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1 aceae (Acidobacteria) and Xanthobacteraceae (Alphaproteobacteria).
2 seobacter clade within the Rhodobacteraceae (Alphaproteobacteria).
3 in magnetic and nonmagnetic spirilla-shaped Alphaproteobacteria.
4 ation and rearrangements in the Epsilon- and Alphaproteobacteria.
5 ique component of the lipopolysaccharides of alphaproteobacteria.
6 ces was found to covary with tRNA(His) among alphaproteobacteria.
7 cteria, Verrucomicrobia, Planctomycetes, and Alphaproteobacteria.
8 ddition to the well-known endosymbiosis with alphaproteobacteria.
9 phy is likely to occur within members of the Alphaproteobacteria.
10 component system is conserved among multiple Alphaproteobacteria.
11 ression led to enlarged ICMs in both studied alphaproteobacteria.
12 chanistically studied in only two species of Alphaproteobacteria.
13 nd novel environmental diversity, within the Alphaproteobacteria.
14 roposal for the higher-level taxonomy of the Alphaproteobacteria.
15 adaptation and host-microbe interactions in Alphaproteobacteria.
16 orter for bacterial DMSP synthesis in marine Alphaproteobacteria.
17 to be involved in formaldehyde oxidation in Alphaproteobacteria.
18 y that mitochondria originated once from the Alphaproteobacteria.
19 M, a DNA methyltransferase conserved in most Alphaproteobacteria.
20 C. crescentus and, presumably, of many other Alphaproteobacteria.
21 hat this notion might also be true for other Alphaproteobacteria.
22 ECF15 family of sigma factors found only in alphaproteobacteria.
23 regulators of the general stress response in alphaproteobacteria.
24 ed aerobic species affiliated with the class Alphaproteobacteria.
25 e-target) VPEID-CTERM/exosortase E system in alphaproteobacteria.
26 the major iron-responsive regulators in the alphaproteobacteria.
27 lobally significant Roseobacter clade of the Alphaproteobacteria.
28 percent sequence identity to Rsh proteins of alphaproteobacteria.
30 eptidoglycan chemical diversity in the Class Alphaproteobacteria, a group of Gram negative bacteria t
31 ydrocarbon degradation (Gammaproteobacteria, Alphaproteobacteria, Actinobacteria) developed in the SO
32 enriched in the hyphosphere and dominated by Alphaproteobacteria, Actinobacteria, and Gammaproteobact
33 m smegmatis and Corynebacterium glutamicum), Alphaproteobacteria (Agrobacterium tumefaciens and Caulo
34 in C. crescentus, the essential genes of two Alphaproteobacteria, Agrobacterium tumefaciens (Rhizobia
37 species restricted to a dozen genera of the Alphaproteobacteria and Betaproteobacteria, suggesting i
39 t the microbial communities are dominated by Alphaproteobacteria and Gammaproteobacteria using the Ca
40 predominant indoors, whereas Actinobacteria, Alphaproteobacteria and Gammaproteobacteria were the mos
42 mic units belonging to the Ruegeria genus of Alphaproteobacteria and NS9 marine group of Flavobacteri
43 The core symbiotic community was composed of Alphaproteobacteria and Opitutae (a class of Verrucomicr
45 d independently in at least four lineages of Alphaproteobacteria and that all methylotrophy modules s
46 stabactin is widespread among methanotrophic alphaproteobacteria and that it can be used by another m
47 waters were dominated by the SAR11 clade of Alphaproteobacteria and the cyanobacterium Synechococcus
50 s from the prolific Roseobacter clade in the Alphaproteobacteria are beginning to reveal the genetic
51 ing of many plasmids and some chromosomes of alphaproteobacteria are directed by their repABC operons
53 ria of the genus Bartonella, a member of the Alphaproteobacteria, are fastidious, gram-negative, aero
54 tous clade of very small and highly abundant Alphaproteobacteria, are known to devote much of their e
55 ers of the marine Roseobacter clade (MRC) of Alphaproteobacteria as the likely metabolizers of TMA an
56 er sp. TM1040 uses components found in other Alphaproteobacteria, as well as novel molecular mechanis
57 earchers to compare the GSR across different Alphaproteobacteria, as well as study the interplay betw
58 to contain a diverse assemblage of bacteria (Alphaproteobacteria, Betaproteobacteria and Gammaproteob
59 oth methylotrophs and non-methylotrophs from Alphaproteobacteria, Betaproteobacteria and Gammaproteob
60 cterial classes, including Verrucomicrobiae, Alphaproteobacteria, Betaproteobacteria, and Gammaproteo
61 ccurring in many, but not all, genera in the Alphaproteobacteria, Betaproteobacteria, Gammaproteobact
62 ntus cell cycle genes are conserved in other Alphaproteobacteria, but it is not clear to what extent
64 obacter group, an abundant lineage of marine Alphaproteobacteria, can constitute large proportions of
65 ost other members of the SAR 11 clade of the Alphaproteobacteria, can evade filtration by slipping th
