Mitochondria as we don't know them

Trends in Biochemical Sciences

Volumn 27, Issue 11, 2002, Pages 564-572

  Tielens, Aloysius G M ^a   Rotte, Carmen ^b   Van Hellemond, Jaap J ^a   Martin, William ^b  

^a UTRECHT UNIVERSITY   (Netherlands)

^b HEINRICH HEINE UNIVERSITY   (Germany)

Author keywords

[No Author keywords available]

Indexed keywords

ADENOSINE TRIPHOSPHATE; CARBOHYDRATE; FUMARATE REDUCTASE; OXYGEN; PROTON PUMP; SUCCINATE DEHYDROGENASE;

ANAEROBIC METABOLISM; BIOCHEMISTRY; CELL FUNCTION; CELL ORGANELLE; ELECTRON TRANSPORT; ENERGY RESOURCE; EUKARYOTE; FUNGAL STRAIN; METAZOON; MITOCHONDRIAL RESPIRATION; MOLECULAR EVOLUTION; NONHUMAN; OXIDATION; PRIORITY JOURNAL; RESPIRATORY CHAIN; REVIEW;

ADENOSINE TRIPHOSPHATE; ANIMALS; ELECTRON TRANSPORT; ENERGY METABOLISM; EUKARYOTIC CELLS; MITOCHONDRIA; OXYGEN; PHYLOGENY; PROTON PUMPS; SUCCINATE DEHYDROGENASE;

EUKARYOTA; METAZOA; PROTISTA;

EID: 0036849127     PISSN: 09680004     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0968-0004(02)02193-X     Document Type: Review

References (57)

