220654-32-0Relevant articles and documents
Seven-enzyme in vitro cascade to (3R)-3-hydroxybutyryl-CoA
Valencia, Luis E.,Zhang, Zhicheng,Cepeda, Alexis J.,Keatinge-Clay, Adrian T.
, p. 1375 - 1378 (2019)
Economical and environmentally-friendly routes to convert feedstock chemicals like acetate into valuable chiral products such as (R)-3-hydroxybutyrate are in demand. Here, seven enzymes (CoaA, CoaD, CoaE, ACS, BktB, PhaB, and GDH) are employed in a one-pot, in vitro, biocatalytic synthesis of (3R)-3-hydroxybutyryl-CoA, which was readily isolated. This platform generates not only chiral diketide building blocks but also desirable CoA derivatives.
Enediyne polyketide synthases stereoselectively reduce the β-ketoacyl intermediates to β- D -hydroxyacyl intermediates in enediyne core biosynthesis
Ge, Hui-Ming,Huang, Tingting,Rudolf, Jeffrey D.,Lohman, Jeremy R.,Huang, Sheng-Xiong,Guo, Xun,Shen, Ben
supporting information, p. 3958 - 3961 (2014/08/18)
PKSE biosynthesizes an enediyne core precursor from decarboxylative condensation of eight malonyl-CoAs. The KR domain of PKSE is responsible for iterative β-ketoreduction in each round of polyketide chain elongation. KRs from selected PKSEs were investiga