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Development of an l-rhamnose bioluminescent microbial biosensor for analysis of food ingredients

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dc.contributor.author Lukasiak, J en
dc.contributor.author Georgiou, CA en
dc.contributor.author Olsen, K en
dc.contributor.author Georgakopoulos, DG en
dc.date.accessioned 2014-06-06T06:51:42Z
dc.date.available 2014-06-06T06:51:42Z
dc.date.issued 2012 en
dc.identifier.issn 14382377 en
dc.identifier.uri http://dx.doi.org/10.1007/s00217-012-1789-5 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/5648
dc.subject Bioluminescence en
dc.subject l-rhamnose en
dc.subject Microbial biosensor en
dc.subject Pectin en
dc.subject Signal enhancement en
dc.subject.other Analytes en
dc.subject.other Calibration curves en
dc.subject.other Chemical method en
dc.subject.other Food ingredients en
dc.subject.other Food process en
dc.subject.other L-rhamnose en
dc.subject.other Microbial biosensor en
dc.subject.other Pectin en
dc.subject.other Promoter region en
dc.subject.other Signal enhancement en
dc.subject.other Vibrio fischeri en
dc.subject.other Bioluminescence en
dc.subject.other Carbohydrates en
dc.subject.other Chemical analysis en
dc.subject.other Escherichia coli en
dc.subject.other Genes en
dc.subject.other Phosphorescence en
dc.subject.other Biosensors en
dc.subject.other Escherichia coli en
dc.subject.other Vibrio fischeri en
dc.title Development of an l-rhamnose bioluminescent microbial biosensor for analysis of food ingredients en
heal.type journalArticle en
heal.identifier.primary 10.1007/s00217-012-1789-5 en
heal.publicationDate 2012 en
heal.abstract A bioluminescent microbial biosensor induced specifically by l-rhamnose was developed and optimized, to monitor food processes where pectin is involved. The biosensor was developed by fusing the Escherichia coli promoter P rhaB to the promoterless luxCDABE genes of Vibrio fischeri within plasmid pUCD615. Escherichia coli carrying this construct responded positively to l-rhamnose, but, because of low reporter signal, the enhancement of bioluminescence levels was required. The response was improved by promoter region length manipulation and resulted in 86-fold increase in response ratio. The specificity of the biosensor (80 times higher ratio response to l-rhamnose compared to other carbohydrates) and quantitative response to the target analyte were confirmed. The potential of this biosensor to monitor the hydrolysis of various types of pectin was demonstrated and a calibration curve was acquired. Our study presents a novel l-rhamnose-inducible microbial biosensor as a fast and economical alternative to chemical methods of pectin analysis. © 2012 Springer-Verlag. en
heal.journalName European Food Research and Technology en
dc.identifier.issue 3 en
dc.identifier.volume 235 en
dc.identifier.doi 10.1007/s00217-012-1789-5 en
dc.identifier.spage 573 en
dc.identifier.epage 579 en


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