Verma S C, Ladha J K, Tripathi A K
School of Biotechnology, Faculty of Science, Banaras Hindu University, 221005, Varanasi, India.
J Biotechnol. 2001 Oct 4;91(2-3):127-41. doi: 10.1016/s0168-1656(01)00333-9.
A study of the diversity of endophytic bacteria present in seeds of a deepwater rice variety revealed the presence of seven types of BOX-PCR fingerprints. In order to evaluate the plant growth promoting potential the presence of nitrogenase, indole acetic acid production and mineral phosphate solubilization were estimated in the representative BOX-PCR types. The seven representatives of BOX-PCR types produced indole acetic acid, reduced acetylene and showed specific immunological cross-reaction with anti-dinitrogenase reductase antibody. Only four types showed mineral phosphate solubilizing ability. Comparison of cellulase and pectinase activities showed differences among different BOX-PCR types. PCR fingerprinting data showed that one strain isolated from the surface sterilized seeds as well as the aerial parts of the seedlings of rice variety showed low cellulase and pectinase but relatively high ARA. On the basis of 16S rDNA nucleotide sequence and BIOLOG system of bacterial identification, this strain was identified as Pantoea agglomerans. For studying the endophytic colonization this strain was genetically tagged with the reporter gene, gusA. Histochemical analysis of the seedling grown in hydroponics showed that the tagged strain colonized the root surface, root hairs, root cap, points of lateral root emergence, root cortex and the stelar region. Treatment of the roots with 2,4-D produced short thickened lateral roots which showed better colonization by P. agglomerans.
一项对深水稻品种种子中内生细菌多样性的研究揭示了七种BOX-PCR指纹类型的存在。为了评估促进植物生长的潜力,对代表性的BOX-PCR类型进行了固氮酶、吲哚乙酸产生和矿物磷酸盐溶解能力的测定。BOX-PCR类型的七个代表产生了吲哚乙酸,还原了乙炔,并与抗二氮酶还原酶抗体表现出特异性免疫交叉反应。只有四种类型表现出矿物磷酸盐溶解能力。纤维素酶和果胶酶活性的比较显示不同BOX-PCR类型之间存在差异。PCR指纹数据表明,从水稻品种表面消毒种子以及幼苗地上部分分离出的一个菌株纤维素酶和果胶酶活性较低,但ARA相对较高。基于16S rDNA核苷酸序列和细菌鉴定的BIOLOG系统,该菌株被鉴定为成团泛菌。为了研究内生定殖,该菌株用报告基因gusA进行了基因标记。对水培生长的幼苗进行组织化学分析表明,标记菌株定殖在根表面、根毛、根冠、侧根出现点、根皮层和中柱区域。用2,4-D处理根部产生了短而粗的侧根,这些侧根显示出成团泛菌更好的定殖。