ライフサイエンスコーパス: formate dehydrogenase

1 (420)-nonreducing hydrogenase or formate via formate dehydrogenase.

2 ogenase, F(420)-nonreducing hydrogenase, and formate dehydrogenase.

3 s, such as carbon monoxide dehydrogenase and formate dehydrogenase.

4 tory ribulose monophosphate cycles, and by a formate dehydrogenase.

5 uring the amount of released formate using a formate dehydrogenase.

6 a subset of the Mo trait, presumably due to formate dehydrogenase, a Mo- and selenium-containing pro

7 ulation of phosphate-dependent repression of formate dehydrogenase-a key enzyme in the methanogenesis

8 hicus and S. wolfei had both hydrogenase and formate dehydrogenase activities.

9 he soluble Fe(III) reductase did not possess formate dehydrogenase activity.

10 The first gene cluster encodes homologs of formate dehydrogenase alpha (FdhA) and beta (FdhB) subun

11 sharing relatively low similarity with known formate dehydrogenase alpha subunits.

12 upled to H(+)/CO(2) reduction by periplasmic formate dehydrogenase and hydrogenase via a flavin-based

13 cinate requires their oxidation by the Fdh-N formate dehydrogenase and succinate dehydrogenase respec

14 li strains as model organisms indicated that formate dehydrogenase and terminal oxidase genes provide

15 ampylobacter jejuni, possesses a periplasmic formate dehydrogenase and two terminal oxidases, which s

16 ron transfer could proceed via a periplasmic formate dehydrogenase and/or hydrogenase, allowing energ

17 that all molybdenum- and tungsten-containing formate dehydrogenases and related enzymes likely operat

18 doxins from Acetobacterium and hydrogenases, formate dehydrogenase, and cytochromes of Desulfovibrio

19 int assay based on the coupled reaction with formate dehydrogenase, and measuring consumption of O(2)

20 ific activities of GSH-FDH, an NAD-dependent formate dehydrogenase, and the key Calvin-Benson-Bassham

21 sigma(E) and cytoplasmic membrane-associated formate dehydrogenase are required for the protective ef

22 effects on the oxidation of formate by yeast formate dehydrogenase as expressed on the kinetic parame

23 ecting multiple periplasmic hydrogenases and formate dehydrogenases, as a key feature of its energy m

24 , the ability of Desulfovibrio desulfuricans formate dehydrogenase (Dd FDH) to reduce carbon dioxide

25 Analyzing a formate dehydrogenase domain that is evolutionarily rela

26 The formate dehydrogenase-encoding fdhCAB operon and flankin

27 rode allowed the targeted orientation of the formate dehydrogenase enzyme from Rhodobacter capsulatus

28 Escherichia coli possesses three distinct formate dehydrogenase enzymes encoded by the fdnGHI, fdh

29 ron transfer flavoproteins, hydrogenases and formate dehydrogenases essential for syntrophic metaboli

30 Surprisingly, formate dehydrogenase (FDH) activity was decreased appro

31 fatty acids, dissimilatory sulfur oxidation, formate dehydrogenase (FDH) and a nitrite reductase (Nir

32 torquens AM1 with lesions in genes for three formate dehydrogenase (FDH) enzymes was previously descr

33 Furthermore, co-expressing formate dehydrogenase (Fdh) from Candida boidinii increa

34 al transcriptomics revealed that 2 of the 23 formate dehydrogenase (FDH) genes known in the system ac

35 Formate dehydrogenase (FDH) has been studied in bacteria

36 reaction come from either formate or H2 via formate dehydrogenase (Fdh) or Hdr-associated hydrogenas

37 We report a study of formate dehydrogenase (FDH) that compares the temperatur

38 products, including CO2 This organism lacks formate dehydrogenase (Fdh), which catalyzes the reducti

39 cription and activity of the donor complexes formate dehydrogenase (FdhABC) and hydrogenase (HydABCD)

40 homologs of fdhF encoding hydrogenase-linked formate dehydrogenases (FDHH ) and all other components

41 dhD, a protein essential for the activity of formate dehydrogenases (FDHs), which are iron/molybdenum

42 The ability of the FdsABG formate dehydrogenase from Cupriavidus necator (formerly

43 d identity to the respective subunits of the formate dehydrogenase from Moorella thermoacetica, but t

44 lybdenum-containing, NAD(+)-dependent FdsABG formate dehydrogenase from Ralstonia eutropha.

