Alternative oxidase

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The alternative oxidase shown as part of the complete electron transport chain. UQ is ubiquinol/ubiquinone, C is cytochrome c and AOX is the alternative oxidase. AOX.png
The alternative oxidase shown as part of the complete electron transport chain. UQ is ubiquinol/ubiquinone, C is cytochrome c and AOX is the alternative oxidase.
AOX
Identifiers
SymbolAOX
Pfam PF01786
InterPro IPR002680
OPM superfamily 357
OPM protein 3w54
Available protein structures:
Pfam   structures / ECOD  
PDB RCSB PDB; PDBe; PDBj
PDBsum structure summary

The alternative oxidase (AOX) is an enzyme that forms part of the electron transport chain in mitochondria of different organisms. [1] [2] Proteins homologous to the mitochondrial oxidase and the related plastid terminal oxidase have also been identified in bacterial genomes. [3] [4]

Contents

The oxidase provides an alternative route for electrons passing through the electron transport chain to reduce oxygen. However, as several proton-pumping steps are bypassed in this alternative pathway, activation of the oxidase reduces ATP generation. This enzyme was first identified as a distinct oxidase pathway from cytochrome c oxidase as the alternative oxidase is resistant to inhibition by the poison cyanide. [5]

Function

The fungicide azoxystrobin. Azoxystrobin-2D-skeletal.png
The fungicide azoxystrobin.

This metabolic pathway leading to the alternative oxidase diverges from the cytochrome-linked electron transport chain at the ubiquinone pool. [6] Alternative pathway respiration only produces proton translocation at Complex 1 (NADH dehydrogenase) and so has a lower ATP yield than the full pathway. The expression of the alternative oxidase gene AOX is influenced by stresses such as cold, reactive oxygen species and infection by pathogens, as well as other factors that reduce electron flow through the cytochrome pathway of respiration. [7] [8] Although the benefit conferred by this activity remains uncertain, it may enhance an organism's ability to resist these stresses by maintaining the oxidized state of the upstream electron-transport components, thereby reducing the level of oxidative stress induced by overreduced electron carriers. [9]

Unusually, the bloodstream form of the protozoan parasite Trypanosoma brucei , which is the cause of sleeping sickness, depends entirely on the alternative oxidase pathway for cellular respiration through its electron transport chain. [10] [11] This major metabolic difference between the parasite and its human host has made the T. brucei alternative oxidase an attractive target for drug design. [12] [13] Of the known inhibitors of alternative oxidases, the antibiotic ascofuranone inhibits the T. brucei enzyme and cures infection in mice. [14] [15]

In fungi, the ability of the alternative oxidase to bypass inhibition of parts of the electron transport chain can contribute to fungicide resistance. This is seen in the strobilurin fungicides that target complex III, such as azoxystrobin, picoxystrobin and fluoxastrobin. [16] However, even though the alternative pathway generates less ATP, these fungicides are still effective in preventing spore germination, as this is an energy-intensive process. [17]

Structure and mechanism

The alternative oxidase is an integral monotopic membrane protein that is tightly bound to the inner mitochondrial membrane from matrix side [18] The enzyme has been predicted to contain a coupled diiron center on the basis of a conserved sequence motif consisting of the proposed iron ligands, four glutamate and two histidine amino acid residues. [19] The electron spin resonance study of Arabidopsis thaliana alternative oxidase AOX1a showed that the enzyme contains a hydroxo-bridged mixed-valent Fe(II)/Fe(III) binuclear iron center. [20] A catalytic cycle has been proposed that involves this di-iron center and at least one transient protein-derived free radical, which is probably formed on a tyrosine residue. [21]

