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Spanning high-dimensional expression space using ribosome-binding site combinatorics

Protein levels are a dominant factor shaping natural and synthetic biological systems. Although proper functioning of metabolic pathways relies on precise control of enzyme levels, the experimental ability to balance the levels of many genes in parallel is a major outstanding challenge. Here, we int...

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Autores principales: Zelcbuch, Lior, Antonovsky, Niv, Bar-Even, Arren, Levin-Karp, Ayelet, Barenholz, Uri, Dayagi, Michal, Liebermeister, Wolfram, Flamholz, Avi, Noor, Elad, Amram, Shira, Brandis, Alexander, Bareia, Tasneem, Yofe, Ido, Jubran, Halim, Milo, Ron
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3643573/
https://www.ncbi.nlm.nih.gov/pubmed/23470993
http://dx.doi.org/10.1093/nar/gkt151
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author Zelcbuch, Lior
Antonovsky, Niv
Bar-Even, Arren
Levin-Karp, Ayelet
Barenholz, Uri
Dayagi, Michal
Liebermeister, Wolfram
Flamholz, Avi
Noor, Elad
Amram, Shira
Brandis, Alexander
Bareia, Tasneem
Yofe, Ido
Jubran, Halim
Milo, Ron
author_facet Zelcbuch, Lior
Antonovsky, Niv
Bar-Even, Arren
Levin-Karp, Ayelet
Barenholz, Uri
Dayagi, Michal
Liebermeister, Wolfram
Flamholz, Avi
Noor, Elad
Amram, Shira
Brandis, Alexander
Bareia, Tasneem
Yofe, Ido
Jubran, Halim
Milo, Ron
author_sort Zelcbuch, Lior
collection PubMed
description Protein levels are a dominant factor shaping natural and synthetic biological systems. Although proper functioning of metabolic pathways relies on precise control of enzyme levels, the experimental ability to balance the levels of many genes in parallel is a major outstanding challenge. Here, we introduce a rapid and modular method to span the expression space of several proteins in parallel. By combinatorially pairing genes with a compact set of ribosome-binding sites, we modulate protein abundance by several orders of magnitude. We demonstrate our strategy by using a synthetic operon containing fluorescent proteins to span a 3D color space. Using the same approach, we modulate a recombinant carotenoid biosynthesis pathway in Escherichia coli to reveal a diversity of phenotypes, each characterized by a distinct carotenoid accumulation profile. In a single combinatorial assembly, we achieve a yield of the industrially valuable compound astaxanthin 4-fold higher than previously reported. The methodology presented here provides an efficient tool for exploring a high-dimensional expression space to locate desirable phenotypes.
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spelling pubmed-36435732013-05-03 Spanning high-dimensional expression space using ribosome-binding site combinatorics Zelcbuch, Lior Antonovsky, Niv Bar-Even, Arren Levin-Karp, Ayelet Barenholz, Uri Dayagi, Michal Liebermeister, Wolfram Flamholz, Avi Noor, Elad Amram, Shira Brandis, Alexander Bareia, Tasneem Yofe, Ido Jubran, Halim Milo, Ron Nucleic Acids Res Methods Online Protein levels are a dominant factor shaping natural and synthetic biological systems. Although proper functioning of metabolic pathways relies on precise control of enzyme levels, the experimental ability to balance the levels of many genes in parallel is a major outstanding challenge. Here, we introduce a rapid and modular method to span the expression space of several proteins in parallel. By combinatorially pairing genes with a compact set of ribosome-binding sites, we modulate protein abundance by several orders of magnitude. We demonstrate our strategy by using a synthetic operon containing fluorescent proteins to span a 3D color space. Using the same approach, we modulate a recombinant carotenoid biosynthesis pathway in Escherichia coli to reveal a diversity of phenotypes, each characterized by a distinct carotenoid accumulation profile. In a single combinatorial assembly, we achieve a yield of the industrially valuable compound astaxanthin 4-fold higher than previously reported. The methodology presented here provides an efficient tool for exploring a high-dimensional expression space to locate desirable phenotypes. Oxford University Press 2013-05 2013-03-06 /pmc/articles/PMC3643573/ /pubmed/23470993 http://dx.doi.org/10.1093/nar/gkt151 Text en © The Author(s) 2013. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0/), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Methods Online
Zelcbuch, Lior
Antonovsky, Niv
Bar-Even, Arren
Levin-Karp, Ayelet
Barenholz, Uri
Dayagi, Michal
Liebermeister, Wolfram
Flamholz, Avi
Noor, Elad
Amram, Shira
Brandis, Alexander
Bareia, Tasneem
Yofe, Ido
Jubran, Halim
Milo, Ron
Spanning high-dimensional expression space using ribosome-binding site combinatorics
title Spanning high-dimensional expression space using ribosome-binding site combinatorics
title_full Spanning high-dimensional expression space using ribosome-binding site combinatorics
title_fullStr Spanning high-dimensional expression space using ribosome-binding site combinatorics
title_full_unstemmed Spanning high-dimensional expression space using ribosome-binding site combinatorics
title_short Spanning high-dimensional expression space using ribosome-binding site combinatorics
title_sort spanning high-dimensional expression space using ribosome-binding site combinatorics
topic Methods Online
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3643573/
https://www.ncbi.nlm.nih.gov/pubmed/23470993
http://dx.doi.org/10.1093/nar/gkt151
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