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1 act occurs in Asticcacaulis biprosthecum and Agrobacterium tumefaciens.
2 in encoded by the tumour-inducing plasmid of Agrobacterium tumefaciens.
3 stance (SAR) on crown gall disease caused by Agrobacterium tumefaciens.
4 nal structure of AiiB, an AHL lactonase from Agrobacterium tumefaciens.
5 icotiana benthamiana plants using engineered Agrobacterium tumefaciens.
6 cient transformation of Arabidopsis roots by Agrobacterium tumefaciens.
7 ents found in Gram-negative bacteria such as Agrobacterium tumefaciens.
8 conserved in another alpha-proteobacterium, Agrobacterium tumefaciens.
9 rminal domain (residues 425-789) of VirB4 of Agrobacterium tumefaciens.
10 herichia coli, Bordetella bronchiseptica and Agrobacterium tumefaciens.
11 -inducing (Ti) plasmid in the plant pathogen Agrobacterium tumefaciens.
12 ana tabacum) cells from lines transformed by Agrobacterium tumefaciens.
13 B/D4 conjugation system of the phytopathogen Agrobacterium tumefaciens.
14 s, and have also been found in the bacterium Agrobacterium tumefaciens.
15 a is sufficient to suppress tumorigenesis by Agrobacterium tumefaciens.
16 motility, and virulence of the phytopathogen Agrobacterium tumefaciens.
17 Escherichia coli, Salmonella typhimurium and Agrobacterium tumefaciens.
18 plexes to cell division sites of E. coli and Agrobacterium tumefaciens.
19 ) plasmid have been previously identified in Agrobacterium tumefaciens.
20 ducing (Ti)-plasmid virulence (vir) genes of Agrobacterium tumefaciens.
21 of the bioBFDAZ operon in the plant pathogen Agrobacterium tumefaciens.
22 tested this prediction in the plant pathogen Agrobacterium tumefaciens.
23 tricately co-regulated in the soil bacterium Agrobacterium tumefaciens.
26 d microbes Pseudomonas aeruginosa (P.a.) and Agrobacterium tumefaciens (A.t.) as a tractable system t
30 -type quorum-sensing transcription factor in Agrobacterium tumefaciens, activates genes required for
33 growth of several phytopathogenic bacteria (Agrobacterium tumefaciens, Agrobacterium radiobacter, Se
34 acter crescentus (CAUCR), the plant pathogen Agrobacterium tumefaciens (AGRTU), and the mammalian pat
38 ted point mutations into the genomes of both Agrobacterium tumefaciens and Agrobacterium rhizogenes A
41 fold similar to the T4SS VirB8 proteins from Agrobacterium tumefaciens and Brucella suis (G-) and to
42 milar to the well-studied model systems from Agrobacterium tumefaciens and Brucella suis Here, we stu
43 tes of corn seedlings inhibit both growth of Agrobacterium tumefaciens and induction of its Ti plasmi
44 gative species, including Coxiella burnetii, Agrobacterium tumefaciens and Legionella pneumophila.
45 we characterized TssM in the plant pathogen Agrobacterium tumefaciens and provided the first biochem
46 am-negative bacterial species: the pathogens Agrobacterium tumefaciens and Pseudomonas aeruginosa; th
47 xidation by two heterotrophic soil bacteria (Agrobacterium tumefaciens and Pseudomonas fluorescens) a
48 Genetic transformation of host plants by Agrobacterium tumefaciens and related species represents
50 nely performed with the pathogenic bacterium Agrobacterium tumefaciens and similar pathogens (e.g. Ba
51 of the replicons in the alpha proteobacteria Agrobacterium tumefaciens and Sinorhizobium meliloti and
52 to transform in vitro-grown endosperms using Agrobacterium tumefaciens and standard binary vectors.
