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液泡型钠氢逆向转运蛋白基因TaNHX2赋予转基因紫花苜蓿(Medicago sativa)耐盐性。

The vacuolar Na-H antiport gene TaNHX2 confers salt tolerance on transgenic alfalfa (Medicago sativa).

作者信息

Zhang Yan-Min, Liu Zi-Hui, Wen Zhi-Yu, Zhang Hong-Mei, Yang Fan, Guo Xiu-Lin

机构信息

Institute of Genetics and Physiology, Hebei Academy of Agriculture and Forestry Sciences, Plant Genetic Engineering Center of Hebei Province, Shijiazhuang 050051, China.

出版信息

Funct Plant Biol. 2012 Sep;39(8):708-716. doi: 10.1071/FP12095.

Abstract

TaNHX2, a vacuolar Na+-H+ antiport gene from wheat (Triticum aestivum L.), was transformed into alfalfa (Medicago sativa L.) via Agrobacterium-mediated transformation to evaluate the role of vacuolar energy providers in plant salt stress responses. PCR and Southern blotting analysis showed that the target gene was integrated into the Medicago genome. Reverse transcription-PCR indicated that gene TaNHX2 was expressed at the transcriptional level. The relative electrical conductivity in the T2 transgenic plants was lower and the osmotic potential was higher compared to the wild-type plants under salt stress conditions. The tonoplast H+-ATPase, H+-pyrophosphatase (PPase) hydrolysis activities and ATP-dependent proton pump activities in transgenic plants were all higher than those of wild-type plants, and the enzyme activities could be induced by salt stress. The PPi-dependent proton pump activities decreased when NaCl concentrations increased from 100mM to 200mM, especially in transgenic plants. The vacuolar Na+-H+ antiport activities of transgenic plants were 2-3 times higher than those of the wild -type plants under 0mM and 100mM NaCl stress. Na+-H+ antiport activity was not detectable for wild-type plants under 200mM NaCl, but for transgenic plants, it was further increased with an increment in salt stress intensity. These results demonstrated that expression of the foreign TaNHX2 gene enhanced salt tolerance in transgenic alfalfa.

摘要

TaNHX2是从小麦(Triticum aestivum L.)中分离得到的一个液泡Na⁺-H⁺逆向转运蛋白基因,通过农杆菌介导的转化方法将其导入苜蓿(Medicago sativa L.)中,以评估液泡能量供应者在植物盐胁迫响应中的作用。PCR和Southern杂交分析表明,目标基因已整合到苜蓿基因组中。逆转录PCR结果显示,TaNHX2基因在转录水平上表达。在盐胁迫条件下,与野生型植株相比,T2代转基因植株的相对电导率较低,渗透势较高。转基因植株的液泡膜H⁺-ATP酶、H⁺-焦磷酸酶(PPase)水解活性以及依赖ATP的质子泵活性均高于野生型植株,并且这些酶活性能够被盐胁迫诱导。当NaCl浓度从100mM增加到200mM时,尤其是转基因植株,依赖PPi的质子泵活性降低。在0mM和100mM NaCl胁迫下,转基因植株的液泡Na⁺-H⁺逆向转运活性比野生型植株高2至3倍。在200mM NaCl条件下,野生型植株未检测到Na⁺-H⁺逆向转运活性,但转基因植株的该活性随着盐胁迫强度的增加而进一步升高。这些结果表明,外源TaNHX2基因的表达增强了转基因苜蓿的耐盐性。

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