4.4 Article

Structure and biosynthesis of fumosorinone, a new protein tyrosine phosphatase 1B inhibitor firstly isolated from the entomogenous fungus Isaria fumosorosea

Journal

FUNGAL GENETICS AND BIOLOGY
Volume 81, Issue -, Pages 191-200

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.fgb.2015.03.009

Keywords

Natural product; Isaria fumosorosea; Fumosorinone; Protein tyrosine phosphatase 1B inhibitor; PKS-NPRS; Biosynthesis

Funding

  1. National Natural Science Foundation of China [31171885, 31371957]
  2. Changjiang Scholars and Innovative Research Team in University [IRT1124]
  3. Ph.D. Programs Foundation Ministry of Education of China [20121301110006]
  4. Key Projects in the Hebei Province Science Technology [13226508D]

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Fumosorinone, isolated from the entomogenous fungus Isaria fumosorosea, is a new 2-pyridone alkaloid which is elucidated by HRESIMS 1D and 2DNMR. Fumosorinone is structurally similar to tenellin and desmethylbassianin but it differs in chain length and degree of methylation. It is characterized by a classic noncompetitive inhibitor of protein tyrosine phosphatase 1B (IC(50)14.04 mu M) which was implicated as a negative regulator of insulin receptor signaling and a potential drug target for the treatment of type II diabetes and other associated metabolic syndromes. For further study, we identified the biosynthetic gene cluster of fumosorinone from ongoing genome sequencing project, and it was verified by a direct knock-out strategy, reported for the first time in L fumosorosea, using the Agrobacterium-mediated transformation in conjunction with linear deletion cassettes. The biosynthetic gene cluster includes a hybrid polyketide synthase-nonribosomal peptide synthetase gene, two cytochrome P450 enzyme genes, a trans-enoyl reductase gene, and other two transcription regulatory genes. Comparison of fumosorinone biosynthetic cluster with known gene clusters gives further insight into biosynthesis of pyridone alkaloids and provides the foundation for combinatorial biosynthesis for new fumosorinone derivatives. (C) 2015 Elsevier Inc. All rights reserved.

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