戻る
「早戻しボタン」を押すと検索画面に戻ります。 [閉じる]

コーパス検索結果 (left1)

通し番号をクリックするとPubMedの該当ページを表示します
1                                              A. vinelandii also encodes a protein designated NfuA, wh
2                                              A. vinelandii dsbA mutant strains were impossible to cha
3                        NifX purified from an A. vinelandii nifB strain showed a different electrophor
4  Here, we report a systematic analysis of an A. vinelandii UW97 mutant and show that, unlike A. vinel
5                         Here we show that an A. vinelandii strain expressing the V-nitrogenase is cap
6                       This contrasts with an A. vinelandii strain described previously which is unabl
7 rity of the vnfEN genes of A. variabilis and A. vinelandii was not strong.
8 ype Fe protein to the crude extracts made by A. vinelandii UW97.
9 olic regulon, was replaced by the contiguous A. vinelandii iscS, iscU, iscA, hscB, hscA, fdx, and isc
10 on required crude extract of the DeltanifHDK A. vinelandii strain CA12, Fe protein and MgATP.
11       We also find that the newly discovered A. vinelandii siderophore vibrioferrin is almost complet
12  non-polar insertion mutations within either A. vinelandii iscS or hscA revealed that such mutations
13 nhibition, which is also exhibited by extant A. vinelandii nitrogenase isozymes.
14                           In addition to Fe, A. vinelandii siderophores are used for the acquisition
15 tudy of siderophore production in N2 -fixing A. vinelandii under a variety of trace metal conditions.
16 e its electron-flux inhibition with all four A. vinelandii nitrogenases, supporting the suggestion th
17 n transfer, to a similar extent for all four A. vinelandii nitrogenases.
18 alysis of the purified apodinitrogenase from A. vinelandii DJ54.
19 tion of a fully active species of FeVco from A. vinelandii.
20 cy results from reduction of Fe protein from A. vinelandii (Av2) to the all-ferrous oxidation state (
21 geneous, His-tagged form of VFe protein from A. vinelandii.
22 on of His-tagged MoFe proteins purified from A. vinelandii nifZ and nifZ/nifB deletion strains DJ1182
23 mutant forms of dinitrogenase reductase from A. vinelandii that are affected in various protein activ
24 ature of the iscSUA gene cluster region from A. vinelandii is that E. coli genes previously designate
25                                           In A. vinelandii, NifQ was preferentially metalated by NifU
26                   Molybdenum biochemistry in A. vinelandii reveals unexpected mechanisms and a new ro
27  IscS, IscU, HscBA, and Fdx are essential in A. vinelandii and that their depletion results in a defi
28                  Here, BchL was expressed in A. vinelandii and purified to homogeneity using an engin
29  sulfur for iron-sulfur cluster formation in A. vinelandii is supported by the presence of a cysE-lik
30 in encoded by nifD-K translational fusion in A. vinelandii is a large protein (as determined by Weste
31 hat glnK, like glnA, is an essential gene in A. vinelandii.
32  a general purpose monothiol glutaredoxin in A. vinelandii, was monitored by circular dichroism spect
33 pparent co-expression of iscSUA and hscBA in A. vinelandii indicate that the proposed chaperone funct
34 existence of a redox regulatory mechanism in A. vinelandii that controls the rate of expression and m
35 e stress or modification of Fe metabolism in A. vinelandii.
36 ployed to confirm that the Nif- phenotype in A. vinelandii UW97 is exclusively due to the substitutio
37 at there is a putative regulatory protein in A. vinelandii that binds specifically upstream of the -3
38       The presence of a V storage protein in A. vinelandii was also investigated.
39 -dependent regulation and gene redundancy in A. vinelandii, it has been difficult to determine the pr
40      Here, the roles of GlnK and GlnK-UMP in A. vinelandii were studied to determine whether the Nif
41  of nitrogenase genes (nif, anf, and vnf) in A. vinelandii, and one ammonia monooxygenase gene (amoA)
42 r new prospects for the wider application of A. vinelandii as a host for the production and character
43 ne contained within the major nif cluster of A. vinelandii previously designated orf6.
44  also located within the nif gene cluster of A. vinelandii.
