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1 of nitrogenase Fe protein from R. rubrum or Azotobacter vinelandii.
2 eported for the closely related protein from Azotobacter vinelandii.
3 cofactor of the molybdenum nitrogenase from Azotobacter vinelandii.
4 MoFe protein) from a nifB-deletion mutant of Azotobacter vinelandii.
5 e bd quinol oxidases of Escherichia coli and Azotobacter vinelandii.
6 rome bd from its counterparts in E. coli and Azotobacter vinelandii.
7 nvestigated for alginic acid biosynthesis in Azotobacter vinelandii.
8 genes that are similar to the vnfEN genes of Azotobacter vinelandii.
9 response to oxygen in the model diazotroph, Azotobacter vinelandii.
10 on of a His-tagged NifEN-B fusion protein of Azotobacter vinelandii.
11 fixation in the model diazotrophic bacterium Azotobacter vinelandii.
12 NifB-co while bound to the NifX protein from Azotobacter vinelandii.
13 mologous to oxidases in Escherichia coli and Azotobacter vinelandii.
14 f rnf genes in the nitrogen-fixing bacterium Azotobacter vinelandii.
15 d the extracellular mannuronan epimerases of Azotobacter vinelandii.
16 eudomonas fluorescens, Pseudomonas putida or Azotobacter vinelandii.
18 he ferricyanide-oxidized [4Fe-4S] cluster in Azotobacter vinelandii 7Fe ferredoxin, the spectroscopic
19 ic ancestral nitrogenases into the genome of Azotobacter vinelandii, a genetically tractable, nitroge
20 lting from nifH and nifB deletion strains of Azotobacter vinelandii, a novel [Fe-S] cluster is identi
21 ification of the V nitrogenase proteins from Azotobacter vinelandii, an increase in resolution was ob
23 in vitro analysis of two CooA homologs from Azotobacter vinelandii and Carboxydothermus hydrogenofor
24 is presented that nitrogenases isolated from Azotobacter vinelandii and Clostridium pasteurianum can
25 , crystal structures of the Fe-proteins from Azotobacter vinelandii and Clostridium pasteurianum have
26 s-NifEN protein from a DeltanifHDK strain of Azotobacter vinelandii and have found that the amounts o
27 and Pseudomonas putidabut not as strictly in Azotobacter vinelandii and not at all in P. aeruginosa.
28 lity we analyzed the genome of the bacterium Azotobacter vinelandii and show that genes that code for
31 th ptsP orthologs of Pseudomonas aeruginosa, Azotobacter vinelandii, and Escherichia coli, with nearl
32 genes (aefA from Escherichia coli, pstP from Azotobacter vinelandii, and mtrR from Neisseria gonorrho
33 fferent diazotrophs (Sinorhizobium meliloti, Azotobacter vinelandii, and Rahnella aquatilis) cultured
34 ement with the measured value of -0.042 V in Azotobacter vinelandii; and (3) average Mossbauer isomer
35 of the catalytic MoFe protein component from Azotobacter vinelandii are prepared under turnover condi
39 udies on MoFeP from two different organisms, Azotobacter vinelandii ( Av) and Gluconacetobacter diazo
42 lysis of the two-component protein system of Azotobacter vinelandii (Av) nitrogenase is reported.
