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Volumn 7, Issue 2, 2014, Pages 715-719

FeFe hydrogenase reductive inactivation and implication for catalysis

(8) Hajj, Viviane a,d Baffert, Carole a Sybirna, Kateryna b Meynial Salles, Isabelle c Soucaille, Philippe c Bottin, Hervé b Fourmond, Vincent a Léger, Christophe a

a AIX MARSEILLE UNIVERSITY (France)

b CEA (France)

c UNIVERSITÉ DE TOULOUSE (France)

d PENNSYLVANIA STATE UNIVERSITY (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ENVIRONMENTAL ENGINEERING; RENEWABLE ENERGY RESOURCES;

ACTIVE SITE; CATALYTIC CYCLES; COMPLEX PROCESSES; H-CLUSTER; HYDROGENASES; OXIDATIVE CONDITIONS; PHOTOPRODUCTIONS; PROTON ACTIVITY;

PHOTOSENSITIZERS;

CATALYSIS; ELECTRON; ENZYME ACTIVITY; OXIDATION;

EID: 84893088473 PISSN: 17545692 EISSN: 17545706 Source Type: Journal
DOI: 10.1039/c3ee42075b Document Type: Article

Times cited : (35)

References (28)

1
- 35748930865
- See also the 2013 themed issue of Chem. Commun. on Electrocatalytic Hydrogen Evolution
- J. C. Fontecilla-Camps A. Volbeda C. Cavazza Y. Nicolet Chem. Rev. 2007 107 4273 4303
- (2007) Chem. Rev. , vol.107 , pp. 4273-4303
- Fontecilla-Camps, J.C.¹ Volbeda, A.² Cavazza, C.³ Nicolet, Y.⁴

2
- 68349101212
- A. Silakov B. Wenk E. Reijerse W. Lubitz Phys. Chem. Chem. Phys. 2009 11 6592 6599
- (2009) Phys. Chem. Chem. Phys. , vol.11 , pp. 6592-6599
- Silakov, A.¹ Wenk, B.² Reijerse, E.³ Lubitz, W.⁴

3
- 41549166890
- A. S. Pandey T. V. Harris L. J. Giles J. W. Peters R. K. Szilagyi J. Am. Chem. Soc. 2008 130 4533 4540
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 4533-4540
- Pandey, A.S.¹ Harris, T.V.² Giles, L.J.³ Peters, J.W.⁴ Szilagyi, R.K.⁵

4
- 77952428962
- D. W. Mulder E. S. Boyd R. Sarma R. K. Lange J. A. Endrizzi J. B. Broderick J. W. Peters Nature 2010 465 248 251
- (2010) Nature , vol.465 , pp. 248-251
- Mulder, D.W.¹ Boyd, E.S.² Sarma, R.³ Lange, R.K.⁴ Endrizzi, J.A.⁵ Broderick, J.B.⁶ Peters, J.W.⁷

5
- 0037042289
- Z.-P. Liu P. Hu J. Am. Chem. Soc. 2002 124 5175 5182
- (2002) J. Am. Chem. Soc. , vol.124 , pp. 5175-5182
- Liu, Z.-P.¹ Hu, P.²

6
- 0034822720
- H.-J. Fan M. B. Hall J. Am. Chem. Soc. 2001 123 3828 3829
- (2001) J. Am. Chem. Soc. , vol.123 , pp. 3828-3829
- Fan, H.-J.¹ Hall, M.B.²

7
- 34547651339
- C. Greco M. Bruschi L. De Gioia U. Ryde Inorg. Chem. 2007 46 5911 5921
- (2007) Inorg. Chem. , vol.46 , pp. 5911-5921
- Greco, C.¹ Bruschi, M.² De Gioia, L.³ Ryde, U.⁴

8
- 35748942883
- P. E. M. Siegbahn J. W. Tye M. B. Hall Chem. Rev. 2007 107 4414 4435
- (2007) Chem. Rev. , vol.107 , pp. 4414-4435
- Siegbahn, P.E.M.¹ Tye, J.W.² Hall, M.B.³

9
- 47949116193
- M. Bruschi C. Greco P. Fantucci L. De Gioia Inorg. chem. 2008 47 6056 6071
- (2008) Inorg. Chem. , vol.47 , pp. 6056-6071
- Bruschi, M.¹ Greco, C.² Fantucci, P.³ De Gioia, L.⁴

10
- 84868533696
- A. Adamska A. Silakov C. Lambertz O. Rüdiger T. Happe E. Reijerse W. Lubitz Angew. Chem., Int. Ed. 2012 51 11458 11462
- (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 11458-11462
- Adamska, A.¹ Silakov, A.² Lambertz, C.³ Rüdiger, O.⁴ Happe, T.⁵ Reijerse, E.⁶ Lubitz, W.⁷

