The plant biotin synthase reaction - Identification and characterization of essential mitochondrial accessory protein components

被引:67
作者
Picciocchi, A [1 ]
Douce, R [1 ]
Alban, C [1 ]
机构
[1] Bayer CropSci, Lab Mixte Rech,CNRS, INRA, UMR 1932, F-69263 Lyon 9, France
关键词
D O I
10.1074/jbc.M302154200
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
In plants, the last step of the biotin biosynthetic pathway is localized in mitochondria. This chemically complex reaction is catalyzed by the biotin synthase protein, encoded by the bio2 gene in Arabidopsis thaliana. Unidentified mitochondrial proteins in addition to the bio2 gene product are obligatory for the reaction to occur. In order to identify these additional proteins, potato mitochondrial matrix was fractionated onto different successive chromatographic columns. Combination experiments using purified Bio2 protein and the resulting mitochondrial matrix subfractions together with a genomic based research allowed us to identify mitochondrial adrenodoxin, adrenodoxin reductase, and cysteine desulfurase (Nfs1) proteins as essential components for the plant biotin synthase reaction. Arabidopsis cDNAs encoding these proteins were cloned, and the corresponding proteins were expressed in Escherichia coli cells and purified. Purified recombinant adrenodoxin and adrenodoxin reductase proteins formed in vitro an efficient low potential electron transfer chain that interacted with the bio2 gene product to reconstitute a functional plant biotin synthase complex. Bio2 from Arabidopsis is the first identified protein partner for this specific plant mitochondrial redox chain.
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页码:24966 / 24975
页数:10
相关论文
共 53 条
[11]  
Bui BTS, 2000, EUR J BIOCHEM, V267, P2688
[12]  
Chua N. H., 1980, METHOD ENZYMOL, V69, P434
[13]  
DOUCE R, 1987, METHOD ENZYMOL, V148, P403
[14]  
EISENBERG MA, 1987, CELLULAR MOL BIOL, P544
[15]   LAMBDA-YES - A MULTIFUNCTIONAL CDNA EXPRESSION VECTOR FOR THE ISOLATION OF GENES BY COMPLEMENTATION OF YEAST AND ESCHERICHIA-COLI MUTATIONS [J].
ELLEDGE, SJ ;
MULLIGAN, JT ;
RAMER, SW ;
SPOTTSWOOD, M ;
DAVIS, RW .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1991, 88 (05) :1731-1735
[16]   Interaction between the lipoamide-containing H-protein and the lipoamide dehydrogenase (L-protein) of the glycine decarboxylase multienzyme system - 2. Crystal structures of H- and L-proteins [J].
Faure, M ;
Bourguignon, J ;
Neuburger, M ;
Macherel, D ;
Sieker, L ;
Ober, R ;
Kahn, R ;
Cohen-Addad, C ;
Douce, R .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 2000, 267 (10) :2890-2898
[17]   Transfer of sulfur to biotin from biotin synthase (BioB protein) [J].
Gibson, KJ ;
Pelletier, DA ;
Turner, IM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 254 (03) :632-635
[18]   Biotin synthase, a new member of the family of enzymes which uses S-adenosylmethionine as a source of deoxyadenosyl radical (vol 236, pg 402, 1997) [J].
Guianvarc'h, D ;
Florentin, D ;
Bui, BTS ;
Nunzi, F ;
Marquet, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1997, 240 (01) :246-246
[19]   Mutagenesis of the proposed iron-sulfur cluster binding ligands in Escherichia coli biotin synthase [J].
Hewitson, KS ;
Baldwin, JE ;
Shaw, NM ;
Roach, PL .
FEBS LETTERS, 2000, 466 (2-3) :372-376
[20]   FLAVODOXIN IS REQUIRED FOR CONVERSION OF DETHIOBIOTIN TO BIOTIN IN ESCHERICHIA-COLI [J].
IFUKU, O ;
KOGA, N ;
HAZE, S ;
KISHIMOTO, J ;
WACHI, Y .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 224 (01) :173-178