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1 s to the transcriptional regulator CarD from Myxococcus xanthus.
2 al movements for the two motility systems in Myxococcus xanthus.
3 used to examine fruiting body development of Myxococcus xanthus.
4 s to understand the developmental biology of Myxococcus xanthus.
5 showing that cAG is present in surface-grown Myxococcus xanthus.
6 uses defects in fruiting body development in Myxococcus xanthus.
7 g the multicellular developmental process of Myxococcus xanthus.
8 d gene function in the delta proteobacterium Myxococcus xanthus.
9 from the social and developmental bacterium Myxococcus xanthus.
10 (IPTG)-inducible promoter was constructed in Myxococcus xanthus.
11 is and gene expression during development of Myxococcus xanthus.
12 ophage Mx9 is a temperate phage that infects Myxococcus xanthus.
13 pili-mediated (S) gliding and development of Myxococcus xanthus.
14 aces is found in the nonpathogenic bacterium Myxococcus xanthus.
15 quired for starvation-induced development in Myxococcus xanthus.
16 ein required for motility and development in Myxococcus xanthus.
17 orrhoeae, and for social gliding motility in Myxococcus xanthus.
18 S) production in the Gram-negative bacterium Myxococcus xanthus.
19 k shows significant identity with the Ndk of Myxococcus xanthus.
20 the growth and multicellular development of Myxococcus xanthus.
21 cillus subtilis, Caulobacter crescentus, and Myxococcus xanthus.
22 ion, motility, and polarity in the bacterium Myxococcus xanthus.
23 o be required for social gliding motility in Myxococcus xanthus.
24 to multicellular fruiting body formation in Myxococcus xanthus.
25 are required for social gliding motility in Myxococcus xanthus.
26 peron is important for normal development of Myxococcus xanthus.
27 c called TA (myxovirescin), which is made by Myxococcus xanthus.
28 secretion system in the crowded interior of Myxococcus xanthus.
29 ding the social Gram-negative soil bacterium Myxococcus xanthus.
30 ion of many important developmental genes in Myxococcus xanthus.
31 he behavior of the biofilm-forming bacterium Myxococcus xanthus.
32 r bacteria with complex life-styles, such as Myxococcus xanthus.
33 bly absent from spore-forming, Gram-negative Myxococcus xanthus.
34 _7475 (BacM), one of the four bactofilins of Myxococcus xanthus.
35 ulates exopolysaccharide (EPS) production in Myxococcus xanthus.
36 ental programme in the social soil bacterium Myxococcus xanthus.
37 ively regulates fruiting body development in Myxococcus xanthus.
38 we investigate swarms of the myxobacterium, Myxococcus xanthus.
39 ruiting body development-associated genes in Myxococcus xanthus.
40 fferentiation is the gram-negative bacterium 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
45 ellular filamentation on gliding motility of Myxococcus xanthus, a Gram-negative social bacterium, wa
50 eonine kinases (PSTKs) has been performed in Myxococcus xanthus, a soil bacterium with a complex life
53 biological evidence, however, suggests that Myxococcus xanthus aggregation is the consequence of dir
54 developmental requirement for B-signaling in Myxococcus xanthus, also bypass the requirement for A-si
55 oteins of enterics and the gliding bacterium Myxococcus xanthus and are thought to be part of a signa
57 n and purification of PHD from the bacterium Myxococcus xanthus and demonstrate the presence of nonco
60 iments between kin discriminating strains of Myxococcus xanthus and Proteus mirabilis, we found the r
61 smaller nozzle-like structures are found in Myxococcus xanthus and that they are clustered at both c
62 ese movements are known as social gliding in Myxococcus xanthus and twitching in organisms such as Ps
63 1.0+/-0.1 microM for the enzymes from human, Myxococcus xanthus, and Aquifex aeolicus, respectively.
67 extracellular fibrils of the myxobacterium, Myxococcus xanthus, are capable of carrying out ADP-ribo
69 starvation, a dense population of rod-shaped Myxococcus xanthus bacteria coordinate their movements t
73 unrelated proteins (spore coat protein from Myxococcus xanthus, beta-B2 and gamma-B crystallins from
75 sensory system controls directed motility in Myxococcus xanthus by regulating cellular reversal frequ
76 a preferred locus on the genome of its host, Myxococcus xanthus, by a mechanism of site-specific reco
80 and a mammalian pathogen -Escherichia coli, Myxococcus xanthus, Caulobacter crescentus, and Mycobact
81 the z axis has opened a window in studies of Myxococcus xanthus cell ultrastructure and biofilm commu
86 nts, we observed slime deposition by gliding Myxococcus xanthus cells at unprecedented resolution.
