首页> 外文期刊>Plant physiology >Induction and functional analysis of two reduced nicotinamide adenine dinucleotide phosphate-dependent glutathione peroxidase-like proteins in Synechocystis PCC 6803 during the progression of oxidative stress
【24h】

Induction and functional analysis of two reduced nicotinamide adenine dinucleotide phosphate-dependent glutathione peroxidase-like proteins in Synechocystis PCC 6803 during the progression of oxidative stress

机译:氧化应激过程中Synechocystis PCC 6803中两种还原的烟酰胺腺嘌呤二核苷酸磷酸依赖性谷胱甘肽过氧化物酶样蛋白的诱导和功能分析

获取原文
获取原文并翻译 | 示例
           

摘要

Synechocystis PCC 6803 contains two types of glutathione peroxidase-like proteins (GPX-1 and GPX-2) that utilize NADPH but not reduced glutathione and unsaturated fatty acid hydroperoxides or alkyl hydroperoxides. The steady-state transcript level of gpx-1 gradually increased under oxidative stress conditions imposed by high light intensity, high salinity, or application of methylviologen or t-butyl hydroperoxide in the wild-type and GPX-2 knock-out mutant (gpx-2Delta) cells. To examine the ability of GPX-1, GPX-2, and thioredoxin peroxidase to scavenge lipid hydroperoxide in vivo, we measured the photosynthetic evolution of O-2 and the level of lipid peroxidation in the wild-type and each type of mutant cell after the application of t-butyl hydroperoxide or H2O2. The data reported here indicate that GPX-1 and GPX-2 are essential for the removal of lipid hydroperoxides under normal and stress conditions, leading to the protection of membrane integrity.
机译:集胞藻PCC 6803包含两种类型的谷胱甘肽过氧化物酶样蛋白(GPX-1和GPX-2),它们利用NADPH但不还原谷胱甘肽和不饱和脂肪酸氢过氧化物或烷基氢过氧化物。 gpx-1的稳态转录水平在高光强度,高盐度或在野生型GPX-2基因敲除突变体(gpx- 2Delta)细胞。为了检查GPX-1,GPX-2和硫氧还蛋白过氧化物酶清除体内脂质过氧化氢的能力,我们测量了野生型和每种突变型细胞后O-2的光合作用演变以及脂质过氧化的水平。叔丁基过氧化氢或过氧化氢的应用。此处报告的数据表明,GPX-1和GPX-2对于在正常和压力条件下去除脂质氢过氧化物至关重要,从而保护了膜的完整性。

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