Song Xing Shun, Hu Wen Hai, Mao Wei Hua, Ogweno Joshua Otieno, Zhou Yan Hong, Yu Jing Quan
Department of Horticulture, Huajiachi Campus, Zhejiang University, Kaixuan Road 268, Hangzhou, China 310029.
Plant Physiol Biochem. 2005 Dec;43(12):1082-8. doi: 10.1016/j.plaphy.2005.11.003. Epub 2005 Dec 5.
Ascorbate peroxidase (APX) isoenzymes, distributing in at least four distinct cell compartments, the chloroplastic stroma (sAPX) and thylakoid membrane (tAPX), microbody (mAPX) and cytosol (cAPX), catalyze the reduction of H(2)O(2) to water by using ascorbic acid (AsA) as specific electron donor. In order to better clarify the response of APX isoenzymes and AsA regeneration enzymes to abiotic stresses, the activities of APX isoenzymes as well as monodehydroascorbate reductase (MDAR), glutathione reductase (GR) and dehydroascorbate reductase (DHAR) were investigated in cucumber plants after heat, methyl viologen (MV) and H(2)O(2) treatments. The activities of cAPX, sAPX, mAPX increased after a slight decline throughout the experiment. Consistent closely with sAPX activity, the expression of sAPX followed a similar change pattern, indicating that sAPX was regulated at the transcriptional level. In contrast, constitutive expression was observed in tAPX activity and no significant changes in tAPX activity were found throughout the experiment. The increases in MDAR and GR were accompanied with enhanced level of AsA/DHA, implying that the AsA regeneration system plays an essential role in compensating AsA degradation.
抗坏血酸过氧化物酶(APX)同工酶分布于至少四个不同的细胞区室,即叶绿体基质(sAPX)、类囊体膜(tAPX)、微体(mAPX)和细胞质(cAPX),它以抗坏血酸(AsA)作为特定电子供体,催化将H₂O₂还原为水。为了更好地阐明APX同工酶和AsA再生酶对非生物胁迫的响应,研究了黄瓜植株在热、甲基紫精(MV)和H₂O₂处理后APX同工酶以及单脱氢抗坏血酸还原酶(MDAR)、谷胱甘肽还原酶(GR)和脱氢抗坏血酸还原酶(DHAR)的活性。在整个实验过程中,cAPX、sAPX、mAPX的活性在略有下降后上升。sAPX的表达与sAPX活性密切一致,呈现相似的变化模式,表明sAPX在转录水平受到调控。相反,tAPX活性呈组成型表达,在整个实验过程中tAPX活性未发现显著变化。MDAR和GR的增加伴随着AsA/DHA水平的提高,这意味着AsA再生系统在补偿AsA降解方面起着至关重要的作用。