Genetic dereplication of Trichoderma hypoxylon reveals two novel polycyclic lactones.
暂无分享,去创建一个
Shihua Wang | Wenzhao Wang | Jinwei Ren | Huan Liu | W. Yin | Erwei Li | Lin Chen | HongBo Wu
[1] Lin Chen,et al. Deletion of a global regulator LaeB leads to the discovery of novel polyketides in Aspergillus nidulans. , 2018, Organic & biomolecular chemistry.
[2] Yang Teng,et al. Hebecarposides A-K, antiproliferative lanostane-type triterpene glycosides from the leaves of Lyonia ovalifolia var. hebecarpa. , 2018, Phytochemistry.
[3] Wei Li,et al. A highly efficient genetic system for the identification of a harzianum B biosynthetic gene cluster in Trichoderma hypoxylon. , 2018, Microbiology.
[4] Ying Huang,et al. Genetic Manipulation of the COP9 Signalosome Subunit PfCsnE Leads to the Discovery of Pestaloficins in Pestalotiopsis fici. , 2017, Organic letters.
[5] Xingzhong Liu,et al. Trichoderpyrone, a Unique Polyketide Hybrid with a Cyclopentenone-Pyrone Skeleton from the Plant Endophytic Fungus Trichoderma gamsii. , 2017, Journal of natural products.
[6] Peng Zhang,et al. Deletion of a Histone Acetyltransferase Leads to the Pleiotropic Activation of Natural Products in Metarhizium robertsii. , 2017, Organic letters.
[7] Nicholas H Oberlies,et al. Fungal Identification Using Molecular Tools: A Primer for the Natural Products Research Community , 2017, Journal of natural products.
[8] G. Cerqueira,et al. Discovery of McrA, a master regulator of Aspergillus secondary metabolism , 2017, Molecular microbiology.
[9] Wei Li,et al. A new species of Trichoderma hypoxylon harbours abundant secondary metabolites , 2016, Scientific Reports.
[10] S. Zeilinger,et al. Secondary metabolism in Trichoderma – Chemistry meets genomics , 2016 .
[11] Wei Li,et al. Polyketide Production of Pestaloficiols and Macrodiolide Ficiolides Revealed by Manipulations of Epigenetic Regulators in an Endophytic Fungus. , 2016, Organic letters.
[12] Clay C C Wang,et al. Development of Genetic Dereplication Strains in Aspergillus nidulans Results in the Discovery of Aspercryptin. , 2016, Angewandte Chemie.
[13] Xingzhong Liu,et al. Trichodermates A–F, New Cytotoxic Trichothecenes from the Plant Pathogenic Fungus Trichoderma sp. , 2016 .
[14] M. Hashimoto,et al. Use of a biosynthetic intermediate to explore the chemical diversity of pseudo-natural fungal polyketides. , 2015, Nature chemistry.
[15] T. Anke,et al. Fungal natural products in research and development. , 2014, Natural product reports.
[16] Xingzhong Liu,et al. Stereochemical determination of new cytochalasans from the plant endophytic fungus Trichoderma gamsii. , 2014, Fitoterapia.
[17] Lin Chen,et al. Trichoderones A and B: Two Pentacyclic Cytochalasans from the Plant Endophytic Fungus Trichoderma gamsii , 2012 .
[18] Xingzhong Liu,et al. Trichalasins C and D from the plant endophytic fungus Trichoderma gamsii. , 2012, Fitoterapia.
[19] Xingzhong Liu,et al. Cytochalasans with different amino-acid origin from the plant endophytic fungus Trichoderma gamsii , 2012, The Journal of Antibiotics.
[20] J. Bok,et al. Fast and easy method for construction of plasmid vectors using modified quick-change mutagenesis. , 2012, Methods in molecular biology.
[21] N. A. Stover,et al. Trichothecenes: From Simple to Complex Mycotoxins , 2011, Toxins.
[22] A. Stierle,et al. Anticancer compounds derived from fungal endophytes: their importance and future challenges. , 2011, Natural product reports.
[23] Jian Huang,et al. Trichodermatides A-D, novel polyketides from the marine-derived fungus Trichoderma reesei. , 2008, Organic letters.