ライフサイエンスコーパス: acetobutylicum

1 rmation and oxidative stress tolerance in C. acetobutylicum.

2 h from acidogenesis to solventogenesis in C. acetobutylicum.

3 FeFe]-hydrogenase (H(2)ase) from Clostridium acetobutylicum.

4 hogenesis and solventogenesis in Clostridium acetobutylicum.

5 f the TCA cycle and central metabolism of C. acetobutylicum.

6 same as that in B. subtilis and Clostridium acetobutylicum.

7 ydF, and hydG from the bacterium Clostridium acetobutylicum.

8 on of solvent formation genes in Clostridium acetobutylicum.

9 the highest (ca. 200 mM) ever reported in C. acetobutylicum.

10 racis, Staphylococcus aureus and Clostridium acetobutylicum.

11 cterization of Rex-mediated regulation in C. acetobutylicum.

12 yrate kinase, respectively, from Clostridium acetobutylicum.

13 operons of Bacillus subtilis and Clostridium acetobutylicum.

14 le in the solventogenic shift of Clostridium acetobutylicum.

15 in reaction mixtures containing Clostridium acetobutylicum 2[4Fe-4S]-ferredoxin and [Fe-Fe]-hydrogen

16 ADHE of Escherichia coli (49%), Clostridium acetobutylicum (44%), and E. histolytica (43%) and lesse

17 Importantly, analysis of the proteome of C. acetobutylicum 824 by electrospray ionization-mass spect

18 The genome of Clostridium acetobutylicum 824 contains two genes encoding NAD+, Mn2

19 and related O-alpha-linked glucosides by C. acetobutylicum 824.

20 ly map the metabolic pathways of Clostridium acetobutylicum, a soil bacterium whose major fermentatio

21 Acetoacetate decarboxylase from Clostridium acetobutylicum (AAD) catalyzes the decarboxylation of ac

22 n vitro gel retardation experiments using C. acetobutylicum adc and C. beijerinckii ptb promoter frag

23 ative to the anaerobic bacterium Clostridium acetobutylicum, an organism well-known for its historica

24 the onset of solventogenesis in Clostridium acetobutylicum and C. beijerinckii.

25 tional copies were identified in Clostridium acetobutylicum and Staphylococcus aureus, indicating con

26 arity to a glucanohydrolase from Clostridium acetobutylicum and SusG had high similarity to amylases

27 eumoniae, Staphylococcus aureus, Clostridium acetobutylicum, and Clostridium perfringens.

28 itive bacteria, in particular to Clostridium acetobutylicum, and mycoplasmas.

29 oli, the cell adhesion domain of Clostridium acetobutylicum, and the invasin of Yersinia pestis.

30 ryl-CoA dehydrogenase (BCD) from Clostridium acetobutylicum are responsible for the formation of buty

31 First, we generated three strains, C. acetobutylicum ATCC 824 (pADC38AS), 824(pADC68AS), and 8

32 ase the butanol/acetone ratio of Clostridium acetobutylicum ATCC 824 fermentations.

33 the solvent-producing bacterium Clostridium acetobutylicum ATCC 824 has been determined by the shotg

34 The Clostridium acetobutylicum ATCC 824 spo0A gene was cloned, and two r

35 ype and spo0A-deleted strains of Clostridium acetobutylicum ATCC 824.

36 TU map for the obligate anaerobe Clostridium acetobutylicum ATCC 824.

37 butanol and acetone formation in Clostridium acetobutylicum ATCC 824.

38 lly reproduce ABE fermentations of the WT C. acetobutylicum (ATCC 824), as well as its mutants, using

39 ated endospore-forming bacterium Clostridium acetobutylicum, attesting to their importance in the fun

40 iation of endospore formation in Clostridium acetobutylicum, but genes encoding key phosphorelay comp

41 L from Escherichia coli (Ec) and Clostridium acetobutylicum (Ca), respectively.

42 The enzyme, Clostridium acetobutylicum (CaADH), recently expressed by our group,

43 ty of an [FeFe]-hydrogenase from Clostridium acetobutylicum (CaH2ase) immobilized on single-wall carb

44 dy of an [FeFe]-hydrogenase from Clostridium acetobutylicum (CaHydA), we now report electrochemical a

45 s) and [FeFe]-hydrogenase I from Clostridium acetobutylicum (CaI).