11
- 84877255197
- D. W. Mulder M. W. Ratzloff E. M. Shepard A. S. Byer S. M. Noone J. W. Peters J. B. Broderick P. W. King J. Am. Chem. Soc. 2013 135 6921 6929
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 6921-6929
- Mulder, D.W.¹ Ratzloff, M.W.² Shepard, E.M.³ Byer, A.S.⁴ Noone, S.M.⁵ Peters, J.W.⁶ Broderick, J.B.⁷ King, P.W.⁸

12
- 29544438599
- W. Roseboom A. De Lacey V. Fernandez E. Hatchikian S. Albracht J. Biol. Inorg. Chem. 2006 11 102 118
- (2006) J. Biol. Inorg. Chem. , vol.11 , pp. 102-118
- Roseboom, W.¹ De Lacey, A.² Fernandez, V.³ Hatchikian, E.⁴ Albracht, S.⁵

13
- 69049116388
- A. Silakov C. Kamp E. Reijerse T. Happe W. Lubitz Biochemistry 2009 48 7780 7786
- (2009) Biochemistry , vol.48 , pp. 7780-7786
- Silakov, A.¹ Kamp, C.² Reijerse, E.³ Happe, T.⁴ Lubitz, W.⁵

14
- 79951841772
- C. Baffert L. Bertini T. Lautier C. Greco K. Sybirna P. Ezanno E. Etienne P. Soucaille P. Bertrand H. Bottin I. Meynial-Salles L. De Gioia C. Léger J. Am. Chem. Soc. 2011 133 2096 2099
- (2011) J. Am. Chem. Soc. , vol.133 , pp. 2096-2099
- Baffert, C.¹ Bertini, L.² Lautier, T.³ Greco, C.⁴ Sybirna, K.⁵ Ezanno, P.⁶ Etienne, E.⁷ Soucaille, P.⁸ Bertrand, P.⁹ Bottin, H.¹⁰ Meynial-Salles, I.¹¹ De Gioia, L.¹² Léger, C.¹³

15
- 49049115593
- C. Léger P. Bertrand Chem. Rev. 2008 108 2379 2438
- (2008) Chem. Rev. , vol.108 , pp. 2379-2438
- Léger, C.¹ Bertrand, P.²

16
- 84874992451
- V. Fourmond C. Baffert K. Sybirna T. Lautier A. Abou Hamdan S. Dementin P. Soucaille I. Meynial-Salles H. Bottin C. Léger J. Am. Chem. Soc. 2013 135 3926 3938
- (2013) J. Am. Chem. Soc. , vol.135 , pp. 3926-3938
- Fourmond, V.¹ Baffert, C.² Sybirna, K.³ Lautier, T.⁴ Abou Hamdan, A.⁵ Dementin, S.⁶ Soucaille, P.⁷ Meynial-Salles, I.⁸ Bottin, H.⁹ Léger, C.¹⁰

17
- 84870589774
- A. A. Hamdan P.-P. Liebgott V. Fourmond O. Gutiérrez-Sanz A. L. De Lacey P. Infossi M. Rousset S. Dementin C. Léger Proc. Natl. Acad. Sci. U. S. A. 2012 109 19916 19921
- (2012) Proc. Natl. Acad. Sci. U. S. A. , vol.109 , pp. 19916-19921
- Hamdan, A.A.¹ Liebgott, P.-P.² Fourmond, V.³ Gutiérrez-Sanz, O.⁴ De Lacey, A.L.⁵ Infossi, P.⁶ Rousset, M.⁷ Dementin, S.⁸ Léger, C.⁹

18
- 84866393229
- The carbon-carbon bonds formed upon electrode modification are stable in the range -2 to + 1.8 V (ref. 21); we therefore expect that the low potentials used in the experiments described below should not affect the protein/electrode interaction, and indeed, experiments carried out with the enzyme adsorbed (rather than covalently attached) on the electrode give similar results (not shown)
- C. Baffert K. Sybirna P. Ezanno T. Lautier V. Hajj I. Meynial-Salles P. Soucaille H. Bottin C. Léger Anal. Chem. 2012 84 7999 8005
- (2012) Anal. Chem. , vol.84 , pp. 7999-8005
- Baffert, C.¹ Sybirna, K.² Ezanno, P.³ Lautier, T.⁴ Hajj, V.⁵ Meynial-Salles, I.⁶ Soucaille, P.⁷ Bottin, H.⁸ Léger, C.⁹

