Literature DB >> 32357274

Probing Selectivity and Creating Structural Diversity Through Hybrid Polyketide Synthases.

Aaron A Koch1, Jennifer J Schmidt1, Andrew N Lowell1,2, Douglas A Hansen1, Katherine M Coburn1, Joseph A Chemler1, David H Sherman1,3.   

Abstract

Engineering polyketide synthases (PKS) to produce new metabolites requires an understanding of catalytic points of failure during substrate processing. Growing evidence indicates the thioesterase (TE) domain as a significant bottleneck within engineered PKS systems. We created a series of hybrid PKS modules bearing exchanged TE domains from heterologous pathways and challenged them with both native and non-native polyketide substrates. Reactions pairing wildtype PKS modules with non-native substrates primarily resulted in poor conversions to anticipated macrolactones. Likewise, product formation with native substrates and hybrid PKS modules bearing non-cognate TE domains was severely reduced. In contrast, non-native substrates were converted by most hybrid modules containing a substrate compatible TE, directly implicating this domain as the major catalytic gatekeeper and highlighting its value as a target for protein engineering to improve analog production in PKS pathways.
© 2020 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  PKS engineering; biocatalysis; biosynthesis; natural products; polyketides

Mesh:

Substances:

Year:  2020        PMID: 32357274      PMCID: PMC7395861          DOI: 10.1002/anie.202004991

Source DB:  PubMed          Journal:  Angew Chem Int Ed Engl        ISSN: 1433-7851            Impact factor:   15.336


  25 in total

1.  Multiple genetic modifications of the erythromycin polyketide synthase to produce a library of novel "unnatural" natural products.

Authors:  R McDaniel; A Thamchaipenet; C Gustafsson; H Fu; M Betlach; G Ashley
Journal:  Proc Natl Acad Sci U S A       Date:  1999-03-02       Impact factor: 11.205

Review 2.  Genetic engineering of modular PKSs: from combinatorial biosynthesis to synthetic biology.

Authors:  Kira J Weissman
Journal:  Nat Prod Rep       Date:  2016-02       Impact factor: 13.423

Review 3.  Developing tools for engineering hybrid polyketide synthetic pathways.

Authors:  Jeffrey D Kittendorf; David H Sherman
Journal:  Curr Opin Biotechnol       Date:  2006-10-12       Impact factor: 9.740

4.  Engineering the Substrate Specificity of a Modular Polyketide Synthase for Installation of Consecutive Non-Natural Extender Units.

Authors:  Edward Kalkreuter; Jared M CroweTipton; Andrew N Lowell; David H Sherman; Gavin J Williams
Journal:  J Am Chem Soc       Date:  2019-01-24       Impact factor: 15.419

Review 5.  Engineering enzymatic assembly lines for the production of new antimicrobials.

Authors:  Edward Kalkreuter; Gavin J Williams
Journal:  Curr Opin Microbiol       Date:  2018-05-04       Impact factor: 7.934

6.  Identification of a Thioesterase Bottleneck in the Pikromycin Pathway through Full-Module Processing of Unnatural Pentaketides.

Authors:  Douglas A Hansen; Aaron A Koch; David H Sherman
Journal:  J Am Chem Soc       Date:  2017-09-19       Impact factor: 15.419

7.  Diversity-oriented combinatorial biosynthesis of benzenediol lactone scaffolds by subunit shuffling of fungal polyketide synthases.

Authors:  Yuquan Xu; Tong Zhou; Shuwei Zhang; Patricia Espinosa-Artiles; Luoyi Wang; Wei Zhang; Min Lin; A A Leslie Gunatilaka; Jixun Zhan; István Molnár
Journal:  Proc Natl Acad Sci U S A       Date:  2014-07-21       Impact factor: 11.205

8.  Synthesis and biochemical analysis of complex chain-elongation intermediates for interrogation of molecular specificity in the erythromycin and pikromycin polyketide synthases.

Authors:  Jonathan D Mortison; Jeffrey D Kittendorf; David H Sherman
Journal:  J Am Chem Soc       Date:  2009-11-04       Impact factor: 15.419

9.  The methymycin/pikromycin pathway: a model for metabolic diversity in natural product biosynthesis.

Authors:  Jeffrey D Kittendorf; David H Sherman
Journal:  Bioorg Med Chem       Date:  2008-11-05       Impact factor: 3.641

10.  Systematic domain swaps of iterative, nonreducing polyketide synthases provide a mechanistic understanding and rationale for catalytic reprogramming.

Authors:  Adam G Newman; Anna L Vagstad; Philip A Storm; Craig A Townsend
Journal:  J Am Chem Soc       Date:  2014-05-09       Impact factor: 15.419

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  2 in total

1.  Biosynthetic Cyclization Catalysts for the Assembly of Peptide and Polyketide Natural Products.

Authors:  Maria L Adrover-Castellano; Jennifer J Schmidt; David H Sherman
Journal:  ChemCatChem       Date:  2021-01-28       Impact factor: 5.686

2.  Intrinsic and Extrinsic Programming of Product Chain Length and Release Mode in Fungal Collaborating Iterative Polyketide Synthases.

Authors:  Chen Wang; Xiaojing Wang; Liwen Zhang; Qun Yue; Qingpei Liu; Ya-Ming Xu; A A Leslie Gunatilaka; Xiaoyi Wei; Yuquan Xu; István Molnár
Journal:  J Am Chem Soc       Date:  2020-09-23       Impact factor: 15.419

  2 in total

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