1. Müller M. The hydrogenosome. J. Gen. Microbiol. 139:1993;2879-2889.
2. Embley T.M., et al. Multiple origins of anaerobic ciliates with hydrogenosomes within the radiation of aerobic ciliates. Proc. R. Soc. Lond. Ser. B Biol. Sci. 262:1995;87-935.
3. Hackstein J.H., et al. Hydrogenosomes: eukaryotic adaptations to anaerobic environments. Trends Microbiol. 7:1999;441-447.
4. Kulda J. Trichomonads, hydrogenosomes and drug resistance. Int. J. Parasitol. 29:1999;199-212.
5. Hackstein J.H., et al. Hydrogenosomes: convergent adaptations of mitochondria to anaerobic environments. Zoology. 104:2001;290-302.
6. Van der Giezen M., et al. Conserved properties of hydrogenosomal and mitochondrial ADP/ATP carriers: a common origin for both organelles. EMBO J. 21:2002;572-579.
7. Voncken F.G.H., et al. Multiple origins of hydrogenosomes: functional and phylogenetic evidence from the ADP/ATP carrier of the anaerobic chytrid Neocallimastix sp. Mol. Microbiol. 44:2002;1441-1454.
8. Finlay B.J., et al. Nitrate respiration in primitive eukaryotes. Nature. 303:1983;333-336.
9. Kobayashi M., et al. Denitrification, a novel type of respiratory metabolism in fungal mitochondrion. J. Biol. Chem. 271:1996;16263-16267.
10. Takaya N., et al. Cytochrome p450nor, a novel class of mitochondrial cytochrome P450 involved in nitrate respiration in the fungus Fusarium oxysporum. Arch. Biochem. Biophys. 372:1999;340-346.
11. Zumft W.G. Cell biology and molecular basis of denitrification. Microbiol. Mol. Biol. Rev. 61:1997;533-616.
12. Tielens A.G.M. Energy generation in parasitic helminths. Parasitol. Today. 10:1994;346-352.
13. Kita K. Electron-transfer complexes of mitochondria in Ascaris suum. Parasitol. Today. 8:1992;155-159.
14. Tielens A.G.M., Van Hellemond J.J. The electron transport chain in anaerobically functioning eukaryotes. Biochim. Biophys. Acta. 1365:1998;71-78.
15. Komuniecki, R. and Harris, B.G. (1995) Carbohydrate and energy metabolism in helminths. In: Biochemistry and Molecular Biology of Parasites (Marr, J.J. and Müller, M., eds.), pp. 49-66, Academic Press.
16. Van Hellemond J.J., et al. Trypanosomatidae produce acetate via a mitochondrial acetate:succinate CoA transferase. Proc. Natl. Acad. Sci. U. S. A. 95:1998;3036-3041.
17. Rich P.R. Electron and proton transfers through quinones and cytochrome bc complexes. Biochim. Biophys. Acta. 768:1984;53-79.
18. Ackrell, B.A.C. et al. (1992) Structure and function of succinate dehydrogenase and fumarate reductase. In: Chemistry and Biochemistry of Flavoenzymes (Vol. 3) (Muller, F., ed.), pp. 229-297, CRC Press.
19. Wissenbach U., et al. An Escherichia coli mutant containing only demethylmenaquinone, but no menaquinone: effects on fumarate, dimethylsulfoxide, trimethylamine N-oxide and nitrate respiration. Arch. Microbiol. 158:1992;68-73.
20. Van Hellemond J.J., Tielens A.G.M. Expression and functional properties of fumarate reductase. Biochem. J. 304:1994;321-331.
21. Van Hellemond J.J., et al. Rhodoquinone and complex II of the electron transport chain in anaerobically functioning eukaryotes. J. Biol. Chem. 270:1995;31065-31070.
22. Ellis J.E., et al. Detection of ubiquinone in parasitic and free-living protozoa, including species devoid of mitochondria. Mol. Biochem. Parasitol. 65:1994;213-224.
23. Hederstedt, L. and Ohnishi, T. (1992) Progress in succinate:quinone oxidoreductase research. In Molecular Mechanisms in Bioenergetics (Ernster, L., ed.), pp. 16-198, Elsevier Science.
24. Lancaster C.R.D. Succinate:quinone oxidoreductases: an overview. Biochim. Biophys. Acta. 1553:2002;1-6.
25. Roos M.H., Tielens A.G.M. Differential expression of two succinate dehydrogenase subunit-B genes and a transition in energy metabolism during the development of the parasitic nematode Haemonchus contortus. Mol. Biochem. Parasitol. 66:1994;273-281.
26. Amino H., et al. Stage-specific isoforms of Ascaris suum complex II: the fumarate reductase of the parasitic adult and the succinate dehydrogenase of free-living larvae share a common iron-sulfur subunit. Mol. Biochem. Parasitol. 106:2000;63-76.
27. Hagerhall C. Succinate: quinone oxidoreductases. Variations on a conserved theme. Biochim. Biophys. Acta. 1320:1997;107-141.
28. Hagerhall C., Hederstedt L. A structural model for the membrane-integral domain of succinate: quinone oxidoreductases. FEBS Lett. 389:1996;25-31.
