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1,5-二磷酸核酮糖羧化酶的发育与特性研究:表明蓖麻种子萌发时胚乳中二氧化碳固定缺乏羧化酶功能的证据

Development and Characterization of Ribulose-1,5-bisphosphate Carboxylase : Evidence Indicating a Lack of Carboxylase Function in CO(2) Fixation in Endosperm of Germinating Castor Bean Seedlings.

作者信息

Wong J H, Benedict C R

机构信息

Department of Plant Sciences, Texas A & M University, College Station, Texas 77843.

出版信息

Plant Physiol. 1983 May;72(1):37-43. doi: 10.1104/pp.72.1.37.

Abstract

Ribulose-1,5-bisphosphate carboxylase activity was found in endosperm of germinating castor bean seed Ricinus communis and was localized in proplastids. The endosperm carboxylase has been extensively purified and is composed of two different subunits. The molecular weights of the native carboxylase and its subunits were 560,000, 55,000, and 15,000 daltons, respectively. The Michaelis-Menten constants, K(m), for the endosperm carboxylase with respect to ribulose 1,5-bisphosphate, bicarbonate, CO(2), and magnesium in millimolar are 0.54, 13.60, 0.92, and 0.57, respectively. The endosperm carboxylase was activated by Mg(2+) and HCO(3) (-). The preincubation of the carboxylase with 1 millimolar HCO(3) (-) and 5 millimolar MgCl(2) resulted in activation by low and inhibition by high concentrations of 6-phosphogluconate.In studies of dark (14)CO(2) fixation by endosperm slices, [(14)C]malate and [(14)C]citrate were the predominantly labeled products after 30 seconds of exposure of the tissue to H(14)CO(3) (-). In pulse-chase experiments, 87% of the label is malate, and citrate was transferred to sugars after a 60-minute chase with a small amount of the label appearing in the incubation medium as (14)CO(2). The minimal incorporation of the label from (14)CO(2) into phosphoglyceric acid indicated a lack of the endosperm ribulose-1,5-bisphosphate carboxylase participation in the endosperm's CO(2) fixation system. The activities of key Calvin cycle enzymes were examined in the endosperms and cotyledons of dark-grown castor bean seedlings. Many of these autotrophic enzymes develop in the dark in these tissues. The synthesis of ribulose-1,5-bisphosphate carboxylase in the nonphotosynthetic endosperms is not repressed in the dark, and high levels of enzymic activity appear with germination. All of the Calvin cycle enzymes are present in the castor bean endosperm except NADP-linked glyceraldehyde 3-P dehydrogenase, and the absence of this dehydrogenase probably prevents the functioning of these series of reactions in dark CO(2) fixation.

摘要

在萌发的蓖麻种子(Ricinus communis)胚乳中发现了1,5-二磷酸核酮糖羧化酶活性,其定位于前质体中。胚乳羧化酶已被广泛纯化,由两种不同的亚基组成。天然羧化酶及其亚基的分子量分别为560,000、55,000和15,000道尔顿。胚乳羧化酶对1,5-二磷酸核酮糖、碳酸氢盐、CO₂和镁的米氏常数(K(m))(以毫摩尔计)分别为0.54、13.60、0.92和0.57。胚乳羧化酶被Mg²⁺和HCO₃⁻激活。羧化酶与1毫摩尔HCO₃⁻和5毫摩尔MgCl₂预孵育导致低浓度时被激活,而高浓度的6-磷酸葡萄糖酸会产生抑制作用。在胚乳切片的暗(¹⁴)CO₂固定研究中,组织暴露于H¹⁴CO₃⁻30秒后,[¹⁴C]苹果酸和[¹⁴C]柠檬酸是主要的标记产物。在脉冲追踪实验中,87%的标记物是苹果酸,在60分钟追踪后,柠檬酸被转化为糖类,少量标记物以(¹⁴)CO₂形式出现在孵育培养基中。从(¹⁴)CO₂到磷酸甘油酸的标记物掺入极少,这表明胚乳1,5-二磷酸核酮糖羧化酶不参与胚乳的CO₂固定系统。在黑暗中生长的蓖麻幼苗的胚乳和子叶中检测了关键卡尔文循环酶的活性。这些自养酶中的许多在这些组织的黑暗环境中发育。非光合胚乳中1,5-二磷酸核酮糖羧化酶的合成在黑暗中不受抑制,并且随着萌发出现高水平的酶活性。除了NADP连接的甘油醛3-磷酸脱氢酶外,所有卡尔文循环酶都存在于蓖麻胚乳中,而这种脱氢酶的缺失可能阻止了这些系列反应在暗CO₂固定中的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d645/1066165/9ae85845c0ce/plntphys00561-0047-a.jpg

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