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首页> 外文期刊>Scientia horticulturae >Overexpression of the rice phosphate transporter gene OsPT6 enhances tolerance to low phosphorus stress in vegetable soybean
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Overexpression of the rice phosphate transporter gene OsPT6 enhances tolerance to low phosphorus stress in vegetable soybean

机译:水稻磷酸转运蛋白基因OsPT6的过表达增强了蔬菜大豆对低磷胁迫的耐受性

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摘要

Low phosphorus (P) availability is a major constraint in the growth and production of vegetable soybean. To improve P efficiency in vegetable soybean, a rice (Oryza sativa L) phosphate transporter gene, OsPT6, was transferred into the vegetable soybean cultivar 'NY-1001' using an Agrobacterium-mediated cotyledonary-node transformation system. OsPT6 was driven by the constitutive cauliflower mosaic virus (CaMV) 35S promoter in the binary vector pCAMBIA3301-OsPT6. Two independent fertile T-0 transgenic plants (12PT6-1 and 12PT6-2) were obtained and confirmed by PCR and Southern blotting analyses. The overexpression of the OsPT6 gene of the T-2 transgenic plants was detected by quantitative RT-PCR analysis. The tolerance of the T-2 transgenic lines overexpressing OsPT6 to low concentrations of phosphate (low-Pi; 10 mu M Pi) was evaluated by hydroponic culture using a modified Hoagland's nutrient solution. The P contents in leaves, stems, and roots of the transgenic plants were significantly higher than those of the non-transformed (NT) plants under the concentrations of both low- and normal-Pi of standard Hoagland's nutrient solution. Under low-Pi stress, the transgenic plants grew better and exhibited significant increases in plant height, root length, root weight, number of pods and seeds, and seed weight per plant compared with the NT plants. Our data indicate that the overexpression of OsPT6 in transgenic vegetable soybean lines improves P accumulation and growth performance and thereby represents a promising approach for the improvement of P efficiency in vegetable soybean
机译:磷(P)利用率低是蔬菜大豆生长和生产的主要限制因素。为了提高蔬菜大豆中的磷效率,使用农杆菌介导的子叶节点转化系统将水稻(Oryza sativa L)磷酸转运蛋白基因OsPT6转移到蔬菜大豆品种“ NY-1001”中。 OsPT6由二元载体pCAMBIA3301-OsPT6中的本构性花椰菜花叶病毒(CaMV)35S启动子驱动。获得了两个独立的可育T-0转基因植物(12PT6-1和12PT6-2),并通过PCR和Southern印迹分析进行了证实。通过定量RT-PCR分析检测到T-2转基因植物的OsPT6基因的过表达。通过使用改良的Hoagland营养液进行水培培养,评估了过表达OsPT6的T-2转基因株系对低浓度磷酸盐(低Pi; 10μM Pi)的耐受性。在标准Hoagland营养液的低Pi和正常Pi浓度下,转基因植物的叶,茎和根中的P含量均显着高于非转化(NT)植物。在低Pi胁迫下,与NT植物相比,转基因植物生长得更好,并且植物高度,根长,根重,豆荚和种子的数量以及每株种子的重量显着增加。我们的数据表明,OsPT6在转基因蔬菜大豆品系中的过表达改善了P的积累和生长性能,从而代表了改善蔬菜大豆P效率的有前途的方法

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