ライフサイエンスコーパス: extorquens

1 metabolism by the bacterium Methylobacterium extorquens.

2 species, also occurring in Methylobacterium extorquens AM1 (Me).

3 he facultative methylotroph Methylobacterium extorquens AM1 and shown to be the major regulator of th

4 ication and characterization of FtfL from M. extorquens AM1 and the confirmation that this enzyme is

5 ol revealed that while cells of wild-type M. extorquens AM1 as well as cells of all the single and th

6 PA1, a strain that is closely related to M. extorquens AM1 but is lacking methylamine dehydrogenase,

7 none-containing enzyme from Methylobacterium extorquens AM1 by high resolution x-ray crystallography

8 at the analogous H(4)F pathway present in M. extorquens AM1 cannot fulfill the formaldehyde detoxific

9 ents, and (13)C-labeling experiments that M. extorquens AM1 contains an additional malyl-CoA/beta-met

10 e serine cycle methylotroph Methylobacterium extorquens AM1 contains two pterin-dependent pathways fo

11 ingle-carbon compounds-like Methylobacterium extorquens AM1 encode two routes for methylamine oxidati

12 The Methylobacterium extorquens AM1 genome contains two homologs of MxaF, Xox

13 s revealed that the protein repertoire of M. extorquens AM1 grown on acetate is similar to that of ce

14 he methylotrophic bacterium Methylobacterium extorquens AM1 involves high carbon flux through the eth

15 Methylobacterium extorquens AM1 is a facultative methylotroph capable of

16 n of common pathways during the growth of M. extorquens AM1 on C1 and C2 compounds, but with a major

17 enases is sufficient to sustain growth of M. extorquens AM1 on formate, while surprisingly, none is r

18 The methylotroph Methylobacterium extorquens AM1 oxidizes methanol and methylamine to form

19 hylotrophic proteobacterium Methylobacterium extorquens AM1 possesses tetrahydromethanopterin (H(4)MP

20 he facultative methylotroph Methylobacterium extorquens AM1 possesses two pterin-dependent pathways f

21 M. extorquens AM1 pqqE complemented a K. pneumoniae pqqF mu

22 Methylobacterium extorquens AM1 pqqEF are genes required for synthesis of

23 luding PqqF of Klebsiella pneumoniae, and M. extorquens AM1 PqqF has low identity with the same endop

24 robic alpha-proteobacterium Methylobacterium extorquens AM1 synthesizes the tetrahydromethanopterin (

25 Methylobacterium extorquens AM1 uses dedicated cofactors for one-carbon u

26 Methylobacterium extorquens AM1 was used to explore the genetics of depho

27 l-type" genes linked on the chromosome of M. extorquens AM1 were analyzed for the ability to synthesi

28 he facultative methylotroph Methylobacterium extorquens AM1 were identified from a transposon mutagen

29 he facultative methylotroph Methylobacterium extorquens AM1 whose expression is affected by either mo

30 A mutant of Methylobacterium extorquens AM1 with lesions in genes for three formate d

31 In Methylobacterium extorquens AM1, a mutant defective in the MMAA homolog m

32 Methylobacterium extorquens AM1, a serine cycle facultative methylotroph,

33 1), C(2), and heterotrophic metabolism in M. extorquens AM1, as well as the entry metabolite for the

34 xF is not required for methanol growth in M. extorquens AM1, but here we show that when both xoxF hom

35 In Methylobacterium extorquens AM1, MaDH is essential for methylamine growth

36 In Methylobacterium extorquens AM1, the best-studied aerobic methylotroph, a

37 c methylotrophic bacterium, Methylobacterium extorquens AM1, was found to contain a cluster of genes

38 he facultative methylotroph Methylobacterium extorquens AM1, which lacks isocitrate lyase, the key en

39 in replicate populations of Methylobacterium extorquens AM1.

40 C(1) and C(2) compounds in Methylobacterium extorquens AM1.

41 the absence of ccrR compared to wild-type M. extorquens AM1.

42 ch point for methylotrophic metabolism in M. extorquens AM1.

43 problem was investigated in Methylobacterium extorquens AM1.

44 he facultative methylotroph Methylobacterium extorquens AM1.

45 in the regulation of the serine cycle in M. extorquens AM1.

46 similatory C1 metabolism in Methylobacterium extorquens AM1.

47 ld-type and mutant cells of Methylobacterium extorquens AM1.

48 e oxidation and detoxification pathway in M. extorquens AM1.

49 ared to the activities found in wild-type M. extorquens AM1.

50 the key formaldehyde oxidation pathway in M. extorquens AM1.

51 le facultative methylotroph Methylobacterium extorquens AM1.

52 ved in formaldehyde oxidation to CO(2) in M. extorquens AM1.

53 e serine cycle methylotroph Methylobacterium extorquens AM1.

54 mes of three methylotrophs, Methylobacterium extorquens (an alphaproteobacterium, 7 Mbp), Methylibium

55 homolog has previously been reported for M. extorquens and assigned as the putative H2MPT reductase

56 dy, we have mimicked in the Methylobacterium extorquens ATR, a C-terminal truncation mutation, D180X,

57 ed from tRNA, we mutated the miaA gene of M. extorquens by single exchange of an internal miaA fragme

58 Wild-type M. extorquens cells were grown at steady state on a limitin

59 Methylobacterium extorquens DM4 expresses a dichloromethane dehalogenase

60 cture of cytochrome cL from Methylobacterium extorquens has been determined by X-ray crystallography

61 he methylotrophic bacterium Methylobacterium extorquens have been modified by site-directed mutagenes

62 he methylotrophic bacterium Methylobacterium extorquens have indicated that an uncharacterized archae

63 l methylotrophy pathways in Methylobacterium extorquens involved in glyoxylate generation and acetyl-

64 ncoding a potential beta-RFAP synthase in M. extorquens is the first report of a putative methanopter

65 sequence similarity to the Methylobacterium extorquens MeaB, which is a chaperone for methylmalonyl-

66 Furthermore, analysis of M. extorquens PA1 mutants with defects in methylotrophy-spe

67 influences the yield during the growth of M. extorquens PA1 on methylamine.

68 In this study, we used M. extorquens PA1, a strain that is closely related to M. e

69 These results demonstrate that in M. extorquens, physiological heterogeneity at the single-ce

70 and meaA (62% identity) of Methylobacterium extorquens, respectively.

71 ore similar to those in M. capsulatus and M. extorquens than to the ones in the more closely related

72 aize, and soybean) and of a Methylobacterium extorquens type culture originally recovered as a soil i

73 MeaB and methylmalonyl-CoA mutase from M. extorquens were cloned and purified in their active form

74 mutant of the gram-negative Methylobacterium extorquens, which introduces a link between membrane ord

75 onstrated that the ATR from Methylobacterium extorquens, which supports methylmalonyl-CoA mutase acti