45 These results might suggest that extracts of A. vinelandii contain a physiological source of reductan
46 lementation of these assays with extracts of A. vinelandii DJ42.48 (DeltanifENX DeltavnfE) results in
47  species of VNFG are observed in extracts of A. vinelandii strains that accumulate dinitrogenase 2, w
48 or intact cluster transfer to an apo form of A. vinelandii aconitase A, a member of the monomeric deh
49 own that the [4Fe-4S] cluster-loaded form of A. vinelandii IscU, but not the [2Fe-2S] cluster-loaded
50  The redox and nitrogen-sensing functions of A. vinelandii NIFL are therefore separable and are discr
51  unlike A. vinelandii DJ54, the nifH gene of A. vinelandii UW97 has no deletion in either coding sequ
52                            Purified GroEL of A. vinelandii alone or in combination with MgATP and Fe
53 ave no effects on the diazotrophic growth of A. vinelandii while WO(3) NPs are highly detrimental to
54  L clusters to the biosynthetic machinery of A. vinelandii for further maturation into the M clusters
55 elective pressure against the maintenance of A. vinelandii iscS or hscA knock-out mutations and sugge
56 erefore, it seems that the Nif- phenotype of A. vinelandii UW97 is caused by a general structural dis
57 tation responsible for the Nif- phenotype of A. vinelandii UW97 is the substitution of a non-conserve
58  alanine did not affect the Nif phenotype of A. vinelandii.
59       Genome-wide transcription profiling of A. vinelandii cultured under nitrogen-fixing conditions
60               Therefore, the in vivo role of A. vinelandii DsbA is unknown, but it may function to fo
61 re we report the complete genome sequence of A. vinelandii DJ, which has a single circular genome of
62 aining extracts from a DeltanifHDK strain of A. vinelandii CA12 along with FeMoco, Fe protein, and Mg
63 ntroduced into wild type and FdI- strains of A. vinelandii.
64  in both wild-type and delta nifW strains of A. vinelandii.
65 d DNA sequence analysis of a 7,886-base pair A. vinelandii genomic segment that includes the iscS gen
66 with exquisitely oxygen-sensitive processes, A. vinelandii is specialized in terms of its complement
67 rologous Clostridium pasteurianum Fe protein-A. vinelandii MoFe protein complex.
68                                        Since A. vinelandii DJ54 is a delta nifH strain, this strain i
69 E2oCD 24mer in comparison to the less stable A. vinelandii E2pCD 24mer.
70                                 We show that A. vinelandii has two clusters of rnf-like genes: rnf1,
71 eam of Escherichia coli fpr, suggesting that A. vinelandii may have a SoxS-like regulatory system and
72                                          The A. vinelandii dsbA gene was expressed in Escherichia col
73                                          The A. vinelandii DsbA protein contains the well-conserved m
74 ans nifB, nifS, and nifU genes alongside the A. vinelandii fdxN gene, in E. coli.
75               As described initially for the A. vinelandii Fe-protein in a different crystal form at
76 on of reductant is required, however, if the A. vinelandii cell-free extract is chemically oxidized p
77 gene, herein designated fdxD, that is in the A. vinelandii iscSUA operon that encodes proteins involv
78 rrangement observed in the structures of the A. vinelandii and C. pasteurianum Fe-proteins indicate t
79 eporter gene was placed under control of the A. vinelandii fpr promoter and introduced into wild type
80                            Inspection of the A. vinelandii genome indicates that such recruitment of
81  was used for the functional analysis of the A. vinelandii isc genes, whose products are involved in
82    Here, we report the identification of the A. vinelandii protein that binds specifically to the par
83 dients during turnover demonstrates that the A. vinelandii cytochrome bd oxidase is coupled to energy
84 to the vnfDK genes just upstream than to the A. vinelandii vnfEN genes.
85 sults show that the toxicity of WO(3) NPs to A. vinelandii is due to an interference with the catecho
86 350 times tighter than that of the wild-type A. vinelandii nitrogenase complex and at least 20 times
87 ructure of the complex between the wild-type A. vinelandii nitrogenase proteins stabilized with ADP.A
88 vinelandii UW97 mutant and show that, unlike A. vinelandii DJ54, the nifH gene of A. vinelandii UW97
89 e relative levels of FdIV and FdI in various A. vinelandii strains leading to the conclusion that FdI
90 coexpressing M. thermautotrophicus NifB with A. vinelandii NifU, NifS, and FdxN, and engineered yeast