Involvement of fumarase C and NADH oxidase in metabolic adaptation of Pseudomonas fluorescens cells evoked by aluminum and gallium toxicity

被引:38
作者
Chenier, Daniel [1 ]
Beriault, Robin [1 ]
Mailloux, Ryan [1 ]
Baquie, Mathurin [1 ]
Abramia, Gia [2 ]
Lemire, Joseph [1 ]
Appanna, Vasu [1 ]
机构
[1] Laurentian Univ, Dept Chem & Biochem, Sudbury, ON P3E 2C6, Canada
[2] Int Ctr Environm Res, GE-380079 Tbilisi, Georgia
关键词
D O I
10.1128/AEM.02702-07
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Iron (Fe) is a critical element in all aerobic organisms as it participates in a variety of metabolic networks. In this study, aluminum (Al) and gallium (Ga), two Fe mimetics, severely impeded the ability of the soil microbe Pseudomonas fluorescens to perform oxidative phosphorylation. This was achieved by disrupting the activity and expression of complexes I, II, and IV. These toxic metals also inactivated aconitase (ACN) and fumarase A (FUM A), two tricarboxylic acid cycle enzymes dependent on Fe for their catalytic activity, while FUM C, an Fe-independent enzyme, displayed an increase in activity and expression under these stressed situations. Furthermore, in the Al- and Ga-exposed cells, the activity and expression of an H2O-forming NADH oxidase were markedly increased. The incubation of the Al- and Ga-challenged cells in an Fe-containing medium led to the recovery of the affected enzymatic activities. Taken together, these data provide novel insights into how environmental pollutants such as A] and Ga interfere with cellular Fe metabolism and also illustrate the ability of Pseudomonas fluorescens to modulate metabolic networks to combat this situation.
引用
收藏
页码:3977 / 3984
页数:8
相关论文
共 36 条
[21]   Iron-dependent changes in cellular energy metabolism: influence on citric acid cycle and oxidative phosphorylation [J].
Oexle, H ;
Gnaiger, E ;
Weiss, G .
BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS, 1999, 1413 (03) :99-107
[22]   Gallium disrupts iron metabolism of mycobacteria residing within human macrophages [J].
Olakanmi, O ;
Britigan, BE ;
Schlesinger, LS .
INFECTION AND IMMUNITY, 2000, 68 (10) :5619-5627
[23]   OXYGEN, IRON, CARBON, AND SUPEROXIDE CONTROL OF THE FUMARASE FUMA AND FUMC GENES OF ESCHERICHIA-COLI - ROLE OF THE ARCA, FNR, AND SOXR GENE-PRODUCTS [J].
PARK, SJ ;
GUNSALUS, RP .
JOURNAL OF BACTERIOLOGY, 1995, 177 (21) :6255-6262
[24]   Iron and the redox status of the lungs [J].
Quinlan, GJ ;
Evans, TW ;
Gutteridge, JMC .
FREE RADICAL BIOLOGY AND MEDICINE, 2002, 33 (10) :1306-1313
[25]   Mechanisms of iron regulation in mycobacteria: role in physiology and virulence [J].
Rodriguez, GM ;
Smith, I .
MOLECULAR MICROBIOLOGY, 2003, 47 (06) :1485-1494
[26]   Molecular system bioenergetics: regulation of substrate supply in response to heart energy demands [J].
Saks, Valdur ;
Favier, Roland ;
Guzun, Rita ;
Schlattner, Uwe ;
Wallimann, Theo .
JOURNAL OF PHYSIOLOGY-LONDON, 2006, 577 (03) :769-777
[27]  
Sapan CV, 1999, BIOTECHNOL APPL BIOC, V29, P99
[28]  
Schägger H, 2001, J BIOL CHEM, V276, P37861
[29]   BLUE NATIVE ELECTROPHORESIS FOR ISOLATION OF MEMBRANE-PROTEIN COMPLEXES IN ENZYMATICALLY ACTIVE FORM [J].
SCHAGGER, H ;
VONJAGOW, G .
ANALYTICAL BIOCHEMISTRY, 1991, 199 (02) :223-231
[30]   Friedreich ataxia: the oxidative stress paradox [J].
Seznec, H ;
Simon, D ;
Bouton, C ;
Reutenauer, L ;
Hertzog, A ;
Golik, P ;
Procaccio, V ;
Patel, M ;
Drapier, JC ;
Koenig, M ;
Puccio, H .
HUMAN MOLECULAR GENETICS, 2005, 14 (04) :463-474