首页> 外文期刊>Pedosphere: A Quarterly Journal of Soil Science >Diversity of Microbial Community in a Paddy Soil with cry1Ac/cpti Transgenic Rice
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Diversity of Microbial Community in a Paddy Soil with cry1Ac/cpti Transgenic Rice

机译:转cry1Ac / cpti水稻水稻土中微生物群落的多样性

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Two types of cry1Ac/cpti transgenic rice (GM1 and GM2) and their parental non-cry1Ac/cpti rice (CK1 and CK2) were planted in the field at Wufeng, Fujian Province, China for four years to investigate the influence of genetically modified rice on diversity of bacterial and fungal community in the paddy soil. The community composition and abundance of bacteria or fungi in the paddy soil were assessed at different growth stages of rice by denaturing gradient gel electrophoresis and real-time polymerase chain reaction based on 16S rRNA gene or SSU rRNA gene in the 4th year after the experimental establishment. The composition of bacterial or fungal community changed during rice growth, while no significant differences were observed between the fields cultivated with GM1 and CK1, or between the fields cultivated with 0M2 and CK2 in either bacterial or fungal community composition. The copy numbers of bacterial 168 rRNA gene in the soils with CK1, CK2, GM1 and GM2 ranged from 5.64 x 10(11) to 6.89 x 10(11) copies g(-1) dry soil at rice growth stages, and those of fungal SSU rRNA gene from 5.24 x 10(8) to 8.68 x 10(8) copies g(-1) dry soil. There were no marked differences in the copies of bacterial 16S rRNA gene or fungal SSU rRNA gene between CK1 and GM1 or between CK2 and GM2 at any growth stage of rice. Planting cry1Ac/cpti transgenic rice had no significant effect on composition and abundance of bacterial and fungal community in paddy soil during the rice growing season at least in the short term.
机译:在中国福建省五丰市的田间种植了两种类型的cry1Ac / cpti转基因水稻(GM1和GM2)及其亲本非cry1Ac / cpti水稻(CK1和CK2)四年,以研究转基因水稻的影响对稻田土壤细菌和真菌群落多样性的影响实验建立后第4年,通过变性梯度凝胶电泳和基于16S rRNA基因或SSU rRNA基因的实时聚合酶链反应,评估水稻在不同生育时期水稻土中细菌或真菌的群落组成和丰度。 。水稻生长过程中细菌或真菌群落的组成发生了变化,而在GM1和CK1栽培的田间或在0M2和CK2栽培的田间,细菌或真菌的群落组成均没有显着差异。在水稻生长阶段,CK1,CK2,GM1和GM2的土壤中细菌168 rRNA基因的拷贝数范围为5.64 x 10(11)至6.89 x 10(11)份g(-1)干燥土壤。真菌SSU rRNA基因从5.24 x 10(8)到8.68 x 10(8)副本g(-1)干燥土壤。在水稻的任何生长阶段,CK1和GM1之间或CK2和GM2之间的细菌16S rRNA基因或真菌SSU rRNA基因的拷贝均无明显差异。至少在短期内,种植cry1Ac / cpti转基因水稻对稻田土壤中细菌和真菌群落的组成和丰度没有明显影响。

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