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Antioxidant enzyme activity in salt tolerant selected clones of stylo 184 (Stylosanthes guianensis CIAT 184), an important forage legume

机译:重要的饲草科植物stylo 184(Stylosanthes guianensis CIAT 184)的耐盐选择克隆中的抗氧化酶活性

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摘要

In vitro shoots from five selected clones-one sensitive (T1) and four salt tolerant (T2, T3, T4 and T5)-of Stylosanthes guianensis CIAT 184 were multiplied in Murashige and Skoog medium with 0, 0.5 and 1% (weight per volume) NaCl for 1 wk followed by transfer to a recovery medium for a further week. Their relative fresh weight (RFW) and antioxidative enzymes-superoxide dismutase (SOD), catalase (CAT) and peroxidase (POX)-were measured after 7 d on the salt medium and again after another 7 d on a recovery medium (without additional NaCl). Exposure to NaCl reduced the growth of all clones at some stage. For the four clones selected as salt tolerant, the reduction in growth was evident after 7 d (up to 45%) on the NaCl media, however, for the clone selected as salt sensitive this reduction (50%) only occurred after 7 d on the recovery medium. Shoots of clones T2, T3 and T5, however, increased their growth on the recovery medium and this was associated with an increase in POX activity (from 0.5% NaCl medium for T2 and 1% NaCl medium for T3 and T5). The SOD activity of these clones was higher than the salt sensitive clone but decreased at 1% NaCl when shoots had been on the recovery medium for 7 d. In T4, the RFW increased to equal that of the control at 0.5% NaCl after recovery while the SOD activity was reduced and the POX activity was stable after both salt treatment and recovery. The NaCl treatments had no effect on the CAT activity for any of the clones. The lowest SOD activity was found in T1 while the tolerant clone, T5, showed the highest CAT and POX activity, providing the ability to distinguish between clones.
机译:在Murashige和Skoog培养基中以0、0.5和1%(每单位重量的重量)繁殖来自五个选定的克隆的茎-敏感(T1)和四个耐盐性(T2,T3,T4和T5)-圭y(Stylosanthes guianensis CIAT 184) 1周的氯化钠溶液,然后再转移至回收介质中一周。在盐培养基上第7天后测量其相对鲜重(RFW)和抗氧化酶-超氧化物歧化酶(SOD),过氧化氢酶(CAT)和过氧化物酶(POX)-再在回收培养基上再测量7天后(不添加额外的NaCl) )。暴露于NaCl会降低某个阶段所有克隆的生长。对于选择为耐盐的四个克隆,在NaCl培养基上培养7 d后(高达45%)明显减少了生长,但是,对于选择为对盐敏感的克隆,仅在培养7 d后才出现了这种降低(50%)。恢复介质。但是,克隆T2,T3和T5的芽增加了它们在回收培养基上的生长,这与POX活性的增加有关(从T2的0.5%NaCl培养基和T3和T5的1%NaCl培养基开始)。这些芽的SOD活性高于盐敏感性克隆,但当芽在回收培养基上停留7 d时,NaCl含量降低至1%。在T4中,回收后RFW增加到与0.5%NaCl的对照相同,而盐处理和回收后SOD活性降低且POX活性稳定。 NaCl处理对任何克隆的CAT活性均无影响。在T1中发现最低的SOD活性,而耐性克隆T5显示出最高的CAT和POX活性,从而提供了区分克隆的能力。

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