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Involvement of protein kinases in the NaCl-induced upregulation of antioxidant enzyme activities in cotton callus

机译:蛋白激酶参与NaCl诱导的棉花愈伤组织抗氧化酶活性的上调

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Antioxidant enzyme activity was measured in salt tolerant callus tissue derived from the cultivar Coker 312 over an 8 hour period following treatment with either 250 mM NaCl, 2 mu M staurosporine, 2 mu M K252a, 5 mu M TMB-8,100 nM A23187, 250 mM NaCl + 2 mu M staurosporine, 250 mM NaCl + 2 mu M K252a, 250 mM NaCl + 5 mu M TMB-8, and 250 mM NaCl + 5 mu M TMB-8 + 100 nM A23187. Staurosporine and K252a have been reported to inhibit plant protein kinase activity. TMB-8 is a putative calcium channel blocker, and A23187 is a calcium ionophore. NaCl induced an up-regulation of catalase, peroxidase, ascorbate peroxidase, and glutathione reductase activities within 1 hour after treatment. The K252a and TMB-8 treatments completely inhibited the NaCl stress-induced increases in the activities of all four enzymes. At the concentration used in this experiment, staurosporine did not completely inhibit the NaCl-induced increases in antioxidant activity; however, it either reduced the responses of ascorbate peroxidase, glutathione reductase, and peroxidase or delayed the response of catalase. Treatment with A23187 increased antioxidant activity in the NaCl-tolerant controls, and treatment with TMB-8 4-A23187 increased antioxidant activity in both the controlsand the NaCl-stressed callus. These data support the hypothesis that protein kinases are involved in the signal transduction pathway associated with the NaCl-induced up-regulation of antioxidant activity and that these protein kinases may be regulated bycalcium.
机译:在用250mM NaCl,2亩半孢子素,2μmK252a,5μmtmb-8,100nm a23187,250mm,50mM k252a,5μm,250mm NaCl + 2 mu m Staurosporine,250mM NaCl +2μmk252a,250mM NaCl +5μmtmb-8和250mM NaCl +5μmtmb-8 + 100nm a23187。据报道,Staurosporine和K252A抑制植物蛋白激酶活性。 TMB-8是推定的钙通道阻断剂,A23187是钙离子载体。 NaCl在处理后1小时内诱导过氧化氢酶,过氧化物酶,抗坏血酸过氧化物酶和谷胱甘肽还原酶活性的上调。 K252A和TMB-8治疗完全抑制了所有四种酶的活性的NaCl胁迫诱导的增加。在该实验中使用的浓度下,Staurosporine没有完全抑制抗氧化活性的NaCl诱导的增加;然而,它可以减少抗坏血酸过氧化物酶,谷胱甘肽还原酶和过氧化物酶的反应或延迟过氧化氢酶的响应。用A23187治疗在NaCl耐受对照中增加的抗氧化活性,并用TMB-8 4-A23187治疗在对照中增加了对照和NaCl胁迫的愈伤组织中的抗氧化活性。这些数据支持蛋白激酶参与与NaCl诱导的抗氧化活性的上调相关的信号转导通路的假设,并且这些蛋白激酶可以通过钙调节。

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