Chooi Yit-Heng, Cacho Ralph, Tang Yi
Department of Chemical and Biomolecular Engineering, University of California, Los Angeles, Los Angeles, CA 90095, USA.
Chem Biol. 2010 May 28;17(5):483-94. doi: 10.1016/j.chembiol.2010.03.015.
Penicillium aethiopicum produces two structurally interesting and biologically active polyketides: the tetracycline-like viridicatumtoxin 1 and the classic antifungal agent griseofulvin 2. Here, we report the concurrent discovery of the two corresponding biosynthetic gene clusters (vrt and gsf) by 454 shotgun sequencing. Gene deletions confirmed that two nonreducing PKSs (NRPKSs), vrtA and gsfA, are required for the biosynthesis of 1 and 2, respectively. Both PKSs share similar domain architectures and lack a C-terminal thioesterase domain. We identified gsfI as the chlorinase involved in the biosynthesis of 2, because deletion of gsfI resulted in the accumulation of decholorogriseofulvin 3. Comparative analysis with the P. chrysogenum genome revealed that both clusters are embedded within conserved syntenic regions of P. aethiopicum chromosomes. Discovery of the vrt and gsf clusters provided the basis for genetic and biochemical studies of the pathways.
四环类的绿灰菌素1和经典抗真菌剂灰黄霉素2。在此,我们报告通过454鸟枪法测序同时发现了两个相应的生物合成基因簇(vrt和gsf)。基因缺失证实,两个非还原型聚酮合酶(NRPKSs),vrtA和gsfA,分别是1和2生物合成所必需的。这两个聚酮合酶具有相似的结构域架构,且缺乏C端硫酯酶结构域。我们鉴定出gsfI为参与2生物合成的氯酶,因为缺失gsfI会导致脱氯灰黄霉素3的积累。与产黄青霉基因组的比较分析表明,这两个基因簇都嵌入在埃塞俄比亚青霉染色体的保守同线区域内。vrt和gsf基因簇的发现为这些途径的遗传和生化研究提供了基础。