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Ancestral Sequence Reconstruction of a Cytochrome P450 Family Involved in Chemical Defense Reveals the Functional Evolution of a Promiscuous, Xenobiotic-Metabolizing Enzyme in Vertebrates

Harris, Kurt L. (författare)
University of Queensland, Australia
Thomson, Raine E. S. (författare)
University of Queensland, Australia
Gumulya, Yosephine (författare)
University of Queensland, Australia
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Foley, Gabriel (författare)
University of Queensland, Australia
Carrera-Pacheco, Saskya E. (författare)
Universidad UTE, Ecuador
Syed, Parnayan (författare)
University of Queensland, Australia
Janosik, Tomasz (författare)
RISE,Kemiska processer och läkemedel
Sandinge, Ann-Sofie (författare)
AstraZeneca, Sweden
Andersson, Shalini (författare)
AstraZeneca, Sweden
Jurva, Ulrik (författare)
AstraZeneca, Sweden
Bodén, Mikael (författare)
University of Queensland, Australia
Gillam, Elizabeth M. J. (författare)
University of Queensland, Australia
visa färre...
 (creator_code:org_t)
2022-05-26
2022
Engelska.
Ingår i: Molecular biology and evolution. - : NLM (Medline). - 0737-4038 .- 1537-1719. ; 39:6
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • The cytochrome P450 family 1 enzymes (CYP1s) are a diverse family of hemoprotein monooxygenases, which metabolize many xenobiotics including numerous environmental carcinogens. However, their historical function and evolution remain largely unstudied. Here we investigate CYP1 evolution via the reconstruction and characterization of the vertebrate CYP1 ancestors. Younger ancestors and extant forms generally demonstrated higher activity toward typical CYP1 xenobiotic and steroid substrates than older ancestors, suggesting significant diversification away from the original CYP1 function. Caffeine metabolism appears to be a recently evolved trait of the CYP1A subfamily, observed in the mammalian CYP1A lineage, and may parallel the recent evolution of caffeine synthesis in multiple separate plant species. Likewise, the aryl hydrocarbon receptor agonist, 6-formylindolo[3,2-b]carbazole (FICZ) was metabolized to a greater extent by certain younger ancestors and extant forms, suggesting that activity toward FICZ increased in specific CYP1 evolutionary branches, a process that may have occurred in parallel to the exploitation of land where UV-exposure was higher than in aquatic environments. As observed with previous reconstructions of P450 enzymes, thermostability correlated with evolutionary age; the oldest ancestor was up to 35 °C more thermostable than the extant forms, with a 10T50 (temperature at which 50% of the hemoprotein remains intact after 10 min) of 71 °C. This robustness may have facilitated evolutionary diversification of the CYP1s by buffering the destabilizing effects of mutations that conferred novel functions, a phenomenon which may also be useful in exploiting the catalytic versatility of these ancestral enzymes for commercial application as biocatalysts.

Ämnesord

TEKNIK OCH TEKNOLOGIER  -- Kemiteknik -- Kemiska processer (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Chemical Engineering -- Chemical Process Engineering (hsv//eng)

Nyckelord

ancestral sequence reconstruction
CYP1A2
CYP1B1
cytochrome P450
drug metabolism
thermostability
caffeine
cytochrome P450 1A1
xenobiotic agent
animal
genetics
mammal
metabolism
vertebrate
Animals
Cytochrome P-450 CYP1A1
Cytochrome P-450 Enzyme System
Mammals
Vertebrates
Xenobiotics

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