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1 gence from its closest phylogenetic neighbor Frankia, a mesophilic plant endosymbiont and soil dwelle
2 ivalent microbial signaling molecules in the Frankia/actinorhizal association remains elusive.
3                                              Frankia alni ACN14a was found to be unable to respire or
4 s in root hairs in response to exudates from Frankia alni, but not to S. fredii NGR234 Nod factors.
5                                    The early Frankia-Alnus symbiotic molecular exchanges were analyze
6 a cellulose synthase was conserved among the Frankia and other actinobacteria such as Streptomyces.
7 ers of the actinomycete genera Streptomyces, Frankia and Rhodococcus, which typically live in soils a
8 s yet unknown molecular interactions between Frankia and their host plants.
9 etagamma-Proteobacteria, and Actinobacteria (Frankia) and provide strong support for the placement of
10 gically active symbiotic signals secreted by Frankia appear to be chemically distinct from the curren
11 are actinorhizal species that associate with Frankia bacteria and we showed that Alnus glutinosa indu
12 omycorrhizal (ECM) fungi and nitrogen-fixing Frankia bacteria and, although their ECM fungal communit
13 y hosting symbiotic diazotrophic rhizobia or Frankia bacteria in root organs known as nodules.
14 -free culture supernatants of the compatible Frankia CcI3 strain are able to elicit sustained high fr
15 how that the signal molecules present in the Frankia CcI3 supernatant are hydrophilic, of low molecul
16                                    For this, Frankia cells were placed in the presence of Alnus roots
17 firmed its close proximity to the Candidatus Frankia datiscae Dg1 genome with the absence of 38 genes
18 f the so far uncultured cluster-2 Candidatus Frankia datiscae Dg1, with cultivated Frankiae has revea
19 anic P acquisition abilities relative to non-Frankia ECM hosts.
20                                          The Frankia genome contains two truncated hemoglobin genes (
21                                          The Frankia genomes have conserved Sec (general secretory) a
22 aride-degrading enzymes present in all three Frankia genomes, suggesting that plant cell wall polysac
23  (N) when compared with ECM fungi on the non-Frankia host Pseudotsuga menziesii.
24 either rhizobia, the symbionts of legumes or Frankia in the case of actinorhizal plants.
25 N expression is correlated with infection by Frankia, including preinfection stages in developing roo
26 odules cgMT1 transcript is present in mature Frankia-infected cells and in the pericycle.
27 nslation of the message were not observed in Frankia-infected tissue where transcript accumulation wa
28  ecology and probably linked, in the case of Frankia microsymbionts to atypical patterns of auxotroph
29  provide strong support for the placement of Frankia nif genes at the base of combined the Cyanobacte
30 ng root nodules of legumes and actinorhizal (Frankia-nodulated) plants.
31 n unusual nitrogen transfer pathway from the Frankia nodule microsymbiont to the plant infected tissu
32 luster-2 strains together at the root of the Frankia radiation.
33 secreted polysaccharide-degrading enzymes in Frankia reflects a strategy used by these bacteria to av
34 es, lipases, and proteases found in the core Frankia secretome might facilitate hyphal penetration th
35  161 orthologous proteins belong to the core Frankia secretome.
36 ns shared among the strains, termed the core Frankia secretome.
37                  The predicted secretomes of Frankia sp. are relatively small and include few hydrola
38 from Micromonospora echinospora and Krm from Frankia sp. Ccl3, were experimentally determined as G140
39                                              Frankia sp. strains, the nitrogen-fixing facultative end
40 es extracellular solute-binding proteins and Frankia-specific hypothetical proteins that may enable t
41 sely related actinobacteria, and are termed "Frankia-specific." The genes encoding these conserved se
42 that establish a symbiosis with diazotrophic Frankia spp. bacteria share an evolutionary origin about
43 actions between plants and the soil bacteria Frankia spp. that lead to the formation of nitrogen-fixi
44                          Oxygen exclusion in Frankia spp., members of an actinomycetal genus that for
45  Our results suggest that auxin signaling in Frankia spp.-infected cells is involved in the long-dist
46 , we analyzed the role of auxin signaling in Frankia spp.-infected cells.
47              The potential secretome of each Frankia strain comprised 4-5% of the total proteome, a l
48 e ProCgNIN:GFP reporter as a function of the Frankia strain tested.
49 ompared the genome-based secretomes of three Frankia strains representing diverse host specificities.
50            With the objective of identifying Frankia symbiotic factors we present a novel approach ba
51                                          The Frankia vesicle envelope thus represents a layer specifi
52 Parasponia (Cannabaceae), and actinobacteria Frankia, which are able to interact with about 260 speci