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Proteogenomics data for deciphering Frankia coriariae interactions with root exudates from three host plants☆

Identifieur interne : 000402 ( Main/Exploration ); précédent : 000401; suivant : 000403

Proteogenomics data for deciphering Frankia coriariae interactions with root exudates from three host plants☆

Auteurs : Guylaine Miotello [France] ; Amir Ktari [Tunisie] ; Abdellatif Gueddou [Tunisie] ; Imen Nouioui [Tunisie] ; Faten Ghodhbane-Gtari [Tunisie] ; Jean Armengaud [France] ; Maher Gtari [Tunisie]

Source :

RBID : PMC:5526514

Abstract

Frankia coriariae BMG5.1 cells were incubated with root exudates derived from compatible (Coriaria myrtifolia), incompatible (Alnus glutinosa) and non-actinorhizal (Cucumis melo) host plants. Bacteria cells and their exoproteomes were analyzed by high-throughput proteomics using a Q-Exactive HF high resolution tandem mass spectrometer incorporating an ultra-high-field orbitrap analyzer. MS/MS spectra were assigned with two protein sequence databases derived from the closely-related genomes from strains BMG5.1 andDg1, the Frankia symbiont of Datisca glomerata. The tandem mass spectrometry data accompanying the manuscript describing the database searches and comparative analysis (Ktari et al., 2017, doi.org/10.3389/fmicb.2017.00720) [1] have been deposited to the ProteomeXchange with identifiers PXD005979 (whole cell proteomes) and PXD005980 (exoproteome data).


Url:
DOI: 10.1016/j.dib.2017.07.009
PubMed: 28765834
PubMed Central: 5526514


Affiliations:


Links toward previous steps (curation, corpus...)


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<p>
<italic>Frankia coriariae</italic>
BMG5.1 cells were incubated with root exudates derived from compatible (
<italic>Coriaria myrtifolia</italic>
), incompatible (
<italic>Alnus glutinosa</italic>
) and non-actinorhizal (
<italic>Cucumis melo</italic>
) host plants. Bacteria cells and their exoproteomes were analyzed by high-throughput proteomics using a Q-Exactive HF high resolution tandem mass spectrometer incorporating an ultra-high-field orbitrap analyzer. MS/MS spectra were assigned with two protein sequence databases derived from the closely-related genomes from strains BMG5.1 andDg1, the
<italic>Frankia</italic>
symbiont of
<italic>Datisca glomerata</italic>
. The tandem mass spectrometry data accompanying the manuscript describing the database searches and comparative analysis (Ktari et al., 2017, doi.org/10.3389/fmicb.2017.00720)
<xref rid="bib1" ref-type="bibr">[1]</xref>
have been deposited to the ProteomeXchange with identifiers PXD005979 (whole cell proteomes) and PXD005980 (exoproteome data).</p>
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<name sortKey="Ktari, A" uniqKey="Ktari A">A. Ktari</name>
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<author>
<name sortKey="Wei, W" uniqKey="Wei W">W. Wei</name>
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<author>
<name sortKey="Scheltema, R A" uniqKey="Scheltema R">R.A. Scheltema</name>
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<name sortKey="Kelstrup, C D" uniqKey="Kelstrup C">C.D. Kelstrup</name>
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<name sortKey="Hartmann, E M" uniqKey="Hartmann E">E.M. Hartmann</name>
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<author>
<name sortKey="Klein, G" uniqKey="Klein G">G. Klein</name>
</author>
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<author>
<name sortKey="Clair, G" uniqKey="Clair G">G. Clair</name>
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<author>
<name sortKey="Armengaud, J" uniqKey="Armengaud J">J. Armengaud</name>
</author>
<author>
<name sortKey="Duport, C" uniqKey="Duport C">C. Duport</name>
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<author>
<name sortKey="Rubiano Labrador, C" uniqKey="Rubiano Labrador C">C. Rubiano-Labrador</name>
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<name sortKey="Sghaier, H" uniqKey="Sghaier H">H. Sghaier</name>
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