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Formate dehydrogenase, an enzyme of anaerobic metabolism, is induced by iron deficiency in barley roots.甲酸脱氢酶是一种无氧代谢酶,在大麦根中受缺铁诱导。
Plant Physiol. 1998 Feb;116(2):725-32. doi: 10.1104/pp.116.2.725.
2
Induced activity of adenine phosphoribosyltransferase (APRT) in iron-deficiency barley roots: a possible role for phytosiderophore production.缺铁大麦根中腺嘌呤磷酸核糖转移酶(APRT)的诱导活性:植物铁载体产生的一种可能作用。
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3
Expression of a gene specific for iron deficiency (Ids3) in the roots of Hordeum vulgare.大麦根部缺铁特异性基因(Ids3)的表达
Plant Cell Physiol. 1993 Apr;34(3):401-10.
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Cloning two genes for nicotianamine aminotransferase, a critical enzyme in iron acquisition (Strategy II) in graminaceous plants.克隆两个与烟酰胺氨基转移酶相关的基因,该酶是禾本科植物铁吸收(策略II)中的关键酶。
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In vivo evidence that Ids3 from Hordeum vulgare encodes a dioxygenase that converts 2'-deoxymugineic acid to mugineic acid in transgenic rice.大麦的Ids3编码一种双加氧酶,该酶在转基因水稻中将2'-脱氧 mugineic 酸转化为 mugineic 酸的体内证据。
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Two dioxygenase genes, Ids3 and Ids2, from Hordeum vulgare are involved in the biosynthesis of mugineic acid family phytosiderophores.来自大麦的两个双加氧酶基因Ids3和Ids2参与了麦根酸家族植物铁载体的生物合成。
Plant Mol Biol. 2000 Sep;44(2):199-207. doi: 10.1023/a:1006491521586.

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Over-expression of the Arabidopsis formate dehydrogenase in chloroplasts enhances formaldehyde uptake and metabolism in transgenic tobacco leaves.拟南芥质体甲酸脱氢酶的过表达增强了转基因烟草叶片中甲醛的摄取和代谢。
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本文引用的文献

1
Biosynthesis of Phytosiderophores : In Vitro Biosynthesis of 2'-Deoxymugineic Acid from l-Methionine and Nicotianamine.植物铁载体的生物合成:从L-蛋氨酸和烟酰胺体外生物合成2'-脱氧麦根酸
Plant Physiol. 1990 Aug;93(4):1497-503. doi: 10.1104/pp.93.4.1497.
2
Chlorophyll Biosynthesis.叶绿素生物合成
Plant Cell. 1995 Jul;7(7):1039-1057. doi: 10.1105/tpc.7.7.1039.
3
Two Related Biosynthetic Pathways of Mugineic Acids in Gramineous Plants.禾本科植物中麦根酸的两条相关生物合成途径。
Plant Physiol. 1993 Jun;102(2):373-378. doi: 10.1104/pp.102.2.373.
4
Iron and copper nutrition-dependent changes in protein expression in a tomato wild type and the nicotianamine-free mutant chloronerva.番茄野生型和无烟酰胺突变体chloronerva中蛋白质表达的铁和铜营养依赖性变化
Plant Physiol. 1996 Jun;111(2):533-40. doi: 10.1104/pp.111.2.533.
5
Site-directed mutagenesis of the formate dehydrogenase active centre: role of the His332-Gln313 pair in enzyme catalysis.甲酸脱氢酶活性中心的定点诱变:His332-Gln313对在酶催化中的作用。
FEBS Lett. 1996 Jul 15;390(1):104-8. doi: 10.1016/0014-5793(96)00641-2.
6
Developmental regulation of the gene for formate dehydrogenase in Neurospora crassa.粗糙脉孢菌中甲酸盐脱氢酶基因的发育调控。
J Bacteriol. 1993 Jun;175(12):3703-9. doi: 10.1128/jb.175.12.3703-3709.1993.
7
Identification of a major soluble protein in mitochondria from nonphotosynthetic tissues as NAD-dependent formate dehydrogenase.鉴定非光合组织线粒体中的一种主要可溶性蛋白为NAD依赖型甲酸脱氢酶。
Plant Physiol. 1993 Aug;102(4):1171-7. doi: 10.1104/pp.102.4.1171.
8
High resolution structures of holo and apo formate dehydrogenase.全酶和脱辅基甲酸脱氢酶的高分辨率结构。
J Mol Biol. 1994 Feb 25;236(3):759-85. doi: 10.1006/jmbi.1994.1188.
9
A dioxygenase gene (Ids2) expressed under iron deficiency conditions in the roots of Hordeum vulgare.一个在大麦根中铁缺乏条件下表达的双加氧酶基因(Ids2)。
Plant Mol Biol. 1994 Jul;25(4):705-19. doi: 10.1007/BF00029608.
10
NAD(+)-dependent formate dehydrogenase.烟酰胺腺嘌呤二核苷酸(NAD⁺)依赖性甲酸脱氢酶
Biochem J. 1994 Aug 1;301 ( Pt 3)(Pt 3):625-43. doi: 10.1042/bj3010625.

甲酸脱氢酶是一种无氧代谢酶,在大麦根中受缺铁诱导。

Formate dehydrogenase, an enzyme of anaerobic metabolism, is induced by iron deficiency in barley roots.

作者信息

Suzuki K, Itai R, Suzuki K, Nakanishi H, Nishizawa N K, Yoshimura E, Mori S

机构信息

Department of Applied Biological Chemistry, University of Tokyo, Japan.

出版信息

Plant Physiol. 1998 Feb;116(2):725-32. doi: 10.1104/pp.116.2.725.

DOI:10.1104/pp.116.2.725
PMID:9489019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC35132/
Abstract

To identify the proteins induced by Fe deficiency, we have compared the proteins of Fe-sufficient and Fe-deficient barley (Hordeum vulgare L.) roots by two-dimensional polyacrylamide gel electrophoresis. Peptide sequence analysis of induced proteins revealed that formate dehydrogenase (FDH), adenine phosphoribosyltransferase, and the lds3 gene product (for Fe deficiency-specific) increased in Fe-deficient roots. FDH enzyme activity was detected in Fe-deficient roots but not in Fe-sufficient roots. A cDNA encoding FDH (Fdh) was cloned and sequenced. Fdh expression was induced by Fe deficiency. Fdh was also expressed under anaerobic stress and its expression was more rapid than that induced by Fe deficiency. Thus, the expression of Fdh observed in Fe-deficient barley roots appeared to be a secondary effect caused by oxygen deficiency in Fe-deficient plants.

摘要

为了鉴定缺铁诱导产生的蛋白质,我们通过二维聚丙烯酰胺凝胶电泳比较了铁充足和缺铁大麦(Hordeum vulgare L.)根系的蛋白质。对诱导蛋白的肽序列分析表明,甲酸脱氢酶(FDH)、腺嘌呤磷酸核糖转移酶和lds3基因产物(缺铁特异性)在缺铁根系中增加。在缺铁根系中检测到了FDH酶活性,而在铁充足的根系中未检测到。克隆并测序了编码FDH(Fdh)的cDNA。Fdh的表达受缺铁诱导。Fdh在厌氧胁迫下也有表达,且其表达比缺铁诱导的表达更快。因此,在缺铁大麦根系中观察到的Fdh表达似乎是缺铁植物中缺氧引起的次生效应。