29. Iverson T.M., et al. Structure of the Escherichia coli fumarate reductase respiratory complex. Science. 284:1999;1961-1966.
30. Lancaster C.R., et al. Structure of fumarate reductase from Wolinella succinogenes at 2.2 A resolution. Nature. 402:1999;377-385.
31. Buetow, D.E. (1989) The mitochondrion. In The Biology of Euglena, Vol. 4. Subcellular Biochemistry and Molecular Biology (Buetow, D.E., ed), pp. 247-314, Academic Press.
32. Schneider T., Betz A. Wax ester fermentation in Euglena gracilis T. Factors favouring the synthesis of odd-numbered fatty acids and alcohols. Planta. 166:1985;67-73.
33. 2-inactivation of the enzyme and its stability in the aerobe. Arch. Biochem. Biophys. 280:1990;292-298.
34. Rotte C., et al. Pyruvate:NADP+ oxidoreductase from the mitochondrion of Euglena gracilis and from the apicomplexan Cryptosporidium parvum: A fusion of pyruvate:ferredoxin oxidoreductase and NADPH-cytochrome P450 reductase. Mol. Biol. Evol. 18:2001;710-720.
35. Yokota A., et al. Mechanism of metabolic regulation in photoassimilation of propionate in Euglena gracilis Z. Arch. Biochem. Biophys. 213:1982;530-537.
36. Shigeoka S., Nakano Y. Characterization and molecular properties of 2-oxoglutarate decarboxylase from Euglena gracilis. Arch. Biochem. Biophys. 288:1991;22-28.
37. Green L.S., et al. Catabolism of alpha-ketoglutarate by a sucA mutant of Bradyrhizobium japonicum: evidence for an alternative tricarboxylic acid cycle. J. Bacteriol. 182:2000;2838-2844.
38. Kitaoka, S. et al. (1989) Enzymes and their functional localization. In The Biology of Euglena, Vol. 4. Subcellular Biochemistry and Molecular Biology (Buetow, D.E., ed.) pp. 2-135, Academic Press.
39. Clayton C.E., Michels P. Metabolic compartmentation in African trypanosomes. Parasitol. Today. 12:1996;465-471.
40. Siedow J.N., Umbach A.L. The mitochondrial cyanide-resistant oxidase: structural conservation amid regulatory diversity. Biochim. Biophys. Acta. 1459:2000;432-439.
41. Völkel S., Grieshaber M.K. Sulphide oxidation and oxidative phosphorylation in the mitochondria of the lugworm Arenicola marina. J. Exp. Biol. 200:1997;83-92.
42. Grieshaber M.K., Völkel S. Animal adaptations for tolerance and exploitation of poisonous sulfide. Annu. Rev. Physiol. 60:1998;33-53.
43. Hahlbeck E., et al. Sulphide detoxification in Hediste diversicolor and Marenzelleria viridis, two dominant polychaete worms within the shallow coastal waters of the southern Baltic Sea. Comp. Biochem. Physiol. B Biochem. Mol. Biol. 125:2000;457-471.
44. Doeller J.E., et al. Chemolithoheterotrophy in a metazoan tissue: thiosulfate production matches ATP demand in ciliated mussel gills. J. Exp. Biol. 204:2001;3755-3764.
45. Doeller J.E., et al. Chemolithoheterotrophy in a metazoan tissue: sulfide supports cellular work in ciliated mussel gills. J. Exp. Biol. 202:1999;1953-1961.
46. Martin W., et al. An overview of endosymbiotic models for the origin of eukaryotes, their ATP-producing organelles (mitochondria and hydrogenosomes), and their heterotrophic lifestyle. Biol. Chem. 382:2001;1521-1539.
47. Kurland C.G., Andersson S.G.E. Origin and evolution of the mitochondrial proteome. Microbiol. Mol. Biol. Rev. 64:2000;786-820.
48. Rotte C., et al. Origins of hydrogenosomes and mitochondria. Curr. Opin. Microbiol. 3:2000;481-486.
49. Martin W., Müller M. The hydrogen hypothesis for the first eukaryote. Nature. 392:1998;37-41.
50. Akhmanova A., et al. A hydrogenosome with a genome. Nature. 396:1998;527-528.
51. Horner D.S., et al. Iron hydrogenases-ancient enzymes in modern eukaryotes. Trends Biochem. Sci. 27:2002;148-153.
52. Voncken F.G.J., et al. A hydrogenosomal [Fe]-hydrogenase from the anaerobic chytrid Neocallimastix sp. L2. Gene. 284:2002;103-112.
53. Gray M.W., et al. Mitochondrial evolution. Science. 283:1999;1476-1481.
54. Tovar J., et al. The mitosome, a novel organelle related to mitochondria in the amitochondrial parasite Entamoeba histolytica. Mol. Microbiol. 32:1999;1013-1021.
55. Blaxter M.L., et al. A molecular evolutionary framework for the phylum Nematoda. Nature. 392:1998;71-75.
56. Nelson, D.L. and Cox, M.M. (2000) Lehninger Principles of Biochemistry (3rd edn), Worth Publishers.
57. De Zwaan, A. (1991) Molluscs. In Metazoan Life without Oxygen (Bryant, C., ed), pp. 186-217, Chapman and Hall.