Waditee Rungaroon, Hibino Takashi, Nakamura Tatsunosuke, Incharoensakdi Aran, Takabe Teruhiro
Research Institute and Department of Chemistry, Meijo University, Nagoya 468-8502, Japan.
Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):4109-14. doi: 10.1073/pnas.052576899. Epub 2002 Mar 12.
The salt tolerance of a freshwater cyanobacterium, Synechococcus sp. PCC 7942, transformed with genes involved in the synthesis of a Na(+)/H(+) antiporter, betaine, catalase, and a chaperone was examined. Compared with the expression of betaine, catalase, and the chaperone, the expression of the Na(+)/H(+) antiporter gene from a halotolerant cyanobacterium (ApNhaP) drastically improved the salt tolerance of the freshwater cyanobacterium. The Synechococcus cells expressing ApNhaP could grow in BG11 medium containing 0.5 M NaCl as well as in sea water, whereas those expressing betaine, catalase, and the chaperone could not grow under those conditions. The coexpression of ApNhaP with catalase or ApNhaP with catalase and betaine did not further enhance the salt tolerance of Synechococcus cells expressing ApNhaP alone when grown in BG11 medium containing 0.5 M NaCl. Interestingly, the coexpression of ApNhaP with catalase resulted in enhanced salt tolerance of cells grown in sea water. These results demonstrate a key role of sodium ion exclusion by the Na(+)/H(+) antiporter for the salt tolerance of photosynthetic organisms.
对一株经与钠离子/氢离子反向转运蛋白、甜菜碱、过氧化氢酶和一种伴侣蛋白合成相关基因转化的淡水蓝藻——聚球藻属PCC 7942的耐盐性进行了检测。与甜菜碱、过氧化氢酶和伴侣蛋白的表达相比,来自耐盐蓝藻(ApNhaP)的钠离子/氢离子反向转运蛋白基因的表达极大地提高了该淡水蓝藻的耐盐性。表达ApNhaP的聚球藻细胞能够在含有0.5 M氯化钠的BG11培养基以及海水中生长,而表达甜菜碱、过氧化氢酶和伴侣蛋白的细胞在这些条件下无法生长。当在含有0.5 M氯化钠的BG11培养基中生长时,ApNhaP与过氧化氢酶共表达或ApNhaP与过氧化氢酶和甜菜碱共表达并不会进一步提高单独表达ApNhaP的聚球藻细胞的耐盐性。有趣的是,ApNhaP与过氧化氢酶共表达导致在海水中生长的细胞耐盐性增强。这些结果证明了钠离子/氢离子反向转运蛋白对钠离子的排出在光合生物耐盐性方面起着关键作用。