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1 ental programme in the social soil bacterium Myxococcus xanthus.
2 ively regulates fruiting body development in Myxococcus xanthus.
3 we investigate swarms of the myxobacterium, Myxococcus xanthus.
4 ruiting body development-associated genes in Myxococcus xanthus.
5 fferentiation is the gram-negative bacterium Myxococcus xanthus.
6 s to the transcriptional regulator CarD from Myxococcus xanthus.
7 al movements for the two motility systems in Myxococcus xanthus.
8 us to chromosome segregation and motility in Myxococcus xanthus.
9 used to examine fruiting body development of Myxococcus xanthus.
10 s to understand the developmental biology of Myxococcus xanthus.
11 uses defects in fruiting body development in Myxococcus xanthus.
12 g the multicellular developmental process of Myxococcus xanthus.
13 d gene function in the delta proteobacterium Myxococcus xanthus.
14 from the social and developmental bacterium Myxococcus xanthus.
15 (IPTG)-inducible promoter was constructed in Myxococcus xanthus.
16 is and gene expression during development of Myxococcus xanthus.
17 ophage Mx9 is a temperate phage that infects Myxococcus xanthus.
18 pili-mediated (S) gliding and development of Myxococcus xanthus.
19 aces is found in the nonpathogenic bacterium Myxococcus xanthus.
20 quired for starvation-induced development in Myxococcus xanthus.
21 ein required for motility and development in Myxococcus xanthus.
22 orrhoeae, and for social gliding motility in Myxococcus xanthus.
23 he behavior of the biofilm-forming bacterium Myxococcus xanthus.
24 k shows significant identity with the Ndk of Myxococcus xanthus.
25 the growth and multicellular development of Myxococcus xanthus.
26 activator of the Hypr GGDEF enzyme GacB from Myxococcus xanthus.
27 showing that cAG is present in surface-grown Myxococcus xanthus.
28 S) production in the Gram-negative bacterium Myxococcus xanthus.
29 cillus subtilis, Caulobacter crescentus, and Myxococcus xanthus.
30 ion, motility, and polarity in the bacterium Myxococcus xanthus.
31 peron is important for normal development of Myxococcus xanthus.
32 c called TA (myxovirescin), which is made by Myxococcus xanthus.
33 secretion system in the crowded interior of Myxococcus xanthus.
34 ding the social Gram-negative soil bacterium Myxococcus xanthus.
35 ion of many important developmental genes in Myxococcus xanthus.
36 r bacteria with complex life-styles, such as Myxococcus xanthus.
37 bly absent from spore-forming, Gram-negative Myxococcus xanthus.
38 on-helix-helix family that binds c-di-GMP in Myxococcus xanthus.
39 _7475 (BacM), one of the four bactofilins of Myxococcus xanthus.
40 ulates exopolysaccharide (EPS) production in Myxococcus xanthus.
42 asmic-function (ECF) sigma factor (RpoE1) in Myxococcus xanthus, a bacterium which has a complex life
43 haracterized the Che7 chemosensory system of Myxococcus xanthus, a common soil bacterium which displa
46 ellular filamentation on gliding motility of Myxococcus xanthus, a Gram-negative social bacterium, wa
52 eonine kinases (PSTKs) has been performed in Myxococcus xanthus, a soil bacterium with a complex life
55 biological evidence, however, suggests that Myxococcus xanthus aggregation is the consequence of dir
56 developmental requirement for B-signaling in Myxococcus xanthus, also bypass the requirement for A-si
57 n and purification of PHD from the bacterium Myxococcus xanthus and demonstrate the presence of nonco
59 ystems, are essential for pilus extension in Myxococcus xanthus and form a complex that is an integra
61 iments between kin discriminating strains of Myxococcus xanthus and Proteus mirabilis, we found the r
62 smaller nozzle-like structures are found in Myxococcus xanthus and that they are clustered at both c
63 ese movements are known as social gliding in Myxococcus xanthus and twitching in organisms such as Ps
64 1.0+/-0.1 microM for the enzymes from human, Myxococcus xanthus, and Aquifex aeolicus, respectively.
68 nduced spores of the Gram-negative bacterium Myxococcus xanthus are peptidoglycan (PG)-deficient.
70 coevolving bacterial communities composed of Myxococcus xanthus as predator and Escherichia coli as p
71 starvation, a dense population of rod-shaped Myxococcus xanthus bacteria coordinate their movements t
75 unrelated proteins (spore coat protein from Myxococcus xanthus, beta-B2 and gamma-B crystallins from
77 sensory system controls directed motility in Myxococcus xanthus by regulating cellular reversal frequ
78 a preferred locus on the genome of its host, Myxococcus xanthus, by a mechanism of site-specific reco
82 and a mammalian pathogen -Escherichia coli, Myxococcus xanthus, Caulobacter crescentus, and Mycobact
83 the z axis has opened a window in studies of Myxococcus xanthus cell ultrastructure and biofilm commu
87 nts, we observed slime deposition by gliding Myxococcus xanthus cells at unprecedented resolution.
