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在玉米根的质膜中有两种不同的硝酸盐还原活性的证据。

Evidence for two different nitrate-reducing activities at the plasma membrane in roots of Zea mays L.

出版信息

Planta. 1994;194(4):557-64. doi: 10.1007/BF00714470.

DOI:10.1007/BF00714470
PMID:24624488
Abstract

Plasma-membrane (PM) vesicles isolated from 6-d-old corn roots by sucrose gradient centrifugation or two-phase partitioning showed an NADH-dependent nitrate reductase (NR) activity averaging at 40 nmol per milligram PM protein per hour. This membrane-associated NR activity could not be removed from two-phase partitioned PM vesicles by salt washing, osmotic shock treatment, sonication, or freeze-thawing to reverse vesicle sidedness. Therefore, it could not be attributed to contamination of membrane vesicles by the soluble, cytosolic NR. Plasma-membrane vesicles reduced NO~ in the presence of the electron donors NADH or NADPH at an activity ratio of 2.2. The NADH- and NADPH-dependent NR activities of outside-out oriented PM vesicles differed in their sensitivity toward the detergent Brij 58,leading to a latency of 65% or 29% using NADH or NADPH as electron donor, respectively. The activities of NO 3 reduction in the presence of saturating concentrations of NADH and NADPH were additive. Furthermore,both activities were characterized by a different pH dependence with a pH optimum of 7.5 for the NADH-dependent activity and of 6.8 for the NADPH-dependent activity. The membrane-associated NAD(P)H-dependent NR activities responded to different nitrogen nutrition of plants in a manner different from the soluble forms of the enzyme. The data confirm the existence of a corn PM NR and suggest that there may be two different NO₃-reducing enzymes located at the PM of corn roots.

摘要

通过蔗糖梯度离心或双相分配从 6 天大的玉米根中分离的质膜(PM)小泡显示出 NADH 依赖性硝酸还原酶(NR)活性,平均每毫克 PM 蛋白每小时 40nmol。这种膜相关的 NR 活性不能通过盐洗、渗透压休克处理、超声处理或冻融来逆转小泡的侧面从双相分配的 PM 小泡中去除,因此不能归因于膜小泡被可溶性细胞质 NR 污染。在电子供体 NADH 或 NADPH 的存在下,PM 小泡还原 NO~,活性比为 2.2。向外定向的 PM 小泡的 NADH 和 NADPH 依赖性 NR 活性对去污剂 Brij 58 的敏感性不同,分别使用 NADH 或 NADPH 作为电子供体时,潜伏期为 65%或 29%。在 NADH 和 NADPH 的饱和浓度存在下,NO 3 还原的活性是相加的。此外,两种活性的 pH 依赖性不同,NADH 依赖性活性的最佳 pH 为 7.5,NADPH 依赖性活性的最佳 pH 为 6.8。膜结合的 NAD(P)H 依赖性 NR 活性对植物的不同氮营养的反应方式与酶的可溶性形式不同。这些数据证实了玉米 PM NR 的存在,并表明可能有两种不同的位于玉米根质膜上的 NO₃还原酶。

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本文引用的文献

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2
NADH-Ferricyanide Reductase of Leaf Plasma Membranes : Partial Purification and Immunological Relation to Potato Tuber Microsomal NADH-Ferricyanide Reductase and Spinach Leaf NADH-Nitrate Reductase.叶片质膜的NADH-铁氰化物还原酶:部分纯化及其与马铃薯块茎微粒体NADH-铁氰化物还原酶和菠菜叶片NADH-硝酸盐还原酶的免疫学关系。
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Biochemical and Immunological Characterization of Nitrate Reductase Deficient nia Mutants of Nicotiana plumbaginifolia.硝酸还原酶缺陷的菸草 nia 突变体的生化和免疫特性。
Plant Physiol. 1990 Mar;92(3):659-65. doi: 10.1104/pp.92.3.659.
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