Literature DB >> 259502

The living state and cancer.

A Szent-Györgyi.   

Abstract

The surrounding world can be divided into two parts: alive and inanimate. What makes the difference is the subtle reactivity of living systems. The difference is so great that it is reasonable to suppose that what underlies life is a specific physical state, 'the living state'. Living systems are built mainly of nucleic acids and proteins. The former are the guardians of the basic blueprint while the business of life is carried on by proteins. Proteins thus have to share the subtle reactivity of living systems. A closed-shell protein molecule, however, has no electronic mobility, and has but a low chemical reactivity. Its orbitals are occupied by electron pairs which are held firmly. The situation can be changed by taking single electrons out of the system. This unpairs electrons, leaves half-occupied orbitals with positive electron holes, making the molecules into highly reactive paramagnetic free radicals. The reactivity of the system depends on the degree of its electronic desaturation. Electrons can be taken out of protein molecules by 'electron aceptors' in 'cahrge transfer'. When life began, our globe was covered by dense water vapour. There was no light and no free oxygen. Electron acceptors could be made out of trioses by concentrating their carbon atoms as carbonyls at one end of the molecule. The resulting methylglyoxal is a weak acceptor which made a low level of development possible. When light appeared, free oxygen was generated by the energy of photons. Oxygen is a strong electron acceptor. Its appearance opened the way to the present level of development. The transfer of electrons from protein to oxygen is effected by a complex chemical mechanism which involves ascorbic acid.

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Year:  1978        PMID: 259502     DOI: 10.1002/9780470720493.ch2

Source DB:  PubMed          Journal:  Ciba Found Symp        ISSN: 0300-5208


  4 in total

1.  Similar nature of inhibition of mitochondrial respiration of heart tissue and malignant cells by methylglyoxal. A vital clue to understand the biochemical basis of malignancy.

Authors:  S Ray; S Biswas; M Ray
Journal:  Mol Cell Biochem       Date:  1997-06       Impact factor: 3.396

2.  Reduction of methylglyoxal in Escherichia coli K12 by an aldehyde reductase and alcohol dehydrogenase.

Authors:  K Misra; A B Banerjee; S Ray; M Ray
Journal:  Mol Cell Biochem       Date:  1996-03-23       Impact factor: 3.396

3.  Inhibition of astrocyte glutamate uptake by reactive oxygen species: role of antioxidant enzymes.

Authors:  O Sorg; T F Horn; N Yu; D L Gruol; F E Bloom
Journal:  Mol Med       Date:  1997-07       Impact factor: 6.354

4.  Inhibition of electron flow through complex I of the mitochondrial respiratory chain of Ehrlich ascites carcinoma cells by methylglyoxal.

Authors:  S Ray; S Dutta; J Halder; M Ray
Journal:  Biochem J       Date:  1994-10-01       Impact factor: 3.857

  4 in total

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