Arcuri Helen Andrade, Canduri Fernanda, Pereira José Henrique, da Silveira Nelson José Freitas, Camera Júnior João Carlos, de Oliveira Jaim Simões, Basso Luiz Augusto, Palma Mário Sérgio, Santos Diógenes Santiago, de Azevedo Júnior Walter Filgueira
Department of Physics IBILCE/UNESP, São José do Rio Preto, SP 15054-000, Brazil.
Biochem Biophys Res Commun. 2004 Jul 30;320(3):979-91. doi: 10.1016/j.bbrc.2004.05.220.
The Xylella fastidiosa is a bacterium that is the cause of citrus variegated chlorosis (CVC). The shikimate pathway is of pivotal importance for production of a plethora of aromatic compounds in plants, bacteria, and fungi. Putative structural differences in the enzymes from the shikimate pathway, between the proteins of bacterial origin and those of plants, could be used for the development of a drug for the control of CVC. However, inhibitors for shikimate pathway enzymes should have high specificity for X. fastidiosa enzymes, since they are also present in plants. In order to pave the way for structural and functional efforts towards antimicrobial agent development, here we describe the molecular modeling of seven enzymes of the shikimate pathway of X. fastidiosa. The structural models of shikimate pathway enzymes, complexed with inhibitors, strongly indicate that the previously identified inhibitors may also inhibit the X. fastidiosa enzymes.
木质部难养菌是引起柑橘杂色黄化病(CVC)的一种细菌。莽草酸途径对于植物、细菌和真菌中大量芳香族化合物的产生至关重要。细菌来源的蛋白质与植物来源的蛋白质在莽草酸途径酶方面的假定结构差异,可用于开发控制柑橘杂色黄化病的药物。然而,莽草酸途径酶的抑制剂应对木质部难养菌的酶具有高特异性,因为这些酶在植物中也存在。为了为抗微生物剂开发的结构和功能研究铺平道路,我们在此描述了木质部难养菌莽草酸途径七种酶的分子建模。与抑制剂复合的莽草酸途径酶的结构模型强烈表明,先前鉴定出的抑制剂也可能抑制木质部难养菌的酶。