DISTINCT REDOX BEHAVIOR OF PROSTHETIC GROUPS IN READY AND UNREADY HYDROGENASE FROM CHROMATIUM-VINOSUM

被引:83
作者
COREMANS, JMCC
VANDERZWAAN, JW
ALBRACHT, SPJ
机构
[1] UNIV AMSTERDAM,EC SLATER INST BIOCHEM,PLANTAGE MUIDERGRACHT 12,1018 TV AMSTERDAM,NETHERLANDS
[2] UNIV AMSTERDAM,CTR BIOTECHNOL,1018 TV AMSTERDAM,NETHERLANDS
关键词
HYDROGENASE; NICKEL; IRON-SULFUR CLUSTER; REDOX POTENTIAL; (C-VINOSUM);
D O I
10.1016/0167-4838(92)90386-R
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The redox behaviour of the Ni(III)/Ni(II) transition in hydrogenase from Chromatium vinosum is described and compared with the redox behaviour of the nickel ion in the F420-nonreducing hydrogenase from Methanobacterium thermoautotrophicum. Analogous to the situation in the oxidised hydrogenase of Desulfovibrio gigas (Fernandez, V.M., Hatchikian, E.C., Patil, D.S. and Cammack, R. (1986) Biochim. Biophys. Acta 883, 145-154), the C. vinosum enzyme can also exist in two forms: the 'unready' form (EPR characteristics of Ni(III): g(x,y,z) = 2.32, 2.24, 2.01) and the 'ready' form (EPR characteristics Ni(III): g(x,y,z) = 2.34, 2.16, 2.01). Like in the oxidised enzyme of M. thermoautotrophicum the Ni(III)/Ni(II) transition for the unready form titrated completely reversible (both at pH 6.0 and pH 8.0). In contrast, the reversibility of the Ni(III)/Ni(II) transition in the ready enzyme was strongly dependent on pH and temperature. At pH 6.0 and 2-degrees-C reduction of Ni(III) in ready enzyme was completely irreversible, whereas at pH 8.0 and 30-degrees-C Ni(III) in both ready and unready enzyme titrated with E0' = -115 mV (n = 1). Hampered redox equilibration between the ready enzyme and the mediating dyes is interpreted in terms of an obstruction of the electron transfer from nickel at the active site to the artificial electron acceptors in solution. The origin of this obstruction might be related to possible changes in the protein structure induced by the activation process. The E0'-value of the Ni(III)/Ni(II) equilibrium was pH sensitive (-60 mV/DELTA-pH) indicating that reduction of nickel is coupled to a protonation. A similar pH-dependence was observed for the titration of the spin-spin interaction of Ni(III) and a special form of the [3Fe-4S]+ cluster (E0' = +150 mV, pH 8.0, 30-degrees-C). Redox equilibration of this coupling was extremely sensitive to pH and temperature. The uncoupled [3Fe-4S]+ cluster titrated pH-independently with E0' = -10 mV (pH 8.0, 30-degrees-C).
引用
收藏
页码:157 / 168
页数:12
相关论文
共 34 条
[1]   THE REDOX PROPERTIES AND ACTIVATION OF THE F420-NON-REACTIVE HYDROGENASE OF METHANOBACTERIUM-FORMICICUM [J].
ADAMS, MWW ;
JIN, SLC ;
CHEN, JS ;
MORTENSON, LE .
BIOCHIMICA ET BIOPHYSICA ACTA, 1986, 869 (01) :37-47
[2]   MAGNETIC INTERACTION OF NICKEL(III) AND THE IRON-SULFUR CLUSTER IN HYDROGENASE FROM CHROMATIUM-VINOSUM [J].
ALBRACHT, SPJ ;
KALKMAN, ML ;
SLATER, EC .
BIOCHIMICA ET BIOPHYSICA ACTA, 1983, 724 (03) :309-316
[3]   ELECTRON-PARAMAGNETIC-RES SPECTRUM AT 4, 9 AND 35 GHZ OF HYDROGENASE FROM CHROMATIUM-VINOSUM - DIRECT EVIDENCE FOR SPIN-SPIN INTERACTION BETWEEN NI(III) AND THE IRON-SULFUR CLUSTER [J].
ALBRACHT, SPJ ;
VANDERZWAAN, JW ;
FONTIJN, RD .
BIOCHIMICA ET BIOPHYSICA ACTA, 1984, 766 (01) :245-258
[4]  
ALBRACHT SPJ, 1984, CURR TOP BIOENERG, V13, P79
[5]   THE ELECTRON-PARAMAGNETIC-RES PROPERTIES OF NICKEL IN HYDROGENASE FROM METHANOBACTERIUM-THERMOAUTOTROPHICUM [J].
ALBRACHT, SPJ ;
GRAF, EG ;
THAUER, RK .
FEBS LETTERS, 1982, 140 (02) :311-313
[6]  
[Anonymous], BIOORGANIC CHEM NICK
[7]  
[Anonymous], 1985, ENZYME STRUCTURE MEC
[8]   NEW INSIGHTS, IDEAS AND UNANSWERED QUESTIONS CONCERNING IRON-SULFUR CLUSTERS IN MITOCHONDRIA [J].
BEINERT, H ;
ALBRACHT, SPJ .
BIOCHIMICA ET BIOPHYSICA ACTA, 1982, 683 (3-4) :245-277
[9]   REDOX PROPERTIES OF THE ESR-DETECTABLE NICKEL IN HYDROGENASE FROM DESULFOVIBRIO-GIGAS [J].
CAMMACK, R ;
PATIL, D ;
AGUIRRE, R ;
HATCHIKIAN, EC .
FEBS LETTERS, 1982, 142 (02) :289-292
[10]   THE REDOX PROPERTIES OF THE IRON-SULFUR CLUSTER IN HYDROGENASE FROM CHROMATIUM-VINOSUM, STRAIN-D [J].
CAMMACK, R ;
RAO, KK ;
SERRA, J ;
LLAMA, MJ .
BIOCHIMIE, 1986, 68 (01) :93-96