53 ns, the causative agent of crown gall tumors Agrobacterium tumefaciens and the parasitic plant Striga
54 Pseudomonas aeruginosa, Pseudomonas putida, Agrobacterium tumefaciens, and Acinetobacter calcoacetic
55 mbinant tadA proteins from Escherichia coli, Agrobacterium tumefaciens, and Aquifex aeolicus, as well
56 oach to Escherichia coli, Bacillus subtilis, Agrobacterium tumefaciens, and Mesoplasma florum, reveal
57 rt a prokaryotic (6-4) photolyase, PhrB from Agrobacterium tumefaciens, and propose that (6-4) photol
58 t Sinorhizobium meliloti, the plant pathogen Agrobacterium tumefaciens, and the animal pathogen Bruce
59 en Rickettsia prowazekii, the plant pathogen Agrobacterium tumefaciens, and the bovine and human path
60 used on two organisms, Bacillus subtilis and Agrobacterium tumefaciens, and two experimental systems,
61 omologous to several virB genes and virD4 of Agrobacterium tumefaciens are found in an intravacuolar
62 ding the enzyme isopentenyl transferase from Agrobacterium tumefaciens, as a positive selectable mark
63 how enhanced susceptibility to the bacterium Agrobacterium tumefaciens, as revealed by a higher effic
64 ortholog of LpxQ is present in the genome of Agrobacterium tumefaciens, as shown by heterologous expr
66 -dimensional crystal structures of HutI from Agrobacterium tumefaciens (At-HutI) and an environmental
67 The replicator regions of the Ti plasmids of Agrobacterium tumefaciens belong to the repABC family of
69 Ns and their corresponding target sites into Agrobacterium tumefaciens binary plasmids, allowing effi
70 ormed on 63 of the identified cDNAs using an Agrobacterium tumefaciens binary vector carrying the pot
72 duced by several bacterial pathogens such as Agrobacterium tumefaciens, Bordetella pertussis, Brucell
73 at several pathogens of plants and mammals - Agrobacterium tumefaciens, Bordetella pertussis, Helicob
74 re we describe a new family with homology to Agrobacterium tumefaciens BphP2, an HK first discovered
75 significant LpxXL orthologues are present in Agrobacterium tumefaciens, Brucella melitensis, and all
77 e 5.67-megabase genome of the plant pathogen Agrobacterium tumefaciens C58 consists of a circular chr
79 A citrate synthase (CS) deletion mutant of Agrobacterium tumefaciens C58 is highly attenuated in vi
80 -glycine repeat protein G (VgrG) paralogs in Agrobacterium tumefaciens C58 specifically control the s
84 des available in the extracellular milieu of Agrobacterium tumefaciens can be transported into the cy
92 ere generated by co-infiltrating plants with Agrobacterium tumefaciens cells harboring engineered RNA
93 acterize the dynamic localization of several Agrobacterium tumefaciens components during the cell cyc
96 biotic alpha-rhizobia and the plant pathogen Agrobacterium tumefaciens differed in their ability to f
99 Here, we demonstrate that two Ti plasmids of Agrobacterium tumefaciens encode robust entry exclusion
102 fructose 1,6-bisphosphate (FBP), whereas the Agrobacterium tumefaciens enzyme is activated by fructos
104 on inoculation of N. benthamiana leaves with Agrobacterium tumefaciens expressing RPS2, a rapid hyper
105 NV) minireplicon (MR) reporter cassettes for Agrobacterium tumefaciens expression in Nicotiana bentha
107 s FtsZ linker with a 249-residue linker from Agrobacterium tumefaciens FtsZ interfered with cell divi
108 We demonstrate that the rod-shaped bacterium Agrobacterium tumefaciens grows unidirectionally from th
112 f pyrrhocoricin against Escherichia coli and Agrobacterium tumefaciens identified the N-terminal half
113 glucose pyrophosphorylase from the bacterium Agrobacterium tumefaciens, identifying a previously elus
115 plore the role of early division proteins of Agrobacterium tumefaciens including three FtsZ homologs,
116 nes from the tumor-inducing (Ti) plasmids of Agrobacterium tumefaciens, including homologues of the T
118 es also drive reporter gene expression in an Agrobacterium tumefaciens infection assay in Nicotiana b
120 aryotic fruiting and combined the assay with Agrobacterium tumefaciens insertional mutagenesis to scr
138 Conjugative transfer of the Ti plasmids of Agrobacterium tumefaciens is controlled by a quorum-sens
143 typical of transgenic plants expressing the Agrobacterium tumefaciens isopentenyltransferase (ipt) g
145 co (Nicotiana tabacum) NT1 cell lines, using Agrobacterium tumefaciens-mediated DNA delivery of a bin
146 research has taken me from bacteriophage to Agrobacterium tumefaciens-mediated DNA transfer to plant
149 ogy, that three independent groups described Agrobacterium tumefaciens-mediated genetic transformatio
151 ired for intracellular survival, we utilized Agrobacterium tumefaciens-mediated mutagenesis, and scre
152 ors are an indispensable component of modern Agrobacterium tumefaciens-mediated plant genetic transfo
153 psis thaliana histone H2A-1 is important for Agrobacterium tumefaciens-mediated plant transformation.
