摘要
将胡杨Na+/H+逆向转运蛋白基因PeNhaD1,分别转入对盐敏感的缺失质膜和缺失液泡膜Na+/H+逆向转运蛋白基因的酵母突变菌株ANT3和GX1中。结果表明,在pH6.0、Na+浓度为80mmol/L(固体培养基)或400mmol/L(液体培养基)的条件下,转化具有目的基因的酵母ANT3具有更高的耐盐性,而将目的基因转化到突变株GX1时,却不能提高其耐盐性。实验结果说明PeNhaD1可能是通过编码质膜Na+/H+逆向转运蛋白而提高酵母的耐盐性的,推测其在胡杨耐盐机制中的作用可能是提高拒盐性。
Yeast complementation experiments were carried out to define the possible function of PeNhaD1, a Na^+/H^+ antiporter gene from Populus euphratica Oliv., a salt resistant tree. PeNhaD1 was introduced to the Saccharomyces cerevisiae mutant strain ANT3 (△enal-4∷HIS3 Anhal∷LEU2), which lacks the plasma membrane Na^+/H^+ antiporter gene ScNHA1 or GX 1 (△nhx 1∷TRP1), which lacks tonoplast Na^+/H^+ antiporter gene ScNHX1 (Figs.1, 2). Our results showed that PeNhaD1 rescued the normal growth of ANT3 in the presence of high salt (80 mmol/L NaCl on solid medium or 400 mmol/L in liquid medium, pH 6.0) (Figs.3, 5), but not that of GX1 (Figs.4, 6), suggesting that PeNhaD1 may play a role in salt tolerance of Populus euphratica by maintaining the capacity for salt exclusion under saline condition.
出处
《植物生理与分子生物学学报》
CAS
CSCD
北大核心
2007年第2期173-178,共6页
Journal Of Plant Physiology and Molecular Biology
基金
国家自然科学基金重点项目(No.30430430)
国家高技术研究和发展(863)计划项目(2006AA10Z131)资助~~