首页> 外文OA文献 >Effect of Nitrogen Starvation on Polypeptide Composition, Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase, and Thylakoid Carotenoprotein Content of Synechocystis sp. Strain PCC6308 1
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Effect of Nitrogen Starvation on Polypeptide Composition, Ribulose-1,5-Bisphosphate Carboxylase/Oxygenase, and Thylakoid Carotenoprotein Content of Synechocystis sp. Strain PCC6308 1

机译:氮饥饿对蓝藻藻多肽多肽组成,核糖-1,5-二磷酸羧化酶/加氧酶和类囊体类胡萝卜素蛋白含量的影响。株PCC6308 1

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摘要

Synechocystis sp. strain PCC6308 cells were starved for nitrogen for 5 days. The polypeptide compositions of whole cell extracts and washed membranes of nitrogen-replete and nitrogen-starved cells were compared by one- and two-dimensional electrophoresis. Immunoblotting of one-dimensional gels indicated that pelletable ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) was depleted in cells starved for nitrogen, while levels of soluble Rubisco were comparable in nitrogen-starved and nitrogen-replete cells. This is consistent with the hypothesis that pelletable Rubisco may serve as a nitrogen reserve in Synechocystis 6308. Other polypeptides were differentially enriched in the membrane or soluble fractions of nitrogen-replete cells or nitrogen-starved cells, suggesting nitrogen starvation may alter partitioning of polypeptides into soluble and membrane fractions. Degradation of abundant polypeptides during nitrogen starvation appeared to cause an effective magnification of less abundant polypeptides in the molecular mass range of 20 to 40 kilodaltons, as shown by two-dimensional electrophoresis. A 42-kilodalton thylakoid carotenoid protein identified by immunoblotting was conserved in membranes from nitrogen-starved cells. This may be functional for cells depleted of pigment and thus exposed to higher light levels because of decreased self-shading.
机译:集胞藻使菌株PCC6308细胞缺乏氮5天。通过一维和二维电泳比较全细胞提取物的多肽组成以及富氮和缺氮细胞的洗涤膜。一维凝胶的免疫印迹表明,在缺乏氮的细胞中,可沉淀的核糖-1,5-双磷酸核糖羧化酶/加氧酶(Rubisco)耗竭,而在饥饿和富氮的细胞中可溶性Rubisco的水平相当。这与可沉淀的Rubisco可能在Synechocystis 6308中充当氮储备的假设相吻合。其他多肽在富氮细胞或缺氮细胞的膜或可溶级分中差异富集,表明氮饥饿可能会改变多肽的分配可溶性和膜级分。如二维电泳所示,氮饥饿期间丰富多肽的降解似乎会导致分子质量范围为20至40道尔顿的次丰富多肽的有效放大。通过免疫印迹鉴定的42千达尔顿类囊体类胡萝卜素蛋白在氮饥饿细胞的膜中保守。这对于缺乏色素的细胞可能是起作用的,并且由于减少了自身阴影,因此暴露于较高的光照水平。

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