The detection of food soils and cells on stainless steel using industrial methods: UV illumination and ATP bioluminescence
Open food contact surfaces were subjected to organic soiling to provide a source for transfer of microbial cells. Rapid industrial methods used for the detection of residual cells and soil e.g. ATP (adenosine triphosphate) bioluminescence and an ultraviolet (UV) light detection method were assessed...
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description | Open food contact surfaces were subjected to organic soiling to provide a source for transfer of microbial cells. Rapid industrial methods used for the detection of residual cells and soil e.g. ATP (adenosine triphosphate) bioluminescence and an ultraviolet (UV) light detection method were assessed for their ability to detect organic soils, or organic soil–cell mix on surfaces. A range of soils (complex [meat extract, fish extract, cottage cheese extract]; oils [cholesterol, fish oil, mixed fatty acids]; proteins [bovine serum albumin, fish peptones casein]; carbohydrates [glycogen, starch, lactose]); was used. Under UV, oily soils, mixed fatty acids, cholesterol and casein were detected at low concentrations, with detection levels ranging from 1% to 0.001% for different substances. Glycogen was the most difficult substance to detect at lower concentrations. Using UV wavelength bands (
λ) of 330–380 nm, 510–560 nm and 590–650 nm, wavelength bands of 330–380 nm, illuminated most of the soils well, whilst the wavelength band of 510–560 nm illuminated the fish extract, cholesterol and fatty acids; the 590–650 nm wavelength band illuminated the lactose. Soils at all concentrations were detected by the ATP bioluminescence method; the complex soils gave the highest readings. When complex soils were combined with
Listeria monocytogenes Scott A or a non-pathogenic
Escherichia coli O157:H7, ATP measurements increased by 1–2 logs
. For UV illumination, the
L. monocytogenes and cheese combination was the most intensely illuminated, with
E. coli and meat the least.
UV illumination is a simple well established method for detecting food soil, with little change in findings when microorganisms are included. Performance can be enhanced in certain circumstances by altering the wavelength. ATP bioluminescence is a proven system for hygienic assessment being especially useful in the presence of microorganisms rather than organic soil alone. |
doi_str_mv | 10.1016/j.ijfoodmicro.2008.06.019 |
format | Article |
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λ) of 330–380 nm, 510–560 nm and 590–650 nm, wavelength bands of 330–380 nm, illuminated most of the soils well, whilst the wavelength band of 510–560 nm illuminated the fish extract, cholesterol and fatty acids; the 590–650 nm wavelength band illuminated the lactose. Soils at all concentrations were detected by the ATP bioluminescence method; the complex soils gave the highest readings. When complex soils were combined with
Listeria monocytogenes Scott A or a non-pathogenic
Escherichia coli O157:H7, ATP measurements increased by 1–2 logs
. For UV illumination, the
L. monocytogenes and cheese combination was the most intensely illuminated, with
E. coli and meat the least.
UV illumination is a simple well established method for detecting food soil, with little change in findings when microorganisms are included. Performance can be enhanced in certain circumstances by altering the wavelength. ATP bioluminescence is a proven system for hygienic assessment being especially useful in the presence of microorganisms rather than organic soil alone.</description><identifier>ISSN: 0168-1605</identifier><identifier>EISSN: 1879-3460</identifier><identifier>DOI: 10.1016/j.ijfoodmicro.2008.06.019</identifier><identifier>PMID: 18678428</identifier><identifier>CODEN: IJFMDD</identifier><language>eng</language><publisher>Amsterdam: Elsevier B.V</publisher><subject>adenosine triphosphate ; Adenosine Triphosphate - analysis ; ATP bioluminescence ; biofilm ; Biological and medical sciences ; bioluminescence ; Colony Count, Microbial ; Conditioning film ; Equipment Contamination ; Escherichia coli ; Escherichia coli O157:H7 ; Food ; food contact surfaces ; Food industries ; Food Industry - standards ; Food Microbiology ; food pathogens ; food processing equipment ; food processing plants ; food sanitation ; Fundamental and applied biological sciences. Psychology ; General aspects ; Hygiene - standards ; Listeria monocytogenes ; Luminescence ; Luminescent Measurements - methods ; Methods of analysis, processing and quality control, regulation, standards ; microbial detection ; nonpathogenic strains ; Soil ; Soil Microbiology ; stainless steel ; Stainless Steel - analysis ; Surface ; ultraviolet radiation ; Ultraviolet Rays ; UV light</subject><ispartof>International journal of food microbiology, 2008-09, Vol.127 (1), p.121-128</ispartof><rights>2008 Elsevier B.V.</rights><rights>2008 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c526t-7cf81acab634df4b0f77da9fbc54cd883ab07b47a1340e0c0bf932c40be37a5a3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/j.ijfoodmicro.2008.06.019$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,777,781,3538,27906,27907,45977</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20679434$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18678428$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Whitehead, Kathryn A.