Mitochondrial function and critical temperature in the Antarctic bivalve, Laternula elliptica

Comparative Biochemistry and Physiology - A Molecular and Integrative Physiology

Volumn 124, Issue 2, 1999, Pages 179-189

  Pörtner, Hans O ^a   Hardewig, Iris ^a   Peck, Lloyd S ^b  

^a ALFRED WEGENER INSTITUTE FOR POLAR AND MARINE RESEARCH   (Germany)

^b BRITISH ANTARCTIC SURVEY   (United Kingdom)

Author keywords

Activation energy; Antarctic bivalve; Cold adaptation; Critical temperature; Isocitrate dehydrogenase; Laternula elliptica; Mitochondria; Proton leak

Indexed keywords

ISOCITRATE DEHYDROGENASE; NICOTINAMIDE ADENINE DINUCLEOTIDE PHOSPHATE; OLIGOMYCIN;

ANIMAL TISSUE; ANTARCTICA; ARTICLE; CLAM; COLD ACCLIMATIZATION; CONTROLLED STUDY; GILL; INHALATIONAL DRUG ADMINISTRATION; MITOCHONDRIAL RESPIRATION; NONHUMAN; OXIDATIVE PHOSPHORYLATION; OXYGEN CONSUMPTION; PROTON TRANSPORT; TEMPERATURE;

LATERNULA ELLIPTICA;

EID: 0038206002     PISSN: 10956433     EISSN: None     Source Type: Journal    
DOI: 10.1016/S1095-6433(99)00105-1     Document Type: Article

References (53)

