Literature DB >> 16887508

Isolation and preliminary characterization of a soluble nitrate reductase from the sulfate reducing organism Desulfovibrio desulfuricans ATCC 27774.

S Bursakov1, M Y Liu, W J Payne, J LeGall, I Moura, J J Moura.   

Abstract

Desulfovibrio desulfuricans ATCC 27774 is a sulfate reducer that can adapt to nitrate respiration, inducing the enzymes required to utilize this alternative metabolic pathway. Nitrite reductase from this organism has been previously isolated and characterized, but no information was available on the enzyme involved in the reduction of nitrate. This is the first report of purification to homogeneity of a nitrate reductase from a sulfate reducing organism, thus completing the enzymatic system required to convert nitrate (through nitrite) to ammonia. D. desulfuricans nitrate reductase is a monomeric (circa 70 kDa) periplasmic enzyme with a specific activity of 5.4 K(m) for nitrate was estimated to be 20 microM. EPR signals due to one [4Fe-4S] cluster and Mo(V) were identified in dithionite reduced samples and in the presence of nitrate.

Entities:  

Year:  1995        PMID: 16887508     DOI: 10.1016/s1075-9964(95)80444-7

Source DB:  PubMed          Journal:  Anaerobe        ISSN: 1075-9964            Impact factor:   3.331


  12 in total

Review 1.  Mo and W bis-MGD enzymes: nitrate reductases and formate dehydrogenases.

Authors:  José J G Moura; Carlos D Brondino; José Trincão; Maria João Romão
Journal:  J Biol Inorg Chem       Date:  2004-08-12       Impact factor: 3.358

2.  EPR and redox properties of periplasmic nitrate reductase from Desulfovibrio desulfuricans ATCC 27774.

Authors:  Pablo J González; María G Rivas; Carlos D Brondino; Sergey A Bursakov; Isabel Moura; José J G Moura
Journal:  J Biol Inorg Chem       Date:  2006-05-09       Impact factor: 3.358

3.  Molybdenum- and tungsten-containing formate dehydrogenases and formylmethanofuran dehydrogenases: Structure, mechanism, and cofactor insertion.

Authors:  Dimitri Niks; Russ Hille
Journal:  Protein Sci       Date:  2018-10-31       Impact factor: 6.725

4.  Kinetic consequences of the endogenous ligand to molybdenum in the DMSO reductase family: a case study with periplasmic nitrate reductase.

Authors:  Breeanna Mintmier; Jennifer M McGarry; Daniel J Bain; Partha Basu
Journal:  J Biol Inorg Chem       Date:  2020-11-01       Impact factor: 3.358

5.  Isolation and preliminary characterization of a respiratory nitrate reductase from hydrocarbon-degrading bacterium Gordonia alkanivorans S7.

Authors:  Irena Romanowska; Ewa Kwapisz; Magdalena Mitka; Stanisław Bielecki
Journal:  J Ind Microbiol Biotechnol       Date:  2010-04-09       Impact factor: 3.346

Review 6.  Molybdenum and tungsten-dependent formate dehydrogenases.

Authors:  Luisa B Maia; José J G Moura; Isabel Moura
Journal:  J Biol Inorg Chem       Date:  2014-12-05       Impact factor: 3.358

7.  Inhibition of Sulfate Reduction and Cell Division by Desulfovibrio desulfuricans Coated in Palladium Metal.

Authors:  Robert J Barnes; Stephen P Voegtlin; Shiv R Naik; Renessa Gomes; Casey R J Hubert; Stephen R Larter; Steven L Bryant
Journal:  Appl Environ Microbiol       Date:  2022-05-31       Impact factor: 5.005

8.  Incorporation of either molybdenum or tungsten into formate dehydrogenase from Desulfovibrio alaskensis NCIMB 13491; EPR assignment of the proximal iron-sulfur cluster to the pterin cofactor in formate dehydrogenases from sulfate-reducing bacteria.

Authors:  Carlos D Brondino; Mario C G Passeggi; Jorge Caldeira; Maria J Almendra; Maria J Feio; Jose J G Moura; Isabel Moura
Journal:  J Biol Inorg Chem       Date:  2003-12-11       Impact factor: 3.358

Review 9.  Nitrate and periplasmic nitrate reductases.

Authors:  Courtney Sparacino-Watkins; John F Stolz; Partha Basu
Journal:  Chem Soc Rev       Date:  2014-01-21       Impact factor: 54.564

10.  The napEDABC gene cluster encoding the periplasmic nitrate reductase system of Thiosphaera pantotropha.

Authors:  B C Berks; D J Richardson; A Reilly; A C Willis; S J Ferguson
Journal:  Biochem J       Date:  1995-08-01       Impact factor: 3.857

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