</creatorcontrib><creatorcontrib>Smith, Lindsay A.</creatorcontrib><creatorcontrib>Verran, Joanna</creatorcontrib><title>The detection of food soils and cells on stainless steel using industrial methods: UV illumination and ATP bioluminescence</title><title>International journal of food microbiology</title><addtitle>Int J Food Microbiol</addtitle><description>Open food contact surfaces were subjected to organic soiling to provide a source for transfer of microbial cells. Rapid industrial methods used for the detection of residual cells and soil e.g. ATP (adenosine triphosphate) bioluminescence and an ultraviolet (UV) light detection method were assessed for their ability to detect organic soils, or organic soil–cell mix on surfaces. A range of soils (complex [meat extract, fish extract, cottage cheese extract]; oils [cholesterol, fish oil, mixed fatty acids]; proteins [bovine serum albumin, fish peptones casein]; carbohydrates [glycogen, starch, lactose]); was used. Under UV, oily soils, mixed fatty acids, cholesterol and casein were detected at low concentrations, with detection levels ranging from 1% to 0.001% for different substances. Glycogen was the most difficult substance to detect at lower concentrations. Using UV wavelength bands (
λ) of 330–380 nm, 510–560 nm and 590–650 nm, wavelength bands of 330–380 nm, illuminated most of the soils well, whilst the wavelength band of 510–560 nm illuminated the fish extract, cholesterol and fatty acids; the 590–650 nm wavelength band illuminated the lactose. Soils at all concentrations were detected by the ATP bioluminescence method; the complex soils gave the highest readings. When complex soils were combined with
Listeria monocytogenes Scott A or a non-pathogenic
Escherichia coli O157:H7, ATP measurements increased by 1–2 logs
. For UV illumination, the
L. monocytogenes and cheese combination was the most intensely illuminated, with
E. coli and meat the least.
UV illumination is a simple well established method for detecting food soil, with little change in findings when microorganisms are included. Performance can be enhanced in certain circumstances by altering the wavelength. ATP bioluminescence is a proven system for hygienic assessment being especially useful in the presence of microorganisms rather than organic soil alone.</description><subject>adenosine triphosphate</subject><subject>Adenosine Triphosphate - analysis</subject><subject>ATP bioluminescence</subject><subject>biofilm</subject><subject>Biological and medical sciences</subject><subject>bioluminescence</subject><subject>Colony Count, Microbial</subject><subject>Conditioning film</subject><subject>Equipment Contamination</subject><subject>Escherichia coli</subject><subject>Escherichia coli O157:H7</subject><subject>Food</subject><subject>food contact surfaces</subject><subject>Food industries</subject><subject>Food Industry - standards</subject><subject>Food Microbiology</subject><subject>food pathogens</subject><subject>food processing equipment</subject><subject>food processing plants</subject><subject>food sanitation</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>General aspects</subject><subject>Hygiene - standards</subject><subject>Listeria monocytogenes</subject><subject>Luminescence</subject><subject>Luminescent Measurements - methods</subject><subject>Methods of analysis, processing and quality control, regulation, standards</subject><subject>microbial detection</subject><subject>nonpathogenic strains</subject><subject>Soil</subject><subject>Soil Microbiology</subject><subject>stainless steel</subject><subject>Stainless Steel - analysis</subject><subject>Surface</subject><subject>ultraviolet radiation</subject><subject>Ultraviolet Rays</subject><subject>UV light</subject><issn>0168-1605</issn><issn>1879-3460</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkV2P1CAUhonRuOPqX1C80LuOh0IL9W4z8SvZRBNnvCUUDrtM2rJCa6K_XrozUS-94gSe8x54IOQlgy0D1r45bsPRx-jGYFPc1gBqC-0WWPeAbJiSXcVFCw_JprCqYi00F-RJzkcAaDiHx-SCqVYqUasN-bW_RepwRjuHONHo6RpMcwxDpmZy1OJQqnKUZxOmAXMuFeJAlxymGxomt-Q5BTPQEefb6PJbevhGwzAsY5jMfegac7X_QvsQ73cxW5wsPiWPvBkyPjuvl-Tw_t1-97G6_vzh0-7qurJN3c6VtF4xY03fcuG86MFL6Uzne9sI65TipgfZC2kYF4Bgofcdr62AHrk0jeGX5PUp9y7F7wvmWY8hr88yE8Yla9YpEAJ4AbsTWKzmnNDruxRGk35qBnoVr4_6H_F6Fa-h1UV86X1-HrL0I7q_nWfTBXh1Bky2ZvDJTDbkP1wNrewEF4V7ceK8idrcpMIcvtbAOLCGy6ZZk3YnAou0HwGTzjasQl1I5Ru1i-E_Lvwbz_azkA</recordid><startdate>20080930</startdate><enddate>20080930</enddate><creator>Whitehead, Kathryn A.</creator><creator>Smith, Lindsay A.</creator><creator>Verran, Joanna</creator><general>Elsevier B.V</general><general>[Amsterdam; New York, NY]: Elsevier Science</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</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>7QL</scope><scope>7QO</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>20080930</creationdate><title>The detection of food soils and cells on stainless steel using industrial methods: UV illumination and ATP bioluminescence</title><author>Whitehead, Kathryn A. ; Smith, Lindsay A. ; Verran, Joanna</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c526t-7cf81acab634df4b0f77da9fbc54cd883ab07b47a1340e0c0bf932c40be37a5a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>adenosine triphosphate</topic><topic>Adenosine Triphosphate - analysis</topic><topic>ATP