Ramírez-Mata Alberto, López-Lara Lilia I, Xiqui-Vázquez Ma Luisa, Jijón-Moreno Saúl, Romero-Osorio Angelica, Baca Beatriz E
Centro de Investigaciones en Ciencias Microbiológicas, Instituto de Ciencias, Benemérita Universidad Autónoma de Puebla, Edif. 103J, Av. San Claudio S/N, Col. San Manuel, Puebla Pue CP 72570, Mexico.
Res Microbiol. 2016 Apr;167(3):190-201. doi: 10.1016/j.resmic.2015.12.004. Epub 2015 Dec 18.
In bacteria, proteins containing GGDEF domains are involved in production of the second messenger c-di-GMP. Here we report that the cdgA gene encoding diguanylate cyclase A (CdgA) is involved in biofilm formation and exopolysaccharide (EPS) production in Azospirillum brasilense Sp7. Biofilm quantification using crystal violet staining revealed that inactivation of cdgA decreased biofilm formation. In addition, confocal laser scanning microscopy analysis of green-fluorescent protein-labeled bacteria showed that, during static growth, the biofilms had differential levels of development: bacteria harboring a cdgA mutation exhibited biofilms with considerably reduced thickness compared with those of the wild-type Sp7 strain. Moreover, DNA-specific staining and treatment with DNase I, and epifluorescence studies demonstrated that extracellular DNA and EPS are components of the biofilm matrix in Azospirillum. After expression and purification of the CdgA protein, diguanylate cyclase activity was detected. The enzymatic activity of CdgA-producing cyclic c-di-GMP was determined using GTP as a substrate and flavin adenine dinucleotide (FAD(+)) and Mg(2)(+) as cofactors. Together, our results revealed that A. brasilense possesses a functional c-di-GMP biosynthesis pathway.
在细菌中,含有GGDEF结构域的蛋白质参与第二信使环二鸟苷酸(c-di-GMP)的产生。在此,我们报道编码双鸟苷酸环化酶A(CdgA)的cdgA基因参与巴西固氮螺菌Sp7的生物膜形成和胞外多糖(EPS)产生。使用结晶紫染色进行生物膜定量分析表明,cdgA基因失活会减少生物膜的形成。此外,对绿色荧光蛋白标记细菌的共聚焦激光扫描显微镜分析显示,在静态生长期间,生物膜的发育水平存在差异:与野生型Sp7菌株相比,携带cdgA突变的细菌所形成的生物膜厚度显著降低。此外,DNA特异性染色、用脱氧核糖核酸酶I处理以及落射荧光研究表明,胞外DNA和EPS是固氮螺菌生物膜基质的组成成分。在对CdgA蛋白进行表达和纯化后,检测到了双鸟苷酸环化酶活性。以GTP作为底物、黄素腺嘌呤二核苷酸(FAD(+))和Mg(2)(+)作为辅因子,测定了CdgA产生环化c-di-GMP的酶活性。我们的研究结果共同表明,巴西固氮螺菌拥有一条功能性的c-di-GMP生物合成途径。