コーパス検索結果 (１語後でソート)
通し番号をクリックするとPubMedの該当ページを表示します
1 as largely driven by changes in diversity of rhizobia.
2 elop from the pocket and become colonized by rhizobia.
3 fense and enable symbiotic associations with rhizobia.
4 ndent on Nod factor production by compatible rhizobia.
5 with nitrogen-fixing soil bacteria known as rhizobia.
6 les in association with nitrogen-fixing soil rhizobia.
7 their cognate avirulence genes derived from rhizobia.
8 oordinated, program that allows infection by rhizobia.
9 led nodules and their infection by symbiotic rhizobia.
10 nts form symbioses with soil bacteria called rhizobia.
11 uptake from AM fungi and fixed nitrogen from rhizobia.
12 nduce nodule organogenesis in the absence of rhizobia.
13 production and carbon regulatory network of rhizobia.
14 ies of C. crescentus and the nitrogen-fixing rhizobia.
15 ngi and nitrogen-fixing soil bacteria called rhizobia.
16 ble mechanism for sanctions against cheating rhizobia.
17 is with bacteria collectively referred to as rhizobia.
18 reversible binding were the FixL proteins of Rhizobia.
19 tch in the FixL/FixJ two-component system of Rhizobia.
20 formation and to form nodules on exposure to rhizobia.
21 dopseudomonas palustris and FixK proteins of rhizobia.
22 I)-siderophore receptor from nitrogen-fixing rhizobia.
23 with nitrogen-fixing soil bacteria known as rhizobia.
24 nitrogen-fixing bacteria collectively called rhizobia.
25 mologous operons recently characterized from rhizobia.
26 s, uninfected root segments, and free-living rhizobia.
27 riation in the symbiosis between legumes and rhizobia.
28 s formed by the legume in its symbiosis with rhizobia.
29 development and infection by nitrogen-fixing rhizobia.
30 host and harbor thousands of nitrogen-fixing rhizobia.
31 rogen-fixing root nodule symbioses with soil rhizobia.
32 on these legumes perform in association with rhizobia.
33 e beneficial interaction with soil bacteria, rhizobia.
34 on of these free fatty acids were unknown in rhizobia.
35 ctions between the plant and nitrogen-fixing rhizobia.
36 wild-type roots 24 h after inoculation with rhizobia.
37 lowed auxin transport control in response to rhizobia.
38 nly when coinoculated with the corresponding rhizobia.
39 ignals present in the surface or secreted by rhizobia.
40 on-related gene expression in the absence of rhizobia.
41 25 (symrk knockout mutant) in the absence of rhizobia.
42 of association with polysomes in response to rhizobia.
43 effect on the binding of purified lectin to rhizobia, a result that will facilitate forthcoming expe
44 whereas, across 14 experiments that compete rhizobia against soil populations or each other, the poo
45 and the root symbioses with nitrogen-fixing rhizobia and arbuscular mycorrhiza were similar to the w
47 thogens, while infection and colonization by rhizobia and arbuscular mycorrhizal fungi was maintained
50 of the Fix network is conserved between the rhizobia and C. crescentus, a free-living aerobe that ca
51 ection threads that were sometimes devoid of rhizobia and formed small nodules with greatly reduced n
53 impact and the selective interaction between rhizobia and legumes culminating in development of funct
59 rol of iron-dependent gene expression in the rhizobia and other taxa of the Alphaproteobacteria is fu
60 he result of the interaction of legumes with rhizobia and requires the mitotic activation and differe
61 strategies, such as persister formation for rhizobia and reversal of spore germination by mycorrhiza
62 P-binding cassette transporters from several rhizobia and Salmonella enterica serovar Typhimurium, bu
63 ed N tissue concentrations in the absence of rhizobia and that this controls lateral root density in
66 FadLSm homologs from related symbiotic alpha-rhizobia and the plant pathogen Agrobacterium tumefacien
67 in the first 72 h of the interaction between rhizobia and their host plants, nodule primordium induct
69 ion in infection threads are normal, whereas rhizobia and their symbiotic plant cells become necrotic
70 evolve de novo, and published data on legume-rhizobia and yucca-moth mutualisms are consistent with P
72 hat mediates O2-dependent differentiation in rhizobia, and therefore hemB expression is under develop
74 hizobium fitness imply that most ineffective rhizobia are 'defective' rather than 'defectors'; this e
77 lant cells become necrotic immediately after rhizobia are released from infection threads into symbio
79 ides further evidence that the K antigens of rhizobia are strain-specific antigens which are produced
80 s toward the developing nodule primordia and rhizobia are taken up into the nodule cells, where they
82 Symbiosis between legumes (e.g. soybean) and rhizobia bacteria (e.g. Bradyrhizobium japonicum) result
84 otype of inhibited or delayed recruitment of rhizobia bacteria to host plant roots, fewer root nodule
85 nitrogen via symbiosis with nitrogen-fixing rhizobia bacteria, in rotation with nonleguminous crops.
