Evidence map›Paper›PMID 27055058›Full record

ArticleInorganic chemistry2016

Nitrite Reductase Activity in Engineered Azurin Variants.

Steven M Berry, Jacob N Strange, Erika L Bladholm, Balabhadra Khatiwada, Christine G Hedstrom, Alexandra M Sauer

Abstract read
In one paragraph

Article in Inorganic chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Catalysis and Electron Transfer inChemical reviews · 2022
    Review
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Steven M BerryDepartment of Chemistry and Biochemistry, University of Minnesota Duluth , 1039 University Drive, Duluth, Minnesota 55812, United States.
Jacob N StrangeDepartment of Chemistry and Biochemistry, University of Minnesota Duluth , 1039 University Drive, Duluth, Minnesota 55812, United States.
Erika L BladholmDepartment of Chemistry and Biochemistry, University of Minnesota Duluth , 1039 University Drive, Duluth, Minnesota 55812, United States.
Balabhadra KhatiwadaDepartment of Chemistry and Biochemistry, University of Minnesota Duluth , 1039 University Drive, Duluth, Minnesota 55812, United States.
Christine G HedstromDepartment of Chemistry and Biochemistry, University of Minnesota Duluth , 1039 University Drive, Duluth, Minnesota 55812, United States.
Alexandra M SauerDepartment of Chemistry and Biochemistry, University of Minnesota Duluth , 1039 University Drive, Duluth, Minnesota 55812, United States.
University of Minnesota, Duluth · US

Funding

Study of copper oxidoreductases through metalloprotein engineeringR15GM097676 · NIGMS · UNIVERSITY OF MINNESOTA DULUTH · PI BERRY, STEVEN M · 2012 to 2012
$311k
NIGMS NIH HHS R15 GM097676
6 · The paper itself

Abstract

Nitrite reductase (NiR) activity was examined in a series of dicopper P.a. azurin variants in which a surface binding copper site was added through site-directed mutagenesis. Four variants were synthesized with copper binding motifs inspired by the catalytic type 2 copper binding sites found in the native noncoupled dinuclear copper enzymes nitrite reductase and peptidylglycine α-hydroxylating monooxygenase. The four azurin variants, denoted Az-NiR, Az-NiR3His, Az-PHM, and Az-PHM3His, maintained the azurin electron transfer copper center, with the second designed copper site located over 13 Å away and consisting of mutations Asn10His,Gln14Asp,Asn16His-azurin, Asn10His,Gln14His,Asn16His-azurin, Gln8Met,Gln14His,Asn16His-azurin, and Gln8His,Gln14His,Asn16His-azurin, respectively. UV-visible absorption spectroscopy, EPR spectroscopy, and electrochemistry of the sites demonstrate copper binding as well as interaction with small exogenous ligands. The nitrite reduction activity of the variants was determined, including the catalytic Michaelis-Menten parameters. The variants showed activity (0.34-0.59 min(-1)) that was slower than that of native NiRs but comparable to that of other model systems. There were small variations in activity of the four variants that correlated with the number of histidines in the added copper site. Catalysis was found to be reversible, with nitrite produced from NO. Reactions starting with reduced azurin variants demonstrated that electrons from both copper centers were used to reduce nitrite, although steady-state catalysis required the T2 copper center and did not require the T1 center. Finally, experiments separating rates of enzyme reduction from rates of reoxidation by nitrite demonstrated that the reaction with nitrite was rate limiting during catalysis.

Indexed as

Ascorbic AcidAzurinBinding SitesCatalysisCopperElectrochemical TechniquesKineticsMutagenesis, Site-DirectedNitrite ReductasesOxidation-ReductionProtein EngineeringSodium NitriteAscorbic AcidAzurinCopperNitrite ReductasesSodium Nitrite

Identifiers

PMID27055058
PMCPMC4894363
OpenAlexW2329280385

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.