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1
Light-mediated Activation of Nitrate Reductase in Synchronous Chlorella.光介导的同步小球藻中硝酸还原酶的激活
Plant Physiol. 1978 Aug;62(2):284-6. doi: 10.1104/pp.62.2.284.
2
[On the induction of nitrate- and nitrite-reductase in synchronized Chlorella cultures].[关于同步化小球藻培养物中硝酸盐和亚硝酸盐还原酶的诱导作用]
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Regulation of Glutamine Synthetase by Light and during Nitrogen Deficiency in Synchronous Chlorella sorokiniana.光照和氮饥饿对同步小球藻谷氨酰胺合成酶的调控。
Plant Physiol. 1980 Nov;66(5):805-8. doi: 10.1104/pp.66.5.805.
4
A comparison of the high-active and low-active form of nitrate reductase in synchronous Chlorella sorokiniana.同步小球藻中硝酸还原酶高活性和低活性形式的比较。
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5
Activation, synthesis and turnover of nitrate reductase controlled by nitrate and ammonium in Chlorella vulgaris.硝酸还原酶在小球藻中受硝酸盐和铵盐调控的激活、合成和周转。
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Purification and characterization of demolybdo nitrate reductase (NADH-cytochrome c oxidoreductase) of Chlorella vulgaris.普通小球藻脱钼硝酸还原酶（NADH-细胞色素c氧化还原酶）的纯化与特性分析
J Biol Chem. 1981 Nov 25;256(22):11527-31.
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Synthesis of Nitrate Reductase in Chlorella: I. EVIDENCE FOR AN INACTIVE PROTEIN PRECURSOR.小球藻硝酸还原酶的合成：I. 无活性蛋白前体的证据。
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8
Reduced nicotinamide adenine dinucleotide-nitrate reductase of Chlorella vulgaris. Purification, prosthetic groups, and molecular properties.普通小球藻的还原型烟酰胺腺嘌呤二核苷酸-硝酸还原酶。纯化、辅基及分子特性。
J Biol Chem. 1975 Jun 10;250(11):4120-7.
9
Molybdenum insertion in vitro in demolybdo nitrate reductase of Chlorella vulgaris.钼在普通小球藻脱钼硝酸还原酶中的体外插入。
J Biol Chem. 1981 Nov 25;256(22):11532-7.
10
Nitrate uptake and nitrate reduction in synchronous Chlorella.同步小球藻中的硝酸盐摄取和硝酸盐还原。
Planta. 1979 Jan;146(3):287-92. doi: 10.1007/BF00387800.

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1
Differences in nitrate reductase activity between species of different stages in old field succession.弃耕地演替不同阶段物种间硝酸还原酶活性的差异。
Oecologia. 1983 Mar;57(1-2):43-48. doi: 10.1007/BF00379560.
2
Nitrate uptake and nitrate reduction in synchronous Chlorella.同步小球藻中的硝酸盐摄取和硝酸盐还原。
Planta. 1979 Jan;146(3):287-92. doi: 10.1007/BF00387800.
3
Activation, synthesis and turnover of nitrate reductase controlled by nitrate and ammonium in Chlorella vulgaris.硝酸还原酶在小球藻中受硝酸盐和铵盐调控的激活、合成和周转。
Planta. 1979 Oct;147(1):63-8. doi: 10.1007/BF00384592.
4
A comparison of the high-active and low-active form of nitrate reductase in synchronous Chlorella sorokiniana.同步小球藻中硝酸还原酶高活性和低活性形式的比较。
Planta. 1984 Jan;160(1):1-5. doi: 10.1007/BF00392458.
5
Nitrate-reductase expression is under the control of a circadian rhythm and is light inducible in Nicotiana tabacum leaves.硝酸还原酶的表达受昼夜节律控制，并且在烟草叶片中受光照诱导。
Planta. 1990 Jan;180(2):257-61. doi: 10.1007/BF00194005.
6
Decrease of Nitrate Reductase Activity in Spinach Leaves during a Light-Dark Transition.光暗转换期间菠菜叶片中硝酸还原酶活性的降低
Plant Physiol. 1992 Feb;98(2):573-7. doi: 10.1104/pp.98.2.573.
7
The role of nitrate and ammonium ions and light on the induction of nitrate reductase in maize leaves.硝酸盐和铵离子以及光照对玉米叶片硝酸还原酶诱导的作用。
Plant Physiol. 1988 Dec;88(4):1067-72. doi: 10.1104/pp.88.4.1067.
8
Regulation of nitrate reductase activity in cultured spinach cells as studied by an enzyme-linked immunosorbent assay.通过酶联免疫吸附测定法研究培养菠菜细胞中硝酸还原酶活性的调节。
Plant Physiol. 1986 Nov;82(3):739-41. doi: 10.1104/pp.82.3.739.
9
Synthesis and degradation of nitrite reductase in pea leaves.亚硝酸还原酶在豌豆叶片中的合成与降解。
Plant Physiol. 1984 May;75(1):251-2. doi: 10.1104/pp.75.1.251.
10
Synthesis and degradation of barley nitrate reductase.大麦硝酸还原酶的合成与降解
Plant Physiol. 1983 Aug;72(4):949-52. doi: 10.1104/pp.72.4.949.

