ライフサイエンスコーパス: clostridia

1 both acid formation and solvent formation by clostridia.

2 cellulosome-localized protease inhibitors in Clostridia.

3 nce factors of various species of pathogenic Clostridia.

4 le in maintaining NADH/NAD(+) homeostasis in clostridia.

5 llulosic biomass degradation in cellulolytic Clostridia.

6 tive production of p-cresol from tyrosine in clostridia.

7 stly highly conserved in the Bacilli and the Clostridia.

8 -Megasphaera-Sporomusa group back within the Clostridia.

9 ower MFC anode communities were dominated by Clostridia.

10 which are conserved among other bacilli and clostridia.

11 of sporulation-specific genes in Bacilli and Clostridia.

12 , the highest detected number in cluster III clostridia.

13 t-related amidases almost exclusively target Clostridia.

14 ad by the strictly anaerobic Bacteroides and Clostridia.

15 a derived cellulolytic organism in the class Clostridia.

16 chnique never used before with solventogenic clostridia.

17 vailable to date on pectate lyase genes from Clostridia.

18 y for purine fermentation in the purinolytic clostridia.

19 ust of Firmicutes (70%) at the phylum level, Clostridia (44%) at the Class level, and Clostridiales a

20 re highly diverse and primarily dominated by Clostridia (48.5%), Bacilli (27.9%), and beta-Proteobact

21 residues), is conserved throughout the class Clostridia, a distribution inconsistent with putative ba

22 Unlike the Gram-positive Bacilli and Clostridia, A. longum spores retain their outer spore me

23 gamma-Proteobacteria, delta-Proteobacteria, Clostridia, Actinobacteria, Deinococcus-Thermus species

24 in Science, Kim et al. (2017) revealed that Clostridia added to mouse infant gut microbiota are suff

25 escribed previously from different groups of clostridia, along with differences in flanking sequences

26 selected strains of high butyrate-producing Clostridia also decreased GVHD.

27 s (BoNTs) are produced by various species of clostridia and are potent neurotoxins which cause the di

28 ng seven bacterial classes with Bacteroidia, Clostridia and Bacilli dominating the microbiota.

29 Diverse families within the Clostridia and Bacteroidetes taxa discriminated human wa

30 Bacterial taxa within Clostridia and Firmicutes could be studied as probiotic

31 ars (PERMANOVA P = .047), with enrichment of Clostridia and Firmicutes in the infant gut microbiome o

32 Clostridia and Fusobacteria, widely pathogenic to other

33 nderstanding of sporulation in solventogenic clostridia and its relationship to solvent formation and

34 ion has been detected in anaerobes, first in clostridia and later in acetogens and methanogens.

35 ram-positive bacteria (Firmicutes), Bacilli, Clostridia and Negativicutes, include numerous members t

36 ude of regulatory function that CaCO3 has in clostridia and provides detailed insights into degenerat

37 e divergence of the branches leading to the 'Clostridia and relatives' and the remaining low-G+C Gram

38 Bacillus and Staphylococcus rather than the 'Clostridia and relatives' as suggested by the sequences

39 sted almost entirely of sequences similar to Clostridia and showed a decrease in bacterial abundance

40 similarities among the F1 subunits from both clostridia and the beta subunit of F1 from E. coli.

41 heifers, and we show that it is dominated by Clostridia and/or Bacilli but also harbors Bacteroidetes

42 iotic-mediated depletion of anaerobes (e.g., Clostridia) and associated decreases in butyrate result

43 deep groundwater, phylum Chloroflexi, class Clostridia, and candidate division OD1 were the major ta

44 es in selective pressure between eukaryotes, Clostridia, and other bacteria, our results are consiste

45 re seen for Proteobacteria, Deferribacteres, Clostridia, and others; however, changes in Enterobacter

46 Anaerobic bacteria of the genus Clostridia are a major threat to human and animal health

47 Clostridia are anaerobic Firmicutes producing a large ar

48 Solventogenic clostridia are strictly anaerobic, endospore forming bac

49 Spores produced by bacilli and clostridia are surrounded by a multilayered protein shel

50 It has recently been proposed that the Clostridia are the oldest Eubacterial class and the ubiq

51 Colonization with clostridia, at the age of 5 and 13 weeks was also associ

52 s was executed and COGs were mostly found in Clostridia, Bacilli (Firmicutes), and in alpha and beta

53 naerobic species affiliated with the classes Clostridia, Bacilli, Gammaproteobacteria, Epsilonproteob

54 Treatment of SMCs with Clostridia botulinum C3 exoenzyme, which inhibits RhoA a

55 Lysine 2,3-aminomutase from Clostridia catalyzes the interconversion of L-lysine and

56 icute phylum, which includes the Bacilli and Clostridia classes, are their ability to form endospores

57 microbiota (increases relative abundance of Clostridia clusters IV and XIVa) and a concomitant incre

58 nally, how does the germination of spores of clostridia compare with that of spores of bacilli?