72 rial envelopes, has been conserved in modern alphaproteobacteria despite more than a billion years of
73 th mats were dominated by Chloroflexi, while Alphaproteobacteria dominated the lower layers of pustul
75 ies Erythrobacteraceae and Rhodobacteraceae (Alphaproteobacteria), Flavobacteriaceae (Bacteriodetes),
76 p II and III archaea and organoheterotrophic Alphaproteobacteria, Flavobacteriia and Planctomycetacia
77 a relationships ruled by Dothideomycetes and Alphaproteobacteria further suggest tight host-microbe i
78 oducing isolates contained dsyB(8), but some alphaproteobacteria, gammaproteobacteria and actinobacte
79 ghest expression of solute transporters were Alphaproteobacteria, Gammaproteobacteria, and Deltaprote
81 mic Bartonella spp., tested using Bartonella Alphaproteobacteria growth medium (BAPGM), were retrospe
84 the endemic Mexican Mimosa species favoured alphaproteobacteria in the genera Rhizobium and Ensifer:
86 enetic studies comparing CtrA sequences from alphaproteobacteria in which the role of CtrA has been e
87 regulatory network, conserved throughout the Alphaproteobacteria, in the magnetotactic bacterium Magn
88 re we announce the genome sequences of eight alphaproteobacteria, including the first genome sequence
91 ying how stalk morphogenesis in a species of Alphaproteobacteria is controlled unveils an interesting
92 formation and surface attachment in multiple Alphaproteobacteria is driven by unipolar polysaccharide
93 ession in the rhizobia and other taxa of the Alphaproteobacteria is fundamentally different from the
94 is indicated that the dddU gene, mainly from Alphaproteobacteria, is widely distributed in the Atlant
95 of hopanoid C-2 methyltransferase (HpnP) in Alphaproteobacteria led to the downfall of this molecula
97 arsR6 [nolR]), and in Brucella, as in other alphaproteobacteria, MucR binds to its own promoter to r
99 With an obligate intracellular lifestyle, Alphaproteobacteria of the order Rickettsiales have inex
101 of cyanobacteria, while the gene appeared in Alphaproteobacteria only around 750 million years ago (M
102 stral contributions from Asgardarchaeota and Alphaproteobacteria operating predominantly in glycolysi
104 P lyase was prevalent in several lineages of Alphaproteobacteria (Pelagibacter, SAR116, Roseobacter a
106 mparison with other sequenced members of the Alphaproteobacteria provides new data on the evolution o
107 EcfG, the general stress response factor of alphaproteobacteria, regulates expression of hpnP under
108 gene Orf52, in two distantly related purple alphaproteobacteria, Rhodobacter sphaeroides and Rhodops
109 Alteromonadaceae and Oceanospirillaceae) and Alphaproteobacteria (Rhodobacteraceae and Hyphomonadacea
110 , Gammaproteobacteria (Piscirickettsiaceae), Alphaproteobacteria (Rhodobacteraceae), and Bacteroidete
112 Further taxonomic assignment of unclassified Alphaproteobacteria sequencing reads allowed for detecti
117 al organization are co-conserved across many alphaproteobacteria species, but there are great differe
118 oteobacteria populations, while copiotrophic Alphaproteobacteria such as the Roseobacter clade, with
119 a coral microbiome with higher abundances of Alphaproteobacteria (such as Rhodobacterales and Sphingo
123 nd 600 Ma probably reflects the expansion of Alphaproteobacteria that coincided with the rise of euka
124 Sinorhizobium meliloti is a member of the Alphaproteobacteria that fixes nitrogen when it is in a
125 a member of the marine Roseobacter clade of Alphaproteobacteria that forms symbioses with unicellula
126 duced by Wolbachia, obligately intracellular alphaproteobacteria that infect approximately half of al
127 ctural basis for complex network assembly in Alphaproteobacteria that is analogous to those formed by
128 ng process identified a set of proteins from Alphaproteobacteria that recognize various benzoate deri
129 vector of "Candidatus Liberibacter" species (Alphaproteobacteria) that cause huanglongbing (citrus gr
131 tructurally conserved in many members of the Alphaproteobacteria, the VtlR/LsrB regulatory circuitry
133 rospiraceae (Bacteroidetes) and Phaeobacter (Alphaproteobacteria) towards the end of the experiment.
134 to nine genera within eight families of the Alphaproteobacteria, two of the families being the newly
141 of ADP-PFK-As in cyanobacteria and in a few alphaproteobacteria, which was confirmed in enzymatic st
142 and that are present in polarly flagellated alphaproteobacteria while being absent in alphaproteobac
143 ed alphaproteobacteria while being absent in alphaproteobacteria with other flagellation patterns.
144 11 are highly abundant, cosmopolitan aquatic Alphaproteobacteria with streamlined, A+T-biased genomes
146 us") diverged after the establishment of the Alphaproteobacteria yet before the betaproteobacteria/ga