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Production of alkenes and novel secondary products by P450 OleTJE using novel H2 O2 -generating fusion protein systems.
Matthews, Sarah; Tee, Kang Lan; Rattray, Nicholas J; McLean, Kirsty J; Leys, David; Parker, David A; Blankley, Richard T; Munro, Andrew W.
Afiliação
  • Matthews S; Manchester Institute of Biotechnology, Centre for Synthetic Biology of Fine and Speciality Chemicals (SYNBIOCHEM), School of Chemistry, The University of Manchester, UK.
  • Tee KL; Manchester Institute of Biotechnology, Centre for Synthetic Biology of Fine and Speciality Chemicals (SYNBIOCHEM), School of Chemistry, The University of Manchester, UK.
  • Rattray NJ; Manchester Institute of Biotechnology, Centre for Synthetic Biology of Fine and Speciality Chemicals (SYNBIOCHEM), School of Chemistry, The University of Manchester, UK.
  • McLean KJ; Manchester Institute of Biotechnology, Centre for Synthetic Biology of Fine and Speciality Chemicals (SYNBIOCHEM), School of Chemistry, The University of Manchester, UK.
  • Leys D; Manchester Institute of Biotechnology, Centre for Synthetic Biology of Fine and Speciality Chemicals (SYNBIOCHEM), School of Chemistry, The University of Manchester, UK.
  • Parker DA; The Westhollow Technology Center, Houston, TX, USA.
  • Blankley RT; Agilent Technologies UK Ltd., Stockport, Cheshire, UK.
  • Munro AW; Manchester Institute of Biotechnology, Centre for Synthetic Biology of Fine and Speciality Chemicals (SYNBIOCHEM), School of Chemistry, The University of Manchester, UK.
FEBS Lett ; 591(5): 737-750, 2017 03.
Article em En | MEDLINE | ID: mdl-28144940
Jeotgalicoccus sp. 8456 OleTJE (CYP152L1) is a fatty acid decarboxylase cytochrome P450 that uses hydrogen peroxide (H2 O2 ) to catalyse production of terminal alkenes, which are industrially important chemicals with biofuel applications. We report enzyme fusion systems in which Streptomyces coelicolor alditol oxidase (AldO) is linked to OleTJE . AldO oxidizes polyols (including glycerol), generating H2 O2 as a coproduct and facilitating its use for efficient OleTJE -dependent fatty acid decarboxylation. AldO activity is regulatable by polyol substrate titration, enabling control over H2 O2 supply to minimize oxidative inactivation of OleTJE and prolong activity for increased alkene production. We also use these fusion systems to generate novel products from secondary turnover of 2-OH and 3-OH myristic acid primary products, expanding the catalytic repertoire of OleTJE .
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbiologia Industrial / Proteínas Recombinantes de Fusão / Sistema Enzimático do Citocromo P-450 / Oxirredutases do Álcool / Alcenos / Ácidos Graxos / Peróxido de Hidrogênio Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Microbiologia Industrial / Proteínas Recombinantes de Fusão / Sistema Enzimático do Citocromo P-450 / Oxirredutases do Álcool / Alcenos / Ácidos Graxos / Peróxido de Hidrogênio Idioma: En Ano de publicação: 2017 Tipo de documento: Article