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Engineered Biosynthesis of Fungal 4-Quinolone Natural Products.
Liu, Mengting; Ohashi, Masao; Tang, Yi.
Affiliation
  • Liu M; Department of Chemical and Biomolecular Engineering and Department of Chemistry and Biochemistry University of California, Los Angeles, California 90095, United States.
  • Ohashi M; Hubei Key Laboratory of Natural Medicinal Chemistry and Resource Evaluation, School of Pharmacy, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430030, China.
  • Tang Y; Department of Chemical and Biomolecular Engineering and Department of Chemistry and Biochemistry University of California, Los Angeles, California 90095, United States.
Org Lett ; 22(16): 6637-6641, 2020 08 21.
Article in En | MEDLINE | ID: mdl-32806159
Quinolone-containing natural products are widely found in bacteria, fungi, and plants. The fungal quinolactacins, which are N-methyl-4-quinolones, display a wide spectrum of biological activities. Here we uncovered a concise nonribosomal peptide synthetase pathway involved in quinolactacin A biosynthesis from Penicillium by using heterologous reconstitution and in vitro enzymatic synthesis. The N-desmethyl analog of quinolactacin A was accessed through the construction of a hybrid bacterial and fungi pathway in the heterologous host.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Penicillium / Peptide Synthases / Quinolones / 4-Quinolones / Fungi Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2020 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Penicillium / Peptide Synthases / Quinolones / 4-Quinolones / Fungi Language: En Journal: Org Lett Journal subject: BIOQUIMICA Year: 2020 Document type: Article Affiliation country: United States Country of publication: United States