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A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells

[Image: see text] Nitrate (NO(3)(–)) is a critical source of nitrogen (N) available to microorganisms and plants. Nitrate sensing activates signaling pathways in the plant system that impinges upon, developmental, molecular, metabolic, and physiological responses locally, and globally. To sustain, t...

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Autores principales: Fatima, Urooj, Ameen, Fuad, Soleja, Neha, Khan, Parvez, Almansob, Abobakr, Ahmad, Altaf
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2020
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689916/
https://www.ncbi.nlm.nih.gov/pubmed/33251465
http://dx.doi.org/10.1021/acsomega.0c04868
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author Fatima, Urooj
Ameen, Fuad
Soleja, Neha
Khan, Parvez
Almansob, Abobakr
Ahmad, Altaf
author_facet Fatima, Urooj
Ameen, Fuad
Soleja, Neha
Khan, Parvez
Almansob, Abobakr
Ahmad, Altaf
author_sort Fatima, Urooj
collection PubMed
description [Image: see text] Nitrate (NO(3)(–)) is a critical source of nitrogen (N) available to microorganisms and plants. Nitrate sensing activates signaling pathways in the plant system that impinges upon, developmental, molecular, metabolic, and physiological responses locally, and globally. To sustain, the high crop productivity and high nutritional value along with the sustainable environment, the study of rate-controlling steps of a metabolic network of N assimilation through fluxomics becomes an attractive strategy. To monitor the flux of nitrate, we developed a non-invasive genetically encoded fluorescence resonance energy transfer (FRET)-based tool named “FLIP-NT” that monitors the real-time uptake of nitrate in the living cells. The developed nanosensor is suitable for real-time monitoring of nitrate flux in living cells at subcellular compartments with high spatio-temporal resolution. The developed FLIP-NT nanosensor was not affected by the pH change and have specificity for nitrate with an affinity constant (K(d)) of ∼5 μM. A series of affinity mutants have also been generated to expand the physiological detection range of the sensor protein with varying K(d) values. It has been found that this sensor successfully detects the dynamics of nitrate fluctuations in bacteria and yeast, without the disruption of cellular organization. This FLIP-NT nanosensor could be a very important tool that will help us to advance the understanding of nitrate signaling.
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spelling pubmed-76899162020-11-27 A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells Fatima, Urooj Ameen, Fuad Soleja, Neha Khan, Parvez Almansob, Abobakr Ahmad, Altaf ACS Omega [Image: see text] Nitrate (NO(3)(–)) is a critical source of nitrogen (N) available to microorganisms and plants. Nitrate sensing activates signaling pathways in the plant system that impinges upon, developmental, molecular, metabolic, and physiological responses locally, and globally. To sustain, the high crop productivity and high nutritional value along with the sustainable environment, the study of rate-controlling steps of a metabolic network of N assimilation through fluxomics becomes an attractive strategy. To monitor the flux of nitrate, we developed a non-invasive genetically encoded fluorescence resonance energy transfer (FRET)-based tool named “FLIP-NT” that monitors the real-time uptake of nitrate in the living cells. The developed nanosensor is suitable for real-time monitoring of nitrate flux in living cells at subcellular compartments with high spatio-temporal resolution. The developed FLIP-NT nanosensor was not affected by the pH change and have specificity for nitrate with an affinity constant (K(d)) of ∼5 μM. A series of affinity mutants have also been generated to expand the physiological detection range of the sensor protein with varying K(d) values. It has been found that this sensor successfully detects the dynamics of nitrate fluctuations in bacteria and yeast, without the disruption of cellular organization. This FLIP-NT nanosensor could be a very important tool that will help us to advance the understanding of nitrate signaling. American Chemical Society 2020-11-12 /pmc/articles/PMC7689916/ /pubmed/33251465 http://dx.doi.org/10.1021/acsomega.0c04868 Text en © 2020 The Authors. Published by American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited.
spellingShingle Fatima, Urooj
Ameen, Fuad
Soleja, Neha
Khan, Parvez
Almansob, Abobakr
Ahmad, Altaf
A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells
title A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells
title_full A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells
title_fullStr A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells
title_full_unstemmed A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells
title_short A Fluorescence Resonance Energy Transfer-Based Analytical Tool for Nitrate Quantification in Living Cells
title_sort fluorescence resonance energy transfer-based analytical tool for nitrate quantification in living cells
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7689916/
https://www.ncbi.nlm.nih.gov/pubmed/33251465
http://dx.doi.org/10.1021/acsomega.0c04868
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