Literature DB >> 10097087

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

Y Shen1, P Yoon, T W Yu, H G Floss, D Hopwood, B S Moore.   

Abstract

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.

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Year:  1999        PMID: 10097087      PMCID: PMC22344          DOI: 10.1073/pnas.96.7.3622

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  15 in total

1.  An unusually large multifunctional polypeptide in the erythromycin-producing polyketide synthase of Saccharopolyspora erythraea.

Authors:  J Cortes; S F Haydock; G A Roberts; D J Bevitt; P F Leadlay
Journal:  Nature       Date:  1990-11-08       Impact factor: 49.962

2.  Antibiotic activity of polyketide products derived from combinatorial biosynthesis: implications for directed evolution.

Authors:  H Fu; C Khosla
Journal:  Mol Divers       Date:  1996-02       Impact factor: 2.943

Review 3.  Combinatorial biosynthesis of 'unnatural' natural products: the polyketide example.

Authors:  C J Tsoi; C Khosla
Journal:  Chem Biol       Date:  1995-06

4.  Biosynthesis of the ansamycin antibiotic rifamycin: deductions from the molecular analysis of the rif biosynthetic gene cluster of Amycolatopsis mediterranei S699.

Authors:  P R August; L Tang; Y J Yoon; S Ning; R Müller; T W Yu; M Taylor; D Hoffmann; C G Kim; X Zhang; C R Hutchinson; H G Floss
Journal:  Chem Biol       Date:  1998-02

5.  Nucleotide sequence and deduced functions of a set of cotranscribed genes of Streptomyces coelicolor A3(2) including the polyketide synthase for the antibiotic actinorhodin.

Authors:  M A Fernández-Moreno; E Martínez; L Boto; D A Hopwood; F Malpartida
Journal:  J Biol Chem       Date:  1992-09-25       Impact factor: 5.157

6.  Engineered biosynthesis of novel polyketides: influence of a downstream enzyme on the catalytic specificity of a minimal aromatic polyketide synthase.

Authors:  R McDaniel; S Ebert-Khosla; H Fu; D A Hopwood; C Khosla
Journal:  Proc Natl Acad Sci U S A       Date:  1994-11-22       Impact factor: 11.205

7.  Ectopic expression of the Streptomyces coelicolor whiE genes for polyketide spore pigment synthesis and their interaction with the act genes for actinorhodin biosynthesis.

Authors:  T W Yu; D A Hopwood
Journal:  Microbiology       Date:  1995-11       Impact factor: 2.777

8.  Engineered biosynthesis of novel polyketides.

Authors:  R McDaniel; S Ebert-Khosla; D A Hopwood; C Khosla
Journal:  Science       Date:  1993-12-03       Impact factor: 47.728

9.  Biosynthesis of fredericamycin A, a new antitumor antibiotic.

Authors:  K M Byrne; B D Hilton; R J White; R Misra; R C Pandey
Journal:  Biochemistry       Date:  1985-01-15       Impact factor: 3.162

10.  Analysis of the nucleotide sequence of the Streptomyces glaucescens tcmI genes provides key information about the enzymology of polyketide antibiotic biosynthesis.

Authors:  M J Bibb; S Biró; H Motamedi; J F Collins; C R Hutchinson
Journal:  EMBO J       Date:  1989-09       Impact factor: 11.598

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  18 in total

Review 1.  Microbial polyketide synthases: more and more prolific.

Authors:  C R Hutchinson
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-30       Impact factor: 11.205

Review 2.  Cyclization of aromatic polyketides from bacteria and fungi.

Authors:  Hui Zhou; Yanran Li; Yi Tang
Journal:  Nat Prod Rep       Date:  2010-03-31       Impact factor: 13.423

3.  Identification of olivetolic acid cyclase from Cannabis sativa reveals a unique catalytic route to plant polyketides.

Authors:  Steve J Gagne; Jake M Stout; Enwu Liu; Zakia Boubakir; Shawn M Clark; Jonathan E Page
Journal:  Proc Natl Acad Sci U S A       Date:  2012-07-16       Impact factor: 11.205

4.  Identification of the novobiocin biosynthetic gene cluster of Streptomyces spheroides NCIB 11891.

Authors:  M Steffensky; A Mühlenweg; Z X Wang; S M Li; L Heide
Journal:  Antimicrob Agents Chemother       Date:  2000-05       Impact factor: 5.191

5.  Insight into the molecular basis of aromatic polyketide cyclization: crystal structure and in vitro characterization of WhiE-ORFVI.

Authors:  Ming-Yue Lee; Brian D Ames; Shiou-Chuan Tsai
Journal:  Biochemistry       Date:  2012-03-30       Impact factor: 3.162

6.  Analysis of the ketosynthase-chain length factor heterodimer from the fredericamycin polyketide synthase.

Authors:  Ping-Hui Szu; Sridhar Govindarajan; Michael J Meehan; Abhirup Das; Don D Nguyen; Pieter C Dorrestein; Jeremy Minshull; Chaitan Khosla
Journal:  Chem Biol       Date:  2011-08-26

7.  Engineered biosynthesis of aklanonic acid analogues.

Authors:  Taek Soon Lee; Chaitan Khosla; Yi Tang
Journal:  J Am Chem Soc       Date:  2005-09-07       Impact factor: 15.419

8.  EncM, a versatile enterocin biosynthetic enzyme involved in Favorskii oxidative rearrangement, aldol condensation, and heterocycle-forming reactions.

Authors:  Longkuan Xiang; John A Kalaitzis; Bradley S Moore
Journal:  Proc Natl Acad Sci U S A       Date:  2004-10-25       Impact factor: 11.205

9.  Crystal structure and functional analysis of tetracenomycin ARO/CYC: implications for cyclization specificity of aromatic polyketides.

Authors:  Brian Douglas Ames; Tyler Paz Korman; Wenjun Zhang; Peter Smith; Thanh Vu; Yi Tang; Shiou-Chuan Tsai
Journal:  Proc Natl Acad Sci U S A       Date:  2008-04-03       Impact factor: 11.205

10.  In vivo and in vitro analysis of the hedamycin polyketide synthase.

Authors:  Abhirup Das; Chaitan Khosla
Journal:  Chem Biol       Date:  2009-11-25
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