bioluminescence</topic><topic>biofilm</topic><topic>Biological and medical sciences</topic><topic>bioluminescence</topic><topic>Colony Count, Microbial</topic><topic>Conditioning film</topic><topic>Equipment Contamination</topic><topic>Escherichia coli</topic><topic>Escherichia coli O157:H7</topic><topic>Food</topic><topic>food contact surfaces</topic><topic>Food industries</topic><topic>Food Industry - standards</topic><topic>Food Microbiology</topic><topic>food pathogens</topic><topic>food processing equipment</topic><topic>food processing plants</topic><topic>food sanitation</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>General aspects</topic><topic>Hygiene - standards</topic><topic>Listeria monocytogenes</topic><topic>Luminescence</topic><topic>Luminescent Measurements - methods</topic><topic>Methods of analysis, processing and quality control, regulation, standards</topic><topic>microbial detection</topic><topic>nonpathogenic strains</topic><topic>Soil</topic><topic>Soil Microbiology</topic><topic>stainless steel</topic><topic>Stainless Steel - analysis</topic><topic>Surface</topic><topic>ultraviolet radiation</topic><topic>Ultraviolet Rays</topic><topic>UV light</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Whitehead, Kathryn A.</creatorcontrib><creatorcontrib>Smith, Lindsay A.</creatorcontrib><creatorcontrib>Verran, Joanna</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Biotechnology Research Abstracts</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><jtitle>International journal of food microbiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Whitehead, Kathryn A.</au><au>Smith, Lindsay A.</au><au>Verran, Joanna</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The detection of food soils and cells on stainless steel using industrial methods: UV illumination and ATP bioluminescence</atitle><jtitle>International journal of food microbiology</jtitle><addtitle>Int J Food Microbiol</addtitle><date>2008-09-30</date><risdate>2008</risdate><volume>127</volume><issue>1</issue><spage>121</spage><epage>128</epage><pages>121-128</pages><issn>0168-1605</issn><eissn>1879-3460</eissn><coden>IJFMDD</coden><abstract>Open food contact surfaces were subjected to organic soiling to provide a source for transfer of microbial cells. Rapid industrial methods used for the detection of residual cells and soil e.g. ATP (adenosine triphosphate) bioluminescence and an ultraviolet (UV) light detection method were assessed for their ability to detect organic soils, or organic soil–cell mix on surfaces. A range of soils (complex [meat extract, fish extract, cottage cheese extract]; oils [cholesterol, fish oil, mixed fatty acids]; proteins [bovine serum albumin, fish peptones casein]; carbohydrates [glycogen, starch, lactose]); was used. Under UV, oily soils, mixed fatty acids, cholesterol and casein were detected at low concentrations, with detection levels ranging from 1% to 0.001% for different substances. Glycogen was the most difficult substance to detect at lower concentrations. Using UV wavelength bands (
λ) of 330–380 nm, 510–560 nm and 590–650 nm, wavelength bands of 330–380 nm, illuminated most of the soils well, whilst the wavelength band of 510–560 nm illuminated the fish extract, cholesterol and fatty acids; the 590–650 nm wavelength band illuminated the lactose. Soils at all concentrations were detected by the ATP bioluminescence method; the complex soils gave the highest readings. When complex soils were combined with
Listeria monocytogenes Scott A or a non-pathogenic
Escherichia coli O157:H7, ATP measurements increased by 1–2 logs
. For UV illumination, the
L. monocytogenes and cheese combination was the most intensely illuminated, with
E. coli and meat the least.
UV illumination is a simple well established method for detecting food soil, with little change in findings when microorganisms are included. Performance can be enhanced in certain circumstances by altering the wavelength. ATP bioluminescence is a proven system for hygienic assessment being especially useful in the presence of microorganisms rather than organic soil alone.</abstract><cop>Amsterdam</cop><pub>Elsevier B.V</pub><pmid>18678428</pmid><doi>10.1016/j.ijfoodmicro.2008.06.019</doi><tpages>8</tpages></addata></record> |
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source | MEDLINE; Elsevier ScienceDirect Journals |
subjects | adenosine triphosphate Adenosine Triphosphate - analysis ATP bioluminescence biofilm Biological and medical sciences bioluminescence Colony Count, Microbial Conditioning film Equipment Contamination Escherichia coli Escherichia coli O157:H7 Food food contact surfaces Food industries Food Industry - standards Food Microbiology food pathogens food processing equipment food processing plants food sanitation Fundamental and applied biological sciences. Psychology General aspects Hygiene - standards Listeria monocytogenes Luminescence Luminescent Measurements - methods Methods of analysis, processing and quality control, regulation, standards microbial detection nonpathogenic strains Soil Soil Microbiology stainless steel Stainless Steel - analysis Surface ultraviolet radiation Ultraviolet Rays UV light |
title | The detection of food soils and cells on stainless steel using industrial methods: UV illumination and ATP bioluminescence |
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