Literature DB >> 7766626

A variable-temperature direct electrochemical study of metalloproteins from hyperthermophilic microorganisms involved in hydrogen production from pyruvate.

E T Smith1, J M Blamey, Z H Zhou, M W Adams.   

Abstract

The hyperthermophilic bacterium Thermotoga maritima and the hyperthermophilic archaeon Pyrococcus furiosus grow optimally at 80 and 100 degrees C, respectively, by the fermentation of carbohydrates to organic acids, CO2, and H2. Pyruvate is a major source of reductant for H2 production during fermentation, and pyruvate ferredoxin oxidoreductase (POR), a 4Fe-type ferredoxin, and hydrogenase have been previously purified from both species. P. furiosus utilizes a copper-iron-containing POR and a nickel-iron-containing hydrogenase, whereas the POR of T. maritima lacks copper and its hydrogenase lacks nickel. For all four enzymes and for the two ferredoxins, we have determined their reduction potentials (E degrees') and, where possible, thermodynamic parameters associated with electron transfer (delta S degrees and delta H degrees), using differential pulse voltammetry at temperatures ranging from 25 to 95 degrees C. At ambient temperature, the E degrees' values for all six proteins were comparable and spanned less than 50 mV, but their temperature dependence varied dramatically, even between analogous proteins, such that in the physiological-relevant temperature range the E degrees' values became widely separated. In most cases, transition points were observed in E degrees'/temperature profiles, and these generally corresponded with significant increases in catalytic activity, but occurred at lower temperatures in T. maritima than in P. furiosus. The two ferredoxins (and also P. furiosus rubredoxin) had much more negative entropy terms than were calculated for POR and hydrogenase, and these values were also more negative than those previously reported for mesophilic redox proteins. The reduction potentials measured at high temperatures and likely efficiencies of electron transfer between the various proteins were consistent with in vitro activity measurements.(ABSTRACT TRUNCATED AT 250 WORDS)

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Year:  1995        PMID: 7766626     DOI: 10.1021/bi00021a030

Source DB:  PubMed          Journal:  Biochemistry        ISSN: 0006-2960            Impact factor:   3.162


  12 in total

1.  Ferredoxins as interchangeable redox components in support of MiaB, a radical S-adenosylmethionine methylthiotransferase.

Authors:  Arthur J Arcinas; Stephanie J Maiocco; Sean J Elliott; Alexey Silakov; Squire J Booker
Journal:  Protein Sci       Date:  2019-01       Impact factor: 6.725

2.  Geometric and electrostatic study of the [4Fe-4S] cluster of adenosine-5'-phosphosulfate reductase from broken symmetry density functional calculations and extended X-ray absorption fine structure spectroscopy.

Authors:  Devayani P Bhave; Wen-Ge Han; Samuel Pazicni; James E Penner-Hahn; Kate S Carroll; Louis Noodleman
Journal:  Inorg Chem       Date:  2011-06-16       Impact factor: 5.165

3.  Parsing redox potentials of five ferredoxins found within Thermotoga maritima.

Authors:  Stephanie J Maiocco; Arthur J Arcinas; Squire J Booker; Sean J Elliott
Journal:  Protein Sci       Date:  2019-01       Impact factor: 6.725

4.  Crystal structures of the all-cysteinyl-coordinated D14C variant of Pyrococcus furiosus ferredoxin: [4Fe-4S] ↔ [3Fe-4S] cluster conversion.

Authors:  Monika Nøhr Løvgreen; Maja Martic; Michael S Windahl; Hans E M Christensen; Pernille Harris
Journal:  J Biol Inorg Chem       Date:  2011-04-12       Impact factor: 3.358

5.  Expression of Shewanella oneidensis MR-1 [FeFe]-hydrogenase genes in Anabaena sp. strain PCC 7120.

Authors:  Katrin Gärtner; Sigal Lechno-Yossef; Adam J Cornish; C Peter Wolk; Eric L Hegg
Journal:  Appl Environ Microbiol       Date:  2012-09-28       Impact factor: 4.792

6.  Insights into Flavin-based Electron Bifurcation via the NADH-dependent Reduced Ferredoxin:NADP Oxidoreductase Structure.

Authors:  Julius K Demmer; Haiyan Huang; Shuning Wang; Ulrike Demmer; Rudolf K Thauer; Ulrich Ermler
Journal:  J Biol Chem       Date:  2015-07-02       Impact factor: 5.157

7.  Voltammetric studies of the reactions of iron-sulphur clusters ([3Fe-4S] or [M3Fe-4S]) formed in Pyrococcus furiosus ferredoxin.

Authors:  S E Fawcett; D Davis; J L Breton; A J Thomson; F A Armstrong
Journal:  Biochem J       Date:  1998-10-15       Impact factor: 3.857

8.  The iron-hydrogenase of Thermotoga maritima utilizes ferredoxin and NADH synergistically: a new perspective on anaerobic hydrogen production.

Authors:  Gerrit J Schut; Michael W W Adams
Journal:  J Bacteriol       Date:  2009-05-01       Impact factor: 3.490

Review 9.  Physiological characteristics of the extreme thermophile Caldicellulosiruptor saccharolyticus: an efficient hydrogen cell factory.

Authors:  Karin Willquist; Ahmad A Zeidan; Ed W J van Niel
Journal:  Microb Cell Fact       Date:  2010-11-22       Impact factor: 5.328

10.  Mutational Analyses of the Enzymes Involved in the Metabolism of Hydrogen by the Hyperthermophilic Archaeon Pyrococcus furiosus.

Authors:  Gerrit J Schut; William J Nixon; Gina L Lipscomb; Robert A Scott; Michael W W Adams
Journal:  Front Microbiol       Date:  2012-05-01       Impact factor: 5.640

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