1. +-linked isocitrate dehydrogenase in muscle from vertebrates and invertebrates. Biochem. J. 154:1976;689-700.
2. Arntz W.E., Brey T., Gallardo V.A. Antarctic Zoobenthos. Oceanogr. Mar. Biol.: Ann. Rev. 32:1994;241-304.
3. Ballantyne J.S., Moyes C.D. The effects of salinity acclimation on the osmotic properties of mitochondria from the gill of Crassostrea gigas. J. Exp. Biol. 133:1987;449-456.
4. Blier P.U., Guderley H. Mitochondrial activity in rainbow trout red muscle: the effect of temperature on the ADP-dependence of ATP synthesis. J. Exp. Biol. 176:1993;145-157.
5. Brand M.D. The contribution of the leak of protons across the mitochondrial inner membrane to standard metabolic rate. J. Theor. Biol. 145:1990;267-286.
6. Brand M.D., Couture P., Else P.L., Withers K.W., Hulbert A.J. Evolution of energy metabolism. Proton permeability of the inner membrane of liver mitochondria is greater in a mammal than in a reptile. Biochem. J. 275:1991;81-86.
7. Brand M.D., Chien L.-F., Ainscow E.K., Rolfe D.F.S., Porter R.K. The causes and functions of mitochondrial proton leak. Biochim. Biophys. Acta. 1187:1994;132-139.
8. Brookes P.S., Rolfe D.F.S., Brand M.D. The proton permeability of liposomes made from mitochondrial inner membrane phospholipids: comparison with intact mitochondria. J. Membr. Biol. 155:1997;167-173.
9. Brookes P.S., Buckingham J.A., Tenreiro A.M., Hulbert A.J., Brand M.D. The proton permeability of the inner membrane of liver mitochondria from ectothermic and endothermic vertebrates and from obese rats: correlations with standard metabolic rate and phospholipid fatty acid composition. Comp. Biochem. Physiol. 119B:1998;325-334.
10. Burcham J.M., Paynter K.T., Bishop S.H. Coupled mitochondria from oyster gill tissue. Mar. Biol. Lett. 4:1983;349-356.
11. Burcham J.M., Ritchie A.L., Bishop S.H. Preparation and some respiratory properties of coupled mitochondria from ribbed mussel (Modiolus demissus) gill tissue. J. Exp. Zool. 229:1984;55-67.
12. Chance B., Williams G.R. The respiratory chain and oxidative phosphorylation. Adv. Enzymol. 17:1956;65-134.
13. Clarke A. Temperature and energetics: an introduction to cold ocean physiology. Pörtner H.O., Playle R. Cold Ocean Physiology. 1998;3-30 Cambridge University Press.
14. Crockett E.L., Sidell B.D. Some pathways of energy metabolism are cold adapted in Antarctic fishes. Physiol. Zool. 63:1990;472-488.
15. Dahlhoff E., O'Brien J., Somero G.N., Vetter R.D. Temperature effects on mitochondria from hydrothermal vent invertebrates: evidence for adaptation to elevated and variable habitat temperatures. Physiol. Zool. 64:1991;1490-1518.
16. Davis E.J., Davis-van Thienen W.I.A. An assessment of the role of proton leaks in the mechanistic stoichiometry of oxidative phosphorylation. Arch. Biochem. Biophys. 289:1991;184-186.
17. Dufour S., Rousse N., Canioni P., Diolez P. Top-down control analysis of temperature effect on oxidative phosphorylation. Biochem. J. 314:1996;743-751.
18. Dunn J.F. Low-temperature adaptation of oxidative energy production in cold-water fishes. Can. J. Zool. 66:1988;1098-1104.
19. J.C. Ellory, A.C. Hall, Temperature effects on red cell membrane transport processes, in: K. Bowler, B.J. Fuller (Eds.), Temperature and Animal Cells. Symp. Soc. Exp. Biol., Vol. 31, pp. 53-66.
20. Greenbaum N.L., Wilson D.F. Role of intramitochondrial pH in the energetics and regulation of mitochondrial oxidative phosphorylation. Biochim. Biophys. Acta. 1058:1991;11-120.
21. Guderley H., Johnston I.A. Plasticity of fish muscle mitochondria with thermal acclimation. J. Exp. Biol. 199:1996;1311-1317.
22. Guderley H. Temperature and growth rates as modulators of the metabolic capacities of fish muscle. Pörtner H.O., Playle R. Cold Ocean Physiology. 1998;58-87 Cambridge University Press.
23. Hardewig I, Peck LS, Pörtner HO. Thermal sensitivity of mitochondrial function in the Antarctic Notothenioid Lepidonotothen nudifrons. J. Comp. Physiol. B. 1999 (in press).
24. Hardy P. Biomass estimates from shallow water infaunal communities at Signy Island, South Orkney Islands. Br. Antarctic Survey Bull. 31:1972;93-106.
25. Houlihan D.F., Allan D. Oxygen consumption of some Antarctic and British gastropods: an evaluation of cold adaptation. Comp. Biochem. Physiol. 73A:1982;383-387.
26. Howlett R.A., Willis W.T. Fiber-type-related differences in the enzymes of a proposed substrate cycle. Biochim. Biophys. Acta. 1363:1998;224-230.
27. Hummel H., Sommer A., Bogaards R.H., Pörtner H.O. Variation in genetic traits of the lugworm Arenicola marina: temperature related expression of mitochondrial allozymes? Mar. Ecol. Prog. Ser. 159:1997;189-195.
28. Johnston I.A., Guderley H., Franklin C.E., Crockford T., Kamunde C. Are mitochondria subject to evolutionary temperature adaptations? J. Exp. Biol. 195:1994;293-306.
