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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
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
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
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
25 positions 3, 4, 6, 7, and 8 of this motif in Rhizobium meliloti DctD disrupted transcriptional activa
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
34 symbiotically important exopolysaccharide of Rhizobium meliloti, is composed of polymerized octasacch
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
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
51 In Sinorhizobium meliloti (also known as Rhizobium meliloti), these molecules are highly modified
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