首页> 外文OA文献 >Photosynthesis in Polyploid Tall Fescue 1: II. PHOTOSYNTHESIS AND RIBULOSE-1, 5-BISPHOSPHATE CARBOXYLASE OF POLYPLOID TALL FESCUE
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Photosynthesis in Polyploid Tall Fescue 1: II. PHOTOSYNTHESIS AND RIBULOSE-1, 5-BISPHOSPHATE CARBOXYLASE OF POLYPLOID TALL FESCUE

机译:多倍体高羊茅的光合作用1:II。多聚壁高羊茅的光合作用和核糖1,5-双磷酸羧化酶

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摘要

Net photosynthesis on a leaf area and leaf weight basis increased significantly with ploidy in a 4X, 6X, 8X and 10X allopolyploid series of tail fescue (Festuca arundinacea Schreb.). Total protein did not increase significantly with ploidy. Rocket immunoelectrophoresis was used to quantitate ribulose-1, 5-bisphosphate carboxylase (RuBPCase) protein. RuBPCase content, expressed on both a concentration basis and as a percentage of total protein increased significantly with ploidy in both field and greenhouse experiments. The range of RuBPCase content was 16 to 73% of total protein and 2.8 and 6.5 mg/ml of extract. Specific activity of RuBPCase did not increase significantly with ploidy. Chlorophyll concentration increased as a quadratic function of ploidy, with the mean for 8X genotypes representing maximal chlorophyll content. Evidence is presented that increasing concentrations of RuBPCase are associated with higher net photosynthesis rates in tall fescue. This suggests that RuBPCase may represent a marker for increased net photosynthesis. RuBPCase was extracted in a partially active state or inhibited state and must be fully activated by Mg2+ and HCO3− to measure maximal activities. Polyploidization appeared to increase selectively the allocation of total protein for synthesis of RuBPCase; however, there was also a range for carboxylase content among the genotypes within a given ploidy level.
机译:在4倍,6倍,8倍和10倍同种多倍体尾部羊茅(Festuca arundinacea Schreb。)上,倍性显着提高了叶面积和叶重的净光合作用。总蛋白没有随着倍性显着增加。火箭免疫电泳用于定量核糖-1,5-双磷酸羧化酶(RuBPCase)蛋白。在田间和温室实验中,RuBPCase的含量(以浓度和总蛋白质的百分比表示)均随着倍性显着增加。 RuBPCase含量范围为总蛋白的16%至73%,提取物的含量为2.8和6.5 mg / ml。 RuBPCase的比活性没有随倍性显着增加。叶绿素浓度以二次方函数形式增加,8X基因型的平均值代表最大叶绿素含量。有证据表明,在高羊茅中,RuBPCase的浓度增加与净光合作用速率较高有关。这表明RuBPCase可能代表净光合作用增加的标志。 RuBPCase以部分活性状态或抑制状态提取,必须被Mg2 +和HCO3-完全激活才能测量最大活性。多倍体化似乎可以选择性增加用于合成RuBPCase的总蛋白质的分配。然而,在给定的倍数水平内,基因型之间的羧化酶含量也有一个范围。

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