本文引用的文献

1
Effect of light and glucose on the induction of nitrate reductase and on the distribution of nitrate in etiolated barley leaves.光和葡萄糖对黄化大麦叶片中硝酸还原酶诱导及硝酸盐分布的影响。
Plant Physiol. 1976 Oct;58(4):588-91. doi: 10.1104/pp.58.4.588.
2
Nitrate Absorption by Barley: II. Influence of Nitrate Reductase Activity.硝酸根在大麦中的吸收：II. 硝酸还原酶活性的影响。
Plant Physiol. 1976 Jan;57(1):59-62. doi: 10.1104/pp.57.1.59.
3
Influence of Ionic Strength, pH, and Chelation of Divalent Metals on Isolation of Polyribosomes from Tobacco Leaves.离子强度、pH 值和二价金属螯合对从烟草叶片中分离多核糖体的影响。
Plant Physiol. 1976 Jan;57(1):5-10. doi: 10.1104/pp.57.1.5.
4
Protein measurement with the Folin phenol reagent.使用福林酚试剂进行蛋白质测定。
J Biol Chem. 1951 Nov;193(1):265-75.
5
Separation of labeled from unlabeled proteins by equilibrium density gradient sedimentation.通过平衡密度梯度沉降法分离标记蛋白和未标记蛋白。
Anal Biochem. 1962 Dec;4:489-504. doi: 10.1016/0003-2697(62)90129-x.
6
Regulation of the nitrate assimilation pathway in cultured tobacco cells. 3. The nitrate uptake system.培养烟草细胞中硝酸盐同化途径的调控。3. 硝酸盐吸收系统。
Biochim Biophys Acta. 1971 Feb 23;230(2):362-72. doi: 10.1016/0304-4165(71)90223-6.
7
Induction of aryl-beta-glucosidase in Fomes annosus by cellobiose.纤维二糖对黄丝层孔菌中芳基-β-葡萄糖苷酶的诱导作用。
Arch Mikrobiol. 1973 Nov 2;93(3):195-204. doi: 10.1007/BF00412019.
8
Aminopeptidases of Physarum polycephalum. Activity, isoenzyme pattern, and synthesis during differentiation.多头绒泡菌的氨肽酶。分化过程中的活性、同工酶模式及合成
J Biol Chem. 1975 Sep 25;250(18):7420-7.
9
Synthesis of acetylcholine receptors by cultured chick myotubes and denervated mouse extensor digitorum longus muscles.培养的鸡肌管和去神经支配的小鼠趾长伸肌合成乙酰胆碱受体。
Proc Natl Acad Sci U S A. 1976 Jan;73(1):161-4. doi: 10.1073/pnas.73.1.161.
10
Studies on metrizamide-protein interactions.关于甲泛葡胺-蛋白质相互作用的研究。
Biochim Biophys Acta. 1976 Nov 26;453(1):176-84. doi: 10.1016/0005-2795(76)90261-0.

光介导的同步小球藻中硝酸还原酶的激活

Light-mediated Activation of Nitrate Reductase in Synchronous Chlorella.

机构信息

Pflanzenphysiologisches Institut der Universität Göttingen, Germany.

出版信息

Plant Physiol. 1978 Aug;62(2):284-6. doi: 10.1104/pp.62.2.284.

DOI:10.1104/pp.62.2.284
PMID:16660502
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1092106/
Abstract

The mechanism underlying the sharp increase in activity of nitrate reductase (EC 1.6.6.1) in Chlorella vulgaris forma tertia (strain 211 8k) during the first hour of the 7 hours/5 hours light/dark cycle was investigated. Using the method of density labeling and isopycnic centrifugation, it could be demonstrated that this rapid increase in activity is based on light-mediated activation rather than de novo synthesis of the enzyme. The problematic nature of cycloheximide specificity and models of nitrate reductase activation are discussed.

摘要

研究了在 7 小时/5 小时光/暗循环的第一个小时内，小球藻变种（菌株 211 8k）中硝酸还原酶（EC 1.6.6.1）活性急剧增加的机制。使用密度标记和等密度离心的方法，可以证明这种活性的快速增加是基于光介导的激活，而不是酶的从头合成。本文还讨论了环己酰亚胺特异性的问题和硝酸还原酶激活的模型。