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MarH, a Bifunctional Enzyme Involved in the Condensation and Hydroxylation Steps of the Marineosin Biosynthetic Pathway.
Lu, Wanli; Kancharla, Papireddy; Reynolds, Kevin A.
Afiliação
  • Lu W; Department of Chemistry, Portland State University , Portland, Oregon 97201, United States.
  • Kancharla P; Department of Chemistry, Portland State University , Portland, Oregon 97201, United States.
  • Reynolds KA; Department of Chemistry, Portland State University , Portland, Oregon 97201, United States.
Org Lett ; 19(6): 1298-1301, 2017 03 17.
Article em En | MEDLINE | ID: mdl-28271893
ABSTRACT
A novel bifunctional enzyme, MarH, has been identified, and its key functional role in the marineosin biosynthesis successfully probed. MarH catalyzes (1) a condensation step between 4-methoxy-2,2'-bipyrrole-5-carboxaldehyde (MBC) and 2-undecylpyrrole (UP) to form undecylprodiginine (UPG) and (2) hydroxylation of the alkyl chain of UPG to form the (S)-23-hydroxyundecylprodiginine (HUPG), which is essential for MarG catalyzed bicyclization toward the formation of an unusual spiro-tetrahydropyran-aminal ring of marineosins. The final enigmatic steps in the marineosin biosynthesis have now been deciphered.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piranos / Pirróis / Compostos de Espiro / Streptomyces / Proteínas de Bactérias Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Piranos / Pirróis / Compostos de Espiro / Streptomyces / Proteínas de Bactérias Idioma: En Revista: Org Lett Assunto da revista: BIOQUIMICA Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Estados Unidos