Wang Ying, Hu Pengjie, Pan Yuanyuan, Zhu Yaxin, Liu Xingzhong, Che Yongsheng, Liu Gang
State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China; University of Chinese Academy of Sciences, Beijing 100049, China.
State Key Laboratory of Mycology, Institute of Microbiology, Chinese Academy of Sciences, Beijing 100101, China.
Fungal Genet Biol. 2017 Jun;103:25-33. doi: 10.1016/j.fgb.2017.03.007. Epub 2017 Apr 1.
Verticillin is one of the dimeric epipolythiodioxopiperazines (ETPs) which are toxic secondary metabolites produced only by fungi. ETPs have received substantial attention since its complex molecular architecture and a wide range of biological activities. Although biosynthesis of the monomeric gliotoxin has been studied extensively, the biosynthetic pathway of dimeric ETPs is far from being studied. To investigate the biosynthesis of dimeric ETPs and expand our understanding of their dimerization, the verticillin biosynthetic gene cluster (ver) was identified and cloned from a genomic DNA fosmid library of the Cordyceps-colonizing fungus Clonostachys rogersoniana with the designed primers based on the sequence of a nonribosomal peptide synthetase (NRPS) ChaP which was predicted to be responsible for chaetocin biosynthesis in Chaetomium virescens. To validate it, the chaP homologous gene verP in the ver cluster was disrupted. HPLC-MS analysis demonstrated that the verP disruption mutant (ΔverP) completely abolished verticillin production, and it could be restored by introducing a copy of the wild-type verP gene. Further gene disruptions and chemical analysis demonstrated that most genes of this ver cluster were essential for verticillin biosynthesis. Intriguingly, disruption of verP almost abolished the conidiation of Clonostachys rogersoniana and it was partially restored by addition of the fermentation extract which contains verticillin, implying that verticillin or its intermediate plays a role in the Cordyceps-colonizing fungal morphological differentiation.
绿胶霉素是二聚体环多硫二氧哌嗪(ETPs)之一,ETPs是仅由真菌产生的有毒次生代谢产物。由于其复杂的分子结构和广泛的生物活性,ETPs受到了广泛关注。尽管单体gliotoxin的生物合成已被广泛研究,但二聚体ETPs的生物合成途径仍远未被研究。为了研究二聚体ETPs的生物合成并扩展我们对其环化作用的理解,基于预测负责绿僵菌中chaetocin生物合成的非核糖体肽合成酶(NRPS)ChaP的序列,设计引物从定殖于虫草的真菌罗氏轮枝菌的基因组DNA fosmid文库中鉴定并克隆了绿胶霉素生物合成基因簇(ver)。为了验证它,ver簇中的chaP同源基因verP被破坏。HPLC-MS分析表明,verP破坏突变体(ΔverP)完全消除了绿胶霉素的产生,并且通过引入野生型verP基因的一个拷贝可以恢复。进一步的基因破坏和化学分析表明,该ver簇的大多数基因对于绿胶霉素的生物合成是必不可少的。有趣的是,verP的破坏几乎消除了罗氏轮枝菌的分生孢子形成,并且通过添加含有绿胶霉素的发酵提取物部分恢复,这意味着绿胶霉素或其中间体在定殖于虫草的真菌形态分化中起作用。