Comparative genomics and proteogenomics highlight key molecular players involved in Frankia sporulation.
Actinorhizal symbiosis
Desiccation
Frankia sporulation
Secondary metabolites
Starvation
Journal
Research in microbiology
ISSN: 1769-7123
Titre abrégé: Res Microbiol
Pays: France
ID NLM: 8907468
Informations de publication
Date de publication:
Historique:
received:
30
11
2018
revised:
15
04
2019
accepted:
16
04
2019
pubmed:
25
4
2019
medline:
10
8
2019
entrez:
25
4
2019
Statut:
ppublish
Résumé
Sporulation is a microbial adaptive strategy to resist inhospitable conditions for vegetative growth and to disperse to colonise more favourable environments. This microbial trait is widespread in Actinobacteria. Among them, Frankia strains are able to differentiate sporangia in pure culture, while others can sporulate even when in symbiosis with sporulation occurring within host cells. The molecular determinants controlling Frankia sporulation have not been yet described. In order to highlight, for the first time, the molecular players potentially involved in Frankia sporulation, we conducted (i) a comparison of protein contents between Frankia spores and hyphae and (ii) a comparative genomic analysis of Frankia proteomes with sporulating and non-sporulating Actinobacteria. Among the main results, glycogen-metabolism related proteins, as well as oxidative stress response and protease-like proteins were overdetected in hyphae, recalling lytic processes that allow Streptomyces cells to erect sporogenic hyphae. Several genes encoding transcriptional regulators, including GntR-like, appeared up-regulated in spores, as well as tyrosinase, suggesting their potential role in mature spore metabolism. Finally, our results highlighted new proteins potentially involved in Frankia sporulation, including a pyrophosphate-energized proton pump and YaaT, described as involved in the phosphorelay allowing sporulation in Bacillus subtilis, leading us to discuss the role of a phosphorelay in Frankia sporulation.
Identifiants
pubmed: 31018159
pii: S0923-2508(19)30038-5
doi: 10.1016/j.resmic.2019.04.002
pii:
doi:
Substances chimiques
Bacterial Proteins
0
DNA-Binding Proteins
0
Proteome
0
Monophenol Monooxygenase
EC 1.14.18.1
Types de publication
Journal Article
Langues
eng
Pagination
202-213Informations de copyright
Copyright © 2019 Institut Pasteur. Published by Elsevier Masson SAS. All rights reserved.