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Development of a Pigment-Based Whole-Cell Zinc Biosensor for Human Serum

[Image: see text] Deficiencies in vitamins and minerals (micronutrients) are a critical global health concern, in part due to logistical difficulties in assessing population micronutrient status. Whole-cell biosensors offer a unique opportunity to address this issue, with the potential to move sampl...

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Autores principales: Watstein, Daniel M., Styczynski, Mark P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2017
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778388/
https://www.ncbi.nlm.nih.gov/pubmed/29202581
http://dx.doi.org/10.1021/acssynbio.7b00292
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author Watstein, Daniel M.
Styczynski, Mark P.
author_facet Watstein, Daniel M.
Styczynski, Mark P.
author_sort Watstein, Daniel M.
collection PubMed
description [Image: see text] Deficiencies in vitamins and minerals (micronutrients) are a critical global health concern, in part due to logistical difficulties in assessing population micronutrient status. Whole-cell biosensors offer a unique opportunity to address this issue, with the potential to move sample analysis from centralized, resource-intensive clinics to minimal-resource, on-site measurement. Here, we present a proof-of-concept whole-cell biosensor in Escherichia coli for detecting zinc, a micronutrient for which deficiencies are a significant public health burden. Importantly, the whole-cell biosensor produces readouts (pigments) that are visible to the naked eye, mitigating the need for measurement equipment and thus increasing feasibility for sensor field-friendliness and affordability at a global scale. Two zinc-responsive promoter/transcription factor systems are used to differentially control production of three distinctly colored pigments in response to zinc levels in culture. We demonstrate strategies for tuning each zinc-responsive system to turn production of the different pigments on and off at different zinc levels, and we demonstrate production of three distinct color regimes over a concentration range relevant to human health. We also demonstrate the ability of the sensor cells to grow and produce pigment when cultured in human serum, the ultimate target matrix for assessing zinc nutritional status. Specifically, we present approaches to overcome innate immune responses that would otherwise hinder bacterial sensor survival, and we demonstrate production of multiple pigment regimes in human serum with different zinc levels. This work provides proof of principle for the development of low-cost, minimal-equipment, field-deployable biosensors for nutritional epidemiology applications.
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spelling pubmed-57783882018-01-25 Development of a Pigment-Based Whole-Cell Zinc Biosensor for Human Serum Watstein, Daniel M. Styczynski, Mark P. ACS Synth Biol [Image: see text] Deficiencies in vitamins and minerals (micronutrients) are a critical global health concern, in part due to logistical difficulties in assessing population micronutrient status. Whole-cell biosensors offer a unique opportunity to address this issue, with the potential to move sample analysis from centralized, resource-intensive clinics to minimal-resource, on-site measurement. Here, we present a proof-of-concept whole-cell biosensor in Escherichia coli for detecting zinc, a micronutrient for which deficiencies are a significant public health burden. Importantly, the whole-cell biosensor produces readouts (pigments) that are visible to the naked eye, mitigating the need for measurement equipment and thus increasing feasibility for sensor field-friendliness and affordability at a global scale. Two zinc-responsive promoter/transcription factor systems are used to differentially control production of three distinctly colored pigments in response to zinc levels in culture. We demonstrate strategies for tuning each zinc-responsive system to turn production of the different pigments on and off at different zinc levels, and we demonstrate production of three distinct color regimes over a concentration range relevant to human health. We also demonstrate the ability of the sensor cells to grow and produce pigment when cultured in human serum, the ultimate target matrix for assessing zinc nutritional status. Specifically, we present approaches to overcome innate immune responses that would otherwise hinder bacterial sensor survival, and we demonstrate production of multiple pigment regimes in human serum with different zinc levels. This work provides proof of principle for the development of low-cost, minimal-equipment, field-deployable biosensors for nutritional epidemiology applications. American Chemical Society 2017-12-05 2018-01-19 /pmc/articles/PMC5778388/ /pubmed/29202581 http://dx.doi.org/10.1021/acssynbio.7b00292 Text en Copyright © 2017 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 Watstein, Daniel M.
Styczynski, Mark P.
Development of a Pigment-Based Whole-Cell Zinc Biosensor for Human Serum
title Development of a Pigment-Based Whole-Cell Zinc Biosensor for Human Serum
title_full Development of a Pigment-Based Whole-Cell Zinc Biosensor for Human Serum
title_fullStr Development of a Pigment-Based Whole-Cell Zinc Biosensor for Human Serum
title_full_unstemmed Development of a Pigment-Based Whole-Cell Zinc Biosensor for Human Serum
title_short Development of a Pigment-Based Whole-Cell Zinc Biosensor for Human Serum
title_sort development of a pigment-based whole-cell zinc biosensor for human serum
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5778388/
https://www.ncbi.nlm.nih.gov/pubmed/29202581
http://dx.doi.org/10.1021/acssynbio.7b00292
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