Switch to
| Predicate | Object |
|---|---|
| rdf:type | |
| lifeskim:mentions | |
| pubmed:issue |
1
|
| pubmed:dateCreated |
1996-6-5
|
| pubmed:abstractText |
The C-terminal 268 residues of the spinach assimilatory NADH:nitrate reductase amino acid sequence that correspond to the flavin-containing domain of the enzyme have been selectively amplified and expressed as a recombinant protein in Escherichia coli. The recombinant protein, which was produced in both soluble and insoluble forms, was purified to homogeneity using a combination of ammonium sulfate precipitation, affinity chromatography on 5'-ADP-agarose and FPLC gel filtration. The purified domain exhibited a molecular weight of approximately 30 kDa, estimated by polyacrylamide gel electrophoresis, and a molecular mass of 30,169 for the apoprotein determined by mass spectrometry, which also confirmed the presence of FAD. The UV/visible spectrum was typical of a flavoprotein, with maxima at 272, 386, and 461 nm in the oxidized form while CD spectroscopy yielded both positive and negative maxima at 313 and 382 nm and 461 and 484 nm, respectively. The purified domain showed immunological cross-reactivity with anti-spinach nitrate reductase polyclonal antibodies while both N-terminal and internal amino acid sequencing of isolated peptides confirmed the fidelity of the domain's primary sequence. The protein retained NADH-ferricyanide reductase activity (Vmax=84 micromol NADH consumer/min/nmol FAD) with Km's of 17 and 34 microM for NADH and ferricyanide, respectively, with a pH optimum of approximately 6.5 A variety of NADH-analogs could also function as electron donors, though with decreased efficiency, the most effective being reduced nicotinamide hypoxanthine dinucleotide (V(max) = 35 micromol NHDH consumer/min/nmol FAD) and Km = 22 microM). NAD+ was demonstrated to be a competitive inhibitor (Ki = 1.9 mM) while analysis of inhibition by a variety of NAD+-analogs indicated the most efficient inhibitor to be ADP (Ki = 0.2 mM), with analogs devoid of either the phosphate, ribose, or adenine moieties proving to be markedly less-efficient inhibitors. The isolated domain was also capable of reducing cytochrome b5 directly (V(max) = 1.2 micromol NADH consumed/min/nmol FAD, Km (cyt. b5) = 6 microM), supporting the FAD -> b557 -> Mo electron transfer sequence in spinach nitrate reductase.
|
| pubmed:grant | |
| pubmed:language |
eng
|
| pubmed:journal | |
| pubmed:citationSubset |
IM
|
| pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/Cyanogen Bromide,
http://linkedlifedata.com/resource/pubmed/chemical/DNA Primers,
http://linkedlifedata.com/resource/pubmed/chemical/Flavin-Adenine Dinucleotide,
http://linkedlifedata.com/resource/pubmed/chemical/NAD,
http://linkedlifedata.com/resource/pubmed/chemical/NADH, NADPH Oxidoreductases,
http://linkedlifedata.com/resource/pubmed/chemical/Nitrate Reductase (NADH),
http://linkedlifedata.com/resource/pubmed/chemical/Nitrate Reductases,
http://linkedlifedata.com/resource/pubmed/chemical/Peptide Fragments,
http://linkedlifedata.com/resource/pubmed/chemical/Recombinant Proteins,
http://linkedlifedata.com/resource/pubmed/chemical/Serine Endopeptidases,
http://linkedlifedata.com/resource/pubmed/chemical/ferricyanide reductase,
http://linkedlifedata.com/resource/pubmed/chemical/glutamyl endopeptidase
|
| pubmed:status |
MEDLINE
|
| pubmed:month |
Mar
|
| pubmed:issn |
0003-9861
|
| pubmed:author | |
| pubmed:issnType |
Print
|
| pubmed:day |
1
|
| pubmed:volume |
327
|
| pubmed:owner |
NLM
|
| pubmed:authorsComplete |
Y
|
| pubmed:pagination |
151-60
|
| pubmed:dateRevised |
2007-11-14
|
| pubmed:meshHeading |
pubmed-meshheading:8615685-Amino Acid Sequence,
pubmed-meshheading:8615685-Base Sequence,
pubmed-meshheading:8615685-Binding Sites,
pubmed-meshheading:8615685-Chromatography, Affinity,
pubmed-meshheading:8615685-Chromatography, Gel,
pubmed-meshheading:8615685-Circular Dichroism,
pubmed-meshheading:8615685-Cloning, Molecular,
pubmed-meshheading:8615685-Cyanogen Bromide,
pubmed-meshheading:8615685-DNA Primers,
pubmed-meshheading:8615685-Escherichia coli,
pubmed-meshheading:8615685-Flavin-Adenine Dinucleotide,
pubmed-meshheading:8615685-Kinetics,
pubmed-meshheading:8615685-Molecular Sequence Data,
pubmed-meshheading:8615685-Molecular Weight,
pubmed-meshheading:8615685-Mutagenesis, Site-Directed,
pubmed-meshheading:8615685-NAD,
pubmed-meshheading:8615685-NADH, NADPH Oxidoreductases,
pubmed-meshheading:8615685-Nitrate Reductase (NADH),
pubmed-meshheading:8615685-Nitrate Reductases,
pubmed-meshheading:8615685-Peptide Fragments,
pubmed-meshheading:8615685-Plasmids,
pubmed-meshheading:8615685-Protein Conformation,
pubmed-meshheading:8615685-Recombinant Proteins,
pubmed-meshheading:8615685-Restriction Mapping,
pubmed-meshheading:8615685-Serine Endopeptidases,
pubmed-meshheading:8615685-Spectrophotometry,
pubmed-meshheading:8615685-Spinacia oleracea,
pubmed-meshheading:8615685-Substrate Specificity
|
| pubmed:year |
1996
|
| pubmed:articleTitle |
Spectroscopic and kinetic properties of a recombinant form of the flavin domain of spinach NADH: nitrate reductase.
|
| pubmed:affiliation |
Department of Biochemistry and Molecular Biology, University of South Florida College of Medicine, Tampa, USA.
|
| pubmed:publicationType |
Journal Article,
Research Support, U.S. Gov't, P.H.S.,
Research Support, U.S. Gov't, Non-P.H.S.
|