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1 hydrolases from Burkholderia caryophylli and Rhizobium leguminosarum.
2  siderophore made by the symbiotic bacterium Rhizobium leguminosarum.
3 tein, (13)C, (15)N-labeled NodF protein from Rhizobium leguminosarum.
4 orum-sensing signalling molecule produced by Rhizobium leguminosarum.
5 t region from the homologous cpn60-1 gene of Rhizobium leguminosarum.
6  M, P), has been cloned and characterized in Rhizobium leguminosarum.
7 ation of nitrogen-fixing pea root nodules by Rhizobium leguminosarum.
8  Pseudomonas brassicacearum and rhizospheric Rhizobium leguminosarum.
9                                            A Rhizobium leguminosarum 3841 acpXL mutant (named here Rl
10 lysaccharide (OPS) isolated from free living Rhizobium leguminosarum 3841, a symbiont of Pisum sativu
11 nd core regions of the lipopolysaccharide in Rhizobium leguminosarum, a nitrogen-fixing plant endosym
12                                   Lipid A of Rhizobium leguminosarum, a nitrogen-fixing plant endosym
13      Two such dual-host strains were tested: Rhizobium leguminosarum A34 in peas and beans and Bradyr
14                                              Rhizobium leguminosarum and Rhizobium etli contain funct
15                            The structures of Rhizobium leguminosarum and Rhizobium etli lipid A are d
16  LpxE, a membrane-bound phosphatase found in Rhizobium leguminosarum and some other Gram-negative bac
17  branched-chain amino acid permease (Bra) of Rhizobium leguminosarum and the histidine permease (His)
18                             The lpcC gene of Rhizobium leguminosarum and the lpsB gene of Sinorhizobi
19                             The pyrE gene of Rhizobium leguminosarum biovar trifolii (Rl) was subclon
20                                              Rhizobium leguminosarum biovar viciae strain 3841 is a m
21   The topology NodC in the inner membrane of Rhizobium leguminosarum biovar viciae was analysed using
22 iens pathogenesis, and common nod genes from Rhizobium leguminosarum bv viciae and Rhizobium meliloti
23  suite of bioreporters has been developed in Rhizobium leguminosarum bv viciae strain 3841, and these
24  inoculated with Bradyrhizobium japonicum or Rhizobium leguminosarum bv viciae, respectively, and the
25 ated phosphotransferase system (PTS(Ntr)) of Rhizobium leguminosarum bv.
26 ese/iron-type superoxide dismutase (SodA) of Rhizobium leguminosarum bv.
27 e-cell Raman spectra (SCRS) to differentiate Rhizobium leguminosarum bv.
28                                              Rhizobium leguminosarum bv. trifolii 4S has a lipopolysa
29 olipooligosaccharides (CLOSs) from wild-type Rhizobium leguminosarum bv. trifolii on development of w
30 eviously, we have shown that tfxABCDEFG from Rhizobium leguminosarum bv. trifolii T24 is sufficient t
31 g this 3.1-kb fragment was used to transform Rhizobium leguminosarum bv. trifolii TA-1JH, a strain wh
32  protein product is highly homologous to the Rhizobium leguminosarum bv. viciae RhiR protein and a nu
33              NodO is a secreted protein from Rhizobium leguminosarum bv. viciae with a role in signal
34                                           In Rhizobium leguminosarum bv. viciae, quorum-sensing is re
35 show that a Cpn60 protein from the bacterium Rhizobium leguminosarum can function to allow E. coli gr
36                                 Membranes of Rhizobium leguminosarum contain a 3-deoxy-D-manno-octulo
37                  The endosymbiotic bacterium Rhizobium leguminosarum contains a single hydrogenase sy
38  potential IHF binding sites adjacent to the Rhizobium leguminosarum dctA promoter.
39 e structure of the nitrogen-fixing bacterium Rhizobium leguminosarum differs from that of Escherichia
40                    The lipopolysaccharide of Rhizobium leguminosarum differs from that of other Gram-
41   Lipid A from the nitrogen-fixing bacterium Rhizobium leguminosarum displays many structural differe
42  Plasmid-ID technology, recently deployed in Rhizobium leguminosarum, facilitates the concurrent asse
43                                              Rhizobium leguminosarum has two high-affinity Mn(2+) tra
44 lorimetry, and other methods that RapA2 from Rhizobium leguminosarum indeed exhibits a cadherin-like
45                                              Rhizobium leguminosarum is a Gram-negative bacterium tha
46                                              Rhizobium leguminosarum is a soil bacterium that infects
47 de (LPS) core of the Gram-negative bacterium Rhizobium leguminosarum is more amenable to enzymatic st
48 m the plant endosymbionts Rhizobium etli and Rhizobium leguminosarum is the presence of a proximal su
49 g slow, tight-binding kinetics) of LpxC from Rhizobium leguminosarum (Ki = 340 nM), a Gram-negative p
50                                              Rhizobium leguminosarum lipid A lacks both phosphates, b
51               Coexpression of FnLpxE and the Rhizobium leguminosarum lipid A oxidase RlLpxQ in E. col
52        The lipid A and inner core regions of Rhizobium leguminosarum lipopolysaccharide contain four
53 cture of the lipid A from Rhizobium etli and Rhizobium leguminosarum lipopolysaccharides (LPSs) lacks
54 the purification and characterization of the Rhizobium leguminosarum mannosyl transferase LpcC, which
55                   In the N2-fixing bacterium Rhizobium leguminosarum, mutations in a homologue of ton
56 e monoester hydrolase/phosphodiesterase from Rhizobium leguminosarum (R/PMH) both structurally and ki
57                 The nitrogen-fixing symbiont Rhizobium leguminosarum reportedly produces at least six
58 nalysis of quorum-sensing (QS) regulation in Rhizobium leguminosarum revealed an unusual type of gene
59 es this acyl chain is present in extracts of Rhizobium leguminosarum, Rhizobium etli, and Sinorhizobi
60 of the family Rhizobiaceae, being present in Rhizobium leguminosarum, Rhizobium fredii, Rhizobium mel
61 with those expressing R. capsulatus CcoA and Rhizobium leguminosarum RibN as bona fide copper and rib
62 onging to three genospecies (gsA,C,E) of the Rhizobium leguminosarum species complex.
63 P encoding EI(Ntr) of the PTS(Ntr) system in Rhizobium leguminosarum strain Rlv3841 caused a pleiotro
64                                 To this end, Rhizobium leguminosarum strains nodulating sympatric spe
65 il, we simultaneously monitored 84 different Rhizobium leguminosarum strains, identifying a supercomp
66 iotic nodules with a large diversity of soil Rhizobium leguminosarum symbiovar viciae (Rlv) bacteria.
67            In contrast to Rhizobium etli and Rhizobium leguminosarum, the NGR234 lipid A contains a b
68 e employed the rarely used heterologous host Rhizobium leguminosarum to invoke the activities of two
69 different steps of the symbiotic interaction Rhizobium leguminosarum-Trifolium repens.
70 hingomonas strain S88 and the pssDE genes of Rhizobium leguminosarum were identified as encoding gluc
71      This applies to the symbiotic bacterium Rhizobium leguminosarum, where motility is driven by fla