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1 tal gene transfer of thymidine kinase from a proteobacterium.
2 (HOT2C01) originated from a planktonic alpha-proteobacterium.
3 nsfer and are probably derived from an alpha-proteobacterium.
4 arboxysome genetic components derived from a proteobacterium.
5 les and Candidatus Stammera capleta, a gamma-proteobacterium.
6 s-related genes from an ancient phototrophic proteobacterium.
7 en an ancestral eukaryotic cell and an alpha-proteobacterium.
8 al role as C and energy storage in this beta-proteobacterium.
9 orhizobium meliloti, a nitrogen-fixing alpha-proteobacterium.
10  crescentus, a monopolarly flagellated alpha-proteobacterium.
11             It appears to be a typical gamma proteobacterium.
12 ity is from an uncultured, unsequenced gamma-proteobacterium.
13 autotrophic, sulfur-compound-oxidizing, beta-proteobacterium.
14 dobacter sphaeroides, a photosynthetic alpha-proteobacterium, a transcriptional response to the react
15 the crystal structure of DddY from the gamma-proteobacterium Acinetobacter bereziniae originally isol
16                                    The delta-proteobacterium Actinobacillus pleuropneumoniae encodes
17 grown Sterolibacterium denitrificans, a beta-proteobacterium, adopts an oxygenase-independent pathway
18                                    The alpha-Proteobacterium Agrobacterium tumefaciens has proteins h
19 c PG synthesis is conserved in another alpha-proteobacterium, Agrobacterium tumefaciens.
20 coded in the genome of an uncultivated gamma-proteobacterium and shared highest amino acid sequence s
21 tid (a cyanobacterium), the mitochondrion (a proteobacterium), and its host (an archaeon)--and carrie
22                           We used this alpha proteobacterium as a model to investigate the global org
23 ter asiaticus" (CLas), an unculturable alpha-proteobacterium associated with citrus Huanglongbing (HL
24  degradation of 3-methylbenzoate in the beta-proteobacterium Azoarcus sp. CIB.
25 d two-component system (HTCS), from the beta-proteobacterium Azoarcus sp. strain CIB that degrades c-
26 he expression of the box cluster in the beta-proteobacterium Azoarcus sp., their cognate transcriptio
27  has previously been reported that the alpha-proteobacterium Azospirillum brasilense undergoes methyl
28  proceed through this mechanism in the alpha-proteobacterium Azospirillum brasilense.
29 isease is caused by infection with the alpha-proteobacterium Bartonella bacilliformis.
30 and nitrogen-fixing life styles of the alpha-proteobacterium Bradyrhizobium japonicum.
31 itional symbiotic association with the gamma-proteobacterium Buchnera aphidicola.
32  microsporus (Rm, Mucoromycotina) and a beta-proteobacterium Burkholderia, which controls host asexua
33            Fusion proteins from marine alpha-proteobacterium Candidatus Pelagibacter ubique, actinoba
34 e Lissoclinum patella with a symbiotic alpha-proteobacterium, Candidatus Endolissoclinum faulkneri, a
35 larization module from the free living alpha-proteobacterium Caulobacter crescentus and an orthologou
36 d daughter cells produced by the model alpha-proteobacterium Caulobacter crescentus can have differen
37 ria and we found that sigma32 from the alpha-proteobacterium Caulobacter crescentus does not need the
38 g one-piece tmRNAs have been lost, the alpha-proteobacterium Caulobacter crescentus produces a functi
39                                    The alpha-proteobacterium Caulobacter crescentus produces a motile
40          Here, we demonstrate that the alpha-proteobacterium Caulobacter crescentus produces bona fid
41 typical two-protein bacteriocin in the alpha-proteobacterium Caulobacter crescentus that is retained
42 the RNA chaperone protein Hfq from the alpha-proteobacterium Caulobacter crescentus to 2.15- angstrom
43 he G(1)->S transition in the polarized alpha-proteobacterium Caulobacter crescentus, a model for cell
44                                 In the alpha-proteobacterium Caulobacter crescentus, cell cycle-regul
45                                 In the alpha-proteobacterium Caulobacter crescentus, regulated protei
46 f an RNA degradosome assembly from the alpha-proteobacterium Caulobacter crescentus, which is a model
47 ome assembly has been described in the alpha-proteobacterium Caulobacter crescentus, with the interac
48 s from a variety of lethal assaults in the a-proteobacterium Caulobacter crescentus.
49 unctions of three hipBA modules in the alpha-proteobacterium Caulobacter crescentus.
50                  The chromosome of the alpha-proteobacterium, Caulobacter crescentus, encodes eight P
51                         Strain CJ2 is a beta proteobacterium closely related to Polaromonas vacuolata
52            Wolbachia, an endosymbiotic alpha-proteobacterium commonly found in insects, can inhibit t
53  species Chloroherpeton thalassium, and beta-proteobacterium D. acidovorans each produce a different
54 amine putrescine by fusion enzymes from beta-proteobacterium Delftia acidovorans and delta-proteobact
55 ng genome fragment from a Monterey Bay gamma-proteobacterium (EBAC31A08).