156 ed in the development of various methods for Agrobacterium tumefaciens-mediated transformation of Ara
157 ed to develop a selectable marker system for Agrobacterium tumefaciens-mediated transformation of mai
158 We present a protocol for high-throughput Agrobacterium tumefaciens-mediated transformation of Pen
159 the roles of plant genes and proteins in the Agrobacterium tumefaciens-mediated transformation proces
169 e of vesicle fusion in this process, we used Agrobacterium tumefaciens-mediated transient coexpressio
171 d genes from diverse organisms, we performed Agrobacterium tumefaciens-mediated transient expression
172 CA1 (RPP1) resistance protein, we adopted an Agrobacterium tumefaciens-mediated transient protein exp
173 N. benthamiana as a model host plant to use Agrobacterium tumefaciens-mediated transient protein exp
175 he virB-encoded type IV transport complex of Agrobacterium tumefaciens mediates the transfer of DNA a
176 tor of the VirA/VirG two-component system in Agrobacterium tumefaciens, mediates the expression of vi
177 g Bartonella henselae Pap31, Brucella Omp31, Agrobacterium tumefaciens Omp25, and neisserial opacity
179 pact on the attraction of the plant pathogen Agrobacterium tumefaciens, or the plant growth promoting
180 and practical importance are reviewed here: Agrobacterium tumefaciens, Pantoea stewartii, Erwinia ca
183 work, we report that the volutin granules of Agrobacterium tumefaciens possess properties similar to
187 have also been reported for homologues from Agrobacterium tumefaciens (Rajashankar et al., unpublish
188 VirA/VirG two-component regulatory system of Agrobacterium tumefaciens regulates expression of the vi
189 ple, VirA, a large integral membrane HK from Agrobacterium tumefaciens, regulates the expression of v
195 ccessful genetic transformation of plants by Agrobacterium tumefaciens requires the import of bacteri
197 The genetic transformation of plant cells by Agrobacterium tumefaciens results from the transfer of D
198 n gall disease, caused by the soil bacterium Agrobacterium tumefaciens, results in significant econom
199 essential genes of two Alphaproteobacteria, Agrobacterium tumefaciens (Rhizobiales) and Brevundimona
200 hich are deeply studied pathogens and pests: Agrobacterium tumefaciens, Rhodococcus fascians, Xanthom
201 a cellulose synthase (CelA) minus mutant of Agrobacterium tumefaciens, showing that the predicted pr
203 transformation of maize (Zea mays) using an Agrobacterium tumefaciens standard binary (non-super bin
206 loping spikes were dipped into a solution of Agrobacterium tumefaciens strain AGL1 harboring the beta
208 ich develop upon infection with the virulent Agrobacterium tumefaciens strain C58, highly expressed A
211 d (1) H NMR to quantify metabolic changes in Agrobacterium tumefaciens (strain 5A) upon exposure to s
216 rating Nicotiana benthamiana leaves with two Agrobacterium tumefaciens strains: one contains the targ
217 ion was expressed in the related denitrifier Agrobacterium tumefaciens, suggesting that the lack of e
219 boratories has suggested that integration of Agrobacterium tumefaciens T-DNA into the plant genome oc
224 s can be devastated by pathogenic strains of Agrobacterium tumefaciens that cause crown gall tumors.