43 n this paper, we compare the interactions of Azotobacter vinelandii (Av) nitrogenase with two diazene
44 two phylogenetically distinct nitrogenases (Azotobacter vinelandii, Av, and Clostridium pasteurianum
47 nite-reduced (at pH 8.0) forms of the native Azotobacter vinelandii bacterioferritin to 2.7 and 2.0 A
49 transcription of nitrogen fixation genes in Azotobacter vinelandii by modulating the activity of the
50 em for the controlled expression of genes in Azotobacter vinelandii by using genomic fusions to the s
51 itrogen fixation by the free-living organism Azotobacter vinelandii can occur through the activity of
53 eMo-co synthesis system is not required when Azotobacter vinelandii cell-free extract is prepared in
57 on-sulfur cluster biosynthesis proteins from Azotobacter vinelandii, contains one [4Fe-4S](2+) cluste
59 xtracts from two different mutant strains of Azotobacter vinelandii defective in the biosynthesis of
63 of this complex generated with proteins from Azotobacter vinelandii (designated the L127Delta-Av2-Av1
64 An IscA homologue within the nif regulon of Azotobacter vinelandii, designated (Nif)IscA, was expres
65 e Anf3 from the model diazotrophic bacterium Azotobacter vinelandii Determining the Anf3 crystal stru
66 e structure of the catalytic domain from the Azotobacter vinelandii dihydrolipoamide acetyltransferas
68 rotein expressed by the nifH deletion strain Azotobacter vinelandii DJ1165 (Delta(nifH) MoFe protein)
70 the cytochrome bd terminating branch of the Azotobacter vinelandii electron transport chain, the pur
72 genome of the diazotrophic bacterial model, Azotobacter vinelandii, enabling an integrated assessmen
73 bacter sphaeroides has been purified from an Azotobacter vinelandii expression system; its interactio
76 ne of the Cys(39)-X-X-Cys(42)-X-X-Cys(45) of Azotobacter vinelandii FdI, which coordinates its [4Fe-4
78 ine (D39N) in the nucleotide binding site of Azotobacter vinelandii Fe protein by site-directed mutag
79 8 (located near the [4Fe-4S] cluster) of the Azotobacter vinelandii Fe protein were changed by means
81 e, it is shown that production of the intact Azotobacter vinelandii [Fe-S] cluster biosynthetic machi
82 ial (E(0)') of the [4Fe-4S](2+/+) cluster of Azotobacter vinelandii ferredoxin I (AvFdI) and related
83 in the [3Fe-4S]+/0 location of native (7Fe) Azotobacter vinelandii ferredoxin I (AvFdI) by providing
88 d a 3Fe to 4Fe cluster conversion variant of Azotobacter vinelandii ferredoxin I (FdI) in which the s
89 fication of site-directed mutant variants of Azotobacter vinelandii ferredoxin I (FdI), a pink protei
93 eport the structural characterization of the Azotobacter vinelandii FeSII-nitrogenase complex by cryo
94 A tungsten-tolerant mutant strain (CA6) of Azotobacter vinelandii first described in 1980 has been
95 ometry, and mutational studies of MoSto from Azotobacter vinelandii First, we show that molybdate, AT
98 ifH mutants in the nitrogen-fixing bacterium Azotobacter vinelandii for mutants that acquired NifM in
100 uctases and most similar to the structure of Azotobacter vinelandii FPR and Escherichia coli flavodox
101 have now shown that in Escherichia coli and Azotobacter vinelandii, GlnK binds to the membrane in an
102 3), was identified in ModE and homologs from Azotobacter vinelandii, Haemophilus influenzae, Rhodobac
103 mation of the Fe protein of nitrogenase from Azotobacter vinelandii has been examined in solution by
105 ructure of the nitrogenase MoFe-protein from Azotobacter vinelandii has been refined to 2.0 A resolut
107 ffects of flagella on deposition dynamics of Azotobacter vinelandii in porous media, independent of m
108 ructure of the nitrogenase iron protein from Azotobacter vinelandii in the all-ferrous [4Fe-4S](0) fo
109 oplasmic molybdate-binding protein ModG from Azotobacter vinelandii in two different crystal forms ha
110 n that an E146D site-directed variant of the Azotobacter vinelandii iron protein (Fe protein) is spec
113 d apodinitrogenase (apodinitrogenase 2) from Azotobacter vinelandii is an alpha2beta2delta2 hexamer.
115 -tune regulation of nitrogenase synthesis in Azotobacter vinelandii, is a potential target for PII-me
116 in the presence of a plasmid that harbors an Azotobacter vinelandii isc operon, which is involved in
119 we present kinetic parameters for an altered Azotobacter vinelandii MoFe protein for which the alphaG
120 EM and chemical analysis of two forms of the Azotobacter vinelandii MoFe-protein - a high pH turnover
121 cupying the S2B site of FeMo-cofactor in the Azotobacter vinelandii MoFe-protein, a position that was
124 ction was carried out with the extract of an Azotobacter vinelandii mutant lacking apodinitrogenase.