56                                 In the gamma-proteobacterium Erwinia carotovora, genes common to phos
57 enchmark datasets for the well-studied gamma-proteobacterium Escherichia coli showed that it outperfo
58 We engineered an obligate NQ-dependent gamma-proteobacterium, Escherichia coli DeltaubiC, and perform
59                                    The gamma-proteobacterium Francisella tularensis is one of the mos
60                                          The proteobacterium Frischella perrara is a widely distribut
61 2 plasmid is distinct from that of the alpha proteobacterium genomic replicon origins but is conserve
62  microbial community, dominated by the gamma-proteobacterium Halomonas sulfidaeris, was detected in s
63     Here we examine the extremely halophilic Proteobacterium Halorhodospira halophila and report that
64 essential and CCM-related genes in the gamma-proteobacterium Halothiobacillus neapolitanus.
65 mplete genome sequence of the deep-sea gamma-proteobacterium, Idiomarina loihiensis, isolated recentl
66 ls with dissolved organic matter and a gamma-proteobacterium in seawater increases Transparent Exopol
67 lbachia, a gram-negative [Formula: see text]-proteobacterium, is an endosymbiont found in some arthro
68 ter crescentus, a Gram-negative alpha-purple proteobacterium, is an oligotroph that lives in aquatic
69 er asiaticus" (CLas), a non-culturable alpha-proteobacterium, is associated with citrus Huanglongbing
70              Pseudomonas aeruginosa, a gamma-proteobacterium, is motile by means of a single polar fl
71 ular, tick-transmitted, gram-negative, alpha-proteobacterium, is the primary etiologic agent of globa
72       Colwellia psychrerythraea 34H, a gamma-proteobacterium isolated from subzero Arctic marine sedi
73 ve agent of Legionnaires' disease, the gamma-proteobacterium Legionella pneumophila, resides and repl
74 omes evolved from the chromosome of an alpha-proteobacterium-like ancestor and developed during evolu
75 component heterodimer protein from the alpha-proteobacterium Methylobacterium (Methylorubrum) extorqu
76                           The methylotrophic proteobacterium Methylobacterium extorquens AM1 possesse
77 one-carbon (C1) compounds, the aerobic alpha-proteobacterium Methylobacterium extorquens AM1 synthesi
78 or a sterol biosynthetic pathway were in the proteobacterium, Methylococcus capsulatus, in which ster
79 glutamate pathway in the methylotrophic beta-proteobacterium Methyloversatilis universalis FAM5.
80 ith an unusual nested arrangement: the gamma-proteobacterium Moranella endobia lives in the cytoplasm
81                                    The delta-proteobacterium Myxococcus xanthus coordinates its motil
82 ein, we demonstrate that in the social delta-proteobacterium Myxococcus xanthus, the secretion of a n
83                                 In the delta-proteobacterium Myxococcus xanthus, TsaP is also importa
84 ant phenotype and gene function in the delta proteobacterium Myxococcus xanthus.
85                                  In the beta-proteobacterium Neisseria gonorrhoeae, the native PilQ s
86 ase in tested actinobacteria and in the beta-proteobacterium Nitrosomonas europaea.
87 rome c oxidase of Rhodobacter sphaeroides, a proteobacterium of the alpha subgroup, is structurally s
88 ment derived from an uncultured marine gamma-proteobacterium of the SAR86 group.
89         The eubacterial organism is either a proteobacterium, or a member of a larger photosynthetic
90           Here, we develop and present the a-proteobacterium Paracoccus denitrificans as a suitable b
91 lution structure of complex I from the alpha-proteobacterium Paracoccus denitrificans, a close relati
92 re of the intact ATP synthase from the alpha-proteobacterium Paracoccus denitrificans, inhibited by i
93 ng Gram-negative bacteria, mostly within the Proteobacterium Phylum.
94 ulates key iron metabolism genes in an alpha-proteobacterium, pointing to a departure from the canoni
95         An ancient endosymbiosis of an alpha-proteobacterium produced a diverse range of organelles i
96 n, C(17) H(28) ) was elucidated in the gamma-proteobacterium Pseudomonas chlororaphis O6.
97 s in their respiratory chains, and the gamma-proteobacterium Pseudomonas stutzeri.
