Literature DB >> 9973342

An unusual oxygen-sensitive, iron- and zinc-containing alcohol dehydrogenase from the hyperthermophilic archaeon Pyrococcus furiosus.

K Ma1, M W Adams.   

Abstract

Pyrococcus furiosus is a hyperthermophilic archaeon that grows optimally at 100 degreesC by the fermentation of peptides and carbohydrates to produce acetate, CO2, and H2, together with minor amounts of ethanol. The organism also generates H2S in the presence of elemental sulfur (S0). Cell extracts contained NADP-dependent alcohol dehydrogenase activity (0.2 to 0.5 U/mg) with ethanol as the substrate, the specific activity of which was comparable in cells grown with and without S0. The enzyme was purified by multistep column chromatography. It has a subunit molecular weight of 48,000 +/- 1,000, appears to be a homohexamer, and contains iron ( approximately 1.0 g-atom/subunit) and zinc ( approximately 1.0 g-atom/subunit) as determined by chemical analysis and plasma emission spectroscopy. Neither other metals nor acid-labile sulfur was detected. Analysis using electron paramagnetic resonance spectroscopy indicated that the iron was present as low-spin Fe(II). The enzyme is oxygen sensitive and has a half-life in air of about 1 h at 23 degreesC. It is stable under anaerobic conditions even at high temperature, with half-lives at 85 and 95 degreesC of 160 and 7 h, respectively. The optimum pH for ethanol oxidation was between 9. 4 and 10.2 (at 80 degreesC), and the apparent Kms (at 80 degreesC) for ethanol, acetaldehyde, NADP, and NAD were 29.4, 0.17, 0.071, and 20 mM, respectively. P. furiosus alcohol dehydrogenase utilizes a range of alcohols and aldehydes, including ethanol, 2-phenylethanol, tryptophol, 1,3-propanediol, acetaldehyde, phenylacetaldehyde, and methyl glyoxal. Kinetic analyses indicated a marked preference for catalyzing aldehyde reduction with NADPH as the electron donor. Accordingly, the proposed physiological role of this unusual alcohol dehydrogenase is in the production of alcohols. This reaction simultaneously disposes of excess reducing equivalents and removes toxic aldehydes, both of which are products of fermentation.

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Year:  1999        PMID: 9973342      PMCID: PMC93493     

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  53 in total

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3.  Three-dimensional structure of horse liver alcohol dehydrogenase at 2-4 A resolution.

Authors:  H Eklund; B Nordström; E Zeppezauer; G Söderlund; I Ohlsson; T Boiwe; B O Söderberg; O Tapia; C I Brändén; A Akeson
Journal:  J Mol Biol       Date:  1976-03-25       Impact factor: 5.469

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Authors:  F T Robb; J B Park; M W Adams
Journal:  Biochim Biophys Acta       Date:  1992-04-17

5.  Role of Polysulfides in Reduction of Elemental Sulfur by the Hyperthermophilic Archaebacterium Pyrococcus furiosus.

Authors:  I I Blumentals; M Itoh; G J Olson; R M Kelly
Journal:  Appl Environ Microbiol       Date:  1990-05       Impact factor: 4.792

6.  Characteristics of short-chain alcohol dehydrogenases and related enzymes.

Authors:  B Persson; M Krook; H Jörnvall
Journal:  Eur J Biochem       Date:  1991-09-01

7.  Ultrastructure and pyruvate formate-lyase radical quenching property of the multienzymic AdhE protein of Escherichia coli.

Authors:  D Kessler; W Herth; J Knappe
Journal:  J Biol Chem       Date:  1992-09-05       Impact factor: 5.157

8.  Thermostable NAD(+)-dependent alcohol dehydrogenase from Sulfolobus solfataricus: gene and protein sequence determination and relationship to other alcohol dehydrogenases.

Authors:  S Ammendola; C A Raia; C Caruso; L Camardella; S D'Auria; M De Rosa; M Rossi
Journal:  Biochemistry       Date:  1992-12-15       Impact factor: 3.162

9.  Purification and properties of F420- and NADP(+)-dependent alcohol dehydrogenases of Methanogenium liminatans and Methanobacterium palustre, specific for secondary alcohols.

Authors:  K Bleicher; J Winter
Journal:  Eur J Biochem       Date:  1991-08-15

10.  The novel tungsten-iron-sulfur protein of the hyperthermophilic archaebacterium, Pyrococcus furiosus, is an aldehyde ferredoxin oxidoreductase. Evidence for its participation in a unique glycolytic pathway.

Authors:  S Mukund; M W Adams
Journal:  J Biol Chem       Date:  1991-08-05       Impact factor: 5.157

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  13 in total

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Journal:  J Bacteriol       Date:  1999-09       Impact factor: 3.490

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Authors:  Ronnie Machielsen; Agustinus R Uria; Servé W M Kengen; John van der Oost
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Authors:  Tianyong Zheng; Daniel G Olson; Sean J Murphy; Xiongjun Shao; Liang Tian; Lee R Lynd
Journal:  J Bacteriol       Date:  2017-01-12       Impact factor: 3.490

5.  Characterization of hydrogenase II from the hyperthermophilic archaeon Pyrococcus furiosus and assessment of its role in sulfur reduction.

Authors:  K Ma; R Weiss; M W Adams
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

6.  Impact of substrate glycoside linkage and elemental sulfur on bioenergetics of and hydrogen production by the hyperthermophilic archaeon Pyrococcus furiosus.

Authors:  Chung-Jung Chou; Keith R Shockley; Shannon B Conners; Derrick L Lewis; Donald A Comfort; Michael W W Adams; Robert M Kelly
Journal:  Appl Environ Microbiol       Date:  2007-09-07       Impact factor: 4.792

7.  Thermostable alcohol dehydrogenase from Thermococcus kodakarensis KOD1 for enantioselective bioconversion of aromatic secondary alcohols.

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Journal:  Appl Environ Microbiol       Date:  2013-01-25       Impact factor: 4.792

8.  Sulfolobus tokodaii ST0053 produces a novel thermostable, NAD-dependent medium-chain alcohol dehydrogenase.

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9.  The electron transfer system of syntrophically grown Desulfovibrio vulgaris.

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Journal:  J Bacteriol       Date:  2009-07-06       Impact factor: 3.490

10.  Molecular characterization of the recombinant iron-containing alcohol dehydrogenase from the hyperthermophilic Archaeon, Thermococcus strain ES1.

Authors:  Xiangxian Ying; Amy M Grunden; Lin Nie; Michael W W Adams; Kesen Ma
Journal:  Extremophiles       Date:  2008-12-25       Impact factor: 2.395

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