Streptothricin-F Inhibition of FtsZ Function: A Promising Approach for Controlling <i>Pseudomonas syringae</i> pv. <i>actinidiae</i>
Hua Wang, Qianqian Mi, Yiru Mao, Yunxiao Tan, Mingming Yang, Wei Liu, Nana Wang, Xiangrong Tian, Lili Huang
Abstract
Pseudomonas syringae pv. actinidiae ( Psa ) is a significant pathogenic bacterium affecting the kiwifruit industry. This study investigated the target sites of streptothricin-F (ST-F), produced by Streptomyces lavendulae gCLA4. The inhibition of ST-F on Psa was examined by the microscopic structural differences of Psa before and after treatment with ST-F, as well as the interaction between ST-F and cell division-related proteins. The results revealed filamentation of Psa after ST-F treatment, and fluorescence microscopy showed that ST-F inhibited the formation of the Z-ring composed of FtsZ protein. In vitro experiments and molecular docking demonstrated that ST-F can bind to FtsZ with a binding energy of 0.4 μM and inhibit FtsZ’s GTP-dependent polymerization reaction. In addition, ST-F does not exert inhibitory effects on cell division in Psa strains overexpressing ftsZ . In conclusion, FtsZ is one of the target sites for ST-F inhibition of Psa, highlighting its potential as a therapeutic target for controlling Psa -induced kiwifruit bacterial canker.