98 with histidine kinase (HK) activity from the proteobacterium Pseudomonas syringae, which were built f
99 ing soluble hydrogenase (SH) of aerobic beta-proteobacterium Ralstonia eutropha strain H16 to accompl
100 cleotidyltransferase, acquired from an alpha-proteobacterium, replaced the ancestral enzyme in Metazo
101 equence of Geobacter sulfurreducens, a delta-proteobacterium, reveals unsuspected capabilities, inclu
102  show that the red-type RbcL subunits in the proteobacterium Rhodobacter sphaeroides also fold with G
103  build a large-scale TRN model for the alpha-Proteobacterium Rhodobacter sphaeroides that comprises 1
104 he strategy used by the photosynthetic alpha-proteobacterium Rhodobacter sphaeroides to procure the c
105            In the facultatively phototrophic proteobacterium Rhodobacter sphaeroides, formation of th
106 NA synthesis in the photoheterotrophic alpha-proteobacterium Rhodobacter sphaeroides, we identified a
107 Surf1p is encoded by the genome of the alpha-proteobacterium Rhodobacter sphaeroides, which synthesiz
108  second RpoH homolog, RpoH(II), in the alpha-proteobacterium Rhodobacter sphaeroides.
109 requirements for photosynthesis in the alpha-proteobacterium Rhodobacter sphaeroides.
110 on pathway much like that found in the alpha-proteobacterium Rhodobacter sphaeroides.
111 .6-Mb genome of the facultative phototrophic proteobacterium, Rhodobacter sphaeroides 2.4.1, was cust
112                                    The alpha-proteobacterium Rhodopseudomonas palustris has three ann
113 tive (photoferrotrophic) growth by the alpha-proteobacterium Rhodopseudomonas palustris TIE-1.
114           In the purple photosynthetic alpha-proteobacterium Rhodopseudomonas palustris, two protein
115  for the growth of the closely related alpha-proteobacterium, Rhodopseudomonas palustris, revealed a
116                Here we report that the alpha-proteobacterium Rhodospirillum centenum secretes cGMP wh
117 tion of carbon monoxide dehydrogenase in the proteobacterium Rhodospirillum rubrum requires three acc
118 e tick-borne infection produced by the alpha-proteobacterium, Rickettsia conorii.
119 at a partner-switching system of the aquatic Proteobacterium Shewanella oneidensis regulates post-tra
120                                    The gamma-proteobacterium Shewanella oneidensis strain MR-1 is a m
121 ess gene function in the Gram negative gamma-proteobacterium Shewanella oneidensis strain MR-1.
122 oarray experiments were performed in a gamma-proteobacterium Shewanella oneidensis.
123                      The soil-dwelling alpha-proteobacterium Sinorhizobium meliloti engages in a symb
124                                    The alpha-proteobacterium Sinorhizobium meliloti establishes a chr
125      However, here we show that in the alpha-proteobacterium Sinorhizobium meliloti expression of the
126 anaerobic cholesterol metabolism in the beta-proteobacterium Sterolibacterium denitrificans is cataly
127 rse organisms, including a plant and a gamma-proteobacterium, suggest an ancient origin for this regu
128 PDH gene by lateral transfer from an epsilon-proteobacterium, suggesting that the parasite enzyme mig
129 roteobacterium Delftia acidovorans and delta-proteobacterium Syntrophus aciditrophicus, in a Deltaspe
130 eptides first reported from the marine alpha-proteobacterium Thalassospira sp. CNJ-328.
131  Sphingopyxis granuli strain TFA is an alpha-proteobacterium that belongs to the sphingomonads, a gro
132  biovar viciae strain 3841 is a motile alpha-proteobacterium that can establish a nitrogen-fixing sym
133 lella fastidiosa (Xf), a xylem-limited gamma-proteobacterium that is responsible for several economic
134 knowledge, the first free-living alpha-class proteobacterium to be sequenced and will serve as a foun
135 a endobia lives in the cytoplasm of the beta-proteobacterium Tremblaya princeps These two bacteria, a
136  additional metabolic features of this alpha-proteobacterium using metabolic modelling and the functi
137 thetic pathway was characterized in the beta-proteobacterium Variovorax boronicumulans PHE5-4, demons
138 genomic sequence of the gram negative, gamma-Proteobacterium Vibrio cholerae El Tor N16961 to be 4,03
139 h are produced by a nearshore isolate, gamma Proteobacterium, Vibrio sp. R-10.
140 Wolbachia is an obligate intracellular alpha-proteobacterium, which commonly infects arthropods and f
141 lobacter crescentus is an oligotrophic alpha-proteobacterium with a complex cell cycle involving sess
142  strain Walvis Bay is a Hg-methylating delta-proteobacterium with a sequenced genome and has unusual
143 ibly an ancestor of the cyanobacterium and a proteobacterium, with an archaeal eocyte (crenarchaea),
144               The maternally inherited alpha-proteobacterium Wolbachia has been proposed as a tool to
145                                    The alpha-proteobacterium Wolbachia is probably the most prevalent
146 terial blight of rice is caused by the gamma-proteobacterium Xanthomonas oryzae pv. oryzae, which uti

 
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