45 Phylogenetic analysis suggested that the two formate dehydrogenase gene sets arose from duplication e

46 trophicus expressed multiple hydrogenase and formate dehydrogenase genes during syntrophic benzoate a

47 To study the latter, we identified the formate dehydrogenase genes of M. maripaludis and found

48 h organisms contain multiple hydrogenase and formate dehydrogenase genes, but lack genes for outer me

49 idase family of enzymes, the 5' deiodinases, formate dehydrogenases, glycine reductase, and a few hyd

50 The selenocysteine-containing formate dehydrogenase H (FDH) is an 80-kDa component of

51 of the oxidized [Mo(VI), Fe4S4(ox)] form of formate dehydrogenase H (with and without bound inhibito

52 differentially regulated genes revealed that formate dehydrogenase H and fumarate reductase are impor

53 mitant decrease in (75)Se incorporation into formate dehydrogenase H and nucleosides of bulk tRNA was

54 2-), failed to synthesize selenium-dependent formate dehydrogenase H and seleno-tRNAs.

55 Molybdenum-containing formate dehydrogenase H from Escherichia coli (EcFDH-H)

56 Formate dehydrogenase H from Escherichia coli contains s

57 ytic properties of the molybdenum-containing formate dehydrogenase H from the model organism Escheric

58 guanine dinucleotide [MGD]) synthesis, or in formate dehydrogenase H synthesis were all defective in

59 icodons enabled E. coli to synthesize active formate dehydrogenase H, a selenoenzyme.

60 Formate dehydrogenase H, FDH(Se), from Escherichia coli

61 ermed Hyd-3), FdhF (the molybdenum-dependent formate dehydrogenase-H), and three iron-sulfur proteins

62 Formate dehydrogenase has traditionally been assumed to

63 teps of methanogenesis, including one of two formate dehydrogenases, increased with H2 starvation but

64 (cyanide and carbon monoxide), but not by a formate dehydrogenase inhibitor (hypophosphite).

65 rinsic kinetic isotope effects of the enzyme formate dehydrogenase is used to examine the distributio

66 he mutants suggest that any one of the three formate dehydrogenases is sufficient to sustain growth o

67 A soluble formate dehydrogenase lends additional ecophysiological

68 r the production of xylitol, coexpression of formate dehydrogenase, mannitol dehydrogenase, and a glu

69 Expression of genes for the second formate dehydrogenase, molybdenum-dependent formylmethan

70 rease in formic acid secretion relative to a formate dehydrogenase mutant (fdh1 fdh2), while formic a

71 The structure of the membrane protein formate dehydrogenase-N (Fdn-N), a major component of Es

72 Formate dehydrogenase-N is a three-subunit membrane-boun

73 port infrared photon echo measurement of the formate dehydrogenase-NAD+-azide ternary complex.

74 e selenocysteine into any of the three known formate dehydrogenases of E. coli.

75 Of the two formate dehydrogenases, only the first could support gro

76 o stimulate or suppress expression of either formate dehydrogenase operon via NarL and NarP.

77 s) among these species, including a complete formate dehydrogenase operon, genes required for N-acety

78 gene expression profiles of the alternative formate dehydrogenase operons suggest that the two enzym

79 necessary for gauging the ability of a given formate dehydrogenase or other CO2-utilizing enzyme to c

80 de reductase are strict molybdoenzymes while formate dehydrogenase prefers tungsten.

81 tory nitrate reductase (QR' = 2-AdS(-)), and formate dehydrogenase (QR' = 2-AdSe(-)).

82 hydrogenase reaction (GndA and GndB) and the formate dehydrogenase reaction (FDH1 and FDH4).

83 The formate dehydrogenase subunit FdoH and the yet uncharact

84 pproach was used to identify three different formate dehydrogenase systems in the facultative methylo

85 These results demonstrated that all three formate dehydrogenase systems must be inactivated in ord

86 iently interconverted by tungsten-containing formate dehydrogenases that surpass current synthetic ca

87 ectrons are channeled from an outward-facing formate dehydrogenase via menaquinones to a fumarate red

88 Hydrogenase-linked formate dehydrogenase was also affected, but not as seve

89 Formate dehydrogenase was present in most selenoproteome

90 ies, we conjugated mannitol dehydrogenase to formate dehydrogenase with the defined active site arran

91 cales of active-site motions in complexes of formate dehydrogenase with the transition-state-analog i