Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection
Food and beverage industries require rapid tests to limit economic losses and one way to do so is via molecular tests. In the present work, DNA capture and secondary probes, were designed to target the ITS (Internal Transcribed) sequences of Brettanomyces bruxellensis, a yeast responsible for the...
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sg-ntu-dr.10356-1054832020-06-01T10:01:40Z Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection Cecchini, Francesca Manzano, Marisa Mandabi, Yohai Perelman, Eddie Marks, Robert S. School of Materials Science & Engineering DRNTU::Engineering::Materials::Biomaterials Food and beverage industries require rapid tests to limit economic losses and one way to do so is via molecular tests. In the present work, DNA capture and secondary probes, were designed to target the ITS (Internal Transcribed) sequences of Brettanomyces bruxellensis, a yeast responsible for the production of off flavours in both wine and beer. ITS1 and ITS2 were found to contain distinct regions with sufficient sequence divergence to make them suitable as specific identification target sites. The dot blot technique was used to determine the sensitivity and specificity of the capture probe. Both probes were, thereafter, adapted to construct an optical fibre genosensor, which produced neither false positives nor false negatives, and was both repeatable and faster with respect to traditional methods, the latter requiring at least one week to detect B. bruxellensis. 2013-11-01T02:49:46Z 2019-12-06T21:52:11Z 2013-11-01T02:49:46Z 2019-12-06T21:52:11Z 2011 2011 Journal Article Cecchini, F., Manzano, M., Mandabi, Y., Perelman, E., & Marks, R. S. (2011). Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection. Journal of biotechnology, 157(1), 25-30. 0168-1656 https://hdl.handle.net/10356/105483 http://hdl.handle.net/10220/17208 10.1016/j.jbiotec.2011.10.004 en Journal of biotechnology |
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DRNTU::Engineering::Materials::Biomaterials Cecchini, Francesca Manzano, Marisa Mandabi, Yohai Perelman, Eddie Marks, Robert S. Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection |
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Food and beverage industries require rapid tests to limit economic losses and one way to do so is via
molecular tests. In the present work, DNA capture and secondary probes, were designed to target the ITS
(Internal Transcribed) sequences of Brettanomyces bruxellensis, a yeast responsible for the production of
off flavours in both wine and beer. ITS1 and ITS2 were found to contain distinct regions with sufficient
sequence divergence to make them suitable as specific identification target sites. The dot blot technique
was used to determine the sensitivity and specificity of the capture probe. Both probes were, thereafter,
adapted to construct an optical fibre genosensor, which produced neither false positives nor false negatives,
and was both repeatable and faster with respect to traditional methods, the latter requiring at least
one week to detect B. bruxellensis. |
author2 |
School of Materials Science & Engineering |
author_facet |
School of Materials Science & Engineering Cecchini, Francesca Manzano, Marisa Mandabi, Yohai Perelman, Eddie Marks, Robert S. |
format |
Article |
author |
Cecchini, Francesca Manzano, Marisa Mandabi, Yohai Perelman, Eddie Marks, Robert S. |
author_sort |
Cecchini, Francesca |
title |
Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection |
title_short |
Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection |
title_full |
Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection |
title_fullStr |
Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection |
title_full_unstemmed |
Chemiluminescent DNA optical fibre sensor for Brettanomyces bruxellensis detection |
title_sort |
chemiluminescent dna optical fibre sensor for brettanomyces bruxellensis detection |
publishDate |
2013 |
url |
https://hdl.handle.net/10356/105483 http://hdl.handle.net/10220/17208 |
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1681058977090109440 |