ライフサイエンスコーパス: methylotrophic

1 rine-isocitrate lyase pathway common to many methylotrophic anaerobes, in which formaldehyde produced

2 ates were S-layer-deficient, non-motile, non-methylotrophic and devoid of iron-oxidation despite the

3 ndent activities were detected in all of the methylotrophic and methanotrophic proteobacteria tested

4 Pink-pigmented facultatively methylotrophic bacteria (PPFMs), classified as Methyloba

5 endent enzyme activities in cell extracts of methylotrophic bacteria from 13 different genera are rep

6 Most serine cycle methylotrophic bacteria lack isocitrate lyase and conver

7 the electron-transfer flavoprotein from the methylotrophic bacteria W3A1 (wETF) in solution.

8 the electron-transfer flavoprotein from the methylotrophic bacteria W3A1 (wETF) were used to advanta

9 sole carbon and energy source by specialised methylotrophic bacteria, isolated from a variety of envi

10 are also known in other plants, animals, and methylotrophic bacteria, suggesting an ancient evolution

11 nethiol oxidase (MTO), related to the MTO in methylotrophic bacteria, that converts methanethiol to H

12 In Gram-negative methylotrophic bacteria, the first step in methylotrophi

13 vide a comprehensive review of metabolism of methylotrophic bacteria.

14 n methanol dehydrogenase in the periplasm of methylotrophic bacteria.

15 -ribulose 5-phosphate in formaldehyde-fixing methylotrophic bacteria.

16 on has not yet been experimentally tested in methylotrophic bacteria.

17 genic archaea, sulfate-reducing archaea, and methylotrophic bacteria.

18 occurs during oxidation of methyl halides by methylotrophic bacteria.

19 hic alpha-proteobacteria or in gram-positive methylotrophic bacteria.

20 lism of one- and two-carbon compounds by the methylotrophic bacterium Methylobacterium extorquens AM1

21 Previous complementation studies with the methylotrophic bacterium Methylobacterium extorquens hav

22 ically involved in methanol oxidation in the methylotrophic bacterium Methylobacterium extorquens hav

23 versatilis universalis FAM5 is a facultative methylotrophic bacterium that has been found in a variet

24 An aerobic methylotrophic bacterium, Methylobacterium extorquens AM

25 ts to control acetyl-CoA flux to PHB in this methylotrophic bacterium.

26 tion of the N-methylglutamate pathway in the methylotrophic beta-proteobacterium Methyloversatilis un

27 e methylotrophic bacteria, the first step in methylotrophic growth is the oxidation of methanol to fo

28 tely halophilic bacterium that is capable of methylotrophic growth on a range of one-carbon compounds

29 genome of Methylobacillus flagellatus during methylotrophic growth.

30 ating methylene H4F from formaldehyde during methylotrophic growth: one involving the reaction of for

31 over, unnatural amino acid expression in the methylotrophic host was systematically optimized by modu

32 We sequenced the genomes of 19 methylotrophic isolates from Lake Washington, which belo

33 is universalis FAM5(T), the first cultivable methylotrophic member of the order.

34 icant overlap, confirming the commonality of methylotrophic metabolism downstream of the primary oxid

35 t formaldehyde, is the main branch point for methylotrophic metabolism in M. extorquens AM1.

36 serine cycle for carbon assimilation during methylotrophic metabolism.

37 ignificant role in biomass production during methylotrophic metabolism.

38 n is the main source of methylene H4F during methylotrophic metabolism.

39 of corrinoid binding by proteins involved in methylotrophic methanogenesis are discussed.

40 drABC appears to be specifically involved in methylotrophic methanogenesis, based on reduced growth a

41 ly correlated with the presence of genes for methylotrophic methanogenesis.

42 n/reduction pathway for hydrogenotrophic and methylotrophic methanogenesis.

43 rogenotrophic Methanomicrobiales, as well as methylotrophic Methanosarcinales, Methanococcales, Metha

44 Non-methylotrophic microorganisms may also utilize methylami

45 The entry of methanol into the methylotrophic pathway of methanogenesis is mediated by

46 conditions are not limited to the classical methylotrophic pathway.

