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Plant Cell. 2005 Aug;17(8):2413-20. doi: 10.1105/tpc.105.033993. Epub 2005 Jun 24.
2
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Measurement of Enzyme Activities.酶活性的测定
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Identification of the gene encoding homoserine kinase from Arabidopsis thaliana and characterization of the recombinant enzyme derived from the gene.拟南芥中高丝氨酸激酶编码基因的鉴定及该基因衍生重组酶的特性分析。
Arch Biochem Biophys. 1999 Dec 1;372(1):135-42. doi: 10.1006/abbi.1999.1481.
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Evolution of enzymes involved in the photorespiratory 2-phosphoglycolate cycle from cyanobacteria via algae toward plants.从蓝藻经藻类到植物中参与光呼吸 2-磷酸甘油酸循环的酶的进化。
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Characterization of an Arabidopsis inositol 1,3,4,5,6-pentakisphosphate 2-kinase (AtIPK1).拟南芥肌醇1,3,4,5,6 - 五磷酸2 - 激酶(AtIPK1)的特性分析
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Two thymidine kinases and one multisubstrate deoxyribonucleoside kinase salvage DNA precursors in Arabidopsis thaliana.拟南芥中有两种胸苷激酶和一种多底物脱氧核苷激酶可回收 DNA 前体。
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Only plant-type (GLYK) glycerate kinases produce d-glycerate 3-phosphate.只有植物型(GLYK)甘油酸激酶能产生3-磷酸-d-甘油酸。
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A cytosolic Arabidopsis D-xylulose kinase catalyzes the phosphorylation of 1-deoxy-D-xylulose into a precursor of the plastidial isoprenoid pathway.一种胞质拟南芥D-木酮糖激酶催化1-脱氧-D-木酮糖磷酸化,生成质体类异戊二烯途径的前体。
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本文引用的文献

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The value of mutants unable to carry out photorespiration.无法进行光呼吸的突变体的价值。
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2
Fixation of O(2) during Photorespiration: Kinetic and Steady-State Studies of the Photorespiratory Carbon Oxidation Cycle with Intact Leaves and Isolated Chloroplasts of C(3) Plants.光呼吸过程中氧气的固定:对C₃植物完整叶片和分离叶绿体光呼吸碳氧化循环的动力学和稳态研究
Plant Physiol. 1978 Dec;62(6):954-67. doi: 10.1104/pp.62.6.954.
3
The glycine decarboxylase complex is not essential for the cyanobacterium Synechocystis sp. strain PCC 6803.甘氨酸脱羧酶复合体对于蓝细菌聚球藻属6803菌株并非必需。
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Cell-specific protein profiling in Arabidopsis thaliana trichomes: identification of trichome-located proteins involved in sulfur metabolism and detoxification.
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Differential metabolic networks unravel the effects of silent plant phenotypes.差异代谢网络揭示了植物隐性表型的影响。
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Linking protein fractionation with multidimensional monolithic reversed-phase peptide chromatography/mass spectrometry enhances protein identification from complex mixtures even in the presence of abundant proteins.将蛋白质分级分离与多维整体反相肽色谱法/质谱联用,即使在存在大量蛋白质的情况下,也能增强从复杂混合物中鉴定蛋白质的能力。
Rapid Commun Mass Spectrom. 2004;18(6):643-50. doi: 10.1002/rcm.1376.
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Crystal structure of the YGR205w protein from Saccharomyces cerevisiae: close structural resemblance to E. coli pantothenate kinase.来自酿酒酵母的YGR205w蛋白的晶体结构:与大肠杆菌泛酸激酶的结构高度相似。
Proteins. 2004 Mar 1;54(4):776-83. doi: 10.1002/prot.10596.
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Process for the integrated extraction, identification and quantification of metabolites, proteins and RNA to reveal their co-regulation in biochemical networks.用于综合提取、鉴定和定量代谢物、蛋白质及RNA以揭示它们在生化网络中的协同调控的方法。
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Formation of serine and glyceric acid by the glycolate pathway.通过乙醇酸途径形成丝氨酸和乙醇酸。
Arch Biochem Biophys. 1962 Jul;98:154-63. doi: 10.1016/0003-9861(62)90161-3.
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D-甘油酸3-激酶是拟南芥光呼吸循环中最后一个未知的酶,属于一个新的激酶家族。

D-GLYCERATE 3-KINASE, the last unknown enzyme in the photorespiratory cycle in Arabidopsis, belongs to a novel kinase family.

作者信息

Boldt Ralf, Edner Christoph, Kolukisaoglu Uner, Hagemann Martin, Weckwerth Wolfram, Wienkoop Stefanie, Morgenthal Katja, Bauwe Hermann

机构信息

University of Rostock, Bioscience Institute, Plant Physiology Department, D-18051 Rostock, Germany.

出版信息

Plant Cell. 2005 Aug;17(8):2413-20. doi: 10.1105/tpc.105.033993. Epub 2005 Jun 24.

DOI:10.1105/tpc.105.033993
PMID:15980259
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1182498/
Abstract

D-GLYCERATE 3-KINASE (GLYK; EC 2.7.1.31) catalyzes the concluding reaction of the photorespiratory C2 cycle, an indispensable ancillary metabolic pathway to the photosynthetic C3 cycle that enables land plants to grow in an oxygen-containing atmosphere. Except for GLYK, all other enzymes that contribute to the C2 cycle are known by their primary structures, and the encoding genes have been identified. We have purified and partially sequenced this yet missing enzyme from Arabidopsis thaliana and identified it as a putative kinase-annotated single-copy gene At1g80380. The exclusive catalytic properties of the gene product were confirmed after heterologous expression in Escherichia coli. Arabidopsis T-DNA insertional knockout mutants show no GLYK activity and are not viable in normal air; however, they grow under elevated CO2, providing direct evidence of the obligatory nature of the ultimate step of the C2 cycle. The newly identified GLYK is both structurally and phylogenetically distinct from known glycerate kinases from bacteria and animals. Orthologous enzymes are present in other plants, fungi, and some cyanobacteria. The metabolic context of GLYK activity in fungi and cyanobacteria remains to be investigated.

摘要

D-甘油酸3-激酶(GLYK;EC 2.7.1.31)催化光呼吸C2循环的最后一步反应,光呼吸C2循环是光合C3循环不可或缺的辅助代谢途径,使陆地植物能够在含氧大气中生长。除了GLYK之外,参与C2循环的所有其他酶的一级结构均已明确,其编码基因也已得到鉴定。我们已从拟南芥中纯化出这种缺失的酶并进行了部分测序,将其鉴定为一个推定的带有激酶注释的单拷贝基因At1g80380。在大肠杆菌中进行异源表达后,证实了该基因产物独特的催化特性。拟南芥T-DNA插入敲除突变体无GLYK活性,在正常空气中无法存活;然而,它们在高浓度二氧化碳条件下能够生长,这为C2循环最后一步的必要性提供了直接证据。新鉴定出的GLYK在结构和系统发育上均与细菌和动物中已知的甘油酸激酶不同。其他植物、真菌和一些蓝细菌中存在直系同源酶。真菌和蓝细菌中GLYK活性的代谢背景仍有待研究。