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Catalysis by Nature's photoenzymes.
Taylor, Aoife; Heyes, Derren J; Scrutton, Nigel S.
Afiliación
  • Taylor A; Future Biomanufacturing Research Hub, Manchester Institute of Biotechnology and Department of Chemistry, School of Natural Sciences, The University of Manchester, M1 7DN, United Kingdom.
  • Heyes DJ; Future Biomanufacturing Research Hub, Manchester Institute of Biotechnology and Department of Chemistry, School of Natural Sciences, The University of Manchester, M1 7DN, United Kingdom. Electronic address: https://twitter.com/DerrenHeyes.
  • Scrutton NS; Future Biomanufacturing Research Hub, Manchester Institute of Biotechnology and Department of Chemistry, School of Natural Sciences, The University of Manchester, M1 7DN, United Kingdom. Electronic address: nigel.scrutton@manchester.ac.uk.
Curr Opin Struct Biol ; 77: 102491, 2022 Dec.
Article en En | MEDLINE | ID: mdl-36323132
ABSTRACT
Photoenzymes use light to initiate biochemical reactions. Although rarely found in nature, their study has advanced understanding of how light energy can be harnessed to facilitate enzyme catalysis, which is also of importance to the design and engineering of man-made photocatalysts. Natural photoenzymes can be assigned to one of two families, based broadly on the nature of the light-sensing chromophores used, those being chlorophyll-like tetrapyrroles or flavins. In all cases, light absorption leads to excited state electron transfer, which in turn initiates photocatalysis. Reviewed here are recent findings relating to the structures and mechanisms of known photoenzymes. We highlight recent advances that have deepened understanding of mechanisms in biological photocatalysis.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Flavinas Límite: Humans Idioma: En Revista: Curr Opin Struct Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Flavinas Límite: Humans Idioma: En Revista: Curr Opin Struct Biol Asunto de la revista: BIOLOGIA MOLECULAR Año: 2022 Tipo del documento: Article País de afiliación: Reino Unido
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