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首页> 外文期刊>Ecotoxicology >Effect of iron stress on Withania somnifera L.: antioxidant enzyme response and nutrient elemental uptake of in vitro grown plants
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Effect of iron stress on Withania somnifera L.: antioxidant enzyme response and nutrient elemental uptake of in vitro grown plants

机译:铁胁迫对Withania somnifera L.的影响:离体生长植物的抗氧化酶反应和营养元素吸收

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In the present study the response of antioxidant enzyme activities and the level of expression of their corresponding genes on bioaccumulation of iron (Fe) were investigated. In vitro germinated Withania somnifera L. were grown in Murashige and Skoog's liquid medium with increasing concentrations (0, 25, 50, 100 and 200 mu M) of FeSO4 for 7 and 14 days. Root and leaf tissues analyzed for catalase (CAT, EC 1.11.1.6), superoxide dismutase (SOD, EC 1.15.1.1) and guaiacol peroxidase (GPX, EC 1.11.1.7), have shown an increase in content with respect to exposure time. Isoforms of CAT, SOD and GPX were separated using non-denaturing polyacrylamide gel electrophoresis and observed that the isoenzymes were greatly affected by higher concentrations of Fe. Reverse transcriptase polymerase chain reaction analysis performed by taking three pairs of genes of CAT (RsCat, Catalase1, Cat1) and SOD (SodCp, TaSOD1.2, MnSOD) to find out the differential expression of antioxidant genes under Fe excess. RsCat from CAT and MnSOD from SOD have exhibited high levels of gene expression under Fe stress, which was consistent with the changes of the activity assayed in solution after 7 days of treatment. Analysis by proton induced X-ray emission exhibited an increasing uptake of Fe in plants by suppressing and expressing of other nutrient elements. The results of the present study suggest that higher concentration of Fe causes disturbance in nutrient balance and induces oxidative stress in plant.
机译:在本研究中,研究了抗氧化酶活性及其相应基因的表达水平对铁(Fe)生物富集的响应。体外发芽的Withania somnifera L.在Murashige和Skoog的液体培养基中生长,其中FeSO4的浓度(0、25、50、100和200μM)增加,持续7天和14天。分析过的过氧化氢酶(CAT,EC 1.11.1.6),超氧化物歧化酶(SOD,EC 1.15.1.1)和愈创木酚过氧化物酶(GPX,EC 1.11.1.7)的根和叶组织显示,其含量随接触时间的增加而增加。使用非变性聚丙烯酰胺凝胶电泳分离了CAT,SOD和GPX的同工型,并观察到同工酶受较高浓度的Fe影响。通过取三对CAT(RsCat,Catalase1,Cat1)和SOD(SodCp,TaSOD1.2,MnSOD)对的基因进行逆转录酶聚合酶链反应分析,找出过量铁胁迫下抗氧化基因的差异表达。在Fe胁迫下,来自CAT的RsCat和来自SOD的MnSOD表现出高水平的基因表达,这与处理7天后在溶液中测定的活性变化一致。质子诱导的X射线发射分析显示,通过抑制和表达其他营养元素,植物体内铁的吸收增加。本研究的结果表明,较高的铁含量会导致营养平衡失调并引起植物的氧化胁迫。

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