ライフサイエンスコーパス: Alphaproteobacteria

1 seobacter clade within the Rhodobacteraceae (Alphaproteobacteria).

2 adaptation and host-microbe interactions in Alphaproteobacteria.

3 to be involved in formaldehyde oxidation in Alphaproteobacteria.

4 y that mitochondria originated once from the Alphaproteobacteria.

5 M, a DNA methyltransferase conserved in most Alphaproteobacteria.

6 C. crescentus and, presumably, of many other Alphaproteobacteria.

7 hat this notion might also be true for other Alphaproteobacteria.

8 ECF15 family of sigma factors found only in alphaproteobacteria.

9 regulators of the general stress response in alphaproteobacteria.

10 ed aerobic species affiliated with the class Alphaproteobacteria.

11 e-target) VPEID-CTERM/exosortase E system in alphaproteobacteria.

12 the major iron-responsive regulators in the alphaproteobacteria.

13 lobally significant Roseobacter clade of the Alphaproteobacteria.

14 percent sequence identity to Rsh proteins of alphaproteobacteria.

15 orter for bacterial DMSP synthesis in marine Alphaproteobacteria.

16 ation and rearrangements in the Epsilon- and Alphaproteobacteria.

17 ique component of the lipopolysaccharides of alphaproteobacteria.

18 ces was found to covary with tRNA(His) among alphaproteobacteria.

19 eptidoglycan chemical diversity in the Class Alphaproteobacteria, a group of Gram negative bacteria t

20 in C. crescentus, the essential genes of two Alphaproteobacteria, Agrobacterium tumefaciens (Rhizobia

21 this extra guanylate, unlike those of other alphaproteobacteria and bacteria in general.

22 ccompanied with known or putative members of Alphaproteobacteria and Bacteroidetes.

23 species restricted to a dozen genera of the Alphaproteobacteria and Betaproteobacteria, suggesting i

24 from independent gene permutation events in alphaproteobacteria and cyanobacteria.

25 mic units belonging to the Ruegeria genus of Alphaproteobacteria and NS9 marine group of Flavobacteri

26 The core symbiotic community was composed of Alphaproteobacteria and Opitutae (a class of Verrucomicr

27 Alphaproteobacteria and plants contain a single Rsh enzy

28 d independently in at least four lineages of Alphaproteobacteria and that all methylotrophy modules s

29 waters were dominated by the SAR11 clade of Alphaproteobacteria and the cyanobacterium Synechococcus

30 ve flavobacteria, one sphingobacterium, four alphaproteobacteria, and one gammaproteobacterium.

31 s from the prolific Roseobacter clade in the Alphaproteobacteria are beginning to reveal the genetic

32 ing of many plasmids and some chromosomes of alphaproteobacteria are directed by their repABC operons

33 ria of the genus Bartonella, a member of the Alphaproteobacteria, are fastidious, gram-negative, aero

34 er sp. TM1040 uses components found in other Alphaproteobacteria, as well as novel molecular mechanis

35 to contain a diverse assemblage of bacteria (Alphaproteobacteria, Betaproteobacteria and Gammaproteob

36 oth methylotrophs and non-methylotrophs from Alphaproteobacteria, Betaproteobacteria and Gammaproteob

37 ccurring in many, but not all, genera in the Alphaproteobacteria, Betaproteobacteria, Gammaproteobact

38 ntus cell cycle genes are conserved in other Alphaproteobacteria, but it is not clear to what extent

39 We addressed this question for alphaproteobacteria by using the polarly flagellated alp

40 obacter group, an abundant lineage of marine Alphaproteobacteria, can constitute large proportions of

41 ost other members of the SAR 11 clade of the Alphaproteobacteria, can evade filtration by slipping th

42 to three distinct groups affiliated with the Alphaproteobacteria class of the Proteobacteria.

