ライフサイエンスコーパス: Methylobacterium

1 thway in the isocitrate lyase (ICL)-negative Methylobacterium.

2 Methylobacterium (19%) and members of Nitrosomonadaceae

3 uite of OTUs, including taxa from the genera Methylobacterium, Acinetobacter and Mycoplasma, appear t

4 ostridium, Lactobacillus, Desulfovibrio, and Methylobacterium and an increased tend of Bacteroides an

5 ria such as Enterobacteriaceae, Haemophilus, Methylobacterium, and Ralstonia species were disproporti

6 ix strains of the alphaproteobacterial genus Methylobacterium, chosen for their key adaptations to di

7 e dichloromethane degradation across diverse Methylobacterium environmental isolates.

8 lation, founded with an engineered strain of Methylobacterium, evolved to grow on methanol.

9 ly sequenced genomes of three methylotrophs, Methylobacterium extorquens (an alphaproteobacterium, 7

10 action transcends species, also occurring in Methylobacterium extorquens AM1 (Me).

11 racterized from the facultative methylotroph Methylobacterium extorquens AM1 and shown to be the majo

12 han tryptophylquinone-containing enzyme from Methylobacterium extorquens AM1 by high resolution x-ray

13 The serine cycle methylotroph Methylobacterium extorquens AM1 contains two pterin-depe

14 grow on reduced single-carbon compounds-like Methylobacterium extorquens AM1 encode two routes for me

15 The Methylobacterium extorquens AM1 genome contains two homo

16 on compounds by the methylotrophic bacterium Methylobacterium extorquens AM1 involves high carbon flu

17 Methylobacterium extorquens AM1 is a facultative methylo

18 The methylotroph Methylobacterium extorquens AM1 oxidizes methanol and me

19 The methylotrophic proteobacterium Methylobacterium extorquens AM1 possesses tetrahydrometh

20 The facultative methylotroph Methylobacterium extorquens AM1 possesses two pterin-dep

21 Methylobacterium extorquens AM1 pqqEF are genes required

22 compounds, the aerobic alpha-proteobacterium Methylobacterium extorquens AM1 synthesizes the tetrahyd

23 Methylobacterium extorquens AM1 uses dedicated cofactors

24 Methylobacterium extorquens AM1 was used to explore the

25 trophy genes of the facultative methylotroph Methylobacterium extorquens AM1 were identified from a t

26 nase systems in the facultative methylotroph Methylobacterium extorquens AM1 whose expression is affe

27 A mutant of Methylobacterium extorquens AM1 with lesions in genes fo

28 In Methylobacterium extorquens AM1, a mutant defective in t

29 Methylobacterium extorquens AM1, a serine cycle facultat

30 In Methylobacterium extorquens AM1, MaDH is essential for m

31 In Methylobacterium extorquens AM1, the best-studied aerobi

32 An aerobic methylotrophic bacterium, Methylobacterium extorquens AM1, was found to contain a

33 e metabolism of the facultative methylotroph Methylobacterium extorquens AM1, which lacks isocitrate

34 e same locus within replicate populations of Methylobacterium extorquens AM1.

35 e assimilation of C(1) and C(2) compounds in Methylobacterium extorquens AM1.

36 This problem was investigated in Methylobacterium extorquens AM1.

37 was assessed in the facultative methylotroph Methylobacterium extorquens AM1.

38 r regulator of assimilatory C1 metabolism in Methylobacterium extorquens AM1.

39 MPT) levels in wild-type and mutant cells of Methylobacterium extorquens AM1.

40 in the serine cycle facultative methylotroph Methylobacterium extorquens AM1.

41 al fragment of the serine cycle methylotroph Methylobacterium extorquens AM1.

42 In this study, we have mimicked in the Methylobacterium extorquens ATR, a C-terminal truncation

43 Methylobacterium extorquens DM4 expresses a dichlorometh

44 The structure of cytochrome cL from Methylobacterium extorquens has been determined by X-ray

45 ol oxidation in the methylotrophic bacterium Methylobacterium extorquens have been modified by site-d

46 on studies with the methylotrophic bacterium Methylobacterium extorquens have indicated that an uncha

47 one of the central methylotrophy pathways in Methylobacterium extorquens involved in glyoxylate gener

48 ain has very high sequence similarity to the Methylobacterium extorquens MeaB, which is a chaperone f

49 dopsis, barley, maize, and soybean) and of a Methylobacterium extorquens type culture originally reco

50 hydrogenase gene, and meaA (62% identity) of Methylobacterium extorquens, respectively.

51 panoid-deficient mutant of the gram-negative Methylobacterium extorquens, which introduces a link bet

52 ve previously demonstrated that the ATR from Methylobacterium extorquens, which supports methylmalony

53 required for C1 metabolism by the bacterium Methylobacterium extorquens.

54 ABA correlated with species of Sphingomonas, Methylobacterium, Frankineae, Variovorax, Micromonospori

55 our cases of central venous catheter-related Methylobacterium radiotolerans infection are presented h

56 HpnP proteins from cyanobacteria, Methylobacterium species, and other alpha-proteobacteria

57 thylotrophic bacteria (PPFMs), classified as Methylobacterium spp., are persistent colonizers of plan

58 We transferred the dcmA gene into six Methylobacterium strains that include both close and dis

59 s issue using dichloromethane consumption in Methylobacterium strains.

60 hingomonas, Streptococcus, Streptophyta, and Methylobacterium-were ubiquitous among the analyzed coho