| Literature DB >> 28133950 |
Lihan Zhang1, Takuya Hashimoto2, Bin Qin1, Junko Hashimoto3, Ikuko Kozone3, Teppei Kawahara3, Masahiro Okada1, Takayoshi Awakawa1, Takuya Ito4, Yoshinori Asakawa4, Masashi Ueki5, Shunji Takahashi5, Hiroyuki Osada5, Toshiyuki Wakimoto1, Haruo Ikeda6, Kazuo Shin-Ya2, Ikuro Abe1.
Abstract
Polyketides form many clinically valuable compounds. However, manipulation of their biosynthesis remains highly challenging. An understanding of gene cluster evolution provides a rationale for reprogramming of the biosynthetic machinery. Herein, we report characterization of giant modular polyketide synthases (PKSs) responsible for the production of aminopolyol polyketides. Heterologous expression of over 150 kbp polyketide gene clusters successfully afforded their products, whose stereochemistry was established by taking advantage of bioinformatic analysis. Furthermore, phylogenetic analysis of highly homologous but functionally diverse domains from the giant PKSs demonstrated the evolutionary mechanism for structural diversification of polyketides. The gene clusters characterized herein, together with their evolutionary insights, are promising genetic building blocks for de novo production of unnatural polyketides.Entities:
Keywords: bioengineering; biosynthesis; polyketides; protein structures
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Year: 2017 PMID: 28133950 DOI: 10.1002/anie.201611371
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336