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1 is gene showed 50.6% identity with GltX from Rhizobium meliloti.
2 egulatory role in Caulobacter crescentus and Rhizobium meliloti.
3 56 from Burkholderia cepacia, and ISRm3 from Rhizobium meliloti.
4 ded by flaA and flaB genes, respectively, in Rhizobium meliloti.
5 his operon is conserved in the same order in Rhizobium meliloti.
6  and homology with glucosamine synthase from Rhizobium meliloti.
7 ntrol of a promoter which is constitutive in Rhizobium meliloti.
8 en 18 h and 24 h after spot inoculation with Rhizobium meliloti.
9  both known and novel gene fragments: 5 from Rhizobium meliloti, 13 from Myxococcus xanthus, and 3 fr
10  Brucella abortus, a mammalian pathogen, and Rhizobium meliloti, a phylogenetically related plant sym
11    For Sinorhizobium meliloti (also known as Rhizobium meliloti) AK631 to establish effective symbios
12           As a first step, the ftsA genes of Rhizobium meliloti and Agrobacterium tumefaciens were is
13 ent of the nitrogen-fixing symbiosis between Rhizobium meliloti and its host plant, Medicago sativa (
14   During the symbiosis between the bacterium Rhizobium meliloti and plants such as alfalfa, the bacte
15                                          The Rhizobium meliloti bacA gene encodes a function that is
16                          The function of the Rhizobium meliloti bacA gene, which is a homolog of the
17 ne from several of these bacteria, including Rhizobium meliloti, Brucella abortus, Agrobacterium tume
18 yme is not present in extracts of E. coli or Rhizobium meliloti, but it is readily demonstrable in me
19 t in the genomes of Pseudomonas syringae and Rhizobium meliloti, but not Neisseria meningitidis.
20                                              Rhizobium meliloti can occupy at least two distinct ecol
21        As a first step in characterizing the Rhizobium meliloti cell division machinery, we tested wh
22  membrane potential depolarizing activity in Rhizobium meliloti cell-free filtrates, a plant response
23 tibodies prepared to the complex flagella of Rhizobium meliloti cross-reacted with the striated flage
24                                              Rhizobium meliloti DctD (C4-dicarboxylate transport prot
25 positions 3, 4, 6, 7, and 8 of this motif in Rhizobium meliloti DctD disrupted transcriptional activa
26                                          The Rhizobium meliloti ExoK and ExsH glycanases have been pr
27                                          The Rhizobium meliloti exoS gene is involved in regulating t
28 utoxidation rate on oxygen concentration for Rhizobium meliloti FixL and Aplysia kurodai myoglobin, w
29 e ferric forms of two soluble truncations of Rhizobium meliloti FixL, FixL (heme and kinase domains,
30  ferrous forms of two soluble truncations of Rhizobium meliloti FixL, FixL* and FixLN, are reported.
31 ous complexes of two deletion derivatives of Rhizobium meliloti FixL, FixLN (the heme domain) and a f
32                                              Rhizobium meliloti harboring the binary system also tran
33                    Primary expression of the Rhizobium meliloti-induced peroxidase gene rip1 occurs p
34 symbiotically important exopolysaccharide of Rhizobium meliloti, is composed of polymerized octasacch
35                                          The Rhizobium meliloti lipid A backbone, like that of Escher
36                                              Rhizobium meliloti mutants defective in EPS production f
37 igate interactions between E sigma54 and the Rhizobium meliloti nifH promoter.
38 ccus pyogenes HasA, Xenopus laevis DG42, and Rhizobium meliloti NodC.
39 ene, is expressed following inoculation with Rhizobium meliloti or by adding R. meliloti-produced nod
40 activity is not present in Escherichia coli, Rhizobium meliloti, or the nodulation-defective mutant 2
41 s from Rhizobium leguminosarum bv viciae and Rhizobium meliloti, required for nodulation of pea (Pisu
42 n Rhizobium leguminosarum, Rhizobium fredii, Rhizobium meliloti, Rhizobium etli, and Rhizobium tropic
43                                              Rhizobium meliloti Rm1021 must be able to synthesize suc
44             Effective invasion of alfalfa by Rhizobium meliloti Rm1021 normally requires the presence
45 uction mechanism of the oxygen receptor from Rhizobium meliloti, RmFixL.
46                                           In Rhizobium meliloti (Sinorhizobium meliloti) cultures, th
47 , and visualized under UV light, colonies of Rhizobium meliloti (Sinorhizobium meliloti) exoK mutants
48 e have cloned and sequenced three genes from Rhizobium meliloti (Sinorhizobium meliloti) that are inv
49 er polysaccharide-secreting bacteria such as Rhizobium meliloti (succinoglycan), Xanthomonas campestr
50                                           In Rhizobium meliloti the syrM regulatory gene positively c
51     In Sinorhizobium meliloti (also known as Rhizobium meliloti), these molecules are highly modified

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