Expression of nitrous oxide reductase from Pseudomonas stutzeri in transgenic tobacco roots using the root‐specific rolD promoter from Agrobacterium rhizogenes

Abstract The nitrous oxide (N2O) reduction pathway from a soil bacterium, Pseudomonas stutzeri, was engineered in plants to reduce N2O emissions. As a proof of principle, transgenic plants expressing nitrous oxide reductase (N2OR) from P. stutzeri, encoded by the nosZ gene, and other transgenic plan...

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Main Authors: Shen Wan, Amanda M. Johnson, Illimar Altosaar
Format: Article
Language:English
Published: Wiley 2012-02-01
Series:Ecology and Evolution
Subjects:
Online Access:https://doi.org/10.1002/ece3.74
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author Shen Wan
Amanda M. Johnson
Illimar Altosaar
author_facet Shen Wan
Amanda M. Johnson
Illimar Altosaar
author_sort Shen Wan
collection DOAJ
description Abstract The nitrous oxide (N2O) reduction pathway from a soil bacterium, Pseudomonas stutzeri, was engineered in plants to reduce N2O emissions. As a proof of principle, transgenic plants expressing nitrous oxide reductase (N2OR) from P. stutzeri, encoded by the nosZ gene, and other transgenic plants expressing N2OR along with the more complete operon from P. stutzeri, encoded by nosFLZDY, were generated. Gene constructs were engineered under the control of a root‐specific promoter and with a secretion signal peptide. Expression and rhizosecretion of the transgene protein were achieved, and N2OR from transgenic Nicotiana tabacum proved functional using the methyl viologen assay. Transgenic plant line 1.10 showed the highest specific activity of 16.7 µmol N2O reduced min−1 g−1 root protein. Another event, plant line 1.9, also demonstrated high specific activity of N2OR, 13.2 µmol N2O reduced min−1 g−1 root protein. The availability now of these transgenic seed stocks may enable canopy studies in field test plots to monitor whole rhizosphere N flux. By incorporating one bacterial gene into genetically modified organism (GMO) crops (e.g., cotton, corn, and soybean) in this way, it may be possible to reduce the atmospheric concentration of N2O that has continued to increase linearly (about 0.26% year−1) over the past half‐century.
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spelling doaj.art-5903fdce32114a98a9f83fcdaa1a76662023-06-22T06:50:39ZengWileyEcology and Evolution2045-77582012-02-012228629710.1002/ece3.74Expression of nitrous oxide reductase from Pseudomonas stutzeri in transgenic tobacco roots using the root‐specific rolD promoter from Agrobacterium rhizogenesShen Wan0Amanda M. Johnson1Illimar Altosaar2Department of Biochemistry, Microbiology and Immunology, Center for Research on Environmental Microbiology – CREM, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Ontario, K1H 8M5, CanadaDepartment of Biochemistry, Microbiology and Immunology, Center for Research on Environmental Microbiology – CREM, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Ontario, K1H 8M5, CanadaDepartment of Biochemistry, Microbiology and Immunology, Center for Research on Environmental Microbiology – CREM, Faculty of Medicine, University of Ottawa, 451 Smyth Road, Ottawa, Ontario, K1H 8M5, CanadaAbstract The nitrous oxide (N2O) reduction pathway from a soil bacterium, Pseudomonas stutzeri, was engineered in plants to reduce N2O emissions. As a proof of principle, transgenic plants expressing nitrous oxide reductase (N2OR) from P. stutzeri, encoded by the nosZ gene, and other transgenic plants expressing N2OR along with the more complete operon from P. stutzeri, encoded by nosFLZDY, were generated. Gene constructs were engineered under the control of a root‐specific promoter and with a secretion signal peptide. Expression and rhizosecretion of the transgene protein were achieved, and N2OR from transgenic Nicotiana tabacum proved functional using the methyl viologen assay. Transgenic plant line 1.10 showed the highest specific activity of 16.7 µmol N2O reduced min−1 g−1 root protein. Another event, plant line 1.9, also demonstrated high specific activity of N2OR, 13.2 µmol N2O reduced min−1 g−1 root protein. The availability now of these transgenic seed stocks may enable canopy studies in field test plots to monitor whole rhizosphere N flux. By incorporating one bacterial gene into genetically modified organism (GMO) crops (e.g., cotton, corn, and soybean) in this way, it may be possible to reduce the atmospheric concentration of N2O that has continued to increase linearly (about 0.26% year−1) over the past half‐century.https://doi.org/10.1002/ece3.74Greenhouse gasnitrous oxidenitrous oxide reductasephytoremediationrhizosecretionroot‐specific expression
spellingShingle Shen Wan
Amanda M. Johnson
Illimar Altosaar
Expression of nitrous oxide reductase from Pseudomonas stutzeri in transgenic tobacco roots using the root‐specific rolD promoter from Agrobacterium rhizogenes
Ecology and Evolution
Greenhouse gas
nitrous oxide
nitrous oxide reductase
phytoremediation
rhizosecretion
root‐specific expression
title Expression of nitrous oxide reductase from Pseudomonas stutzeri in transgenic tobacco roots using the root‐specific rolD promoter from Agrobacterium rhizogenes
title_full Expression of nitrous oxide reductase from Pseudomonas stutzeri in transgenic tobacco roots using the root‐specific rolD promoter from Agrobacterium rhizogenes
title_fullStr Expression of nitrous oxide reductase from Pseudomonas stutzeri in transgenic tobacco roots using the root‐specific rolD promoter from Agrobacterium rhizogenes
title_full_unstemmed Expression of nitrous oxide reductase from Pseudomonas stutzeri in transgenic tobacco roots using the root‐specific rolD promoter from Agrobacterium rhizogenes
title_short Expression of nitrous oxide reductase from Pseudomonas stutzeri in transgenic tobacco roots using the root‐specific rolD promoter from Agrobacterium rhizogenes
title_sort expression of nitrous oxide reductase from pseudomonas stutzeri in transgenic tobacco roots using the root specific rold promoter from agrobacterium rhizogenes
topic Greenhouse gas
nitrous oxide
nitrous oxide reductase
phytoremediation
rhizosecretion
root‐specific expression
url https://doi.org/10.1002/ece3.74
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