CA</cop><pub>SAGE Publications</pub><pmid>29642729</pmid><doi>10.1177/1091581818766318</doi><tpages>22</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Animals Chromosome Aberrations - chemically induced Female Flavoring Agents - adverse effects Glycine max Leghemoglobin - adverse effects Male Meat Mutagenicity Tests Pichia - metabolism Plant Preparations - adverse effects Plants, Genetically Modified Rats Rats, Sprague-Dawley Regular Reproduction - drug effects |
title | Safety Evaluation of Soy Leghemoglobin Protein Preparation Derived From Pichia pastoris, Intended for Use as a Flavor Catalyst in Plant-Based Meat |
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