46 rom Chamydomonas reinhardtii and Clostridium acetobutylicum) can be covalently attached to functional

47 into a clostridial chromosome--here, the C. acetobutylicum chromosome--with the aim of altering cell

48 genesis pathway and of the cellulosome of C. acetobutylicum comprise a new set of metabolic capacitie

49 ol-ethanol (ABE) fermentation by Clostridium acetobutylicum, during which cells convert carbon source

50 es between CdSe nanocrystals and Clostridium acetobutylicum [FeFe] hydrogenase I (CaI) enabled light-

51 The Clostridium acetobutylicum [FeFe]-hydrogenase HydA has been investig

52 mercaptopropionic acid (MPA) and Clostridium acetobutylicum [FeFe]-hydrogenase I (CaI) that photocata

53 CdTe nanocrystals (nc-CdTe) and Clostridium acetobutylicum [FeFe]-hydrogenase I (H(2)ase).

54 ical and genetic approaches, we show that C. acetobutylicum forms Asn and Asn-tRNA(Asn) by tRNA-depen

55 However, the C. acetobutylicum genome also contains a significant number

56 Analysis of the Gram-positive Clostridium acetobutylicum genome reveals an inexplicable level of r

57 analyze cultured T cells and 22 Clostridium acetobutylicum glass arrays.

58 C. acetobutylicum grows on a variety of alpha-linked glucos

59 In C. acetobutylicum harboring the subclone, the activities of

60 e [FeFe] hydrogenase, HydA, from Clostridium acetobutylicum in the non-nitrogen-fixing cyanobacterium

61 r cloning context) into the chromosome of C. acetobutylicum in three steps.

62 est an autostimulatory role for sigmaF in C. acetobutylicum, in contrast to the model organism for en

63 that the five orphan histidine kinases of C. acetobutylicum interact directly with Spo0A to control i

64 Clostridium acetobutylicum is a bacterial species that ferments suga

65 CA_C2195 from Clostridium acetobutylicum is a protein of unknown function.

66 Clostridium acetobutylicum is both a model organism for the understa

67 Extractive fermentation of C. acetobutylicum is operated in fed-batch mode with a conc

68 Coexpression of the C. acetobutylicum maturation proteins with various algal an

69 PHX genes in all these genomes except for C. acetobutylicum (not PHX), and B. subtilis, and B. halodu

70 While Clostridium acetobutylicum Ogg (CacOgg) DNA glycosylase can specific

71 acterization of a bacterial Ogg, Clostridium acetobutylicum Ogg (CacOgg).

72 om Chlamydomonas reinhardtii and Clostridium acetobutylicum, only one of which has a chain of redox r

73 ntative production of acetone by Clostridium acetobutylicum provided a crucial alternative source of

74 When a C. acetobutylicum pSOL1 megaplasmid-deficient strain M5 was

75 om Chlamydomonas reinhardtii and Clostridium acetobutylicum, react with O2 according to the same mech

76 Novel members of the C. acetobutylicum Rex regulon were identified and experimen

77 on was subcloned into an Escherichia coli-C. acetobutylicum shuttle vector.

78 The C. acetobutylicum sigK deletion (DeltasigK) mutant was unab

79 Here we show that the Clostridium acetobutylicum sigma(K) acts both early, prior to Spo0A

80 es from Bacillus, Erwinia carotovora, and C. acetobutylicum species.

81 program of the solvent-tolerant Clostridium acetobutylicum strain 824(pGROE1) and the plasmid contro

82 oenzyme A-transferase [CoAT]) of Clostridium acetobutylicum strain ATCC 824.

83 is of 824(pMSPOA) (a spo0A-overexpressing C. acetobutylicum strain with enhanced sporulation) against

84 e transcriptional program of two Clostridium acetobutylicum strains (SKO1 and M5) relative to that of

85 nt industrial and model organism Clostridium acetobutylicum, the spoIIE gene was successfully disrupt

86 In Clostridium acetobutylicum, the T-box that regulates the operon for

87 Comparison of C. acetobutylicum to Bacillus subtilis reveals significant

88 tion of these proteins can allow Clostridium acetobutylicum to survive and even grow in oxygenated cu

89 Based on the set of known C.acetobutylicum TUs, the presented TU map offers an 88% p

90 Inactivation of solR in C. acetobutylicum via homologous recombination yielded muta

91 Here the sigF gene in C. acetobutylicum was successfully disrupted and silenced.

92 DNA microarray analysis of Clostridium acetobutylicum was used to examine the genomic-scale gen

93 rial biofuel-producing bacterium Clostridium acetobutylicum, which previously lacked robust integrati

94 identified in B. subtilis are missing in C. acetobutylicum, which suggests major differences in the