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1 ti-sigma factors that are found in alpha and gamma proteobacteria.
2 ell as several species belonging to beta and gamma Proteobacteria.
3 ally distinct genes in a set of 22 alpha and gamma proteobacteria.
4 onas species and in many polarly flagellated gamma proteobacteria.
5 lular eukaryotes, Bacillus subtilis, and the gamma proteobacteria.
6 many bacterial species but not in beta- and gamma-proteobacteria.
7 s that appear to have origins other than the gamma-Proteobacteria.
8 etected in all three OH-BDE-producing marine gamma-proteobacteria.
9 ously unreported ejection of polar motors by gamma-proteobacteria.
10 r QseC to promote intestinal colonization of gamma-Proteobacteria.
11 t delta(13)C taxa, with methane-metabolizing gamma-proteobacteria.
12 ative bacteria, NBs are found exclusively in gamma-proteobacteria.
13 atory system which is highly conserved among gamma-proteobacteria.
14 ns in 16S rRNA processing in both alpha- and gamma-proteobacteria.
15 (Dam) is widespread and conserved among the gamma-proteobacteria.
16 ciated DNA binding protein conserved in most gamma-proteobacteria.
17 a bacterial community dominated by beta- and gamma-Proteobacteria.
18 es is longer in alpha-proteobacteria than in gamma-proteobacteria.
19 alizing results from bacteriophage infecting gamma-Proteobacteria.
20 dependent growth inhibition (CDI) systems of gamma-proteobacteria.
21 somal fragments but have been limited to the gamma-proteobacteria.
22 of signals may be widespread among beta- and gamma-proteobacteria.
23 d condensation in Escherichia coli and other gamma-proteobacteria.
24 (GSH), the major competing cellular thiol in gamma-proteobacteria.
25 chromosomal segregation and condensation in gamma-proteobacteria.
26 a residue universally conserved in beta- and gamma-proteobacteria.
27 -dependent genes in alpha-proteobacteria and gamma-proteobacteria.
28 lams that form symbioses with chemosynthetic gamma-proteobacteria.
29 nt represents a new bacterial lineage in the gamma-Proteobacteria.
30 mplexes are phylogenetically conserved among gamma-proteobacteria.
31 en conserved across a broad set of beta- and gamma-Proteobacteria.
32 eudomonas species, although both species are gamma-proteobacteria.
33 tricted to a few groups within the beta- and gamma-Proteobacteria.
34 sting of up to 33 core genes in 16 beta- and gamma-Proteobacteria.
35 ne bacterial taxa, including both alpha- and gamma-proteobacteria.
36 ignificantly greater percentage of the class gamma-proteobacteria (0.07% vs 0.89% of total bacteria,
38 e (APR); in fungi and some cyanobacteria and gamma-proteobacteria, a second activation step, phosphor
39 either Porphyromonas gingivalis or ligature, gamma-proteobacteria accumulate and stimulate host immun
40 the Enterobacteriaceae or in species of the gamma-Proteobacteria agreed well with that of the corres
41 ositions in Hfq form signatures for the beta/gamma proteobacteria, alpha proteobacteria and low GC Gr
42 egulatory system is conserved throughout the gamma-proteobacteria and controls key pathways in centra
43 homologues are present in alpha-, beta-, and gamma-proteobacteria and multiple eukaryotes, including
45 (TF)-binding sites in the genomes of several gamma proteobacteria, and hence describing their transcr
46 ted by these MAGs (Actinomycetia, Alpha- and Gamma- Proteobacteria, and Bacteroidota) are active in t
48 anscription factor (TF) binding sites in the gamma-proteobacteria, and have evaluated the statistical
49 genomes of other P. putida strains, in other gamma-Proteobacteria, and in beta- and alpha-Proteobacte
50 ades, such as Actinobacteria, Firmicutes and gamma-Proteobacteria, and shed light on several open que
51 this isolate is the first to be reported for gamma-proteobacteria, and the first instance of a tRNA(L
52 e found only in the Gram-negative alpha- and gamma-proteobacteria, and thus other anaerobic bacteria
55 cific N2 fixation rates indicates that these gamma-proteobacteria are unlikely to be responsible for
56 acterial classes that are active in the gut (gamma-Proteobacteria, Bacilli and Actinobacteria), all o
57 ontrol samples with Alpha-proteobacteria and Gamma-proteobacteria being the predominant classes detec