90 Gliding movements of individual isolated Myxococcus xanthus cells depend on the genes of the A-mo
95 compared the cellular fatty acid profiles of Myxococcus xanthus cells grown in either a Casitone-base
98 ously reported Tn5lac Omega4469 insertion in Myxococcus xanthus cells is regulated by the starvation
100 Coordinated movement of packs of S-motile Myxococcus xanthus cells relies on extrusion and retract
105 We used cryo-electron tomography of intact Myxococcus xanthus cells to visualize type IVa pili and
107 Under starvation conditions, a swarm of Myxococcus xanthus cells will undergo development, a mul
110 99 is the site of a Tn5 lac insertion in the Myxococcus xanthus chromosome that fuses lacZ expression
118 d homologous to the Streptomyces griseus and Myxococcus xanthus crtB genes encoding phytoene synthase
120 ecific incompatibility in the soil bacterium Myxococcus xanthus demonstrates that the social life of
128 ained nine different laboratories' wild type Myxococcus xanthus DK1622 "sublines" and sequenced each
137 by measuring symmetry breaking in a swarm of Myxococcus xanthus exposed to a two-dimensional nutrient
145 obtained evidence that the type IV pilus of Myxococcus xanthus functions as a motility apparatus.
146 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 encoding the transcription factor sigma54 in Myxococcus xanthus has been cloned using a heterologous
162 se variation between yellow and tan forms of Myxococcus xanthus has been recognized for several decad
165 red natural populations of the model species Myxococcus xanthus have fragmented into a large number o
166 us subtilis and fruiting body development of Myxococcus xanthus have revealed key features of regulat
167 development, the quorum-sensing A-signal in Myxococcus xanthus helps to assess starvation and induce
168 explain the adventurous gliding motility of Myxococcus xanthus: (i) polar secretion of slime and (ii
169 endent Tn5-lac insertions in the S1 locus of Myxococcus xanthus inactivate the sglK gene, which is no
171 lar fruiting body formation in the bacterium Myxococcus xanthus, inhibiting the transition from growt
174 ding motility in the developmental bacterium Myxococcus xanthus involves two genetically distinct mot
214 e extracellular matrix of the soil bacterium Myxococcus xanthus is essential for biofilm formation an
217 ence in a signaling network of myxobacterium Myxococcus xanthus is presented and available at Cytopro
220 Mx8, first isolated from the close relative Myxococcus xanthus, is unable to infect S. aurantiaca ce
221 y use of fluorescent reporters, we show that Myxococcus xanthus isolates produce long narrow filament
222 cially useful in the predatory activities of Myxococcus xanthus; (ix) delta proteobacteria drive many
225 licting models have been proposed to explain Myxococcus xanthus motility on solid surfaces, some favo
235 have demonstrated that fruiting body-derived Myxococcus xanthus myxospores contain two fully replicat
237 The screen was based on the observation that Myxococcus xanthus nonmotile cells, by a Tra-dependent m
241 reviously, it was found that the activity of Myxococcus xanthus PFK increased 2.7-fold upon phosphory
246 e of several sigma(54)-activator proteins in Myxococcus xanthus, produced a mutant defective in fruit
248 irectional motility in the gliding bacterium Myxococcus xanthus requires controlled cell reversals me
250 The multicellular developmental cycle of Myxococcus xanthus requires large-scale changes in gene
253 tion and characterization of a member of the Myxococcus xanthus SdeK signal transduction pathway, Brg
260 rchia coli, can be introduced into wild-type Myxococcus xanthus, strain DK1622, by electroporation.
261 ogy to components of the previously analysed Myxococcus xanthus T4aP machine (T4aPM), we find that th
268 vation causes cells in a dense population of Myxococcus xanthus to change their gliding movements and
269 ural isolates of the highly social bacterium Myxococcus xanthus to show that colony-merger incompatib
272 Under conditions of nutrient deprivation, Myxococcus xanthus undergoes a developmental process tha
277 ts social developmental cycle, the bacterium Myxococcus xanthus uses coordinated movement to generate
280 ned a DNA fragment from a genomic library of Myxococcus xanthus using an oligonucleotide probe repres
287 process of the Gram-negative soil bacterium Myxococcus xanthus, vegetatively growing rod cells diffe
288 In contrast, the inhibitor-bound PEP from Myxococcus xanthus was crystallized (1.5-A resolution) i
290 l acetylornithine deacetylase (argE) gene of Myxococcus xanthus was identified via homology to acetyl
293 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
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