Strategy for the identification of micro-organisms producing food and feed products: Bacteria producing food enzymes as study case
Recent European regulations require safety assessments of food enzymes (FE) before their commercialization. FE are mainly produced by micro-organisms, whose viable strains nor associated DNA can be present in the final products. Currently, no strategy targeting such impurities exists in enforcement...
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Veröffentlicht in: | Food chemistry 2020-02, Vol.305, p.125431-125431, Article 125431 |
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creator | Deckers, Marie Vanneste, Kevin Winand, Raf Keersmaecker, Sigrid C.J. De Denayer, Sarah Heyndrickx, Marc Deforce, Dieter Fraiture, Marie-Alice Roosens, Nancy H.C. |
description | Recent European regulations require safety assessments of food enzymes (FE) before their commercialization. FE are mainly produced by micro-organisms, whose viable strains nor associated DNA can be present in the final products. Currently, no strategy targeting such impurities exists in enforcement laboratories. Therefore, a generic strategy of first line screening was developed to detect and identify, through PCR amplification and sequencing of the 16S-rRNA gene, the potential presence of FE producing bacteria in FE preparations. First, the specificity was verified using all microbial species reported to produce FE. Second, an in-house database, with 16S reference sequences from bacteria producing FE, was constructed for their fast identification through blast analysis. Third, the sensitivity was assessed on a spiked FE preparation. Finally, the applicability was verified using commercial FE preparations. Using straightforward PCR amplifications, Sanger sequencing and blast analysis, the proposed strategy was demonstrated to be convenient for implementation in enforcement laboratories.
•No enforcement laboratory strategies targeting enzyme producing organisms exist.•Therefore, a PCR-based method is proposed to detect enzyme producing bacteria.•Targeted bacterial species are identified with a curated in-house database.•The method specificity, sensitivity and applicability were successfully tested.•The proposed method could also be applied on other food and feed products. |
doi_str_mv | 10.1016/j.foodchem.2019.125431 |
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•No enforcement laboratory strategies targeting enzyme producing organisms exist.•Therefore, a PCR-based method is proposed to detect enzyme producing bacteria.•Targeted bacterial species are identified with a curated in-house database.•The method specificity, sensitivity and applicability were successfully tested.•The proposed method could also be applied on other food and feed products.</description><identifier>ISSN: 0308-8146</identifier><identifier>EISSN: 1873-7072</identifier><identifier>DOI: 10.1016/j.foodchem.2019.125431</identifier><identifier>PMID: 31610425</identifier><language>eng</language><publisher>England: Elsevier Ltd</publisher><subject>16S-rRNA gene sequencing ; Bacteria ; Bacteria - genetics ; Bacteria - isolation & purification ; Bacteria - metabolism ; DNA Barcoding, Taxonomic ; Food enzymes ; Food Handling ; Identification ; PCR technology ; Polymerase Chain Reaction ; Producing organisms ; RNA, Ribosomal, 16S - analysis ; Screening</subject><ispartof>Food chemistry, 2020-02, Vol.305, p.125431-125431, Article 125431</ispartof><rights>2019 Elsevier Ltd</rights><rights>Copyright © 2019 Elsevier Ltd. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c405t-7ba950e06a39739362ce739673caa3257365ee13923e803e21986466020937883</citedby><cites>FETCH-LOGICAL-c405t-7ba950e06a39739362ce739673caa3257365ee13923e803e21986466020937883</cites><orcidid>0000-0002-0635-661X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0308814619315468$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/31610425$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Deckers, Marie</creatorcontrib><creatorcontrib>Vanneste, Kevin</creatorcontrib><creatorcontrib>Winand, Raf</creatorcontrib><creatorcontrib>Keersmaecker, Sigrid C.J. De</creatorcontrib><creatorcontrib>Denayer, Sarah</creatorcontrib><creatorcontrib>Heyndrickx, Marc</creatorcontrib><creatorcontrib>Deforce, Dieter</creatorcontrib><creatorcontrib>Fraiture, Marie-Alice</creatorcontrib><creatorcontrib>Roosens, Nancy H.C.</creatorcontrib><title>Strategy for the identification of micro-organisms producing food and feed products: Bacteria producing food enzymes as study case</title><title>Food chemistry</title><addtitle>Food Chem</addtitle><description>Recent European regulations require safety assessments of food enzymes (FE) before their commercialization. FE are mainly produced by micro-organisms, whose viable strains nor associated DNA can be present in the final products. Currently, no strategy targeting such impurities exists in enforcement laboratories. Therefore, a generic strategy of first line screening was developed to detect and identify, through PCR amplification and sequencing of the 16S-rRNA gene, the potential presence of FE producing bacteria in FE preparations. First, the specificity was verified using all microbial species reported to produce FE. Second, an in-house database, with 16S reference sequences from bacteria producing FE, was constructed for their fast identification through blast analysis. Third, the sensitivity was assessed on a spiked FE preparation. Finally, the applicability was verified using commercial FE preparations. Using straightforward PCR amplifications, Sanger sequencing and blast analysis, the proposed strategy was demonstrated to be convenient for implementation in enforcement laboratories.
