非转基因烟草和转植体烟草的根瘤沉积对土壤细菌群落的影响。

Environmental biosafety research Pub Date : 2008-01-01 Epub Date: 2008-04-03 DOI:10.1051/ebr:2008002
Lorenzo Brusetti, Aurora Rizzi, Alessandro Abruzzese, Gian Attilio Sacchi, Enzio Ragg, Marco Bazzicalupo, Claudia Sorlini, Daniele Daffonchio
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引用次数: 6

摘要

研究了转基因烟草(Nicotiana tabacum)根释放的化合物对土壤细菌群落结构的影响及其支持细菌水平基因转移(HGT)的潜力。研究人员将从转植株烟草和非转基因烟草栽培品种中收集到的根释放化合物暴露于土壤微生态系统中。培养 48 小时后,对土壤细菌群落的自动核糖体基因间距分析(ARISA)图谱进行聚类分析,将转基因栽培品种与非转基因栽培品种区分开来,表明转基因栽培品种的根瘤沉积模式与亲本植物不同。不过,这些差异小于所研究的两个非转基因烟草栽培品种之间的差异。根释放化合物的核磁共振特征显示,转培植体与亲本栽培品种的化学指纹图谱存在一些差异。不过,对细菌群落结构的影响是短暂的,在培养 96 小时后趋于消失。通过使用四种潜在的受体物种,研究了根释放的化合物作为细菌转化 DNA 源的潜力。所有受体接触根释放化合物后都没有获得转化子。根释放化合物与转基因供体 DNA 的混合降低了贝氏不动杆菌菌株 ADP1200 的转化频率,而氮青霉、农杆菌和单胞菌菌株在外部添加转基因源的情况下也未能产生能力。通过 PCR 对质体序列的检测表明,根释放的化合物中含有极少量片段化的质体供体 DNA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effects of rhizodeposition of non-transgenic and transplastomic tobaccos on the soil bacterial community.

The effect of root-released compounds of transplastomic tobacco (Nicotiana tabacum) on the soil bacterial community structure, and their potential to support horizontal gene transfer (HGT) to bacteria have been studied. Soil microcosms were exposed to root-released compounds collected from transplastomic and non-transgenic tobacco cultivars. Cluster analysis of automated ribosomal intergenic spacer analysis (ARISA) profiles of the soil bacterial community after 48 h incubation grouped the transgenic cultivar apart from the non-transgenic, indicating that it had a rhizodeposition pattern different from the parental plants. However, these differences were less than between the two non-transgenic tobacco cultivars studied. NMR characterization of the root-released compounds showed some differences in chemical fingerprinting pattern between the transplastomic and the parental cultivar. However, the effect on bacterial community structure was transient, and tended to disappear after 96 h of incubation. The potential of root-released compounds as a source of transforming DNA for bacteria was investigated by using four potential recipient species. No transformants were obtained following exposure of all the recipients to the root-released compounds. Root-released compounds amended to transgene donor DNA decreased the transformation frequency of Acinetobacter baylyi strain ADP1200, while Azospirillum, Agrobacterium, and Sinorhizobium strains failed to develop competence also in the presence of an external added transgene source. Detection of plastid sequences by PCR suggested that a very low amount of fragmented plastid donor DNA was present in the root-released compounds.

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