Xie Linan, Zang Xin, Cheng Wei, Zhang Zhuan, Zhou Jiahai, Chen Mengbin, Tang Yi
Biotechnology Research Institute, The Chinese Academy of Agricultural Sciences, 12 Zhongguancun South Street, Beijing 100081, P. R. China.
State Key Laboratory of Bio-organic and Natural Products Chemistry, Center for Excellence in Molecular Synthesis, Shanghai Institute of Organic Chemistry, University of Chinese Academy of Sciences, Shanghai 200032, China.
J Am Chem Soc. 2021 Jun 16. doi: 10.1021/jacs.1c03988.
Acetohydroxyacid synthase (AHAS) is the first enzyme in the branched-chain amino acid biosynthetic pathway and is a validated target for herbicide and fungicide development. Here we report harzianic acid (HA, ) produced by the biocontrol fungus t-22 (Tht22) as a natural product inhibitor of AHAS. The biosynthetic pathway of HA was elucidated with heterologous reconstitution. Guided by a putative self-resistance enzyme in the genome, HA was biochemically demonstrated to be a selective inhibitor of fungal AHAS, including those from phytopathogenic fungi. In addition, HA can inhibit a common resistant variant of AHAS in which the active site proline is mutated. Structural analysis of AHAS complexed with HA revealed the molecular basis of competitive inhibition, which differs from all known commercial AHAS inhibitors. The alternative binding mode also rationalizes the selectivity of HA, as well as effectiveness toward resistant mutants. A proposed role of HA biosynthesis by Tht22 in the rhizosphere is discussed based on the data.
乙酰羟酸合酶(AHAS)是支链氨基酸生物合成途径中的首个酶,是除草剂和杀菌剂开发的一个已验证靶点。在此,我们报道了由生防真菌t-22(Tht22)产生的哈茨酸(HA)作为AHAS的一种天然产物抑制剂。通过异源重组阐明了HA的生物合成途径。在基因组中一种假定的自身抗性酶的指导下,生物化学证明HA是真菌AHAS的选择性抑制剂,包括来自植物病原真菌的AHAS。此外,HA可以抑制AHAS的一种常见抗性变体,其中活性位点脯氨酸发生了突变。AHAS与HA复合物的结构分析揭示了竞争性抑制的分子基础,这与所有已知的商业AHAS抑制剂不同。这种替代的结合模式也解释了HA的选择性以及对抗性突变体的有效性。基于这些数据,讨论了Tht22在根际合成HA的一个假定作用。