Nitrite induced transcription of p450nor during denitrification by Fusarium oxysporum correlates with the production of N2O with a high 15N site preference

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  • Johann Heinrich von Thünen-Institut, Bundesforschungsinstitut für Ländliche Räume, Wald und Fischerei
  • Universität Bayreuth
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OriginalspracheEnglisch
Aufsatznummer108043
FachzeitschriftSoil Biology and Biochemistry
Jahrgang151
Frühes Online-Datum7 Okt. 2020
PublikationsstatusVeröffentlicht - Dez. 2020

Abstract

The greenhouse gas nitrous oxide (N2O) is produced in soil as a consequence of complex co-occurring processes conducted by diverse microbial species, including fungi. The fungal p450nor gene encodes a nitric oxide reductase associated with fungal denitrification. We thus hypothesized that p450nor gene expression is a marker for ongoing fungal denitrification. Specific PCR primers and quantitative PCR (qPCR) assays were developed targeting p450nor genes and transcripts. The novel PCR primers successfully amplified p450nor from pure cultures, and were used in an mRNA targeted qPCR to quantify p450nor gene transcription (i.e., gene expression) during denitrification activity in cultures of the fungal model denitrifier Fusarium oxysporum. Gene expression was induced by high (5 mM) and low (0.25 mM) nitrite concentrations. Nitrite stimulated N2O production rates by F. oxysporum, which correlated well with an up to 70-fold increase in p450nor gene expression during the first 12–24 h of anoxic incubation. The relative p450nor gene peak expression and peak N2O production rates declined 20- and 2-fold on average, respectively, towards the later phase of incubation (48–120 h). The 15N site preference of N2O (SP(N2O)) was high for F. oxysporum and independent of reaction progress, confirming the fungal origin of N2O produced. In conclusion, the developed fungal p450nor gene expression assay together with the analysis of SP(N2O) values provide a basis to improve current tools for the identification of fungal denitrification and/or N2O production in natural systems like soils.

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Nitrite induced transcription of p450nor during denitrification by Fusarium oxysporum correlates with the production of N2O with a high 15N site preference. / Rohe, Lena; Oppermann, Timo; Well, Reinhard et al.
in: Soil Biology and Biochemistry, Jahrgang 151, 108043, 12.2020.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

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title = "Nitrite induced transcription of p450nor during denitrification by Fusarium oxysporum correlates with the production of N2O with a high 15N site preference",
abstract = "The greenhouse gas nitrous oxide (N2O) is produced in soil as a consequence of complex co-occurring processes conducted by diverse microbial species, including fungi. The fungal p450nor gene encodes a nitric oxide reductase associated with fungal denitrification. We thus hypothesized that p450nor gene expression is a marker for ongoing fungal denitrification. Specific PCR primers and quantitative PCR (qPCR) assays were developed targeting p450nor genes and transcripts. The novel PCR primers successfully amplified p450nor from pure cultures, and were used in an mRNA targeted qPCR to quantify p450nor gene transcription (i.e., gene expression) during denitrification activity in cultures of the fungal model denitrifier Fusarium oxysporum. Gene expression was induced by high (5 mM) and low (0.25 mM) nitrite concentrations. Nitrite stimulated N2O production rates by F. oxysporum, which correlated well with an up to 70-fold increase in p450nor gene expression during the first 12–24 h of anoxic incubation. The relative p450nor gene peak expression and peak N2O production rates declined 20- and 2-fold on average, respectively, towards the later phase of incubation (48–120 h). The 15N site preference of N2O (SP(N2O)) was high for F. oxysporum and independent of reaction progress, confirming the fungal origin of N2O produced. In conclusion, the developed fungal p450nor gene expression assay together with the analysis of SP(N2O) values provide a basis to improve current tools for the identification of fungal denitrification and/or N2O production in natural systems like soils.",
keywords = "N site Preference, Cytochrome P450nor, Fungal denitrification, Gene expression, NO reduction",
author = "Lena Rohe and Timo Oppermann and Reinhard Well and Horn, {Marcus A.}",
note = "Funding Information: We thank Natalie R{\"o}der (Leibniz University Hannover) for technical support and Christoph Tebbe and his team Karin Trescher, Jana Usarek, and Britta M{\"u}ller (Th{\"u}nen-Institute for Biodiversity) for support with laboratory work. Anette Giesemann and Martina Heuer are acknowledged for IRMS analyses at the Th{\"u}nen-Institute for Climate-Smart Agriculture. This project was funded by the Deutsche Forschungsgemeinschaft ( DFG HO4020/4-1 and WE 1904/8-1 ; ” Role of fungal denitrification in N 2 O fluxes from soils “; grant number 251282570 ) and from the Leibniz University Hannover .",
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doi = "10.15488/15942",
language = "English",
volume = "151",
journal = "Soil Biology and Biochemistry",
issn = "0038-0717",
publisher = "Elsevier Ltd.",

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TY - JOUR

T1 - Nitrite induced transcription of p450nor during denitrification by Fusarium oxysporum correlates with the production of N2O with a high 15N site preference

AU - Rohe, Lena

AU - Oppermann, Timo

AU - Well, Reinhard

AU - Horn, Marcus A.

