首页> 外文期刊>Journal of Plant Physiology >Accumulation of LEA proteins in salt (NaCl) stressed young seedlings of rice (Oryza sativa L.) cultivar Bura Rata and their degradation during recovery from salinity stress
【24h】

Accumulation of LEA proteins in salt (NaCl) stressed young seedlings of rice (Oryza sativa L.) cultivar Bura Rata and their degradation during recovery from salinity stress

机译:盐(NaCl)胁迫的水稻新品种Bura Rata幼苗中LEA蛋白的积累及其在盐分胁迫恢复过程中的降解

获取原文
获取原文并翻译 | 示例
       

摘要

Germination and subsequent hydroponic growth under salt stress (100 mmol/L NaCI) triggered an accumulation of six major stress proteins and resulted in a growth arrest of young seedlings of rice (Oryza sativa L.) cv. Bura Rata. Based on two-dimensional electrophoretic resolution, partial amino acid sequencing and immunodetection techniques, four of the salt stress-induced polypeptides were identified as LEA proteins. Under all experimental conditions wherein seedlings exhibited superior halotolerance, salt stress-induced LEA proteins were expressed at low levels. In contrast, accumulation of LEA proteins was found associated with growth arrest. When returned to non-saline media, seedlings stressed with salt for four days recovered immediately. Longer exposure to 100 mmol/L NaCl, however, progressively delayed recovery and reduced the number of seedlings which could recover from salt stress. Recovery from salt stress was consistently accompanied by degradation of the salt stress-induced LEA proteins. The results of this study show that LEA proteins accumulate during the salinity-triggered growth arrest of young Bura Rata seedlings and are mobilised during the recovery of seedlings from salinity stress.
机译:盐胁迫(100 mmol / L NaCl)下的发芽和随后的水培生长触发了六种主要胁迫蛋白的积累,并导致水稻幼苗的生长停滞。 Bura Rata。基于二维电泳分辨率,部分氨基酸测序和免疫检测技术,盐胁迫诱导的多肽中有四个被鉴定为LEA蛋白。在幼苗表现出优异的耐盐性的所有实验条件下,盐胁迫诱导的LEA蛋白均以低水平表达。相反,发现LEA蛋白的积累与生长停滞有关。当返回非盐培养基时,用盐胁迫四天的幼苗立即恢复。然而,长时间暴露于100 mmol / L NaCl会逐渐延迟恢复并减少可从盐胁迫中恢复的幼苗数量。从盐胁迫中恢复一直伴随着盐胁迫诱导的LEA蛋白降解。这项研究的结果表明,LEA蛋白在盐碱触发的年轻Bura Rata幼苗生长停滞期间积累,并在盐碱胁迫下恢复幼苗期间动员。

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