Toxicity of the bacterial luciferase substrate, n-decyl aldehyde, to Saccharomyces cerevisiae and Caenorhabditis elegans

R. P. Hollis, Cristina Lagido, Jonathan Pettitt, Andrew Justin Radcliffe Porter, Kenneth Stuart Killham, Graeme Iain Paton, Lesley Anne Glover

Research output: Contribution to journalArticle

19 Citations (Scopus)

Abstract

This study determined that the bacterial luciferase fusion gene (luxAB) was not a suitable in vivo gene reporter in the model eukaryotic organisms Saccharomyces cerevisiae and Caenorhabditis elegans. LuxAB expressing S. cerevisiae strains displayed distinctive rapid decays in luminescence upon addition of the bacterial luciferase substrate, n-decyl aldehyde, suggesting a toxic response. Growth studies and toxicity bioassays have subsequently confirmed, that the aldehyde substrate was toxic to both organisms at concentrations well tolerated by Escherichia coh. As the addition of aldehyde is an integral part of the bacterial luciferase activity assay, our results do not support the use of lux reporter genes for in vivo analyses in these model eukaryotic organisms. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.

Original languageEnglish
Pages (from-to)140-142
Number of pages2
JournalFEBS Letters
Volume506
Issue number2
DOIs
Publication statusPublished - 5 Oct 2001

Keywords

  • biosensor
  • luciferase
  • bioluminescence
  • toxicity
  • vibrio-harveyi
  • Escherichia-Coli
  • fused gene
  • expression
  • fusion
  • yeast
  • eukaryotes
  • LUXA
  • DNA

Cite this

Toxicity of the bacterial luciferase substrate, n-decyl aldehyde, to Saccharomyces cerevisiae and Caenorhabditis elegans. / Hollis, R. P.; Lagido, Cristina; Pettitt, Jonathan; Porter, Andrew Justin Radcliffe; Killham, Kenneth Stuart; Paton, Graeme Iain; Glover, Lesley Anne.

In: FEBS Letters, Vol. 506, No. 2, 05.10.2001, p. 140-142.

Research output: Contribution to journalArticle

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abstract = "This study determined that the bacterial luciferase fusion gene (luxAB) was not a suitable in vivo gene reporter in the model eukaryotic organisms Saccharomyces cerevisiae and Caenorhabditis elegans. LuxAB expressing S. cerevisiae strains displayed distinctive rapid decays in luminescence upon addition of the bacterial luciferase substrate, n-decyl aldehyde, suggesting a toxic response. Growth studies and toxicity bioassays have subsequently confirmed, that the aldehyde substrate was toxic to both organisms at concentrations well tolerated by Escherichia coh. As the addition of aldehyde is an integral part of the bacterial luciferase activity assay, our results do not support the use of lux reporter genes for in vivo analyses in these model eukaryotic organisms. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.",
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AU - Hollis, R. P.

AU - Lagido, Cristina

AU - Pettitt, Jonathan

AU - Porter, Andrew Justin Radcliffe

AU - Killham, Kenneth Stuart

AU - Paton, Graeme Iain

AU - Glover, Lesley Anne

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AB - This study determined that the bacterial luciferase fusion gene (luxAB) was not a suitable in vivo gene reporter in the model eukaryotic organisms Saccharomyces cerevisiae and Caenorhabditis elegans. LuxAB expressing S. cerevisiae strains displayed distinctive rapid decays in luminescence upon addition of the bacterial luciferase substrate, n-decyl aldehyde, suggesting a toxic response. Growth studies and toxicity bioassays have subsequently confirmed, that the aldehyde substrate was toxic to both organisms at concentrations well tolerated by Escherichia coh. As the addition of aldehyde is an integral part of the bacterial luciferase activity assay, our results do not support the use of lux reporter genes for in vivo analyses in these model eukaryotic organisms. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.

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