N1 - Funding Information: We thank Natalie Röder (Leibniz University Hannover) for technical support and Christoph Tebbe and his team Karin Trescher, Jana Usarek, and Britta Müller (Thünen-Institute for Biodiversity) for support with laboratory work. Anette Giesemann and Martina Heuer are acknowledged for IRMS analyses at the Thünen-Institute for Climate-Smart Agriculture. This project was funded by the Deutsche Forschungsgemeinschaft ( DFG HO4020/4-1 and WE 1904/8-1 ; ” Role of fungal denitrification in N 2 O fluxes from soils “; grant number 251282570 ) and from the Leibniz University Hannover .

PY - 2020/12

Y1 - 2020/12

N2 - The greenhouse gas nitrous oxide (N2O) is produced in soil as a consequence of complex co-occurring processes conducted by diverse microbial species, including fungi. The fungal p450nor gene encodes a nitric oxide reductase associated with fungal denitrification. We thus hypothesized that p450nor gene expression is a marker for ongoing fungal denitrification. Specific PCR primers and quantitative PCR (qPCR) assays were developed targeting p450nor genes and transcripts. The novel PCR primers successfully amplified p450nor from pure cultures, and were used in an mRNA targeted qPCR to quantify p450nor gene transcription (i.e., gene expression) during denitrification activity in cultures of the fungal model denitrifier Fusarium oxysporum. Gene expression was induced by high (5 mM) and low (0.25 mM) nitrite concentrations. Nitrite stimulated N2O production rates by F. oxysporum, which correlated well with an up to 70-fold increase in p450nor gene expression during the first 12–24 h of anoxic incubation. The relative p450nor gene peak expression and peak N2O production rates declined 20- and 2-fold on average, respectively, towards the later phase of incubation (48–120 h). The 15N site preference of N2O (SP(N2O)) was high for F. oxysporum and independent of reaction progress, confirming the fungal origin of N2O produced. In conclusion, the developed fungal p450nor gene expression assay together with the analysis of SP(N2O) values provide a basis to improve current tools for the identification of fungal denitrification and/or N2O production in natural systems like soils.

AB - The greenhouse gas nitrous oxide (N2O) is produced in soil as a consequence of complex co-occurring processes conducted by diverse microbial species, including fungi. The fungal p450nor gene encodes a nitric oxide reductase associated with fungal denitrification. We thus hypothesized that p450nor gene expression is a marker for ongoing fungal denitrification. Specific PCR primers and quantitative PCR (qPCR) assays were developed targeting p450nor genes and transcripts. The novel PCR primers successfully amplified p450nor from pure cultures, and were used in an mRNA targeted qPCR to quantify p450nor gene transcription (i.e., gene expression) during denitrification activity in cultures of the fungal model denitrifier Fusarium oxysporum. Gene expression was induced by high (5 mM) and low (0.25 mM) nitrite concentrations. Nitrite stimulated N2O production rates by F. oxysporum, which correlated well with an up to 70-fold increase in p450nor gene expression during the first 12–24 h of anoxic incubation. The relative p450nor gene peak expression and peak N2O production rates declined 20- and 2-fold on average, respectively, towards the later phase of incubation (48–120 h). The 15N site preference of N2O (SP(N2O)) was high for F. oxysporum and independent of reaction progress, confirming the fungal origin of N2O produced. In conclusion, the developed fungal p450nor gene expression assay together with the analysis of SP(N2O) values provide a basis to improve current tools for the identification of fungal denitrification and/or N2O production in natural systems like soils.

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KW - Cytochrome P450nor

KW - Fungal denitrification

KW - Gene expression

KW - NO reduction

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U2 - 10.15488/15942

DO - 10.15488/15942

M3 - Article

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VL - 151

JO - Soil Biology and Biochemistry

JF - Soil Biology and Biochemistry

SN - 0038-0717

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ER -

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