A futile cycle, also known as a substrate cycle, occurs when two metabolic pathways run simultaneously in opposite directions and have no overall effect other than to dissipate energy in the form of heat. The reason this cycle was called "futile" cycle was because it appeared that this cycle operated with no net utility for the organism. As such, it was thought of being a quirk of the metabolism and thus named a futile cycle. After further investigation it was seen that futile cycles are very important for regulating the concentrations of metabolites. For example, if glycolysis and gluconeogenesis were to be active at the same time, glucose would be converted to pyruvate by glycolysis and then converted back to glucose by gluconeogenesis, with an overall consumption of ATP. Futile cycles may have a role in metabolic regulation, where a futile cycle would be a system oscillating between two states and very sensitive to small changes in the activity of any of the enzymes involved. The cycle does generate heat, and may be used to maintain thermal homeostasis, for example in the brown adipose tissue of young mammals, or to generate heat rapidly, for example in insect flight muscles and in hibernating animals during periodical arousal from torpor. It has been reported that the glucose metabolism substrate cycle is not a futile cycle but a regulatory process. For example, when energy is suddenly needed, ATP is replaced by AMP, a much more reactive adenine.
But during gluconeogenesis (i.e. synthesis of glucose from pyruvate and other compounds) the reverse reaction takes place, being catalyzed by fructose-1,6-bisphosphatase (FBPase-1).
Giving an overall reaction of:
That is, hydrolysis of ATP without any useful metabolic work being done. Clearly, if these two reactions were allowed to proceed simultaneously at a high rate in the same cell, a large amount of chemical energy would be dissipated as heat. This uneconomical process has therefore been called a futile cycle.
- Schwender J, Ohlrogge J, Shachar-Hill Y (2004). "Understanding flux in plant metabolic networks". Curr Opin Plant Biol. 7 (3): 309–17. doi:10.1016/j.pbi.2004.03.016. PMID 15134752.
- H.,, Garrett, Reginald. Biochemistry. Grisham, Charles M. (Sixth ed.). Boston, MA. p. 767. ISBN 9781305577206. OCLC 914290655.CS1 maint: extra punctuation (link)
- Boiteux A, Hess B (1981). "Design of glycolysis". Philos Trans R Soc Lond B Biol Sci. 293 (1063): 5–22. doi:10.1098/rstb.1981.0056. PMID 6115423.
- Samoilov M, Plyasunov S, Arkin A (2005). "Stochastic amplification and signaling in enzymatic futile cycles through noise-induced bistability with oscillations". Proc Natl Acad Sci USA. 102 (7): 2310–5. doi:10.1073/pnas.0406841102. PMC 548975. PMID 15701703.
- Nelson, D. L., Lehninger, A. L., & Cox, M. M. (2008). Lehninger principles of biochemistry (5th ed., pp. 582-583). New York: W.H. Freeman.
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