29. Johnston I.A., Calvo J., Guderley H., Fernandez D., Palmer L. Latitudinal variation in the abundance and oxidative capacities of muscle mitochondria in perciform fishes. J. Exp. Biol. 201:1998;1-12.
30. Lee C.P., Gu Q., Xiong Y., Michell R.A., Ernster L. P/O ratios reassessed: mitochondrial P/O ratios consistently exceed 1.5 with succinate and 2.5 with NAD-linked substrates. FASEB J. 10:1996;345-350.
31. Masini A., Ceccarelli-Stanzani D., Muscatello U. Phosphorylating efficiency of isolated rat liver mitochondria respiring under the conditions of steady-state 4. Biochim. Biophys. Acta. 724:1983;251-257.
32. Mommsen T.P., Hochachka P.W. Respiratory and enzymatic properties of squid heart mitochondria. Eur. J. Biochem. 120:1981;345-350.
33. Moyes C.D., Moon T.W., Ballantyne J.S. Glutamate metabolism in mitochondria from Mya arenaria mantle: effects of pH on the role of glutamate dehydrogenase. J. Exp. Zool. 236:1985;293-301.
34. Moyes C.D., Buck L.T., Hochachka P.W. Temperature effects on pH of mitochondria isolated from carp red muscle. Am. J. Physiol. 254:1988;R611-R615.
35. Nickerson D.M., Facey D.E., Grossman G.D. Estimating physiological thresholds with continuous two-phase regression. Physiol. Zool. 62:1989;866-887.
36. O'Brien J., Dahlhoff E., Somero G. Thermal resistance of mitochondrial respiration: hydrophobic interactions of membrane proteins may limit thermal resistance. Physiol. Zool. 64:1991;1509-1526.
37. O2(s) in oxyconforming and oxyregulating animals: gas exchange, metabolic rate and the mode of energy production. Bicudo J.E.P.W. The Vertebrate Gas Transport Cascade: Adaptations to Environment and Mode of Life. 1993;330-357 CRC Press, Boca Raton, FL.
38. Pörtner H.O., Hardewig I., Sartoris F.J., van Dijk P. Energetic aspects of cold adaptation: critical temperatures in metabolic, ionic and acid-base regulation? Pörtner H.O., Playle R. Cold Ocean Physiology. 1998;88-120 Cambridge University Press.
39. Pörtner H.O., van Dijk P.L.M., Hardewig I., Sommer A. Levels of metabolic cold adaptation: trade-offs in eurythermal and stenothermal ectotherms. Davison W., Williams C.H. Antarctic Ecosystems: Models for Wider Ecological Understanding. 1999 (in press);Caxton Press, Christchurch, New Zealand.
40. Ralph R., Maxwell J.G.H. Growth of two Antarctic lamellibranchs: Adamussium colbecki and Laternula elliptica. Mar. Biol. 42:1977;171-175.
41. Rolfe D.F.S., Brand M.D. Contribution of mitochondrial proton leak to skeletal muscle respiration and to standard metabolic rate. Am. J. Physiol. 271:1996;C1380-1389.
42. Sazanov L.A., Jackson J.B. Proton-translocating transhydrogenase and NAD- and NADP-linked isocitrate dehydrogenases operate in a substrate cycle which contributes to fine regulation of the tricarboxylic acid cycle activity in mitochondria. FEBS Lett. 344:1994;109-116.
43. Sidell B.D., Hazel J.R. Temperature effects the diffusion of small molecules through cytosol of fish muscle. J. Exp. Biol. 129:1987;191-203.
44. Sommer A., Klein B., Pšrtner H.O. Temperature induced anaerobiosis in two populations of the polychaete worm Arenicola marina. J. Comp. Physiol. 167B:1997;25-35.
45. Sommer A., Pörtner H.O. Exposure of Arenicola marina (L.) to extreme temperatures: adaptive flexibility of a boreal and a subpolar population. Mar. Ecol. Prog. Ser. 181:1999;215-226.
46. Storelli C., Acierno R., Maffia M. Membrane lipids and protein adaptations in Antarctic fish. Pörtner H.O., Playle R. Cold Ocean Physiology. 1998;166-189 Cambridge University Press.
47. P.L.M. van Dijk, C. Tesch, I. Hardewig, H.O. Pörtner, Physiological disturbances at critically high temperatures. A comparison between stenothermal Antarctic, and eurythermal temperate eelpouts (Zoarcidae), J. Exp. Biol. 1999 (in press).
48. Yeager D.P., Ultsch G.R. Physiological regulation and conformation: a BASIC program for the determination of critical points. Physiol. Zool. 62:1989;888-907.
49. Weinstein R.B., Somero G.N. Effects of temperature on mitochondrial function in the Antarctic fish Trematomus bernachii. J. Comp. Physiol. 168:1998;190-196.
50. Wibom R., Lundin A., Hultman E. A sensitive method for measuring ATP-formation in rat muscle mitochondria. Scand. J. Clin. Invest. 50:1990;143-152.
51. Wieser W. Developmental and metabolic constraints of the scope of activity in young rainbow trout (Salmo gairdneri). J. Exp. Biol. 118:1985;133-142.
52. Williams E.E., Hazel J.R. Thermal adaptation in fish membranes: temporal resolution of adaptive mechanisms. Cossins A.R. Temperature Adaptation of Biological Membranes. 1994;91-106 Portland Press, London.
53. Zielinski S., Pörtner H.O. Energy metabolism and ATP free-energy change of the intertidal worm Sipunculus nudus below a critical temperature. J. Comp. Physiol. 166B:1996;492-500.