225 ChvE is a chromosomally encoded protein in Agrobacterium tumefaciens that mediates a sugar-induced
226 is a LysR-type transcriptional regulator of Agrobacterium tumefaciens that positively regulates the
227 is a LysR-type transcriptional regulator of Agrobacterium tumefaciens that positively regulates the
228 s a quorum-sensing transcription factor from Agrobacterium tumefaciens that regulates replication and
231 t of which are homologues of T4SS genes from Agrobacterium tumefaciens, the majority have no known fu
232 s to the well-studied archetypal vir T4SS of Agrobacterium tumefaciens, the Rickettsiales vir homolog
234 such as LuxR of Vibrio fischeri and TraR of Agrobacterium tumefaciens, there is no endogenous autoin
235 replication and for conjugal transfer of the Agrobacterium tumefaciens Ti plasmid are regulated by th
236 TraR, the quorum-sensing activator of the Agrobacterium tumefaciens Ti plasmid conjugation system,
237 re we show that the replication origin of an Agrobacterium tumefaciens Ti plasmid resides fully withi
243 cient T-DNA-based gene delivery system using Agrobacterium tumefaciens to transiently express BMV RNA
255 ene were inserted into the poplar genome via Agrobacterium tumefaciens transformation, where they rev
261 n of ipt, a cytokinin biosynthetic gene from Agrobacterium tumefaciens, under the control of the prom
262 tics and experimental analyses indicate that Agrobacterium tumefaciens uses a pathway involving nonph
266 a subset of alpha-proteobacteria, including Agrobacterium tumefaciens Using an activity-based approa
267 nce for interactions among components of the Agrobacterium tumefaciens vir-encoded T4SS is presented.
271 y showed that T-DNA translocates through the Agrobacterium tumefaciens VirB/D4 T4SS by forming close
272 d that is transferred to plant cells] of the Agrobacterium tumefaciens VirB/D4 T4SS in terms of a ser
275 caps of the Escherichia coli pKM101 Tra and Agrobacterium tumefaciens VirB/VirD4 systems are complet
278 This study characterized the contribution of Agrobacterium tumefaciens VirB6, a polytopic inner membr
280 yellow fluorescent protein- or nVenus-tagged Agrobacterium tumefaciens VirE2 and VirD2 proteins and t
282 s system in which to study the regulation of Agrobacterium tumefaciens virulence genes and the mechan
284 pression of orthologues of these proteins in Agrobacterium tumefaciens was shown to be regulated by t
289 e IVA secretion system homologous to that in Agrobacterium tumefaciens, was required for restoration
290 response to infection and transformation by Agrobacterium tumefaciens, we compared the cDNA-amplifie
291 Using uronate dehydrogenase cloned from Agrobacterium tumefaciens, we developed an assay for D-g
292 rum anthropi, Rhodopseudomonas palustris and Agrobacterium tumefaciens were expressed in Escherichia
293 use monocots are difficult to transform with Agrobacterium tumefaciens, whereas other transgenesis me
294 domonas aeruginosa, Campylobacter jejuni and Agrobacterium tumefaciens, which absolutely require poly
295 um-sensing transcriptional activator TraR of Agrobacterium tumefaciens, which controls the replicatio
296 d by the IspDF fusion and IspE proteins from Agrobacterium tumefaciens, which covert MEP to the corre
297 ion of the nopaline synthase (nos) gene from Agrobacterium tumefaciens, which is often used as the 3'
298 y a mutation in a gene homologous to traM of Agrobacterium tumefaciens, which was able to suppress th
300 is thalictroides) were stably transformed by Agrobacterium tumefaciens with constructs containing the