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1 gence from its closest phylogenetic neighbor Frankia, a mesophilic plant endosymbiont and soil dwelle
3 s in root hairs in response to exudates from Frankia alni, but not to S. fredii NGR234 Nod factors.
4 ers of the actinomycete genera Streptomyces, Frankia and Rhodococcus, which typically live in soils a
6 etagamma-Proteobacteria, and Actinobacteria (Frankia) and provide strong support for the placement of
7 gically active symbiotic signals secreted by Frankia appear to be chemically distinct from the curren
8 are actinorhizal species that associate with Frankia bacteria and we showed that Alnus glutinosa indu
9 omycorrhizal (ECM) fungi and nitrogen-fixing Frankia bacteria and, although their ECM fungal communit
10 -free culture supernatants of the compatible Frankia CcI3 strain are able to elicit sustained high fr
11 how that the signal molecules present in the Frankia CcI3 supernatant are hydrophilic, of low molecul
12 firmed its close proximity to the Candidatus Frankia datiscae Dg1 genome with the absence of 38 genes
13 f the so far uncultured cluster-2 Candidatus Frankia datiscae Dg1, with cultivated Frankiae has revea
17 aride-degrading enzymes present in all three Frankia genomes, suggesting that plant cell wall polysac
20 N expression is correlated with infection by Frankia, including preinfection stages in developing roo
22 nslation of the message were not observed in Frankia-infected tissue where transcript accumulation wa
23 ecology and probably linked, in the case of Frankia microsymbionts to atypical patterns of auxotroph
24 provide strong support for the placement of Frankia nif genes at the base of combined the Cyanobacte
26 n unusual nitrogen transfer pathway from the Frankia nodule microsymbiont to the plant infected tissu
28 secreted polysaccharide-degrading enzymes in Frankia reflects a strategy used by these bacteria to av
29 es, lipases, and proteases found in the core Frankia secretome might facilitate hyphal penetration th
33 from Micromonospora echinospora and Krm from Frankia sp. Ccl3, were experimentally determined as G140
35 es extracellular solute-binding proteins and Frankia-specific hypothetical proteins that may enable t
36 sely related actinobacteria, and are termed "Frankia-specific." The genes encoding these conserved se
37 actions between plants and the soil bacteria Frankia spp. that lead to the formation of nitrogen-fixi
39 Our results suggest that auxin signaling in Frankia spp.-infected cells is involved in the long-dist
43 ompared the genome-based secretomes of three Frankia strains representing diverse host specificities.
46 Parasponia (Cannabaceae), and actinobacteria Frankia, which are able to interact with about 260 speci
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