47 The methylotrophic Pichia angusta VKM Y-2559 and the oleagin

48 methanol dehydrogenase that is widespread in methylotrophic Proteobacteria.

49 The methylotrophic proteobacterium Methylobacterium extorque

50 thanogenesis rates of an hdrA1C1B1 mutant on methylotrophic substrates and downregulation of the gene

51 this strain was transitioning from growth on methylotrophic substrates to growth on acetate.

52 ntous fungus (Aspergillus nidulans) and in a methylotrophic yeast (Pichia pastoris), the latter expre

53 isolated from the gene-engineered strain of methylotrophic yeast Hansenula polymorpha and commercial

54 belled protein, efficiently expressed in the methylotrophic yeast Komagataella (Pichia) pastoris.

55 revisiae (catT) have been co-produced in the methylotrophic yeast Pichia pastoris (Pp).

56 oli (Ec) and then refolded (EcCSP) or in the methylotrophic yeast Pichia pastoris (PpCSP) for structu

57 P3;1, we overexpressed this aquaporin in the methylotrophic yeast Pichia pastoris and purified the he

58 ductase (NR; EC 1.6.6.1) was produced in the methylotrophic yeast Pichia pastoris and purified to nea

59 We used the methylotrophic yeast Pichia pastoris as an expression ho

60 uman liver cDNA library and expressed in the methylotrophic yeast Pichia pastoris at a secretion yiel

61 s of the methanol utilization pathway in the methylotrophic yeast Pichia pastoris by binding to Mxr1p

62 Unlike Saccharomyces cerevisiae, the methylotrophic yeast Pichia pastoris can assimilate amin

63 The methylotrophic yeast Pichia pastoris is a popular host f

64 The pas2 mutant of the methylotrophic yeast Pichia pastoris is characterized by

65 pression of an algal phytochrome cDNA in the methylotrophic yeast Pichia pastoris led to time-depende

66 as a model glycoprotein and expressed in the methylotrophic yeast Pichia pastoris to obtain a post-tr

67 venom were constructed and expressed in the methylotrophic yeast Pichia pastoris to probe for the pr

68 ing the cDNA in frame into the genome of the methylotrophic yeast Pichia pastoris under the control o

69 cids, a recombinant expression system in the methylotrophic yeast Pichia pastoris was developed.

70 1) and the sunflower albumin 8 (SFA8) in the methylotrophic yeast Pichia pastoris.

71 ynthetic genes-ARG4, ADE1, and URA3-from the methylotrophic yeast Pichia pastoris.

72 me-biogenesis-defective (pex) mutants of the methylotrophic yeast Pichia pastoris.

73 ned and was expressed in and secreted by the methylotrophic yeast Pichia pastoris.

74 e essential for peroxisome biogenesis in the methylotrophic yeast Pichia pastoris.

75 oduction of the catalytic domain of CA IX in methylotrophic yeast Pichia pastoris.

76 enzymes were expressed in Pichia pastoris, a methylotrophic yeast strain, and their kinetic parameter

77 Pichia pastoris is a methylotrophic yeast that has been genetically engineere

78 The methylotrophic yeast, Pichia pastoris, has been genetica

79 ble alcohol oxidase I (AOXI) promoter of the methylotrophic yeast, Pichia pastoris, is used widely fo

80 at greater than gram per liter levels in the methylotrophic yeast, Pichia pastoris, using the methano

81 ation and peroxisome biogenesis genes in the methylotrophic yeast, Pichia pastoris.

82 ytosolically expressed in Pichia pastoris, a methylotrophic yeast, using spinach (Spinacia oleracea)

83 toris (Pp) and Hansenula polymorpha (Hp) are methylotrophic yeasts commonly used for industrial purpo

84 The methylotrophic yeasts Hansenula polymorpha and Pichia pa

85 Unlike the intronless alcohol oxidases from methylotrophic yeasts, a genomic fragment of the Hv-p68

86 In methylotrophic yeasts, glutathione-dependent formaldehyd

87 tity (>67%) with the alcohol oxidases of the methylotrophic yeasts.