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Engineered plant control of associative nitrogen fixation

Engineering N(2)-fixing symbioses between cereals and diazotrophic bacteria represents a promising strategy to sustainably deliver biologically fixed nitrogen (N) in agriculture. We previously developed novel transkingdom signaling between plants and bacteria, through plant production of the bacteri...

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Autores principales: Haskett, Timothy L., Paramasivan, Ponraj, Mendes, Marta D., Green, Patrick, Geddes, Barney A., Knights, Hayley E., Jorrin, Beatriz, Ryu, Min-Hyung, Brett, Paul, Voigt, Christopher A., Oldroyd, Giles E. D., Poole, Philip S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169844/
https://www.ncbi.nlm.nih.gov/pubmed/35412890
http://dx.doi.org/10.1073/pnas.2117465119
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author Haskett, Timothy L.
Paramasivan, Ponraj
Mendes, Marta D.
Green, Patrick
Geddes, Barney A.
Knights, Hayley E.
Jorrin, Beatriz
Ryu, Min-Hyung
Brett, Paul
Voigt, Christopher A.
Oldroyd, Giles E. D.
Poole, Philip S.
author_facet Haskett, Timothy L.
Paramasivan, Ponraj
Mendes, Marta D.
Green, Patrick
Geddes, Barney A.
Knights, Hayley E.
Jorrin, Beatriz
Ryu, Min-Hyung
Brett, Paul
Voigt, Christopher A.
Oldroyd, Giles E. D.
Poole, Philip S.
author_sort Haskett, Timothy L.
collection PubMed
description Engineering N(2)-fixing symbioses between cereals and diazotrophic bacteria represents a promising strategy to sustainably deliver biologically fixed nitrogen (N) in agriculture. We previously developed novel transkingdom signaling between plants and bacteria, through plant production of the bacterial signal rhizopine, allowing control of bacterial gene expression in association with the plant. Here, we have developed both a homozygous rhizopine producing (RhiP) barley line and a hybrid rhizopine uptake system that conveys upon our model bacterium Azorhizobium caulinodans ORS571 (Ac) 10(3)-fold improved sensitivity for rhizopine perception. Using this improved genetic circuitry, we established tight rhizopine-dependent transcriptional control of the nitrogenase master regulator nifA and the N metabolism σ-factor rpoN, which drove nitrogenase expression and activity in vitro and in situ by bacteria colonizing RhiP barley roots. Although in situ nitrogenase activity was suboptimally effective relative to the wild-type strain, activation was specific to RhiP barley and was not observed on the roots of wild-type plants. This work represents a key milestone toward the development of a synthetic plant-controlled symbiosis in which the bacteria fix N(2) only when in contact with the desired host plant and are prevented from interaction with nontarget plant species.
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spelling pubmed-91698442022-10-11 Engineered plant control of associative nitrogen fixation Haskett, Timothy L. Paramasivan, Ponraj Mendes, Marta D. Green, Patrick Geddes, Barney A. Knights, Hayley E. Jorrin, Beatriz Ryu, Min-Hyung Brett, Paul Voigt, Christopher A. Oldroyd, Giles E. D. Poole, Philip S. Proc Natl Acad Sci U S A Biological Sciences Engineering N(2)-fixing symbioses between cereals and diazotrophic bacteria represents a promising strategy to sustainably deliver biologically fixed nitrogen (N) in agriculture. We previously developed novel transkingdom signaling between plants and bacteria, through plant production of the bacterial signal rhizopine, allowing control of bacterial gene expression in association with the plant. Here, we have developed both a homozygous rhizopine producing (RhiP) barley line and a hybrid rhizopine uptake system that conveys upon our model bacterium Azorhizobium caulinodans ORS571 (Ac) 10(3)-fold improved sensitivity for rhizopine perception. Using this improved genetic circuitry, we established tight rhizopine-dependent transcriptional control of the nitrogenase master regulator nifA and the N metabolism σ-factor rpoN, which drove nitrogenase expression and activity in vitro and in situ by bacteria colonizing RhiP barley roots. Although in situ nitrogenase activity was suboptimally effective relative to the wild-type strain, activation was specific to RhiP barley and was not observed on the roots of wild-type plants. This work represents a key milestone toward the development of a synthetic plant-controlled symbiosis in which the bacteria fix N(2) only when in contact with the desired host plant and are prevented from interaction with nontarget plant species. National Academy of Sciences 2022-04-11 2022-04-19 /pmc/articles/PMC9169844/ /pubmed/35412890 http://dx.doi.org/10.1073/pnas.2117465119 Text en Copyright © 2022 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/This article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Haskett, Timothy L.
Paramasivan, Ponraj
Mendes, Marta D.
Green, Patrick
Geddes, Barney A.
Knights, Hayley E.
Jorrin, Beatriz
Ryu, Min-Hyung
Brett, Paul
Voigt, Christopher A.
Oldroyd, Giles E. D.
Poole, Philip S.
Engineered plant control of associative nitrogen fixation
title Engineered plant control of associative nitrogen fixation
title_full Engineered plant control of associative nitrogen fixation
title_fullStr Engineered plant control of associative nitrogen fixation
title_full_unstemmed Engineered plant control of associative nitrogen fixation
title_short Engineered plant control of associative nitrogen fixation
title_sort engineered plant control of associative nitrogen fixation
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9169844/
https://www.ncbi.nlm.nih.gov/pubmed/35412890
http://dx.doi.org/10.1073/pnas.2117465119
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