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首页> 外文期刊>European Journal of Soil Biology >Impact of beta-carotene transgenic rice with four synthetic genes on rhizosphere enzyme activities and bacterial communities at different growth stages
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Impact of beta-carotene transgenic rice with four synthetic genes on rhizosphere enzyme activities and bacterial communities at different growth stages

机译:具有四个合成基因的β-胡萝卜素转基因水稻对不同生育期根际酶活性和细菌群落的影响

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A field experiment was carried out to assess the impact of beta-carotene transgenic rice with four synthetic genes on bacterial communities and enzyme activities in the rhizosphere. Soil samples from two neighboring fields cultivated with transgenic rice AH33 and its parental non-transgenic variety Zhonghua 11 were taken at seedling, tillering, heading and maturing stages. There were no significant differences in activities of catalase, sucrase and protease between AH33 and Zhonghua 11 at the same growth stage. Although soil urease activities of AH33 showed significant differences (P 0.05) compared with that of Zhonghua 11 at the heading stage, these differences were transient and disappeared at other stages, indicating that changes in soil enzyme activities were mainly related to plant age. Changes in the bacterial communities throughout different growth stages were monitored and analyzed using denaturing gradient gel electrophoresis (DGGE) and 16S rRNA gene clone library techniques. The resulting dendrograms of DGGE patterns showed four distinct clusters, which were identified to be correlating with the respective growth stages. No effect of the transgenic rice AH33 on dominant bacterial communities at the same growth stage was detectable. This indicated that the impact of crop growth stage outweighed possible alterations due to the genetic modifications. The analyses of DGGE and 16S rRNA gene clone libraries revealed that there were no significant differences (P 0.05) in the Shannon Wiener diversity index (H'), richness (R), and evenness (E) of rhizosphere soil between AH33 and Zhonghua 11 at any of the stages. Thus, there was no indication of altered overall bacterial diversity due to the genetic modification. Sequencing of PCR amplicons indicated that the DGGE profiles were mainly composed of Proteobacteria, Acidobacteria, Gemmatimonadetes, Chloroflexi and Verrucomicrobia, and in addition, the 16S rRNA gene clone libraries indicated the presence of Plantomycetes, Armatimonadetes, Actinobacteria, Chlorobi, Cyanobacteria and Fimicutes. In conclusion, our study based on the analysis of four different soil enzymes and the diversity of rhizosphere bacteria gives no indication that the genetic modification with the four synthetic genes and their expression in the transgenic rice AH33 has any specific effects, related to the genetic modification, on the soils in which they are cultivated. (C) 2014 Elsevier Masson SAS. All rights reserved.
机译:进行了田间试验,以评估具有四个合成基因的β-胡萝卜素转基因水稻对根际细菌群落和酶活性的影响。在转基因水稻AH33及其亲本非转基因品种中华11栽培的两个相邻田地的土壤样品在苗,分er,抽穗和成熟期进行。 AH33和中华11在同一生育期的过氧化氢酶,蔗糖酶和蛋白酶活性无明显差异。虽然抽穗期AH33的土壤脲酶活性与中华11号相比有显着差异(P <0.05),但这些差异是短暂的,在其他阶段则消失了,这表明土壤酶活性的变化主要与植株的年龄有关。使用变性梯度凝胶电泳(DGGE)和16S rRNA基因克隆文库技术来监测和分析整个生长阶段细菌群落的变化。 DGGE模式的结果树状图显示了四个不同的簇,这些簇被确定与各自的生长阶段相关。在相同的生长阶段,未检测到转基因水稻AH33对优势细菌群落的影响。这表明由于基因改变,作物生长阶段的影响超过了可能的变化。 DGGE和16S rRNA基因克隆文库的分析表明,AH33和中华之间根际土壤的香农维纳多样性指数(H'),丰富度(R)和均匀度(E)没有显着差异(P <0.05)。在任何阶段都为11。因此,没有迹象表明由于遗传修饰而改变了总体细菌多样性。 PCR扩增子的测序表明DGGE图谱主要由变形杆菌,酸性细菌,芽孢杆菌,绿弯曲菌和疣状微生物菌组成,此外,16S rRNA基因克隆文库表明存在植物菌,Armatimonadetes,放线菌,Chlorobi,蓝藻和纤毛虫。总而言之,我们基于对四种不同土壤酶和根际细菌多样性的分析而得出的研究结果,没有迹象表明四种合成基因的遗传修饰及其在转基因水稻AH33中的表达具有任何特定的作用,与遗传修饰有关,在种植它们的土壤上。 (C)2014 Elsevier Masson SAS。版权所有。

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