19
- 0038621782
- See ESI section S3 for details about the procedure we used to fit the bi-exponential decays It is a coincidence that this 35% matches the decrease in current in the red trace Indeed, imagine the following extreme situation: if a reversible reductive reaction produced a form of the enzyme that has no reductive activity at low potential, but unaffected H2-oxidation activity under oxidizing conditions, one would detect the reductive inactivation as a decrease in current during the low potential step, but the reactivation at high potential would not appear on the CA trace, because the reactivation has no effect on the turnover rate at high-potential
- M. D'Amour D. Bélanger J. Phys. Chem. B 2003 107 4811 4817
- (2003) J. Phys. Chem. B , vol.107 , pp. 4811-4817
- D'Amour, M.¹ Bélanger, D.²

20
- 0034730073
- R. Camba F. A. Armstrong Biochemistry 2000 39 10587 10598
- (2000) Biochemistry , vol.39 , pp. 10587-10598
- Camba, R.¹ Armstrong, F.A.²

21
- 84871291104
- A. Abou Hamdan B. Burlat O. Gutierrez-Sanz P. Liebgott C. Baffert A. de Lacey M. Rousset B. Guigliarelli C. Leger S. Dementin Nat. Chem. Biol. 2013 9 15 17
- (2013) Nat. Chem. Biol. , vol.9 , pp. 15-17
- Abou Hamdan, A.¹ Burlat, B.² Gutierrez-Sanz, O.³ Liebgott, P.⁴ Baffert, C.⁵ De Lacey, A.⁶ Rousset, M.⁷ Guigliarelli, B.⁸ Leger, C.⁹ Dementin, S.¹⁰

22
- 84861402614
- A. Abou Hamdan S. Dementin P.-P. Liebgott O. Gutierrez-Sanz P. Richaud A. L. De Lacey M. Roussett P. Bertrand L. Cournac C. Léger J. Am. Chem. Soc. 2012 134 8368 8371
- (2012) J. Am. Chem. Soc. , vol.134 , pp. 8368-8371
- Abou Hamdan, A.¹ Dementin, S.² Liebgott, P.-P.³ Gutierrez-Sanz, O.⁴ Richaud, P.⁵ De Lacey, A.L.⁶ Roussett, M.⁷ Bertrand, P.⁸ Cournac, L.⁹ Léger, C.¹⁰

23
- 82155186128
- O. A. Zadvornyy J. E. Lucon R. Gerlach N. A. Zorin T. Douglas T. E. Elgren J. W. Peters J. Inorg. Biochem. 2012 106 151 155
- (2012) J. Inorg. Biochem. , vol.106 , pp. 151-155
- Zadvornyy, O.A.¹ Lucon, J.E.² Gerlach, R.³ Zorin, N.A.⁴ Douglas, T.⁵ Elgren, T.E.⁶ Peters, J.W.⁷

24
- 39049132264
- M. Hambourger M. Gervaldo D. Svedruzic P. W. King D. Gust M. Ghirardi A. L. Moore T. A. Moore J. Am. Chem. Soc. 2008 130 2015 2022
- (2008) J. Am. Chem. Soc. , vol.130 , pp. 2015-2022
- Hambourger, M.¹ Gervaldo, M.² Svedruzic, D.³ King, P.W.⁴ Gust, D.⁵ Ghirardi, M.⁶ Moore, A.L.⁷ Moore, T.A.⁸

25
- 78349259311
- K. A. Brown S. Dayal X. Ai G. Rumbles P. W. King J. Am. Chem. Soc. 2010 132 9672 9680
- (2010) J. Am. Chem. Soc. , vol.132 , pp. 9672-9680
- Brown, K.A.¹ Dayal, S.² Ai, X.³ Rumbles, G.⁴ King, P.W.⁵

26
- 0001114286
- V. Balzani F. Bolletta F. Scandola R. Ballardini Pure Appl. Chem. 1979 51 299 311
- (1979) Pure Appl. Chem. , vol.51 , pp. 299-311
- Balzani, V.¹ Bolletta, F.² Scandola, F.³ Ballardini, R.⁴

27
- 84866716771
- S. Chen L.-W. Wang Chem. Mater. 2012 24 3659 3666
- (2012) Chem. Mater. , vol.24 , pp. 3659-3666
- Chen, S.¹ Wang, L.-W.²

28
- 84882631609
- K. Singh T. McArdle P. R. Sullivan C. F. Blanford Energy Environ. Sci. 2013 6 2460 2464
- (2013) Energy Environ. Sci. , vol.6 , pp. 2460-2464
- Singh, K.¹ McArdle, T.² Sullivan, P.R.³ Blanford, C.F.⁴

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