首页> 外文会议>International Nitrogen Fixation Congress >ISOLATION OF GENES FOR SALT TOLERANCE FROM SINORHIZOBIUMLT 11
【24h】

ISOLATION OF GENES FOR SALT TOLERANCE FROM SINORHIZOBIUMLT 11

机译:Sinorhizobiumlt 11的耐盐基因的分离

获取原文
获取外文期刊封面目录资料

摘要

Almost 40% of area over the world cannot be cultivated because of salinity problems. Salinity does reduce water available for plant growth resulting in decreased productivity of most crop plants. Some of leguminous plants can tolerate up to 0.1 M saltwhile Rhizobium strain that nodulate them are generally sensitive to salt. We have identified a Sinorhizobium strain LT11 from Thailand, which can tolerate up to 0.4 M salt and is effective in N2 fixation. The objective of this work was to isolate genesfor salt tolerance from this strain. The genomic DNA library of LT11 was transferred by conjugation to salt-sensitive rhizobial strain TALI 145 and the transconjugants were selected on YEM agar containing 0.1 M NaCl. Two hundred colonies that grew undersalt were isolated and the recombinant cosmid clones were isolated from twenty-one of those colonies. These cosmid clones were classified into two groups after digestion with HincKIII (Fig. 1). The analysis of sequence at the end of each fragments revealed interesting results. The first group of clones showed a relatively high homology with betaine aldehyde dehydrogenase cluster (betA and betB gene) of S. meliloti. The second group exhibited similarity with methylase, xanthine dehydrogenase, transcriptional regulator syrB (AraC family) and a conserved hypothetical protein (Fig. 2). These two groups of clones were introduced into Bradyrhizobium japonicum THA6 and the growth of the resulting strains was checked under different salt condition. Transconjugants showed better growth than THA6 wild type (Fig. 3).
机译:由于盐度问题,近40%的地区无法培养。盐度确实可以减少可用于植物生长的水,导致大多数作物植物的生产率降低。一些豆类植物可以耐受高达0.1米的盐分菌株,其染色它们通常对盐敏感。我们已经鉴定了泰国的Sinorhizobium rest LT11,可耐受高达0.4米的盐,并在N2固定中有效。这项工作的目的是将基因与这种菌株分离出耐盐性。 LT11的基因组DNA文库通过缀合物与盐敏感的根瘤菌株Tali 145转移,并且在含有0.1M NaCl的YEM琼脂上选择过杂交剂。分离出欠下欠下的两种菌落,并将重组粘性克隆从其中二十二种菌落中分离出来。在用Hinckiii(图1)消化后,将这些粘性克隆分为两组。每个片段末尾的序列分析显示出有趣的结果。第一组克隆与S. Meliloti的甜菜碱醛脱氢酶簇(β和betb基因)显示出相对高的同源性。第二组与甲基酶,黄嘌呤脱氢酶,转录调节调节剂Syrb(ARAC系列)和保守的假设蛋白(图2)表现出相似性(图2)。将这两组克隆引入日本毒液THA6中,并在不同的盐条件下检查所得菌株的生长。经杂交师表现出比THA6野生型更好的生长(图3)。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号