Jijón-Moreno Saúl, Marcos-Jiménez Cynthia, Pedraza Raúl O, Ramírez-Mata Alberto, de Salamone I García, Fernández-Scavino Ana, Vásquez-Hernández Claudia A, Soto-Urzúa Lucia, Baca Beatriz E
Centro de Investigaciones en Ciencias Microbiológicas, Benemérita Universidad Autónoma de Puebla (BUAP), 72000, Puebla, Puebla, Mexico.
Antonie Van Leeuwenhoek. 2015 Jun;107(6):1501-17. doi: 10.1007/s10482-015-0444-0. Epub 2015 Apr 5.
Plant growth-promoting bacteria of the genus Azospirillum are present in the rhizosphere and as endophytes of many crops. In this research we studied 40 Azospirillum strains isolated from different plants and geographic regions. They were first characterized by 16S rDNA restriction analysis, and their phylogenetic position was established by sequencing the genes 16S rDNA, ipdC, hisC1, and hisC2. The latter three genes are involved in the indole-3-pyruvic acid (IPyA) biosynthesis pathway of indole-3-acetic acid (IAA). Furthermore, the suitability of the 16S-23S rDNA intergenic spacer sequence (IGS) for the differentiation of closely related Azospirillum taxa and development of PCR protocols allows for specific detection of strains. The IGS-RFLP analysis enabled intraspecies differentiation, particularly of Azospirillum brasilense and Azospirillum lipoferum strains. Results demonstrated that the ipdC, hisC1, and hisC2 genes are highly conserved in all the assessed A. brasilense isolates, suggesting that these genes can be used as an alternative phylogenetic marker. In addition, IAA production determined by HPLC ranged from 0.17 to 98.2 μg mg(-1) protein. Southern hybridization with the A. brasilense ipdC gene probe did not show, a hybridization signal with A. lipoferum, Azospirillum amazonense, Azospirillum halopreferans and Azospirillum irakense genomic DNA. This suggests that these species produce IAA by other pathways. Because IAA is mainly synthesized via the IPyA pathway in A. brasilense strains, a species that is used worldwide in agriculture, the identification of ipdC, hisC1, and hisC2 genes by PCR may be suitable for selecting exploitable strains.
固氮螺菌属的植物促生细菌存在于许多作物的根际和作为内生菌。在本研究中,我们研究了从不同植物和地理区域分离出的40株固氮螺菌菌株。首先通过16S rDNA限制性分析对它们进行表征,并通过对16S rDNA、ipdC、hisC1和hisC2基因进行测序来确定它们的系统发育位置。后三个基因参与吲哚-3-乙酸(IAA)的吲哚-3-丙酮酸(IPyA)生物合成途径。此外,16S-23S rDNA基因间隔序列(IGS)对于区分密切相关的固氮螺菌分类群和开发PCR方案的适用性使得能够特异性检测菌株。IGS-RFLP分析能够进行种内分化,特别是对于巴西固氮螺菌和脂环固氮螺菌菌株。结果表明,ipdC、hisC1和hisC2基因在所有评估的巴西固氮螺菌分离物中高度保守,表明这些基因可作为替代的系统发育标记。此外,通过HPLC测定的IAA产量范围为0.17至98.2μg mg(-1)蛋白质。用巴西固氮螺菌ipdC基因探针进行的Southern杂交未显示与脂环固氮螺菌、亚马逊固氮螺菌、嗜盐固氮螺菌和伊拉克固氮螺菌基因组DNA的杂交信号。这表明这些物种通过其他途径产生IAA。由于IAA主要通过巴西固氮螺菌菌株中的IPyA途径合成,巴西固氮螺菌是一种在全球农业中使用的物种,通过PCR鉴定ipdC、hisC1和hisC2基因可能适合选择可利用的菌株。