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Recent Advances in the Genome Mining of Secondary Metabolites (covering 2012-2018)

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Journal Medchemcomm
Specialty Chemistry
Date 2019 Jul 16
PMID 31303983
Citations 41
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Abstract

Secondary metabolites (SMs) produced by filamentous fungi possess diverse bioactivities that make them excellent drug candidates. Whole genome sequencing has revealed that fungi have the capacity to produce a far greater number of SMs than have been isolated, since many of the genes involved in SM biosynthesis are either silent or expressed at very low levels in standard laboratory conditions. There has been significant effort to activate SM biosynthetic genes and link them to their downstream products, as the SMs produced by these "cryptic" pathways offer a promising source for new drug discovery. Further, an understanding of the genes involved in SM biosynthesis facilitates product yield optimization of first-generation molecules and genetic engineering of second-generation analogs. This review covers advances made in genome mining SMs produced by , , , and in the past six years (2012-2018). Genetic identification and molecular characterization of SM biosynthetic gene clusters, along with proposed biosynthetic pathways, will be discussed in depth.

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References
1.
Raisanen R, Bjork H, Hynninen P . Two-dimensional TLC separation and mass spectrometric identification of anthraquinones isolated from the fungus Dermocybe sanguinea. Z Naturforsch C J Biosci. 2000; 55(3-4):195-202. DOI: 10.1515/znc-2000-3-410. View

2.
Scherlach K, Schuemann J, Dahse H, Hertweck C . Aspernidine A and B, prenylated isoindolinone alkaloids from the model fungus Aspergillus nidulans. J Antibiot (Tokyo). 2010; 63(7):375-7. DOI: 10.1038/ja.2010.46. View

3.
Shaaban M, Shaaban K, Abdel-Aziz M . Seven naphtho-γ-pyrones from the marine-derived fungus Alternaria alternata: structure elucidation and biological properties. Org Med Chem Lett. 2012; 2:6. PMC: 3350997. DOI: 10.1186/2191-2858-2-6. View

4.
Birse C, CLUTTERBUCK A . N-acetyl-6-hydroxytryptophan oxidase, a developmentally controlled phenol oxidase from Aspergillus nidulans. J Gen Microbiol. 1990; 136(9):1725-30. DOI: 10.1099/00221287-136-9-1725. View

5.
Nielsen M, Nielsen J, Anyaogu D, Anyaogu D, Holm D, Nielsen K . Heterologous reconstitution of the intact geodin gene cluster in Aspergillus nidulans through a simple and versatile PCR based approach. PLoS One. 2013; 8(8):e72871. PMC: 3751827. DOI: 10.1371/journal.pone.0072871. View