125 hown previously to accumulate on VnfX in the Azotobacter vinelandii mutant strain CA11.1 (DeltanifHDK
127 alibration error, single nitrogenase-isoform Azotobacter vinelandii mutants and environmental sample
131 he mechanism of [4Fe-4S] cluster assembly on Azotobacter vinelandii(Nif)IscA, and the ability of (Nif
132 ontaining NifDK protein upon coexpression of Azotobacter vinelandii nifD, nifK, nifH, nifM, and nifZ
137 percent) with Halobacterium salinarium Bat, Azotobacter vinelandii NIFL, Neurospora crassa White Col
140 ystem consisting of l-selenocysteine and the Azotobacter vinelandii NifS protein can replace selenide
142 ecursors and their transfer between purified Azotobacter vinelandii NifX and NifEN proteins was studi
143 se samples bound to the nitrogenase maturase Azotobacter vinelandii NifX reveals differences in the p
144 that the combination of the MoFe protein of Azotobacter vinelandii nitrogenase (Av1) with the Fe pro
147 the effects of MgATP or MgADP binding to the Azotobacter vinelandii nitrogenase Fe protein on the pro
148 dence for primary electron transfer from the Azotobacter vinelandii nitrogenase Fe protein to the MoF
149 present study, the crystal structure of the Azotobacter vinelandii nitrogenase Fe protein variant ha
153 iosynthesis of the FeMo cofactor (FeMoco) of Azotobacter vinelandii nitrogenase presumably starts wit
154 nt EPR signals, designated 1b and 1c, during Azotobacter vinelandii nitrogenase turnover at 23 degree
155 on the FeMo cofactor of the MoFe protein of Azotobacter vinelandii nitrogenase were probed using C(2
156 fully reduced cluster of the iron protein of Azotobacter vinelandii nitrogenase, including a common S
157 the [4Fe-4S](+) cluster in the Fe protein of Azotobacter vinelandii nitrogenase, which exists in two
161 he extracellular alginate epimerase AlgE4 of Azotobacter vinelandii provides a structural rationale f
162 h; (ii) enzymatic, in which NifS protein of Azotobacter vinelandii regenerated active Fe-SoxR in as
163 the MoFe protein isolated from the bacterium Azotobacter vinelandii resulted in an inactive, nondisso
164 resented 1.6 A X-ray structure of MoSto from Azotobacter vinelandii reveals various discrete polyoxom
165 more susceptible than nitrogen fixing (i.e., Azotobacter vinelandii, Rhizobium etli, and Azospirillum
166 strains that have a V-nitrogenase, including Azotobacter vinelandii, Rhodopseudomonas palustris, and
168 instead of alpha-195(His)) from a mutant of Azotobacter vinelandii show, contrary to an earlier repo
169 h were produced in certain mutant strains of Azotobacter vinelandii, showed that the N coordination t
170 (apodinitrogenase 2) has been purified from Azotobacter vinelandii strain CA117.30 (DeltanifKDB), an
174 studies of an N(2)-bound Mo-nitrogenase from Azotobacter vinelandii suggest binding of three N(2) spe
175 ifD product (with the exception of vnfE from Azotobacter vinelandii), suggesting that a gene duplicat
176 oped for the isolation of a mutant strain of Azotobacter vinelandii that exhibits in vivo nitrogenase
181 nt background of the nitrogen-fixing microbe Azotobacter vinelandii These included fully active MoFe
183 ture of the ubiquitous N(2) fixing bacterium Azotobacter vinelandii under Mo replete and Mo limiting
185 zation of the vanadium iron (VFe) protein of Azotobacter vinelandii V-nitrogenase has been focused on
187 nitrogenase (lacking the FeMo cofactor) from Azotobacter vinelandii was extracted from the alternativ
190 ification of a novel ferredoxin (FdIII) from Azotobacter vinelandii which brings to 12 the number of
191 onstrated using a monomeric form of IDH from Azotobacter vinelandii, which can be shown to gain the s
192 s of a two-component nitrogenase analog from Azotobacter vinelandii, which consists of the reductase
194 vestigate mRNA produced by mutant strains of Azotobacter vinelandii with defined deletions in the nif
195 aturation proteins NifU, NifS, and FdxN from Azotobacter vinelandii with NifB from the archaea Methan
196 ucible cluster from Pseudomonas stutzeri and Azotobacter vinelandii yields ammonium tolerance and hig