43 The Alphaproteobacteria comprise morphologically diverse bac

44 The genus Wolbachia (Alphaproteobacteria) comprises the most abundant inherit

45 As in alphaproteobacteria, deletion of BacA in M. tuberculosis

46 th mats were dominated by Chloroflexi, while Alphaproteobacteria dominated the lower layers of pustul

47 ghest expression of solute transporters were Alphaproteobacteria, Gammaproteobacteria, and Deltaprote

48 Within the Alphaproteobacteria, gcrA and ccrM are consistently pres

49 mic Bartonella spp., tested using Bartonella Alphaproteobacteria growth medium (BAPGM), were retrospe

50 On average, Alphaproteobacteria (i.e., Thalassobius), Gammaproteobac

51 the endemic Mexican Mimosa species favoured alphaproteobacteria in the genera Rhizobium and Ensifer:

52 oteobacteria and Betaproteobacteria in RW to Alphaproteobacteria in TW.

53 enetic studies comparing CtrA sequences from alphaproteobacteria in which the role of CtrA has been e

54 regulatory network, conserved throughout the Alphaproteobacteria, in the magnetotactic bacterium Magn

55 re we announce the genome sequences of eight alphaproteobacteria, including the first genome sequence

56 other major iron-responsive regulator in the alphaproteobacteria, Irr.

57 ession in the rhizobia and other taxa of the Alphaproteobacteria is fundamentally different from the

58 Unclassified Gammaproteobacteria and Alphaproteobacteria (Magnetovibrio) largely dominated th

59 arsR6 [nolR]), and in Brucella, as in other alphaproteobacteria, MucR binds to its own promoter to r

60 With an obligate intracellular lifestyle, Alphaproteobacteria of the order Rickettsiales have inex

61 SAR11 Alphaproteobacteria (order Pelagibacterales), the most a

62 These results also demonstrate that Alphaproteobacteria possess a diverse set of transport c

63 mparison with other sequenced members of the Alphaproteobacteria provides new data on the evolution o

64 EcfG, the general stress response factor of alphaproteobacteria, regulates expression of hpnP under

65 Alteromonadaceae and Oceanospirillaceae) and Alphaproteobacteria (Rhodobacteraceae and Hyphomonadacea

66 , Gammaproteobacteria (Piscirickettsiaceae), Alphaproteobacteria (Rhodobacteraceae), and Bacteroidete

67 Among Rickettsia species (Alphaproteobacteria: Rickettsiales), REIS has the larges

68 Within the Alphaproteobacteria, several species extrude thin cellul

69 the general stress response sigma factor in Alphaproteobacteria, sigma(EcfG), was identified.

70 Two related alphaproteobacteria, Sinorhizobium meliloti and Caulobac

71 al organization are co-conserved across many alphaproteobacteria species, but there are great differe

72 a coral microbiome with higher abundances of Alphaproteobacteria (such as Rhodobacterales and Sphingo

73 Recent analyses of marine Alphaproteobacteria suggest that some free-living bacter

74 Sinorhizobium meliloti is a member of the Alphaproteobacteria that fixes nitrogen when it is in a

75 a member of the marine Roseobacter clade of Alphaproteobacteria that forms symbioses with unicellula

76 ng process identified a set of proteins from Alphaproteobacteria that recognize various benzoate deri

77 vector of "Candidatus Liberibacter" species (Alphaproteobacteria) that cause huanglongbing (citrus gr

78 rospiraceae (Bacteroidetes) and Phaeobacter (Alphaproteobacteria) towards the end of the experiment.

79 to nine genera within eight families of the Alphaproteobacteria, two of the families being the newly

80 The Alphaproteobacteria uniquely integrate features of two-c

81 A species tree for 72 alphaproteobacteria was produced from a concatenation of

82 The general stress response (GSR) in Alphaproteobacteria was recently shown to be controlled

83 uggest that its essential functions in other alphaproteobacteria were acquired subsequently.

84 Most of the SAGs, apart from alphaproteobacteria, were phylogenetically distant from

85 and that are present in polarly flagellated alphaproteobacteria while being absent in alphaproteobac

86 ed alphaproteobacteria while being absent in alphaproteobacteria with other flagellation patterns.

87 11 are highly abundant, cosmopolitan aquatic Alphaproteobacteria with streamlined, A+T-biased genomes

88 dalis glossinidius, along with the parasitic Alphaproteobacteria Wolbachia.

89 us") diverged after the establishment of the Alphaproteobacteria yet before the betaproteobacteria/ga