Literature DB >> 3098164

The apparent oxidation of NADH by whole cells of the methylotrophic bacterium Methylophilus methylotrophus. A cautionary tale.

R A Patchett, C W Jones.   

Abstract

Previous reports that whole cells of Methylophilus methylotrophus oxidase exogenous NADH have been investigated. Essentially identical rates of oxygen consumption were observed following the addition of methanol or NADH to whole cells. Both activities were inhibited by EDTA and hydroxylamine, but not by HQNO, and exhibited similar pH optima. Analyses of the reaction stoichiometry with NADH as substrate showed that the expected amount of oxygen was consumed, but also revealed acidification (instead of alkalinisation) and no oxidation of NADH. Further studies showed that commercial NADH is contaminated with ethanol which is oxidised to acetic acid by the low specificity methanol oxidase system present in this organism. The oxidation of exogenous NADH by whole cells of M. methylotrophus reported previously is therefore spurious.

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Year:  1986        PMID: 3098164     DOI: 10.1007/bf00393466

Source DB:  PubMed          Journal:  Antonie Van Leeuwenhoek        ISSN: 0003-6072            Impact factor:   2.271


  9 in total

1.  Hematin enzymes of Hemophilus parainfluenzae.

Authors:  D C WHITE; L SMITH
Journal:  J Biol Chem       Date:  1962-04       Impact factor: 5.157

2.  Purification and properties of methanol dehydrogenase from Hyphomicrobium x.

Authors:  J A Duine; J Frank; J Westerling
Journal:  Biochim Biophys Acta       Date:  1978-06-09

3.  The microbial oxidation of methanol. 1. Isolation and properties of Pseudomonas sp. M27.

Authors:  C Anthony; L J Zatman
Journal:  Biochem J       Date:  1964-09       Impact factor: 3.857

Review 4.  Branched electron-transport systems in bacteria.

Authors:  D C White; P R Sinclair
Journal:  Adv Microb Physiol       Date:  1971       Impact factor: 3.517

5.  The microbial oxidation of methanol. The alcohol dehydrogenase of Pseudomonas sp. M27.

Authors:  C Anthony; L J Zatman
Journal:  Biochem J       Date:  1965-09       Impact factor: 3.857

6.  The effect of EDTA and related chelating agents on the oxidation of methanol by the methylotrophic bacterium, Methylophilus methylotrophus.

Authors:  M A Carver; K M Humphrey; R A Patchett; C W Jones
Journal:  Eur J Biochem       Date:  1984-02-01

7.  Respiration-linked proton translocation in the obligate methylotroph Methylophilus methylotrophus.

Authors:  M J Dawson; C W Jones
Journal:  Biochem J       Date:  1981-03-15       Impact factor: 3.857

8.  The electron-transport chains of the obligate methylotroph Methylophilus methylotrophus.

Authors:  A B Cross; C Anthony
Journal:  Biochem J       Date:  1980-11-15       Impact factor: 3.857

9.  Substrate specificity of the purified primary alcohol dehydrogenases from methanol-oxidizing bacteria.

Authors:  G T Sperl; H S Forrest; D T Gibson
Journal:  J Bacteriol       Date:  1974-05       Impact factor: 3.490

  9 in total
  3 in total

1.  In vivo analysis of the mechanisms for oxidation of cytosolic NADH by Saccharomyces cerevisiae mitochondria.

Authors:  K M Overkamp; B M Bakker; P Kötter; A van Tuijl; S de Vries; J P van Dijken; J T Pronk
Journal:  J Bacteriol       Date:  2000-05       Impact factor: 3.490

2.  Studies on electron transfer from methanol dehydrogenase to cytochrome cL, both purified from Hyphomicrobium X.

Authors:  M Dijkstra; J Frank; J A Duine
Journal:  Biochem J       Date:  1989-01-01       Impact factor: 3.857

3.  The mitochondrial alcohol dehydrogenase Adh3p is involved in a redox shuttle in Saccharomyces cerevisiae.

Authors:  B M Bakker; C Bro; P Kötter; M A Luttik; J P van Dijken; J T Pronk
Journal:  J Bacteriol       Date:  2000-09       Impact factor: 3.490

  3 in total

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