•No enforcement laboratory strategies targeting enzyme producing organisms exist.•Therefore, a PCR-based method is proposed to detect enzyme producing bacteria.•Targeted bacterial species are identified with a curated in-house database.•The method specificity, sensitivity and applicability were successfully tested.•The proposed method could also be applied on other food and feed products.</description><subject>16S-rRNA gene sequencing</subject><subject>Bacteria</subject><subject>Bacteria - genetics</subject><subject>Bacteria - isolation & purification</subject><subject>Bacteria - metabolism</subject><subject>DNA Barcoding, Taxonomic</subject><subject>Food enzymes</subject><subject>Food Handling</subject><subject>Identification</subject><subject>PCR technology</subject><subject>Polymerase Chain Reaction</subject><subject>Producing organisms</subject><subject>RNA, Ribosomal, 16S - analysis</subject><subject>Screening</subject><issn>0308-8146</issn><issn>1873-7072</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkE1PGzEQhq2qqATav4B85LJhbO_au5xKoxaQkDjQni1jzwZH2TXYXqRw5JfjKKEHLpxGGj3z8T6EnDCYM2DybDXvQ3D2AYc5B9bNGW9qwb6QGWuVqBQo_pXMQEBbtayWh-QopRUAFLb9Rg4Fkwxq3szI612OJuNyQ_sQaX5A6h2O2ffemuzDSENPB29jqEJcmtGnIdHHGNxk_bik2x-oGR3tEd2-n9M5_WVsxujNRxTHl82AiZpEU57chlqT8Ds56M064Y99PSb__vz-u7iqbm4vrxcXN5WtocmVujddAwjSiE6JTkhusVSphDVG8EYJ2SAy0XGBLQjkrGtlLWXJ3AnVtuKYnO72lqeeJkxZDz5ZXK_NiGFKmgtoVKdq4AWVO7QETylirx-jH0zcaAZ661-v9Lt_vfWvd_7L4Mn-xnQ_oPs_9i68AD93AJakzx6jTtbjaNH5iDZrF_xnN94Aw0WaQg</recordid><startdate>20200201</startdate><enddate>20200201</enddate><creator>Deckers, Marie</creator><creator>Vanneste, Kevin</creator><creator>Winand, Raf</creator><creator>Keersmaecker, Sigrid C.J. 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De</creatorcontrib><creatorcontrib>Denayer, Sarah</creatorcontrib><creatorcontrib>Heyndrickx, Marc</creatorcontrib><creatorcontrib>Deforce, Dieter</creatorcontrib><creatorcontrib>Fraiture, Marie-Alice</creatorcontrib><creatorcontrib>Roosens, Nancy H.C.</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Food chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Deckers, Marie</au><au>Vanneste, Kevin</au><au>Winand, Raf</au><au>Keersmaecker, Sigrid C.J. De</au><au>Denayer, Sarah</au><au>Heyndrickx, Marc</au><au>Deforce, Dieter</au><au>Fraiture, Marie-Alice</au><au>Roosens, Nancy H.C.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Strategy for the identification of micro-organisms producing food and feed products: Bacteria producing food enzymes as study case</atitle><jtitle>Food chemistry</jtitle><addtitle>Food Chem</addtitle><date>2020-02-01</date><risdate>2020</risdate><volume>305</volume><spage>125431</spage><epage>125431</epage><pages>125431-125431</pages><artnum>125431</artnum><issn>0308-8146</issn><eissn>1873-7072</eissn><abstract>Recent European regulations require safety assessments of food enzymes (FE) before their commercialization. FE are mainly produced by micro-organisms, whose viable strains nor associated DNA can be present in the final products. Currently, no strategy targeting such impurities exists in enforcement laboratories. Therefore, a generic strategy of first line screening was developed to detect and identify, through PCR amplification and sequencing of the 16S-rRNA gene, the potential presence of FE producing bacteria in FE preparations. First, the specificity was verified using all microbial species reported to produce FE. Second, an in-house database, with 16S reference sequences from bacteria producing FE, was constructed for their fast identification through blast analysis. Third, the sensitivity was assessed on a spiked FE preparation. Finally, the applicability was verified using commercial FE preparations. Using straightforward PCR amplifications, Sanger sequencing and blast analysis, the proposed strategy was demonstrated to be convenient for implementation in enforcement laboratories.
•No enforcement laboratory strategies targeting enzyme producing organisms exist.•Therefore, a PCR-based method is proposed to detect enzyme producing bacteria.•Targeted bacterial species are identified with a curated in-house database.•The method specificity, sensitivity and applicability were successfully tested.•The proposed method could also be applied on other food and feed products.</abstract><cop>England</cop><pub>Elsevier Ltd</pub><pmid>31610425</pmid><doi>10.1016/j.foodchem.2019.125431</doi><tpages>1</tpages><orcidid>https://orcid.org/0000-0002-0635-661X</orcidid></addata></record> |
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subjects | 16S-rRNA gene sequencing Bacteria Bacteria - genetics Bacteria - isolation & purification Bacteria - metabolism DNA Barcoding, Taxonomic Food enzymes Food Handling Identification PCR technology Polymerase Chain Reaction Producing organisms RNA, Ribosomal, 16S - analysis Screening |
title | Strategy for the identification of micro-organisms producing food and feed products: Bacteria producing food enzymes as study case |
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