91 Gliding movements of individual isolated Myxococcus xanthus cells depend on the genes of the A-mo
96 compared the cellular fatty acid profiles of Myxococcus xanthus cells grown in either a Casitone-base
99 ously reported Tn5lac Omega4469 insertion in Myxococcus xanthus cells is regulated by the starvation
101 Coordinated movement of packs of S-motile Myxococcus xanthus cells relies on extrusion and retract
106 We used cryo-electron tomography of intact Myxococcus xanthus cells to visualize type IVa pili and
108 Under starvation conditions, a swarm of Myxococcus xanthus cells will undergo development, a mul
112 99 is the site of a Tn5 lac insertion in the Myxococcus xanthus chromosome that fuses lacZ expression
121 ecific incompatibility in the soil bacterium Myxococcus xanthus demonstrates that the social life of
129 ained nine different laboratories' wild type Myxococcus xanthus DK1622 "sublines" and sequenced each
130 uced by the well-studied model myxobacterium Myxococcus xanthus DK1622, which were not accessible pre
138 by measuring symmetry breaking in a swarm of Myxococcus xanthus exposed to a two-dimensional nutrient
146 obtained evidence that the type IV pilus of Myxococcus xanthus functions as a motility apparatus.
147 a model organism database for the bacterium Myxococcus xanthus, functions as a collaborative informa
149 M1genome sequence, which includes 97% of the Myxococcus xanthus genes, identified 53 sequence homolog
150 o a rippling population and, on the basis of Myxococcus xanthus genetic data, we conclude that this p
151 14 is the site of a Tn5 lac insertion in the Myxococcus xanthus genome that fuses lacZ expression to
152 00 is the site of a Tn5 lac insertion in the Myxococcus xanthus genome that fuses lacZ expression to
155 Here, we characterized the dynamics of the Myxococcus xanthus gliding motor protein AglR, a homolog
156 ial groups of the cooperative soil bacterium Myxococcus xanthus harbor internal genetic and phenotypi
160 one of the most primitive social organisms, Myxococcus xanthus has been an ideal model bacterium for
161 se variation between yellow and tan forms of Myxococcus xanthus has been recognized for several decad
164 red natural populations of the model species Myxococcus xanthus have fragmented into a large number o
165 us subtilis and fruiting body development of Myxococcus xanthus have revealed key features of regulat
166 development, the quorum-sensing A-signal in Myxococcus xanthus helps to assess starvation and induce
167 explain the adventurous gliding motility of Myxococcus xanthus: (i) polar secretion of slime and (ii
168 endent Tn5-lac insertions in the S1 locus of Myxococcus xanthus inactivate the sglK gene, which is no
170 lar fruiting body formation in the bacterium Myxococcus xanthus, inhibiting the transition from growt
173 ding motility in the developmental bacterium Myxococcus xanthus involves two genetically distinct mot
211 e extracellular matrix of the soil bacterium Myxococcus xanthus is essential for biofilm formation an
214 ence in a signaling network of myxobacterium Myxococcus xanthus is presented and available at Cytopro
217 Mx8, first isolated from the close relative Myxococcus xanthus, is unable to infect S. aurantiaca ce
218 y use of fluorescent reporters, we show that Myxococcus xanthus isolates produce long narrow filament
219 cially useful in the predatory activities of Myxococcus xanthus; (ix) delta proteobacteria drive many
222 licting models have been proposed to explain Myxococcus xanthus motility on solid surfaces, some favo
231 have demonstrated that fruiting body-derived Myxococcus xanthus myxospores contain two fully replicat
233 The screen was based on the observation that Myxococcus xanthus nonmotile cells, by a Tra-dependent m
237 reviously, it was found that the activity of Myxococcus xanthus PFK increased 2.7-fold upon phosphory
242 e of several sigma(54)-activator proteins in Myxococcus xanthus, produced a mutant defective in fruit
244 irectional motility in the gliding bacterium Myxococcus xanthus requires controlled cell reversals me
246 The multicellular developmental cycle of Myxococcus xanthus requires large-scale changes in gene
248 tion and characterization of a member of the Myxococcus xanthus SdeK signal transduction pathway, Brg
255 rchia coli, can be introduced into wild-type Myxococcus xanthus, strain DK1622, by electroporation.
256 ogy to components of the previously analysed Myxococcus xanthus T4aP machine (T4aPM), we find that th
262 ate that in the social delta-proteobacterium Myxococcus xanthus, the secretion of a novel biosurfacta
265 vation causes cells in a dense population of Myxococcus xanthus to change their gliding movements and
266 ural isolates of the highly social bacterium Myxococcus xanthus to show that colony-merger incompatib
270 Under conditions of nutrient deprivation, Myxococcus xanthus undergoes a developmental process tha
275 ts social developmental cycle, the bacterium Myxococcus xanthus uses coordinated movement to generate
278 eltaproteobacteria, such as the pack hunting Myxococcus xanthus, uses a response regulator protein, R
279 ned a DNA fragment from a genomic library of Myxococcus xanthus using an oligonucleotide probe repres
286 process of the Gram-negative soil bacterium Myxococcus xanthus, vegetatively growing rod cells diffe
287 In contrast, the inhibitor-bound PEP from Myxococcus xanthus was crystallized (1.5-A resolution) i
289 l acetylornithine deacetylase (argE) gene of Myxococcus xanthus was identified via homology to acetyl
292 ranscription of lonD, a heat-shock gene from Myxococcus xanthus, was stimulated in the presence of ex
294 ew steps in the developmental aggregation of Myxococcus xanthus were discovered through a frame-by-fr
296 acterize the encapsulin nanocompartment from Myxococcus xanthus, which consists of a shell protein (E
297 Previously, we identified a gene (aldA) from Myxococcus xanthus, which we suggested encoded the enzym
298 developmental aggregation and sporulation in Myxococcus xanthus while also reducing swarm expansion o