Ectopic expression of the minimal whiE polyketide synthase generates a library of aromatic polyketides of diverse sizes and shapes.

The single recombinant expressing the Streptomyces coelicolor minimal whiE (spore pigment) polyketide synthase (PKS) is uniquely capable of generating a large array of well more than 30 polyketides, many of which, so far, are novel to this recombinant. The characterized polyketides represent a diverse set of molecules that differ in size (chain length) and shape (cyclization pattern). This combinatorial biosynthetic library is, by far, the largest and most complex of its kind described to date and indicates that the minimal whiE PKS does not independently control polyketide chain length nor dictate the first cyclization event. Rather, the minimal PKS enzyme complex must rely on the stabilizing effects of additional subunits (i.e., the cyclase whiE-ORFVI) to ensure that the chain reaches the full 24 carbons and cyclizes correctly. This dramatic loss of control implies that the growing polyketide chain does not remain enzyme bound, resulting in the spontaneous cyclization of the methyl terminus. Among the six characterized dodecaketides, four different first-ring cyclization regiochemistries are represented, including C7/C12, C8/C13, C10/C15, and C13/C15. The dodecaketide TW93h possesses a unique 2,4-dioxaadamantane ring system and represents a new structural class of polyketides with no related structures isolated from natural or engineered organisms, thus supporting the claim that engineered biosynthesis is capable of producing novel chemotypes.

[1]  Yuemao Shen,et al.  Engineered biosynthesis of novel polyketides from Streptomyces spore pigment polyketide synthases , 1998 .

[2]  C R Hutchinson,et al.  Biosynthesis of the ansamycin antibiotic rifamycin: deductions from the molecular analysis of the rif biosynthetic gene cluster of Amycolatopsis mediterranei S699. , 1998, Chemistry & biology.

[3]  D. Hopwood,et al.  Genetic Contributions to Understanding Polyketide Synthases. , 1997, Chemical reviews.

[4]  C. Richard Hutchinson,et al.  RATIONAL DESIGN AND ENGINEERED BIOSYNTHESIS OF A NOVEL 18-CARBON AROMATIC POLYKETIDE , 1997 .

[5]  D. Hopwood,et al.  Ectopic expression of the Streptomyces coelicolor whiE genes for polyketide spore pigment synthesis and their interaction with the act genes for actinorhodin biosynthesis. , 1995, Microbiology.

[6]  Chaitan Khosla,et al.  Rational design of aromatic polyketide natural products by recombinant assembly of enzymatic subunits , 1995, Nature.

[7]  C. Khosla,et al.  Combinatorial biosynthesis of 'unnatural' natural products: the polyketide example. , 1995, Chemistry & biology.

[8]  C. Khosla,et al.  Engineered biosynthesis of novel polyketides: evidence for temporal, but not regiospecific, control of cyclization of an aromatic polyketide precursor. , 1994, Chemistry & biology.

[9]  C. Khosla,et al.  Engineered biosynthesis of novel polyketides: influence of a downstream enzyme on the catalytic specificity of a minimal aromatic polyketide synthase. , 1994, Proceedings of the National Academy of Sciences of the United States of America.

[10]  B. Fraser-Reid,et al.  Armed/disarmed effects in the solvolysis of caged 1,6-anhydro pyranoses , 1994 .

[11]  C. Moonen,et al.  Gradient-enhanced heteronuclear correlation spectroscopy. Theory and experimental aspects , 1992 .

[12]  D. Hopwood,et al.  Nucleotide sequence and deduced functions of a set of cotranscribed genes of Streptomyces coelicolor A3(2) including the polyketide synthase for the antibiotic actinorhodin. , 1992, The Journal of biological chemistry.

[13]  J B McAlpine,et al.  Modular organization of genes required for complex polyketide biosynthesis. , 1991, Science.

[14]  Ralph E. Hurd,et al.  Gradient-enhanced proton-detected heteronuclear multiple-quantum coherence spectroscopy , 1991 .

[15]  P. Leadlay,et al.  An unusually large multifunctional polypeptide in the erythromycin-producing polyketide synthase of Saccharopolyspora erythraea , 1990, Nature.

[16]  K. Chater,et al.  Spore colour in Streptomyces coelicolor A3(2) involves the developmentally regulated synthesis of a compound biosynthetically related to polyketide antibiotics , 1990, Molecular microbiology.

[17]  S. Gould,et al.  Biosynthetic origin of the carbon skeleton of simaomicin α, a hexacyclic xanthone antibiotic , 1989 .

[18]  M. Bibb,et al.  Analysis of the nucleotide sequence of the Streptomyces glaucescens tcmI genes provides key information about the enzymology of polyketide antibiotic biosynthesis. , 1989, The EMBO journal.

[19]  C. Y. Kao,et al.  Tetrodotoxin, saxitoxin, and the molecular biology of the sodium channel. , 1986, Annals of the New York Academy of Sciences.

[20]  C. Y. Kao Structure‐Activity Relations of Tetrodotoxin, Saxitoxin, and Analogues a, b , 1986, Annals of the New York Academy of Sciences.

[21]  C. Ireland,et al.  Muamvatin, a novel tricyclic spiro ketal from the Fijian mollusc Siphonaria normalis , 1986 .

[22]  R. C. Pandey,et al.  Biosynthesis of fredericamycin A, a new antitumor antibiotic. , 1985, Biochemistry.

[23]  David O'Hagan,et al.  The polyketide metabolites , 1991 .