Metabolism theories

The RNA world requires a system capable of self-replication as a precondition for the beginnings of life. In contrast, the surface metabolism theory proposed by Wachtershauser postulates that the initial step is metabolism, from which complex replication systems can evolve later. This metabolism would have occurred at the... 

R. U. Ayres, Industrial Metabolism Theory and Policy. The Greening of Industrial Ecosystems, National Academy Press, Washington, DC, 1994. (Reprinted from Industrial Metabolism, R. Ayers and U. Simonis, Eds., United Nations University Press, Tokyo, Japan, 1993.)... 

R. Amimovin. An analysis of the metabolic theory of the origin of the genetic code. Journal of Molecular Evolution, 44 (1997), 473-6. 

In his metabolic theory of labour and value, Marx excluded the non-human from his definition of human labour. For Marx, labour was an expression of man s metabolic relation with and conversion of nature . Yet this labour is notable not just for its assumed conversion of nature into resource, but also for what it is not. Non-human work does not constitute labour, Marx argues, since nature s work whether the web of the spider or the hive of the bee -has not undergone a prior mental conception that would, for instance, characterize the labour of an architect conceptualizing a building (Marx 1990 283 84). The exclusion of non-human work from theories of labour informs the types of material politics that are possible, since non-humans may not then be recognized as participants in our material lives. 

Backbone (protein), 1028 Backside displacement. reaction and.363-364 von Baeyer, Adolf, 113 Baeyer strain theory, 113-114 Bakelile, structure of, 1218 Banana, esters in, 808 Barton, Derek, H. R., 389 Basal metabolic rate, 1169 Basal metabolism. 1169-1170 Base, Bronsted-Lowry, 49 Lewis, 57, 59-60 organic, 56-57 strengths of, 50-52 Base pair (DNA), 1103-1105 electrostatic potential maps of. 

Hurst (19) discusses the similarity in action of the pyrethrins and of DDT as indicated by a dispersant action on the lipids of insect cuticle and internal tissue. He has developed an elaborate theory of contact insecticidal action but provides no experimental data. Hurst believes that the susceptibility to insecticides depends partially on the cuticular permeability, but more fundamentally on the effects on internal tissue receptors which control oxidative metabolism or oxidative enzyme systems. The access of pyrethrins to insects, for example, is facilitated by adsorption and storage in the lipophilic layers of the epicuticle. The epicuticle is to be regarded as a lipoprotein mosaic consisting of alternating patches of lipid and protein receptors which are sites of oxidase activity. Such a condition exists in both the hydrophilic type of cuticle found in larvae of Calliphora and Phormia and in the waxy cuticle of Tenebrio larvae. Hurst explains pyrethrinization as a preliminary narcosis or knockdown phase in which oxidase action is blocked by adsorption of the insecticide on the lipoprotein tissue components, followed by death when further dispersant action of the insecticide results in an irreversible increase in the phenoloxidase activity as a result of the displacement of protective lipids. This increase in phenoloxidase activity is accompanied by the accumulation of toxic quinoid metabolites in the blood and tissues—for example, O-quinones which would block substrate access to normal enzyme systems. The varying degrees of susceptibility shown by different insect species to an insecticide may be explainable not only in terms of differences in cuticle make-up but also as internal factors associated with the stability of oxidase systems. 

Werner s coordination theory, 1, 6 Whewellite structure, 6, 849 Wickmanite structure, 6, 849 Wilkinson s catalyst, 6, 239 Wilson s disease, 5, 721 copper, 6,648 removal, 6,769 copper complexes, 2,959 copper metabolism, 6,766 radiopharmaceutical agents, 6,968 Wolfram s red salt, 5,427 Wurzite... 

Hafher, R.P., Brown, G.C.. Brand, M.D. (1990). Analysis of the control of respiration rate, phosphorylation rate, proton leak rate and proton motive force in isolated mitochondria using the top-down approach of metabolic control theory. Eur. J. Biochem. 188,313-319. 

This potential, or protonmotive force as it is also called, in turn drives a number of energy-requiring functions which include the synthesis of ATP, the coupling of oxidative processes to phosphorylation, a metabohc sequence called oxidative phosphorylation and the transport and concentration in the cell of metabolites such as sugars and amino acids. This, in a few simple words, is the basis of the chemiosmotic theory linking metabolism to energy-requiring processes. 

D. K. Design of drugs involving the concepts and theories of drug metabolism and pharmacokinetics. 

The wide gap between the two opposing theories, replication first and metabolism first , was analysed by Pross from the Ben Gurion University of the Negev (Israel). Pross concludes that replication came first He is convinced that a causality between the two theories can only be established if it is assumed that the replication-first thesis is correct. His analysis also shows that more of the experimental results and theoretical rationales favour the replication thesis. The author finds his assumption justified that life processes are strongly kinetically controlled and that the development of metabolic pathways can only be understood if life is considered as a manifestation of replicative chemistry (Pross, 2004). 

G. Wachtershauser formulated his suggestions on the initial metabolic processes on the primeval Earth (as described above) in the form of six postulates and eleven theses (Wachtershauser, 1990b). Laboratory experiments planned to check, and perhaps confirm, these theories have already been attempted. The reductive Krebs cycle (rTCA cycle) has recently been the subject of much discussion. Smith and Morowitz consider that the rTCA cycle is a universal, possibly primordial, core process which could have provided substances for the synthesis of biomolecules on the young Earth (Smith and Morowitz, 2004). 

The results obtained appeared quite promising, but the real sensation was the detection of pyruvate, the salt of 2-oxopropanoic acid (pyruvic acid), which is one of the most important substances in contemporary metabolism. Pyruvic acid was first obtained in 1835 by Berzelius from dry distillation of tartaric acid. The labile pyruvate was detected in a reaction mixture containing pure FeS, 1-nonanethiol and formic acid, using simulated hydrothermal conditions (523 K, 200 MPa). The pyruvate yield, 0.7%, was certainly not overwhelming, but still remarkable under the extreme conditions used, and its formation supports Wachtershauser s theory. Cody concludes from these results that life first evolved in a metabolic system prior to the development of replication processes. 

Freeman Dyson considers that any theory on the origin of life which begins with cooperative organisation in a large population of molecules, and makes no provision for short circuits in the metabolic pathways, will be met by the criticism just described (Dyson, 1985). 

He describes molecular populations mathematically in the way physicists calculate classical dynamic systems. Very exact dynamic equations are devised, while the laws of interaction are left very general. This leads to a general theory of molecular systems, which makes it possible to define what is understood by the origin of metabolism (Dyson, 1999). 

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