59 llergy-protective capacity is conferred by a Clostridia-containing microbiota.

60 equenced to date, including actinomycetales, clostridia, corynebacteria, and streptococci.

61 001) populations but significantly decreased clostridia counts (P < 0.001).

62 roides (P = .02) increased, whereas rates of clostridia decreased (P < .001).

63 and recent efforts to metabolically engineer clostridia demonstrate their potential for biofuel and b

64 Clostridia depletion and aerobic Salmonella expansion we

65 acillus subtilis, and most other bacilli and clostridia, DHDPA is oxidized to DPA by the products of

66 the risk of hospital-acquired pneumonia and Clostridia difficile infection.

67 Depletion of butyrate-producing Clostridia, either through oral antibiotic treatment or

68 (containing the type I reaction center) and Clostridia (forming heat-resistant endospores).

69 tment depleted commensal, butyrate-producing Clostridia from the mouse intestinal lumen, leading to d

70 Bacilli and Clostridia generate dormant, highly resistant cells, cal

71 was evidenced in seven species belonging to Clostridia, Halothermothrix, and Tepidanaerobacter.

72 Analysis of the genomes of the clostridia in Cluster I, including the pathogens Clostri

73 substantial differences between bacilli and clostridia in the engulfment and spore coat formation st

74 The class Clostridia in the phylum Firmicutes (formerly low-G+C Gr

75 The reconstructed Rex regulons in clostridia included the genes involved in fermentation,

76 josui, they seem to be typical of mesophilic clostridia, indicating that the large gene clusters may

77 rst step in the establishment of Bacilli and Clostridia infections, we analyzed the requirements for

78 asses from Bacilli to Gammaproteobacteria to Clostridia, interrupted by abrupt population changes.

79 Central to all clostridia is the orchestration of endospore formation (

80 biquity of TFP in this class suggests that a Clostridia-like ancestor possessed TFP, which evolved in

81 range: 0.8 compared with 4.3; P = 0.035) and clostridia (median: 10.4% and 3.7%; interquartile range:

82 the biochemistry of strict anaerobes such as clostridia, methanogens, acetogens, and sulfate-reducing

83 These findings suggest that BCD in clostridia might interact with the electron transfer fla

84 th Negativicutes (p=0.0013) and the combined Clostridia-Negativicutes class (p=0.0051) in infants who

85 s had significantly higher concentrations of clostridia (P = 0.026) and lower concentrations (P = 0.0

86 Histotoxic clostridia produce collagenases responsible for extensiv

87 The clostridia produce more protein toxins than any other ba

88 a previously unidentified mechanism by which Clostridia regulate innate lymphoid cell function and in

89 gut microbiota, specifically a depletion of Clostridia, reprogram host metabolism to perform lactate

90 la; PseudoDB for pseudomonads; ClostriDB for clostridia; RhizoDB for Rhizobium and Sinorhizobium; and

91 rarchical fistulous complexes, enriched with clostridia/segmented filamentous bacteria, running under

92 ts of Lactobacillaceae spp and 3 fold higher Clostridia spp in the sow fed group in comparison to mil

93 nced to date, including the Actinomycetales, clostridia, streptococci, and corynebacteria.

94 ate the existence of a group of cellulolytic clostridia that belong to the family Ruminococcaceae.

95 lesser-known family (the Veillonellaceae) of Clostridia that form endospores but that are surprisingl

96 like proteins may be a common feature of the clostridia that may represent the ancestral state before

97 um hydroxylase enzymes in several species of clostridia that specialize in the fermentation of purine

98 type cell envelopes, was recently moved from Clostridia to a separate class Negativicutes.

99 piraceae and Ruminococcaceae of the class of Clostridia to be associated with high urinary 3-IS level

100 e mechanism: depletion of butyrate-producing Clostridia to elevate epithelial oxygenation, allowing a

101 s of BoNTs, labeled A-G, and toxin-producing clostridia typically only produce one serotype of BoNT.

102 ions such as the classes Sphingobacteria and Clostridia were observed over the entire filter depth.

103 all leachate samples and cluster III and XIV clostridia were the most abundant (1-6% and 1-17% of tot

104 species, with the only exception detected in Clostridia, where the Rex motif deviates in two position

105 bacteria, Geobacter, and to a lesser extent, Clostridia, while low-power MFC anode communities were d

106 ich include important pathogenic Bacilli and Clostridia, whose ability to sporulate contributes to th

107 Comparative genomics of cellulolytic clostridia will provide insight into factors that influe