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1 c factors, including its symbiotic bacterium Pseudonocardia.
2  antagonistic interactions among free-living Pseudonocardia.
3  of free-living actinomycetes from the genus Pseudonocardia.
4 urban locations by the exclusive presence of Pseudonocardia (Actinobacteria) in the biofilm and the a
5                                              Pseudonocardia and Amycolatopsis isolates also show nons
6                                              Pseudonocardia and Amycolatopsis secretions kill or stro
7 Two different bacterial genera are featured, Pseudonocardia and Salinispora, and, although the small-
8                 Within this order, the genus Pseudonocardia and their specialised metabolites have be
9 d previously identified this molecule from a Pseudonocardia associated with Apterostigma dentigerum,
10 , garden-infecting Escovopsis pathogens, and Pseudonocardia bacteria on the ant integument has been p
11 ts are thought to form such a mutualism with Pseudonocardia bacteria to derive antibiotics that speci
12                                              Pseudonocardia can occur on males, suggesting that Pseud
13  popularized as an example of ant-Escovopsis-Pseudonocardia co-evolution.
14 asionally Amycolatopsis (a close relative of Pseudonocardia) co-occur on workers from a single nest,
15 nocardia can occur on males, suggesting that Pseudonocardia could also be horizontally transmitted du
16                                              Pseudonocardia dioxanivorans CB1190 is the first bacteri
17                  In reactors bioaugmented by Pseudonocardia dioxanivorans CB1190 with 3.0 V applied,
18     In this study, we examined autotrophy in Pseudonocardia dioxanivorans CB1190, which can grow usin
19 res on aerobic 1,4-dioxane biodegradation by Pseudonocardia dioxanivorans CB1190.
20 phy in attine ant- and plant root-associated Pseudonocardia discussed.
21       Here we test 4 key assumptions of this Pseudonocardia-Escovopsis coevolution model.
22 nceptual framework to replace the prevailing Pseudonocardia-Escovopsis coevolution model.
23 ,4-dioxane and the first member of the genus Pseudonocardia for which there is an annotated genome se
24                          If association with Pseudonocardia is adaptive to attine ants, alternate rol
25                                              Pseudonocardia is an actinobacterial genus of interest d
26  in phylotypes closely related to the genera Pseudonocardia known to biodegrade 1,4-dioxane.
27 ious finding of a growth-enhancing effect of Pseudonocardia on the cultivars.
28 However, the chemical ecology of free-living Pseudonocardia remains understudied.
29 Streptomyces, Nocardiopsis, Alloalcanivorax, Pseudonocardia, Sinomicrobium, and Lysinibacillus.
30 -pyrosequencing) surveys reveal that several Pseudonocardia species and occasionally Amycolatopsis (a
31 ctrometry-based metabolomic profiles of nine Pseudonocardia species isolated from marine sediments an
32                                         Some Pseudonocardia spp. can grow autotrophically, but the ge
33 and were produced by two different symbiotic Pseudonocardia spp. from ants in the genus Apterostigma
34 ave benefited from horizontal gene transfer, Pseudonocardia spp. have relied on plasmid-based tactics
35 he potential for autotrophic growth of other Pseudonocardia spp. was explored, and the ecological imp
36 -term association with a single, co-evolving Pseudonocardia strain, attine ants accumulate complex, d
37 regarding antibiotic-secreting, integumental Pseudonocardia that co-evolve to specifically suppress E
38 ned the inhibition of the Co-type NHase from Pseudonocardia thermophila JCM 3095 (PtNHase) by boronic
39 cat) and K(m) for the cobalt-type NHase from Pseudonocardia thermophila JCM 3095 (PtNHase) were exami
40 olecules, the genomes of the three producing Pseudonocardia were sequenced and the biosynthetic gene