See also

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References

  1. ↑ McDonald A, Vanlerberghe G (2004). "Branched mitochondrial electron transport in the Animalia: presence of alternative oxidase in several animal phyla". IUBMB Life. 56 (6): 333–41. doi:10.1080/1521-6540400000876. PMID   15370881.
  2. ↑ Sluse FE, Jarmuszkiewicz W (1998). "Alternative oxidase in the branched mitochondrial respiratory network: an overview on structure, function, regulation, and role". Braz. J. Med. Biol. Res. 31 (6): 733–47. doi: 10.1590/S0100-879X1998000600003 . PMID   9698817.
  3. ↑ McDonald AE, Amirsadeghi S, Vanlerberghe GC (2003). "Prokaryotic orthologues of mitochondrial alternative oxidase and plastid terminal oxidase". Plant Mol. Biol. 53 (6): 865–76. doi:10.1023/B:PLAN.0000023669.79465.d2. PMID   15082931. S2CID   41525108.
  4. ↑ Atteia A, van Lis R, van Hellemond JJ, Tielens AG, Martin W, Henze K (2004). "Identification of prokaryotic homologues indicates an endosymbiotic origin for the alternative oxidases of mitochondria (AOX) and chloroplasts (PTOX)". Gene. 330: 143–8. doi:10.1016/j.gene.2004.01.015. PMID   15087133.
  5. ↑ Moore AL, Siedow JN (1991). "The regulation and nature of the cyanide-resistant alternative oxidase of plant mitochondria". Biochim. Biophys. Acta. 1059 (2): 121–40. doi:10.1016/S0005-2728(05)80197-5. PMID   1883834.
  6. ↑ Juszczuk IM, Rychter AM (2003). "Alternative oxidase in higher plants" (PDF). Acta Biochim. Pol. 50 (4): 1257–71. doi: 10.18388/abp.2003_3649 . PMID   14740012.
  7. ↑ Vanlerberghe GC, McIntosh L (1997). "Alternative oxidase: From Gene to Function". Annual Review of Plant Physiology and Plant Molecular Biology. 48: 703–734. doi:10.1146/annurev.arplant.48.1.703. PMID   15012279.
  8. ↑ Ito Y, Saisho D, Nakazono M, Tsutsumi N, Hirai A (1997). "Transcript levels of tandem-arranged alternative oxidase genes in rice are increased by low temperature". Gene. 203 (2): 121–9. doi:10.1016/S0378-1119(97)00502-7. PMID   9426242.
  9. ↑ Maxwell DP, Wang Y, McIntosh L (1999). "The alternative oxidase lowers mitochondrial reactive oxygen production in plant cells". Proc. Natl. Acad. Sci. U.S.A. 96 (14): 8271–6. Bibcode:1999PNAS...96.8271M. doi: 10.1073/pnas.96.14.8271 . PMC   22224 . PMID   10393984.
  10. ↑ Chaudhuri M, Ott RD, Hill GC (2006). "Trypanosome alternative oxidase: from molecule to function". Trends Parasitol. 22 (10): 484–91. doi:10.1016/j.pt.2006.08.007. PMID   16920028.
  11. ↑ Clarkson AB, Bienen EJ, Pollakis G, Grady RW (1989). "Respiration of bloodstream forms of the parasite Trypanosoma brucei brucei is dependent on a plant-like alternative oxidase". J. Biol. Chem. 264 (30): 17770–6. doi: 10.1016/S0021-9258(19)84639-2 . PMID   2808350.
  12. ↑ Nihei C, Fukai Y, Kita K (2002). "Trypanosome alternative oxidase as a target of chemotherapy". Biochim. Biophys. Acta. 1587 (2–3): 234–9. doi: 10.1016/s0925-4439(02)00086-8 . PMID   12084465.
  13. ↑ Grady RW, Bienen EJ, Dieck HA, Saric M, Clarkson AB (1993). "N-n-alkyl-3,4-dihydroxybenzamides as inhibitors of the trypanosome alternative oxidase: activity in vitro and in vivo". Antimicrob. Agents Chemother. 37 (5): 1082–5. doi:10.1128/aac.37.5.1082. PMC   187903 . PMID   8517695.
  14. ↑ Minagawa N, Yabu Y, Kita K, Nagai K, Ohta N, Meguro K, Sakajo S, Yoshimoto A (1997). "An antibiotic, ascofuranone, specifically inhibits respiration and in vitro growth of long slender bloodstream forms of Trypanosoma brucei brucei". Mol. Biochem. Parasitol. 84 (2): 271–80. doi:10.1016/S0166-6851(96)02797-1. PMID   9084049.
  15. ↑ Yabu Y, Yoshida A, Suzuki T, Nihei C, Kawai K, Minagawa N, Hosokawa T, Nagai K, Kita K, Ohta N (2003). "The efficacy of ascofuranone in a consecutive treatment on Trypanosoma brucei brucei in mice". Parasitol. Int. 52 (2): 155–64. doi:10.1016/S1383-5769(03)00012-6. PMID   12798927.
  16. ↑ Miguez M, Reeve C, Wood PM, Hollomon DW (2004). "Alternative oxidase reduces the sensitivity of Mycosphaerella graminicola to QOI fungicides". Pest Manag. Sci. 60 (1): 3–7. doi:10.1002/ps.837. PMID   14727735.
  17. ↑ Avila-Adame C, Köller W (2003). "Impact of alternative respiration and target-site mutations on responses of germinating conidia of Magnaporthe grisea to Qo-inhibiting fungicides". Pest Manag. Sci. 59 (3): 303–9. doi:10.1002/ps.638. PMID   12639047.
  18. ↑ Berthold DA, Stenmark P (2003). "Membrane-bound diiron carboxylate proteins". Annual Review of Plant Biology. 54: 497–517. doi:10.1146/annurev.arplant.54.031902.134915. PMID   14503001.
  19. ↑ Berthold DA, Andersson ME, Nordlund P (2000). "New insight into the structure and function of the alternative oxidase". Biochim. Biophys. Acta. 1460 (2–3): 241–54. doi:10.1016/S0005-2728(00)00149-3. PMID   11106766.
  20. ↑ Berthold DA, Voevodskaya N, Stenmark P, Gräslund A, Nordlund P (2002). "EPR studies of the mitochondrial alternative oxidase. Evidence for a diiron carboxylate center". J. Biol. Chem. 277 (46): 43608–14. doi: 10.1074/jbc.M206724200 . PMID   12215444.
  21. ↑ Affourtit C, Albury MS, Crichton PG, Moore AL (2002). "Exploring the molecular nature of alternative oxidase regulation and catalysis". FEBS Lett. 510 (3): 121–6. doi: 10.1016/S0014-5793(01)03261-6 . PMID   11801238. S2CID   12175724.
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