61 active bacteria in the clouds belong to the gamma-Proteobacteria class, among which the Pseudomonas
62 ized with Citrobacter rodentium or the human gamma-Proteobacteria commensal Escherichia coli HS as a
63 d that the dominant alpha-proteobacteria and gamma-proteobacteria communities in bulk soil and root e
64 a poorly understood protein conserved across gamma-proteobacteria, contains a domain of unknown funct
66 gher phylotype abundances were observed from gamma-Proteobacteria, delta-Proteobacteria, Bacteroidete
67 rches have identified 176 representatives in gamma-Proteobacteria, delta-Proteobacteria, Clostridia,
68 HR, 2.63; 95% CI, 1.22-5.32; P = 0.015), and gamma-proteobacteria domination of fecal microbiota (HR,
69 .30; 95% CI, 1.42-31.80; P = 0.016), whereas gamma-proteobacteria domination predicted PCs postengraf
71 show that in contrast to other characterised Gamma-proteobacteria, E. coli Sxy is positively autoregu
74 w exceptions to this orthodoxy is a group of gamma-proteobacteria flourishing in obligate intracellul
77 nificant homology to Francisella tularensis (gamma-proteobacteria) have been characterized in several
78 and decreased level of Escherichia and other Gamma proteobacteria in children infected with HIV, amon
79 stinct from E. coli, OH-BDE-producing marine gamma-proteobacteria including Marinomonas mediterranea
80 he appearance of relic structures in diverse gamma-proteobacteria including Plesiomonas shigelloides,
81 in RNase E homologues in a subfamily of the gamma-proteobacteria, including enzymes from pathogens s
82 ding sites, but CsrA in bacteria outside the gamma-proteobacteria is antagonized by a protein called
84 ound primarily in Escherichia coli and other gamma proteobacteria, it does not appear to be part of a
86 nt heterotrophic marine bacteria, alpha- and gamma-Proteobacteria, might hydrolyze DOP outside the cy
89 we trace the evolution of the system through gamma-Proteobacteria, pinpointing key evolutionary event
90 hain flavodoxin family that is unique to the gamma-proteobacteria, possesses a 22-residue sequence th
92 their PBP-docking regions are restricted to gamma-proteobacteria, providing models for niche-specifi
93 ing sequence between E. coli and a series of gamma proteobacteria ranging from Salmonella to Vibrio.
95 including Actinobacteria, alpha-,beta-, and gamma-proteobacteria, revealing a common role of this Am
96 son of I. loihiensis to the genomes of other gamma-proteobacteria reveals abundance of amino acid tra
97 In E. coli, and probably many other related gamma-proteobacteria, RhlB associates with the essential
100 Homologs of FlgJ produced by the beta- and gamma-proteobacteria, such as Salmonella enterica, Vibri
101 oflexi, and classes Anaerolineae, Delta- and Gamma- Proteobacteria than the deeper sections, indicati
102 bdus and Photorhabdus spp. are gram negative gamma proteobacteria that form entomopathogenic symbiose
103 chemotaxis operons of many polar-flagellated gamma-proteobacteria that actively promote polar localiz
105 ocarbon plume stimulated deep-sea indigenous gamma-Proteobacteria that are closely related to known p
106 o the Vibrionaceae, a large family of marine gamma-proteobacteria that includes several dozen species
107 of species of non-pathogenic and pathogenic gamma-proteobacteria that infect different hosts, includ
108 ylotypes (one epsilon-proteobacteria and two gamma-proteobacteria) that formed specific associations
109 fic bacterial phylogenetic groups (primarily gamma-proteobacteria) that were rare in ambient waters,
111 cherichia coli and the majority of beta- and gamma-proteobacteria, the fourth step of lipid A biosynt
115 ia coli, Salmonella enterica, and many other gamma-proteobacteria, the transcription factor Crl posit
117 evolved to become hubs, within lineages like gamma-proteobacteria there is strong tendency to retain
120 en as an electron acceptor, thereby allowing gamma-proteobacteria to synthesize heme in both aerobic
121 y, diverse marine Actinobacteria, alpha- and gamma-proteobacteria were shown to initiate DMSP synthes
122 gs might have wide-spread relevance to other gamma-proteobacteria, which conserve both Cra and FruK.
123 s were identified in a variety of alpha- and gamma-proteobacteria, with a significant enrichment in t