Components of the cytochrome P450-dependent monooxygenase system and 'NADPH-independent benzo[a]pyrene hydroxylase' activity in a wide range of marine invertebrate species

  • Solé M
  • Livingstone D
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Levels of components of the cytochrome P450 (CYP)-dependent monooxygenase system were characterised in microsomes of major biotransformation tissues, or whole bodies, of 33 species from six phyla of aquatic invertebrates. The phylogenetic distribution of benzo[a]pyrene hydroxylase (BPH) activity in the absence of added NADPH (so-called 'NADPH-independent BPH activity') and presence of NADPH was also examined. Microsomal protein yield was higher in individual tissues than whole tissues. The main components (total CYP and cytochrome b5; NADPH-dependent cytochrome c (CYP) reductase, NADH-dependent cytochrome c reductase and NADH-dependent ferricyanide (b5) reductase activities) were found in most species of the Porifera, Cnidaria, Mollusca, Polychaeta, Crustacea and Echinodermata examined. The so-called '418-peak' of the carbon-monoxide difference spectrum of reduced microsomes was found in all species, indicating the wide distribution of this protein. Total CYP levels (pmol mg-1protein; mean ± SEM) were similar in molluscs (50 ± 7), crustaceans (61 ± 11) and echinoderms (56 ± 9), with the exception of high levels (223-266) in two crustacean species. NADPH-dependent BPH activity (pmol min-1mg-1protein) was found in 32 species, being lowest in Porifera and Cnidaria (3-4), intermediate in Mollusca (7.8 ± 1.3), and highest in Crustacea (25 ± 4) and Echinodermata (15 ± 4). NADPH-independent BPH activity was evident in 13 out of 15 molluscan species examined, with the addition of NADPH either stimulating (8 species) or inhibiting (5 species) the activity. NADPH-independent BPH activity was also seen in two poriferan species and indicated in three crustacean species, suggesting that the phenomenon is not solely restricted to the Mollusca. © 2005 Elsevier Inc. All rights reserved.

Author-supplied keywords

  • Benzo[a]pyrene hydroxylase
  • CYP1A
  • Cytochrome P450 monooxygenase system
  • Cytochrome b5
  • Marine invertebrates
  • NADPH-independence
  • Reductases
  • Total CYP

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  • Montserrat Solé

  • David R. Livingstone

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