Borges Nuno, Gonçalves Luís G, Rodrigues Marta V, Siopa Filipa, Ventura Rita, Maycock Christopher, Lamosa Pedro, Santos Helena
Biology Division, Instituto de Tecnologia Química e Biológica, Universidade Nova de Lisboa, Rua da Quinta Grande 6, Apartado 127, 2780-156 Oeiras, Portugal.
J Bacteriol. 2006 Dec;188(23):8128-35. doi: 10.1128/JB.01129-06. Epub 2006 Oct 6.
Archaeoglobus fulgidus accumulates di-myo-inositol phosphate (DIP) and diglycerol phosphate (DGP) in response to heat and osmotic stresses, respectively, and the level of glycero-phospho-myo-inositol (GPI) increases primarily when the two stresses are combined. In this work, the pathways for the biosynthesis of these three compatible solutes were established based on the detection of the relevant enzymatic activities and characterization of the intermediate metabolites by nuclear magnetic resonance analysis. The synthesis of DIP proceeds from glucose-6-phosphate via four steps: (i) glucose-6-phosphate was converted into l-myo-inositol 1-phosphate by l-myo-inositol 1-phosphate synthase; (ii) l-myo-inositol 1-phosphate was activated to CDP-inositol at the expense of CTP; this is the first demonstration of CDP-inositol synthesis in a biological system; (iii) CDP-inositol was coupled with l-myo-inositol 1-phosphate to yield a phosphorylated intermediate, 1,1'-di-myo-inosityl phosphate 3-phosphate (DIPP); (iv) finally, DIPP was dephosphorylated into DIP by the action of a phosphatase. The synthesis of the two other polyol-phosphodiesters, DGP and GPI, proceeds via the condensation of CDP-glycerol with the respective phosphorylated polyol, glycerol 3-phosphate for DGP and l-myo-inositol 1-phosphate for GPI, yielding the respective phosphorylated intermediates, 1X,1'X-diglyceryl phosphate 3-phosphate (DGPP) and 1-(1X-glyceryl) myo-inosityl phosphate 3-phosphate (GPIP), which are subsequently dephosphorylated to form the final products. The results disclosed here represent an important step toward the elucidation of the regulatory mechanisms underlying the differential accumulation of these compounds in response to heat and osmotic stresses.
嗜热栖热放线菌分别在热应激和渗透应激下积累二 - 肌醇磷酸(DIP)和甘油磷酸(DGP),而甘油磷酸 - 肌醇(GPI)的水平主要在两种应激联合作用时升高。在这项工作中,基于相关酶活性的检测以及通过核磁共振分析对中间代谢物的表征,确定了这三种相容性溶质的生物合成途径。DIP的合成从6 - 磷酸葡萄糖开始,经过四个步骤:(i)6 - 磷酸葡萄糖被肌醇 - 1 - 磷酸合酶转化为1 - 肌醇磷酸;(ii)1 - 肌醇磷酸以CTP为代价被激活为CDP - 肌醇;这是生物系统中CDP - 肌醇合成的首次证明;(iii)CDP - 肌醇与1 - 肌醇磷酸偶联生成磷酸化中间体1,1'-二 - 肌醇磷酸3 - 磷酸(DIPP);(iv)最后,DIPP在磷酸酶的作用下脱磷酸化为DIP。另外两种多元醇 - 磷酸二酯DGP和GPI的合成是通过CDP - 甘油与各自的磷酸化多元醇缩合进行的,DGP的是甘油3 - 磷酸,GPI的是1 - 肌醇磷酸,生成各自的磷酸化中间体1X,1'X - 甘油磷酸3 - 磷酸(DGPP)和1 - (1X - 甘油基)肌醇磷酸3 - 磷酸(GPIP),随后它们脱磷酸形成最终产物。这里揭示 的结果代表了朝着阐明这些化合物在热应激和渗透应激下差异积累的调控机制迈出的重要一步