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Thioesterase-Mediated Synthesis of Teixobactin Analogues: Mechanism and Substrate Specificity.
Mandalapu, Dhanaraju; Ji, Xinjian; Chen, Jinfeng; Guo, Chuchu; Liu, Wan-Qiu; Ding, Wei; Zhou, Jiahai; Zhang, Qi.
Afiliação
  • Mandalapu D; Department of Chemistry , Fudan University , Shanghai 200438 , China.
  • Ji X; Department of Chemistry , Fudan University , Shanghai 200438 , China.
  • Chen J; State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry , Chinese Academy of Sciences , Shanghai 200032 , China.
  • Guo C; Department of Chemistry , Fudan University , Shanghai 200438 , China.
  • Liu WQ; Department of Chemistry , Fudan University , Shanghai 200438 , China.
  • Ding W; Department of Chemistry , Fudan University , Shanghai 200438 , China.
  • Zhou J; State Key Laboratory of Bioorganic and Natural Products Chemistry, Shanghai Institute of Organic Chemistry , Chinese Academy of Sciences , Shanghai 200032 , China.
  • Zhang Q; Department of Chemistry , Fudan University , Shanghai 200438 , China.
J Org Chem ; 83(13): 7271-7275, 2018 07 06.
Article em En | MEDLINE | ID: mdl-29357665
ABSTRACT
A chemoenzymatic approach for the synthesis of teixobactin analogues has been established by using the tandem thioesterase (TE) of the nonribosomal peptide synthase (NRPS) Txo2. We show that, unlike the closely related counterparts involved in lysobactin biosynthesis (in which the N-terminal TE is solely responsible for the lactonization reaction), the two teixobactin TE domains are functionally exchangeable and likely act synergistically, representing an unprecedented off-loading mechanism in NRPS enzymology. The substrate specificity of this tandem TE was also investigated in this study.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Depsipeptídeos / Esterases Idioma: En Revista: J Org Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Depsipeptídeos / Esterases Idioma: En Revista: J Org Chem Ano de publicação: 2018 Tipo de documento: Article País de afiliação: China