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11 November 2022

Correction: Pujic et al. The Proteogenome of Symbiotic Frankia alni in Alnus glutinosa Nodules. Microorganisms 2022, 10, 651

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1
Ecologie Microbienne, CNRS, UMR5557, Université Lyon 1, Université de Lyon; INRA, UMR1418, 7330 Villeurbanne, France
2
Département Médicaments et Technologies pour la Santé (DMTS), CEA, INRAE, Université Paris-Saclay, SPI, 30200 Bagnols sur Cèze, France
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Authors to whom correspondence should be addressed.
This article belongs to the Section Environmental Microbiology
The authors wish to make the following corrections to this paper [1].

Text Correction

The original version of this article contained an error on the control of the proteogenomic experiment, which was not nitrogen-fixing BAP—grown culture (without NH4+), but a nitrogen-replete BAP+ (containing 5 mM NH4+) culture. We corrected this error by replacing “N-fixing” by “N-replete” throughout the text.
Examples of corrections are given below:
In the Abstract:
A proteogenomic analysis of symbiotic Frankia alni was done by comparing those proteins more and less abundant in Alnus glutinosa nodules relative to N-replete pure cultures with propionate as the carbon source and ammonium as the nitrogen-source. There were 250 proteins that were significantly overabundant in nodules at a fold change (FC) ≥ 2 threshold, and 1429 with the same characteristics in in vitro nitrogen-replete pure culture.
In the Materials and Methods:
As a reference, F. alni cells were inoculated after syringing with a series of needles (21G, 23G, 25G, 27G) and grown for 10 days (corresponding to the end of the exponential phase) in 250 mL of BAP medium with ammonium (5 mM) in agitated 500 mL Erlenmeyer flasks [25] buffered to pH 6.5. No vesicles could be found.
As here in the Results:
The three biological replicates of symbiotic Frankia alni overproduced at a fold change of ≥2250 proteins (Supplementary Table S1) using a nitrogen-replete propionate-fed pure culture as reference, of which 100 had an FC ≥ 4.38 (Table 1).
And here:
Among F. alni proteins, the nitrogenase proteins were the most overabundant with 7 among the 10 highest using as reference a nitrogen-replete pure culture.
As here in the Legend to Figure 1:
Figure 1. Circular map of the genome of Frankia alni with the proteins over-abundant in nodules relative to a nitrogen-replete pure-culture (FC ≥ 2) positioned along the genome.
As here in the Title of Supplementary Materials Table S1:
Table S1: List of Frankia proteins identified in nodules and in a nitrogen-replete pure culture and their spectral counts.
And as here in the Acknowledgments:
Thanks are expressed to Elise Lacroix for Greenhouse management (Université de Lyon) and to Aude Herrera-Belaroussi (Université de Lyon) for the nitrogen-replete Frankia cells.

Reference

Furthermore, reference Clavijo et al. (2015) had been truncated, it should be as:
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Clavijo, F.; Diedhiou, I.; Vaissayre, V.; Brottier, L.; Acolatse, J.; Moukouanga, D.; Crabos, A.; Auguy, F.; Franche, C.; Gherbi, H.; et al. The Casuarina NIN gene is transcriptionally activated throughout Frankia root infection as well as in response to bacterial diffusible signals. New Phytol. 2015, 208, 887–903.
The authors state that the scientific conclusions are unaffected. This correction was approved by the Academic Editor. The original publication has also been updated.

Reference

  1. Pujic, P.; Alloisio, N.; Miotello, G.; Armengaud, J.; Abrouk, D.; Fournier, P.; Normand, P. The Proteogenome of Symbiotic Frankia alni in Alnus glutinosa Nodules. Microorganisms 2022, 10, 651. [Google Scholar] [CrossRef] [PubMed]
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