89 ducer-independent and because all nodulating rhizobia, both alpha- and beta-proteobacteria have commo
90 were not impaired in epidermal responses to rhizobia but had significantly reduced nodule primordium
91 selection consistently favoured cheating by rhizobia, but did not favour legumes that provided less
92 vates nodule organogenesis in the absence of rhizobia, but its ectodomain is required for proper symb
93 ormation in legumes in response to symbiotic rhizobia, but the molecular mechanism(s) of ethylene act
96 We found that in the cre1 mutant, symbiotic rhizobia cannot locally alter acro- and basipetal auxin
100 asma membrane iron transporters move it into rhizobia-containing cells, where iron is used as the cof
101 nsing FixLJ-K system, initially described in rhizobia, controls microaerobic respiration, photophosph
102 etween leguminous plants and nitrogen-fixing rhizobia culminate in the formation of specialized organ
103 mes and nitrogen-fixing soil bacteria called rhizobia culminates in the development of root nodules,
104 symbiosis between leguminous plants and soil rhizobia culminates in the formation of nitrogen-fixing
105 almost all with PPK1 as well); these include rhizobia, cyanobacteria, Streptomyces, and several patho
106 nverted repeat-lacking clade (IRLC) legumes, rhizobia differentiate into nitrogen-fixing bacteroids.
108 of rhizobia in two different hosts where the rhizobia differentiate into swollen nonreproductive bact
118 ly deposited rhizobia into plant host cells; rhizobia failed to differentiate further in these cases.
119 esponse to symbiotic signals produced by the rhizobia, few sites of in vivo phosphorylation have prev
120 zed organs called root nodules, in which the rhizobia fix atmospheric nitrogen and transfer it to the
121 es in the development of root nodules, where rhizobia fix atmospheric nitrogen and transfer it to the
122 ling pathway that is used by AM fungi and by rhizobia for their symbiotic associations with legumes.
123 surface and extracellular polysaccharides of rhizobia function in the infection process that leads to
125 that symbiotic bacteria, collectively called rhizobia, gain access to the interior of roots and root
126 erial nitrogen stress metabolism so that the rhizobia generate "excess" ammonia and release this ammo
129 pressed nodD genes from different species of rhizobia in a strain of S. meliloti lacking endogenous N
134 Here, we compare symbiotic efficiency of rhizobia in two different hosts where the rhizobia diffe
137 sons with primitive actinorhizal nodules and rhizobia-induced nodules on the nonlegume Parasponia and
141 nally upregulated during root symbiosis, and rhizobia inoculated roots ectopically expressing SINA4 s
142 tions between plants and nitrogen (N)-fixing rhizobia intensify with decreasing N supply and come at
143 e genetic elements that convert nonsymbiotic rhizobia into nitrogen-fixing symbionts of leguminous pl
144 ferated abnormally and very rarely deposited rhizobia into plant host cells; rhizobia failed to diffe
145 itrogen-fixing symbiosis between legumes and rhizobia is highly relevant to human society and global
150 ion between legumes and soil bacteria called rhizobia leads to the formation of a new root-derived or
151 During their symbiotic interaction with rhizobia, legume plants develop symbiosis-specific organ
156 oot-associated bacteria that, in addition to rhizobia, likely contribute to plant growth and ecologic
157 he novel iron sensing mechanism found in the rhizobia may be an evolutionary adaptation to the cellul
161 nthesis genes can be elevated in response to rhizobia/Nod LCOs, suggests that Nod LCOs may induce SL
162 ent during invasion of the nascent nodule by rhizobia, normal lateral root elongation, and normal reg
163 mes, root entry of symbiotic nitrogen-fixing rhizobia occurs via host-constructed tubular tip-growing
164 ction, and demonstrates that the dynamics of rhizobia on host species can feed back on plant populati
165 urther facet of the effect of symbiosis with rhizobia on the ecologically important trait of the plan
166 y to induce root hair curling in response to rhizobia or Nod lipochitooligosaccharides (LCOs) and SL-
167 ch are also impaired in the accommodation of rhizobia, our data indicate that ARPC1 and, by inference
169 gs show that, in response to a plant signal, rhizobia play an active role in the control of infection
170 and nodule organogenesis was unaffected but rhizobia remain restricted to the epidermis in infection
174 trogen-fixing bacteria collectively known as rhizobia results in the formation of a unique plant root
175 biotic interaction between legume plants and rhizobia results in the formation of root nodules, in wh
176 ersonii, a nonlegume that can associate with rhizobia, showed Nod factor-induced calcium oscillations
178 nt the infection site on leguminous roots by rhizobia, soil bacteria that establish a nitrogen-fixing
180 st of this ammonium is contributed by legume-rhizobia symbioses, which are initiated by the infection
189 n-fixing Gram-negative proteobacteria called rhizobia that are able to interact with most leguminous
190 nodules, host plant cells are infected with rhizobia that are encapsulated by a plant-derived membra
195 symbiotic relationships with nitrogen-fixing rhizobia that trigger root nodule organogenesis for bact
196 lishing an intimate relationship with either rhizobia, the symbionts of legumes or Frankia in the cas
201 nstrating that this activity is required for rhizobia to penetrate the cell wall and initiate formati
202 nitiated by the binding and stabilization of rhizobia to plant root hairs, mediated in part by a rece
203 ression of the infection canal that conducts rhizobia to the nodule primordium requires a functional
204 ds to symbiotically associated bacteria; the rhizobia use these compounds to reduce (fix) atmospheric
205 Species from the three other major genera of rhizobia were found to have homologous terpene synthase
207 s receive their nitrogen via nitrogen-fixing rhizobia, which exist in a symbiotic relationship with t
208 ampened in plants nodulated by Fix(-) mutant rhizobia, which in most respects metabolically resemble
209 ligosaccharidic signal molecules produced by rhizobia, which play a key role in the rhizobium-legume
210 feature of legumes in their association with rhizobia, while Cercis, a non-nodulating legume, does no
211 s the coordination of epidermal infection by rhizobia with cell divisions in the underlying cortex.
212 icago is nodulated by at least two groups of rhizobia with divergent chromosomes that have been class
WebLSDに未収録の専門用語（用法）は "新規対訳" から投稿できます。