Analysis of the molecular recognition features of individual modules derived from the erythromycin polyketide synthase

被引:70
作者
Wu, N
Kudo, F
Cane, DE
Khosla, C
机构
[1] Brown Univ, Dept Chem, Providence, RI 02912 USA
[2] Stanford Univ, Dept Chem Engn, Stanford, CA 94305 USA
[3] Stanford Univ, Dept Biochem, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Chem, Stanford, CA 94305 USA
关键词
D O I
10.1021/ja000023d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
6-Deoxyerythronolide B synthase (DEBS), the multifunctional enzyme responsible for the biosynthesis of the macrolide aglycon of the antibiotic erythromycin, is an excellent model system for studying the properties of modular polyketide synthases. In these studies, we analyzed the substrate specificity of selected individual modules of DEBS. Unexpectedly, we observed (i) a high degree of similarity in the specificity of all modules tested, despite the diverse structural features of their natural substrates, and (ii) a distinct preference by all modules for syn diketides over anti diketides. The implications of these results are analyzed from an evolutionary and a protein engineering perspective.
引用
收藏
页码:4847 / 4852
页数:6
相关论文
共 27 条
[21]   Multiple genetic modifications of the erythromycin polyketide synthase to produce a library of novel "unnatural" natural products [J].
McDaniel, R ;
Thamchaipenet, A ;
Gustafsson, C ;
Fu, H ;
Betlach, M ;
Betlach, M ;
Ashley, G .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (05) :1846-1851
[22]   A hybrid modular polyketide synthase obtained by domain swapping [J].
Oliynyk, M ;
Brown, MJB ;
Cortes, J ;
Staunton, J ;
Leadlay, PF .
CHEMISTRY & BIOLOGY, 1996, 3 (10) :833-839
[23]  
Pieper R, 1996, BIOCHEMISTRY-US, V35, P2054, DOI 10.1021/bi952860b
[24]   Purification and characterization of bimodular and trimodular derivatives of the erythromycin polyketide synthase [J].
Pieper, R ;
Gokhale, RS ;
Luo, GL ;
Cane, DE ;
Khosla, C .
BIOCHEMISTRY, 1997, 36 (07) :1846-1851
[25]  
PIEPER R, 1995, J AM CHEM SOC, V117, P11383
[26]   Knowledge-based design of bimodular and trimodular polyketide synthases based on domain and module swaps:: a route to simple statin analogues [J].
Ranganathan, A ;
Timoney, M ;
Bycroft, M ;
Cortés, J ;
Thomas, IP ;
Wilkinson, B ;
Kellenberger, L ;
Hanefeld, U ;
Galloway, IS ;
Staunton, J ;
Leadlay, PF .
CHEMISTRY & BIOLOGY, 1999, 6 (10) :731-741
[27]   Evaluating precursor-directed biosynthesis towards novel erythromycins through in vitrostudies on a bimodular polyketide synthase [J].
Weissman, KJ ;
Bycroft, M ;
Cutter, AL ;
Hanefeld, U ;
Frost, EJ ;
Timoney, MC ;
Harris, R ;
Handa, S ;
Roddis, M ;
Staunton, J ;
Leadlay, PF .
CHEMISTRY & BIOLOGY, 1998, 5 (12) :743-754