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玉米叶片硝酸还原酶的调控:II. 酶活性和蛋白质的合成与周转

Regulation of Corn Leaf Nitrate Reductase : II. Synthesis and Turnover of the Enzyme's Activity and Protein.

作者信息

Remmler J L, Campbell W H

机构信息

Department of Biology, State University of New York, College of Environmental Science and Forestry, Syracuse, New York 13210.

出版信息

Plant Physiol. 1986 Feb;80(2):442-7. doi: 10.1104/pp.80.2.442.

Abstract

The appearance and disappearance of NADH:nitrate reductase (NR) in the leaves of corn (Zea mays L. W64A x W182E) were studied using activity assays, an enzyme-linked immunosorbent assay (ELISA) and western blotting. N-starved, etiolated corn plants were treated with nutrients containing either 35 millimolar NH(4)-nitrate or K-nitrate and immediately thereafter given light. The curve for enhancement of NR activity had three phases: 1 hour lag, 5 hour rapid increase, and steady state. The pattern for NR protein, as measured with the ELISA, also had three phases, but the increase was more rapid and the steady state was established earlier. To differentiate the effects of N nutrition from those of light, N-starved etiolated plants were given N nutrients 4 hours before light. During the dark pretreatment, NR activity and protein increased. When the light was turned on the NR activity and protein increased very rapidly without a lag. Western blots of polyacrylamide gels of native and denatured crude extracts showed that NADH:NR polypeptide was absent prior to treatment with N nutrients, but appeared after nitrate was given in dark or light. A low level of NR activity was found in N-starved, etiolated plants and it was shown by western blotting to be an NR form with a different electrophoretic mobility in nondenaturing gels. Since this minor NR form was not influenced by either nitrate or light, it was designated a constitutive NR. Dark decay of NR activity and protein was also studied. After the plants which had been in light with N nutrients for 24 hours were transferred to dark, the NR activity dropped by 30% within 1 hour, but the NR protein did not decrease. This inactivation of NR was further supported by returning the plants to the light after 1.5 hours of dark and finding the activity restored without change in NR protein. After the initial activity drop, a parallel decrease in NR activity and protein was observed, which was likely due to irreversible degradation by proteolysis.

摘要

利用活性测定、酶联免疫吸附测定(ELISA)和蛋白质印迹法,研究了玉米(Zea mays L. W64A×W182E)叶片中NADH:硝酸还原酶(NR)的出现和消失情况。对缺氮黄化的玉米植株施加含有35毫摩尔NH(4)-硝酸盐或硝酸钾的养分,随后立即进行光照处理。NR活性增强曲线有三个阶段:1小时的滞后阶段、5小时的快速增加阶段和稳定阶段。用ELISA测定的NR蛋白模式也有三个阶段,但增加更快且稳定阶段更早建立。为区分氮素营养和光照的影响,在光照前4小时给缺氮黄化植株施加氮素营养。在黑暗预处理期间,NR活性和蛋白增加。当光照开启时,NR活性和蛋白迅速增加且无滞后。对天然和变性粗提物的聚丙烯酰胺凝胶进行蛋白质印迹分析表明,在用氮素营养处理之前不存在NADH:NR多肽,但在黑暗或光照下施加硝酸盐后出现。在缺氮黄化植株中发现了低水平的NR活性,蛋白质印迹法表明这是一种在非变性凝胶中具有不同电泳迁移率的NR形式。由于这种次要的NR形式不受硝酸盐或光照的影响,因此将其指定为组成型NR。还研究了NR活性和蛋白的黑暗衰减情况。在接受氮素营养光照24小时的植株转移到黑暗环境后,NR活性在1小时内下降了30%,但NR蛋白并未减少。在黑暗处理1.5小时后将植株重新置于光照下,发现活性恢复而NR蛋白无变化,这进一步支持了NR的这种失活现象。在最初的活性下降之后,观察到NR活性和蛋白平行下降,这可能是由于蛋白水解导致的不可逆降解。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c4f9/1075132/84d7c19375cf/plntphys00597-0157-a.jpg

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