Phenotypic and biochemical alterations in relation to MT2 gene expression in Plantago ovata Forsk under zinc stress

被引:17
|
作者
Pramanick, Paulami [1 ]
Chakraborty, Anindita [2 ]
Sen Raychaudhuri, Sarmistha [1 ]
机构
[1] Univ Calcutta, Dept Biophys Mol Biol & Bioinformat, 92 APC Rd, Kolkata 700009, India
[2] UGC DAE Consortium Sci Res, Kolkata Ctr, LB-8,Sect 3, Kolkata 700098, India
关键词
Metallothionein; Zinc; Antioxidant; Plantago ovata; Oxidative stress; REACTIVE OXYGEN; METALLOTHIONEIN GENES; CADMIUM TOLERANCE; PROTEIN; ROOTS; ACCUMULATION; DISTINCT; DAMAGE; ROLES; CDNA;
D O I
10.1007/s10534-017-9990-4
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Plantago ovata Forsk is an annual herb with immense medicinal importance, the seed and husk of which is used in the treatment of chronic constipation, irritable bowel syndrome, diarrhea since ancient times. Zinc, an essential metal, is required by plants as they form important components of zinc finger proteins and also aid in synthesis of photosynthetic pigments such as chlorophyll. However, in excess amount Zn causes chlorosis of leaf and shoot tissues and generate reactive oxygen species. The present study is aimed at investigating the changes in expression levels of MT2 gene in Plantago ovata under zinc stress. Data show up to 1.66 fold increase in expression of PoMT2 in 1000 A mu M ZnSO4 center dot 7H(2)O treated sample. Our study also describes alteration of MT2 gene expressions in Plantago ovata as observed through Real time PCR (qPCR) done by method. In this study we have observed an upregulation (or induction) in the PoMT2 gene expression level in 500 and 800 A mu M ZnSO4 center dot 7H(2)O treated samples but found saturation on further increasing the dose to 1000 A mu M of ZnSO4 center dot 7H(2)O. Determination of the phenotypic and biochemical changes in Plantago ovata due to exposure to zinc stress of concentrations 500, 800 and 1000 A mu M revealed oxidative stress. The enhanced expression of MT2 gene in Plantago ovata has a correlation with the increased total antioxidant activity and increased DPPH radical scavenging activity.
引用
收藏
页码:171 / 184
页数:14
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