View source for Phytopathology (2016) 106, 807-813

{{Publication
|Publication authors=Yujun Zhou, Jianqiang Xu, Yuanye Zhu, [[Yabing Duan]] and Mingguo Zhou
|Author Page=Ming-Guo Zhou, Yabing Duan
|Publication date=2016
|dc:title=Mechanism of action of the benzimidazole fungicide on ''[[Fusarium graminearum]]'': Interfering with polymerization of monomeric tubulin but not polymerized microtubule
|Publication journal=Phytopathology
|prism:volume=106 (8)
|prism:startingPage=807
|Last page=813
|DOI=10.1094/PHYTO-08-15-0186-R
|Publication abstract=Tubulins are the proposed target of clinically relevant anticancer drugs, anthelmintic, and fungicide. β<sub>2</sub>-tubulin of the plant pathogen ''Fusarium graminearum'' was considered as the target of benzimidazole compounds by homology modeling in our previous work. In this study, α<sub>1</sub>-, α<sub>2</sub>-, and β<sub>2</sub>-tubulin of ''F. graminearum'' were produced in ''Escherichia coli''. Three benzimidazole compounds (carbendazim, benomyl, and thiabendazole) interacted with the recombinant β<sub>2</sub>-tubulin and reduced the maximum fluorescence intensity of 2 μM β<sub>2</sub>-tubulin 47, 50, and 25%, respectively, at saturation of compound-tubulin complexes. Furthermore, carbendazim significantly inhibited the polymerization of α<sub>1</sub>-/β<sub>2</sub>-tubulins and α<sub>2</sub>-/β<sub>2</sub>-tubulins 90.9 ± 0.4 and 93.5 ± 0.05%, respectively, in vitro. A similar result appeared with benomyl on the polymerization of α<sub>1</sub>-/β<sub>2</sub>-tubulins and α<sub>2</sub>-/β<sub>2</sub>-tubulins at 89.9 ± 0.1% and 92.6 ± 1.2% inhibition ratios, respectively. In addition, thiabendazole inhibited 81.6 ± 1% polymerization of α<sub>1</sub>-/β<sub>2</sub>-tubulins, whereas it had less effect on α<sub>2</sub>-/β<sub>2</sub>-tubulin polymerization, with 20.1 ± 1.9% inhibition ratio. However, the three compounds cannot destabilize the polymerized microtubule. To illuminate the issue, mapping the carbendazim binding sites and β/α subunit interface on β/α-tubulin complexes by homology modeling showed that the two domains were closed to each other. Understanding the nature of the interaction between benzimidazole compounds and ''F. graminearum'' tubulin is fundamental for the development of tubulin-specific anti-''F. graminearum'' compounds.
|AbstractCC=Yes
|Research topic=control - general
|Is book=No
}}
{{Pest record
|Pest=Fusarium graminearum
|Quarantined=No
}}