Comparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.

Reproducibility is a key challenge of synthetic biology, but the foundation of reproducibility is only as solid as the reference materials it is built upon. Here we focus on the reproducibility of fluorescence measurements from bacteria transformed with engineered genetic constructs. This comparativ...

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Autores principales: Jacob Beal, Geoff S Baldwin, Natalie G Farny, Markus Gershater, Traci Haddock-Angelli, Russell Buckley-Taylor, Ari Dwijayanti, Daisuke Kiga, Meagan Lizarazo, John Marken, Kim de Mora, Randy Rettberg, Vishal Sanchania, Vinoo Selvarajah, Abigail Sison, Marko Storch, Christopher T Workman, iGEM Interlab Study Contributors
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Publicado: Public Library of Science (PLoS) 2021
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Acceso en línea:https://doaj.org/article/c7ded86e73e9474f93a3c887a1d5cc76
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spelling oai:doaj.org-article:c7ded86e73e9474f93a3c887a1d5cc762021-12-02T20:03:54ZComparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.1932-620310.1371/journal.pone.0252263https://doaj.org/article/c7ded86e73e9474f93a3c887a1d5cc762021-01-01T00:00:00Zhttps://doi.org/10.1371/journal.pone.0252263https://doaj.org/toc/1932-6203Reproducibility is a key challenge of synthetic biology, but the foundation of reproducibility is only as solid as the reference materials it is built upon. Here we focus on the reproducibility of fluorescence measurements from bacteria transformed with engineered genetic constructs. This comparative analysis comprises three large interlaboratory studies using flow cytometry and plate readers, identical genetic constructs, and compatible unit calibration protocols. Across all three studies, we find similarly high precision in the calibrants used for plate readers. We also find that fluorescence measurements agree closely across the flow cytometry results and two years of plate reader results, with an average standard deviation of 1.52-fold, while the third year of plate reader results are consistently shifted by more than an order of magnitude, with an average shift of 28.9-fold. Analyzing possible sources of error indicates this shift is due to incorrect preparation of the fluorescein calibrant. These findings suggest that measuring fluorescence from engineered constructs is highly reproducible, but also that there is a critical need for access to quality controlled fluorescent calibrants for plate readers.Jacob BealGeoff S BaldwinNatalie G FarnyMarkus GershaterTraci Haddock-AngelliRussell Buckley-TaylorAri DwijayantiDaisuke KigaMeagan LizarazoJohn MarkenKim de MoraRandy RettbergVishal SanchaniaVinoo SelvarajahAbigail SisonMarko StorchChristopher T WorkmaniGEM Interlab Study ContributorsPublic Library of Science (PLoS)articleMedicineRScienceQENPLoS ONE, Vol 16, Iss 6, p e0252263 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Jacob Beal
Geoff S Baldwin
Natalie G Farny
Markus Gershater
Traci Haddock-Angelli
Russell Buckley-Taylor
Ari Dwijayanti
Daisuke Kiga
Meagan Lizarazo
John Marken
Kim de Mora
Randy Rettberg
Vishal Sanchania
Vinoo Selvarajah
Abigail Sison
Marko Storch
Christopher T Workman
iGEM Interlab Study Contributors
Comparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.
description Reproducibility is a key challenge of synthetic biology, but the foundation of reproducibility is only as solid as the reference materials it is built upon. Here we focus on the reproducibility of fluorescence measurements from bacteria transformed with engineered genetic constructs. This comparative analysis comprises three large interlaboratory studies using flow cytometry and plate readers, identical genetic constructs, and compatible unit calibration protocols. Across all three studies, we find similarly high precision in the calibrants used for plate readers. We also find that fluorescence measurements agree closely across the flow cytometry results and two years of plate reader results, with an average standard deviation of 1.52-fold, while the third year of plate reader results are consistently shifted by more than an order of magnitude, with an average shift of 28.9-fold. Analyzing possible sources of error indicates this shift is due to incorrect preparation of the fluorescein calibrant. These findings suggest that measuring fluorescence from engineered constructs is highly reproducible, but also that there is a critical need for access to quality controlled fluorescent calibrants for plate readers.
format article
author Jacob Beal
Geoff S Baldwin
Natalie G Farny
Markus Gershater
Traci Haddock-Angelli
Russell Buckley-Taylor
Ari Dwijayanti
Daisuke Kiga
Meagan Lizarazo
John Marken
Kim de Mora
Randy Rettberg
Vishal Sanchania
Vinoo Selvarajah
Abigail Sison
Marko Storch
Christopher T Workman
iGEM Interlab Study Contributors
author_facet Jacob Beal
Geoff S Baldwin
Natalie G Farny
Markus Gershater
Traci Haddock-Angelli
Russell Buckley-Taylor
Ari Dwijayanti
Daisuke Kiga
Meagan Lizarazo
John Marken
Kim de Mora
Randy Rettberg
Vishal Sanchania
Vinoo Selvarajah
Abigail Sison
Marko Storch
Christopher T Workman
iGEM Interlab Study Contributors
author_sort Jacob Beal
title Comparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.
title_short Comparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.
title_full Comparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.
title_fullStr Comparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.
title_full_unstemmed Comparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.
title_sort comparative analysis of three studies measuring fluorescence from engineered bacterial genetic constructs.
publisher Public Library of Science (PLoS)
publishDate 2021
url https://doaj.org/article/c7ded86e73e9474f93a3c887a1d5cc76
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