Two variants of the assembly factor Surf1 target specific terminal oxidases in Paracoccus denitrificans

被引:30
作者
Bundschuh, Freya A. [1 ]
Hoffmeier, Klaus [2 ]
Ludwig, Bernd [1 ,3 ]
机构
[1] Goethe Univ Frankfurt, Inst Biochem, Abt Mol Genet, D-60438 Frankfurt, Germany
[2] GenXPro GmbH, Frankfurt, Germany
[3] CEF Macromol Complexes, Frankfurt, Germany
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS | 2008年 / 1777卷 / 10期
关键词
Respiratory chain; Heme/copper oxidase; Oxidase biogenesis; Heme a; Binuclear centre; Heme incorporation;
D O I
10.1016/j.bbabio.2008.05.448
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
Biogenesis of cytochrome c oxidase (COX) relies on a large number of assembly proteins, one of them being Surf1. In humans, the loss of Surf1 function is associated with Leigh syndrome, a fatal neurodegenerative disorder. In the soil bacterium Paracoccus denitrificans, homologous genes specifying Surf1 have been identified and located in two operons of terminal oxidases: surf1q is the last gene of the qox operon (coding for a ba(3)-type ubiquinol oxidase), and surf1c is found at the end of the cta operon (encoding subunits of the aa(3)-type cytochrome c oxidase). We introduced chromosomal single and double deletions for both surf1 genes, leading to significantly reduced oxidase activities in membrane. Our experiments on P. denitrificans surf1 single deletion strains show that both Surf1c and Surf1q are functional and act independently for the aa(3)-type cytochrome c oxidase and the ba(3)-type quinol oxidase, respectively. This is the first direct experimental evidence for the involvement of a Surf1 protein in the assembly of a quinol oxidase. Analyzing the heme content of purified cytochrome c oxidase, we conclude that Surf1, though not indispensable for oxidase assembly, is involved in an early step of cofactor insertion into subunit I. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:1336 / 1343
页数:8
相关论文
共 53 条
[1]   Constitutive knockout of Surf1 is associated with high embryonic lethality, mitochondrial disease and cytochrome c oxidase deficiency in mice [J].
Agostino, A ;
Invernizzi, F ;
Tiveron, C ;
Fagiolari, G ;
Prelle, A ;
Lamantea, E ;
Giavazzi, A ;
Battaglia, G ;
Tatangelo, L ;
Tiranti, V ;
Zeviani, M .
HUMAN MOLECULAR GENETICS, 2003, 12 (04) :399-413
[2]  
ALEXEYEV MF, 1995, BIOTECHNIQUES, V18, P52
[3]   Molecular genetics of the genus Paracoccus:: Metabolically versatile bacteria with bioenergetic flexibility [J].
Baker, SC ;
Ferguson, SJ ;
Ludwig, B ;
Page, MD ;
Richter, OMH ;
van Spanning, RJM .
MICROBIOLOGY AND MOLECULAR BIOLOGY REVIEWS, 1998, 62 (04) :1046-+
[4]   Mss51p and Cox14p jointly regulate mitochondrial Cox1p expression in Saccharomyces cerevisiae [J].
Barrientos, A ;
Zambrano, A ;
Tzagoloff, A .
EMBO JOURNAL, 2004, 23 (17) :3472-3482
[5]   Shy1p is necessary for full expression of mitochondrial COX1 in the yeast model of Leigh's syndrome [J].
Barrientos, A ;
Korr, D ;
Tzagoloff, A .
EMBO JOURNAL, 2002, 21 (1-2) :43-52
[6]   Molecular mechanism of proton translocation by cytochrome c oxidase [J].
Belevich, Ilya ;
Verkhovsky, Michael I. .
ANTIOXIDANTS & REDOX SIGNALING, 2008, 10 (01) :1-29
[7]   Metals in the "omics" world:: copper homeostasis and cytochrome c oxidase assembly in a new light [J].
Bertini, Ivano ;
Cavallaro, Gabriele .
JOURNAL OF BIOLOGICAL INORGANIC CHEMISTRY, 2008, 13 (01) :3-14
[8]   Copper trafficking to the mitochondrion and assembly of copper metalloenzymes [J].
Cobine, Paul A. ;
Pierrel, Fabien ;
Winge, Dennis R. .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2006, 1763 (07) :759-772
[9]  
CRANE F. L., 1971, Methods in Enzymology, V18C, P137, DOI 10.1016/S0076-6879(71)18022-6
[10]   THE TERMINAL OXIDASES OF PARACOCCUS-DENITRIFICANS [J].
DEGIER, JWL ;
LUBBEN, M ;
REIJNDERS, WNM ;
TIPKER, CA ;
SLOTBOOM, DJ ;
VANSPANNING, RJM ;
STOUTHAMER, AH ;
VANDEROOST, J .
MOLECULAR MICROBIOLOGY, 1994, 13 (02) :183-196