Acidianus ambivalens type-II NADH dehydrogenase:: genetic characterisation and identification of the flavin moiety as FMN

被引:24
作者
Bandeiras, TM
Salgueiro, C
Kletzin, A
Gomes, CM
Teixeira, M
机构
[1] Univ Nova Lisboa, Inst Tecnol Quim & Biol, P-2780156 Oeiras, Portugal
[2] Univ Nova Lisboa, Dept Quim, Fac Ciencias & Tecnol, P-2825114 Caparica, Portugal
[3] Med Univ Lubeck, Inst Biochem, D-23538 Lubeck, Germany
关键词
type IINADH dehydrogenase; archaea; sulfolobales; FMN; 31P NMR;
D O I
10.1016/S0014-5793(02)03514-7
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 thermoacidophilic archaeon Acidianus ambivalens contains a monomeric 47 kDa type-II NADH dehydrogenase (NDH), which contains a covalently bound flavin. In this work, by a combination of several methods, namely P-31-nuclear magnetic resonance and fluorescence spectroscopies, it is proven that this enzyme contains covalent FMN, a novelty among this family of enzymes, which were so far thought to mainly have the flavin dinucleotide form. Discrimination between several possible covalent flavin linkages was achieved by spectral and fluorescence experiments, which identified an 8alpha-N(1)-histidylflavintype of linkage. Analysis of the gene-deduced amino acid sequence of type-II NDH showed no transmembranar helices and allowed the definition of putative dinucleotide and quinone binding motifs. Further, it is suggested that membrane anchoring can be achieved via amphipatic helices. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:273 / 277
页数:5
相关论文
共 20 条
[1]   PROTEIN DATABASE SEARCHES FOR MULTIPLE ALIGNMENTS [J].
ALTSCHUL, SF ;
LIPMAN, DJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (14) :5509-5513
[2]   Expression and mutagenesis of the NqrC subunit of the NQR respiratory Na+ pump from Vibrio cholerae with covalently attached FMN [J].
Barquera, B ;
Häse, CC ;
Gennis, RB .
FEBS LETTERS, 2001, 492 (1-2) :45-+
[3]   RGS4 binds to membranes through an amphipathic α-helix [J].
Bernstein, LS ;
Grillo, AA ;
Loranger, SS ;
Linder, ME .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (24) :18520-18526
[4]   The membrane association domain of RGS16 contains unique amphipathic features that are conserved in RGS4 and RGS5 [J].
Chen, CH ;
Seow, KT ;
Guo, K ;
Yaw, LP ;
Lin, SC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (28) :19799-19806
[5]   Prediction of transmembrane alpha-helices in prokaryotic membrane proteins: the dense alignment surface method [J].
Cserzo, M ;
Wallin, E ;
Simon, I ;
vonHeijne, G ;
Elofsson, A .
PROTEIN ENGINEERING, 1997, 10 (06) :673-676
[6]   A new type-II NADH dehydrogenase from the archaeon Acidianus ambivalens:: Characterization and in vitro reconstitution of the respiratory chain [J].
Gomes, CM ;
Bandeiras, TM ;
Teixeira, M .
JOURNAL OF BIOENERGETICS AND BIOMEMBRANES, 2001, 33 (01) :1-8
[7]   Conformation and lipid binding properties of four peptides derived from the membrane-binding domain of CTP:phosphocholine cytidylyltransferase [J].
Johnson, JE ;
Rao, NM ;
Hui, SW ;
Cornell, RB .
BIOCHEMISTRY, 1998, 37 (26) :9509-9519
[8]   Hidden Markov models for detecting remote protein homologies [J].
Karplus, K ;
Barrett, C ;
Hughey, R .
BIOINFORMATICS, 1998, 14 (10) :846-856
[9]   Enhanced genome annotation using structural profiles in the program 3D-PSSM [J].
Kelley, LA ;
MacCallum, RM ;
Sternberg, MJE .
JOURNAL OF MOLECULAR BIOLOGY, 2000, 299 (02) :499-520
[10]   Diversity and origin of alternative NADH:ubiquinone oxidoreductases [J].
Kerscher, SJ .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 2000, 1459 (2-3) :274-283