Literature DB >> 33659541

Determination of Flavin Potential in Proteins by Xanthine/Xanthine Oxidase Method.

Elena Maklashina1,2, Gary Cecchini1,2.   

Abstract

This protocol describes a simple xanthine/xanthine oxidase enzymatic equilibration method for determination of the redox potential of a flavin. As an example of the use of this method, we determine the reduction potential of the covalently bound FAD cofactor ( Em = -55 mV) in the SdhA flavoprotein subunit of succinate dehydrogenase from Escherichia coli. In principle, this method can be used routinely to determine the redox potential of flavin cofactors in any simple flavoprotein from equilibrium concentrations with an appropriate reference dye of known Em without the use of sophisticated electrochemical equipment.
Copyright © 2020 The Authors; exclusive licensee Bio-protocol LLC.

Entities:  

Keywords:  Flavin; Flavoprotein; Midpoint potential; Reduction potential; Xanthine oxidase

Year:  2020        PMID: 33659541      PMCID: PMC7853947          DOI: 10.21769/BioProtoc.3571

Source DB:  PubMed          Journal:  Bio Protoc        ISSN: 2331-8325


  8 in total

1.  Methods for determining the reduction potentials of flavin enzymes.

Authors:  Shelbi L Christgen; Sophia M Becker; Donald F Becker
Journal:  Methods Enzymol       Date:  2019-03-29       Impact factor: 1.600

2.  Redox state of flavin adenine dinucleotide drives substrate binding and product release in Escherichia coli succinate dehydrogenase.

Authors:  Victor W T Cheng; Ramanaguru Siva Piragasam; Richard A Rothery; Elena Maklashina; Gary Cecchini; Joel H Weiner
Journal:  Biochemistry       Date:  2015-01-17       Impact factor: 3.162

3.  Electron transfer and catalytic control by the iron-sulfur clusters in a respiratory enzyme, E. coli fumarate reductase.

Authors:  Janette M Hudson; Kerensa Heffron; Violetta Kotlyar; Yelizaveta Sher; Elena Maklashina; Gary Cecchini; Fraser A Armstrong
Journal:  J Am Chem Soc       Date:  2005-05-18       Impact factor: 15.419

4.  Thermodynamic regulation of human short-chain acyl-CoA dehydrogenase by substrate and product binding.

Authors:  Amy K Saenger; Tien V Nguyen; Jerry Vockley; Marian T Stankovich
Journal:  Biochemistry       Date:  2005-12-13       Impact factor: 3.162

5.  Effect of cysteine to serine mutations on the properties of the [4Fe-4S] center in Escherichia coli fumarate reductase.

Authors:  A T Kowal; M T Werth; A Manodori; G Cecchini; I Schröder; R P Gunsalus; M K Johnson
Journal:  Biochemistry       Date:  1995-09-26       Impact factor: 3.162

Review 6.  What's in a covalent bond? On the role and formation of covalently bound flavin cofactors.

Authors:  Dominic P H M Heuts; Nigel S Scrutton; William S McIntire; Marco W Fraaije
Journal:  FEBS J       Date:  2009-05-05       Impact factor: 5.542

7.  The unassembled flavoprotein subunits of human and bacterial complex II have impaired catalytic activity and generate only minor amounts of ROS.

Authors:  Elena Maklashina; Sany Rajagukguk; T M Iverson; Gary Cecchini
Journal:  J Biol Chem       Date:  2018-04-02       Impact factor: 5.157

8.  A simple method for the determination of reduction potentials in heme proteins.

Authors:  Igor Efimov; Gary Parkin; Elizabeth S Millett; Jennifer Glenday; Cheuk K Chan; Holly Weedon; Harpreet Randhawa; Jaswir Basran; Emma L Raven
Journal:  FEBS Lett       Date:  2014-01-17       Impact factor: 4.124

  8 in total
  1 in total

1.  Broadening the Scope of the Flavin-Tag Method by Improving Flavin Incorporation and Incorporating Flavin Analogs.

Authors:  Yapei Tong; Marnix R Loonstra; Marco W Fraaije
Journal:  Chembiochem       Date:  2022-04-19       Impact factor: 3.461

  1 in total

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