Department of Biology, Kyungpook National University, #1370 Sankyuk-dong, Buk-gu, Daegu 702-701, Republic of Korea.
World J Microbiol Biotechnol. 2012 May;28(5):1901-15. doi: 10.1007/s11274-011-0988-8. Epub 2012 Feb 7.
To determine whether the exogenous expression of glutathione reductase (GR) from Brassica rapa subsp. pekinensis (BrGR) can reduce the deleterious effects of unfavorable conditions, we constructed a transgenic Saccharomyces cerevisiae strain bearing the GR gene cloned into the yeast expression vector, pVTU260. BrGR expression was confirmed by semi reverse transcriptase-polymerase chain reaction (RT-PCR) analysis, immunoblotting analysis and an enzyme assay. Ectopic BrGR-expression improved cellular glutathione (GSH) homeostasis after higher GSH accumulation in the transgenic yeast than in the wild-type yeast under H(2)O(2)-induced oxidative stress. The BrGR-expressing yeast strain induced the activation of metabolic enzymes (Hxt, G6PDH, GAPDH and Ald), antioxidant systems (Gpx, Trx2, Trx3, Trr1, Tsa1 and porin) and molecular chaperones (Hsp104, Hsp90, Hsp70, Hsp42, Hsp26, Grp, Sti1 and Zpr1), which led to lower oxidative protein damage after a reduction in the level of cellular ROS in the BrGR-expressing yeast strain exposed to H(2)O(2) than in the wild-type yeast strain. BrGR-expression increased the ability to adapt and recover from H(2)O(2)-induced oxidative stress and various stressors, including heat shock, menadione, tert-butyl hydroperoxide, heavy metals, sodium dodecyl sulfate, ethanol and NaCl, but did not affect fermentation capacity. These results suggest that ectopic BrGR expression confers acquired tolerance by improving proteostasis and redox homeostasis through co-activation of various cell rescue proteins against ROS-induced oxidative stress in yeast cells.
为了确定外源表达来自白菜亚种 Brassica rapa subsp. pekinensis(BrGR)的谷胱甘肽还原酶(GR)是否可以减轻不利条件的有害影响,我们构建了一个携带 GR 基因克隆到酵母表达载体 pVTU260 的转基因酿酒酵母菌株。通过半反转录-聚合酶链反应(RT-PCR)分析、免疫印迹分析和酶测定证实了 BrGR 的表达。在 H2O2 诱导的氧化应激下,与野生型酵母相比,转基因酵母中更高的 GSH 积累导致细胞内谷胱甘肽(GSH)稳态得到改善。BrGR 表达诱导了代谢酶(Hxt、G6PDH、GAPDH 和 Ald)、抗氧化系统(Gpx、Trx2、Trx3、Trr1、Tsa1 和 孔蛋白)和分子伴侣(Hsp104、Hsp90、Hsp70、Hsp42、Hsp26、Grp、Sti1 和 Zpr1)的激活,这导致在 BrGR 表达酵母菌株中细胞 ROS 水平降低后,氧化蛋白损伤降低暴露于 H2O2 比在野生型酵母菌株中。BrGR 表达增加了适应和从 H2O2 诱导的氧化应激和各种应激源(包括热休克、甲萘醌、叔丁基过氧化物、重金属、十二烷基硫酸钠、乙醇和 NaCl)中恢复的能力,但不影响发酵能力。这些结果表明,异位 BrGR 表达通过共同激活各种细胞拯救蛋白来改善蛋白质稳态和氧化还原稳态,从而赋予酵母细胞对 ROS 诱导的氧化应激的获得性耐受。