Crystal structure of the electron transfer complex rubredoxin-rubredoxin reductase of Pseudomonas aeruginosa

被引:59
作者
Hagelueken, Gregor
Wiehlmann, Lutz
Adams, Thorsten M.
Kolmar, Harald
Heinz, Dirk W.
Tuemmler, Burkhard
Schubert, Wolf-Dieter
机构
[1] Helmholtz Ctr Infect Res, Mol Host Pathogen Interact, D-38124 Braunschweig, Germany
[2] Helmholtz Ctr Infect Res, Div Struct Biol, D-38124 Braunschweig, Germany
[3] Hannover Med Sch, Klin Forschergrp OE 6711, D-30625 Hannover, Germany
[4] Tech Univ Darmstadt, Clemens Schoepf Inst Organ Chem & Biochem, D-64287 Darmstadt, Germany
关键词
D O I
10.1073/pnas.0702919104
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Crude oil spills represent a major ecological threat because of the chemical inertness of the constituent n-alkanes. The Gram-negative bacterium Pseudomonas aeruginosa is one of the few bacterial species able to metabolize such compounds. Three chromosomal genes, rubB, rubA1, and rubA2 coding for an NAD(P)H:rubredoxin reductase (RdxR) and two rubredoxins (Rdxs) are indispensable for this ability. They constitute an electron transport (ET) pathway that shuttles reducing equivalents from carbon metabolism to the membrane-bound alkane hydroxylases AlkB1 and AlkB2. The RdxR-Rdx system also is crucial as part of the oxidative stress response in archaea or anaerobic bacteria. The redox couple has been analyzed in detail as a model system for ET processes. We have solved the structure of RdxR of A aeruginosa both alone and in complex with Rdx, without the need for cross-linking, and both structures were refined at 2.40- and 2.45-angstrom resolution, respectively. Rc1xR consists of two cofactor-binding domains and a C-terminal domain essential for the specific recognition of Rdx. Only a small number of direct interactions govern mutual recognition of RdxR and Rdx, corroborating the transient nature of the complex. The shortest distance between the redox centers is observed to be 6.2 angstrom.
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页码:12276 / 12281
页数:6
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