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Molecular Biology of Cytochrome P-450: Evolution, Structure and Regulation

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Book cover Molecular Aspects of Oxidative Drug Metabolizing Enzymes

Part of the book series: NATO ASI Series ((ASIH,volume 90))

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Abstract

Cytochrome P450 is a class of hemoproteins that function as the terminal monooxygenases in microsomal, mitochondrial, or cytosolic NADPH-dependent electron transport pathways. P450 genes are widely distributed in nature from bacteria to higher animals and plants. Each mammalian genome possesses at least 50 P450 genes located on various chromosomes. Mammalian P450s as a whole metabolize an uncountable number of endogenous and exogenous substrates, such as steroids, fatty acids, vitamin D3, drugs, toxicants, environmental pollutants, and so on (Gonzalez 1990). The P450 enzymes involved in biosynthesis of physiologically active compounds (steroid hormones, prostaglandins, bile acids, vitamins, thromboxane, etc) play critical roles in development and maintenance of normal animal life. Other P450s mainly work in detoxication systems to convert lipophilic xenobiotics to more water-soluble forms. Some of the products of these reactions are chemically unstable and often produce DNA adduct which may trigger chemical carcinogenesis.

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© 1995 Springer-Verlag Berlin Heidelberg

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Fujii-Kuriyama, Y., Gotoh, O. (1995). Molecular Biology of Cytochrome P-450: Evolution, Structure and Regulation. In: Arinç, E., Schenkman, J.B., Hodgson, E. (eds) Molecular Aspects of Oxidative Drug Metabolizing Enzymes. NATO ASI Series, vol 90. Springer, Berlin, Heidelberg. https://doi.org/10.1007/978-3-642-79528-2_4

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  • DOI: https://doi.org/10.1007/978-3-642-79528-2_4

  • Publisher Name: Springer, Berlin, Heidelberg

  • Print ISBN: 978-3-642-79530-5

  • Online ISBN: 978-3-642-79528-2

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