ライフサイエンスコーパス: Rhizobium leguminosarum

1 siderophore made by the symbiotic bacterium Rhizobium leguminosarum.

2 Pseudomonas brassicacearum and rhizospheric 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 hydrolases from Burkholderia caryophylli and Rhizobium leguminosarum.

7 M, P), has been cloned and characterized in Rhizobium leguminosarum.

8 ation of nitrogen-fixing pea root nodules by 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 ese/iron-type superoxide dismutase (SodA) of Rhizobium leguminosarum bv.

26 e-cell Raman spectra (SCRS) to differentiate Rhizobium leguminosarum bv.

27 Rhizobium leguminosarum bv. trifolii 4S has a lipopolysa

28 olipooligosaccharides (CLOSs) from wild-type Rhizobium leguminosarum bv. trifolii on development of w

29 eviously, we have shown that tfxABCDEFG from Rhizobium leguminosarum bv. trifolii T24 is sufficient t

30 g this 3.1-kb fragment was used to transform Rhizobium leguminosarum bv. trifolii TA-1JH, a strain wh

31 protein product is highly homologous to the Rhizobium leguminosarum bv. viciae RhiR protein and a nu

32 NodO is a secreted protein from Rhizobium leguminosarum bv. viciae with a role in signal

33 In Rhizobium leguminosarum bv. viciae, quorum-sensing is re

34 show that a Cpn60 protein from the bacterium Rhizobium leguminosarum can function to allow E. coli gr

35 Membranes of Rhizobium leguminosarum contain a 3-deoxy-D-manno-octulo

36 The endosymbiotic bacterium Rhizobium leguminosarum contains a single hydrogenase sy

37 potential IHF binding sites adjacent to the Rhizobium leguminosarum dctA promoter.

38 e structure of the nitrogen-fixing bacterium Rhizobium leguminosarum differs from that of Escherichia

39 The lipopolysaccharide of Rhizobium leguminosarum differs from that of other Gram-

40 Lipid A from the nitrogen-fixing bacterium Rhizobium leguminosarum displays many structural differe

41 Rhizobium leguminosarum has two high-affinity Mn(2+) tra

42 lorimetry, and other methods that RapA2 from Rhizobium leguminosarum indeed exhibits a cadherin-like

43 Rhizobium leguminosarum is a Gram-negative bacterium tha

44 Rhizobium leguminosarum is a soil bacterium that infects

45 de (LPS) core of the Gram-negative bacterium Rhizobium leguminosarum is more amenable to enzymatic st

46 m the plant endosymbionts Rhizobium etli and Rhizobium leguminosarum is the presence of a proximal su

47 g slow, tight-binding kinetics) of LpxC from Rhizobium leguminosarum (Ki = 340 nM), a Gram-negative p

48 Rhizobium leguminosarum lipid A lacks both phosphates, b

49 Coexpression of FnLpxE and the Rhizobium leguminosarum lipid A oxidase RlLpxQ in E. col

50 The lipid A and inner core regions of Rhizobium leguminosarum lipopolysaccharide contain four

51 cture of the lipid A from Rhizobium etli and Rhizobium leguminosarum lipopolysaccharides (LPSs) lacks

52 the purification and characterization of the Rhizobium leguminosarum mannosyl transferase LpcC, which

53 In the N2-fixing bacterium Rhizobium leguminosarum, mutations in a homologue of ton

54 e monoester hydrolase/phosphodiesterase from Rhizobium leguminosarum (R/PMH) both structurally and ki

55 The nitrogen-fixing symbiont Rhizobium leguminosarum reportedly produces at least six

56 nalysis of quorum-sensing (QS) regulation in Rhizobium leguminosarum revealed an unusual type of gene

57 es this acyl chain is present in extracts of Rhizobium leguminosarum, Rhizobium etli, and Sinorhizobi

58 of the family Rhizobiaceae, being present in Rhizobium leguminosarum, Rhizobium fredii, Rhizobium mel

59 P encoding EI(Ntr) of the PTS(Ntr) system in Rhizobium leguminosarum strain Rlv3841 caused a pleiotro

60 To this end, Rhizobium leguminosarum strains nodulating sympatric spe

61 In contrast to Rhizobium etli and Rhizobium leguminosarum, the NGR234 lipid A contains a b

62 e employed the rarely used heterologous host Rhizobium leguminosarum to invoke the activities of two

63 hingomonas strain S88 and the pssDE genes of Rhizobium leguminosarum were identified as encoding gluc