Yin_2003_J.Am.Chem.Soc_125_5671

Reference

Title : Expression and kinetic analysis of the substrate specificity of modules 5 and 6 of the picromycin\/methymycin polyketide synthase - Yin_2003_J.Am.Chem.Soc_125_5671
Author(s) : Yin Y , Lu H , Khosla C , Cane DE
Ref : Journal of the American Chemical Society , 125 :5671 , 2003
Abstract :

Picromycin synthase (PICS) is a multifunctional, modular polyketide synthase (PKS) that catalyzes the conversion of methylmalonyl-CoA to narbonolide and 10-deoxymethynolide, the macrolide aglycone precursors of the antibiotics picromycin and methymycin, respectively. PICS modules 5 and 6 were each expressed in Escherichia coli with a thioesterase domain at the C-terminus to allow release of polyketide products. The substrate specificity of PICS modules 5+TE and 6+TE was investigated using N-acetylcysteamine thioesters of 2-methyl-3-hydroxy-pentanoic acid as diketide analogues of the natural polyketide chain elongation substrates. PICS module 5+TE could catalyze the chain elongation of only the syn diketide (2S,3R)-4, while PICS module 6+TE processed both syn diastereomers, (2S,3R)-4 and (2R,3S)-5, with a 2.5:1 preference in k(cat)/K(m) for 5 but did not turn over either of the two anti diketides. The observed substrate specificity patterns are in contrast to the 15-100:1 preference for 4 over 5 previously established for several modules of the closely related erythromycin PKS, 6-deoxyerythronolide B synthase (DEBS).

PubMedSearch : Yin_2003_J.Am.Chem.Soc_125_5671
PubMedID: 12733905

Related information

Citations formats

Yin Y, Lu H, Khosla C, Cane DE (2003)
Expression and kinetic analysis of the substrate specificity of modules 5 and 6 of the picromycin\/methymycin polyketide synthase
Journal of the American Chemical Society 125 :5671

Yin Y, Lu H, Khosla C, Cane DE (2003)
Journal of the American Chemical Society 125 :5671