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1.
Abstract

A simple procedure is described for the preparation of the title compounds 1, 8 and 9. 3′-3′ or 3′-5′ or 5′-5′ TpT was reacted with a twofold molar excess of TPS in anhydrous DMF, at room temperature, for 5 min, followed by a 1 min in situ treatment of the reaction mixture with excess 7.0 N NH4OH, at 0°C. The alkaline hydrolysis of 1, 8 and 9 proceeds without the assistance of 3′- and 5′-hydroxyl groups resulting in equimolar mixtures of thymidine (4) and thymidine 3′-phosphoramidate (6) (for the 3′-3′ isomer) or thymidine 5′-phosphoramidate (7) (for the 5′-5′ isomer) or 6 and 7 in equal quantities (for the 3′-5′ isomer).  相似文献   

2.
前言8位氚标记脱氧腺嘌呤核苷5'-一磷酸(以下简写为~3H-dAMP)可用于脱氧核糖核酸结构分析及代谢研究,还可以转变成脱氧腺三磷(~3H-dATP)。我们遵照毛主席“独立自主,自力更生”的  相似文献   

3.
Abstract

The solid-phase preparation of oligodeoxyribonucleotides covalently linked via nucleic bases with normal (3′-5′) or inverted (5′-5′) polarities is reported. The key-step of these syntheses is the preparation of the tethered dimers.  相似文献   

4.
5′-核苷酸在农业、食品和医药行业有着广泛的用途。比较了目前5′-核苷酸的工业和实验室合成方法,包括化学合成法,微生物发酵法,酶解法和酶催化法。  相似文献   

5.
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7.
Abstract

We have studied double and triple helix formation between 2′–5′ or 3–5′ linked oligoriboadenylates and oligoribouridylates with chain length 7 or 10 by CD spectrometry. The complex formation depends on the type of linkage of oligoribonucleotides, chain length, concentration and molar ratio of the strands, temperature and the cationic concentration. Mixture of any linkage isomers of oligo(rA) and oligo(rU) in 1:1 molar ratio form duplex at 0.1 M NaCl. The duplex stability largely depends on the type of the linkages and is in the following order; [35′] oligo(rA)·[3′-5′] oligo(rU) > [2′-5′] oligo(rA)'[3′-5′] oligo(rU) > [3′-5′] oligo(rA)·[2′-5′] oligo(rU) > [2–5′] oligo(rA)*[2′-5′] oligo(rU). The higher cationic concentrations, 0.5 M MgCl2, stabilize the complex and either duplex or triplex is formed depending on the input strand ratio and the type of linkage. Thermodynamic parameters, DH and DS, for the complex formation between linkage isomers of oligo(rA) and oligo(rU) showed a linear relationship indicating an enthalpy-entropy compensation phenomena. The duplex and triplex composed of [2′-5′] oligo(rA) and [2′-5′] oligo(rU) exhibit different CD spectra compared to those of any others containing 3–5′ linkage, suggesting that the fully 2–5′ duplex and triplex may possess a unique conformation. We describe prebiological significance of the linkage isomers of RNA and selection of the 3–5′ linkage against 2′-5 linkage.  相似文献   

8.
采用RT-PCR和RACE方法从鹤望兰黄色花萼中克隆到类黄酮生物合成途径关键基因SrF3′5′H。该cDNA全长1 766 bp,具有完整的开放阅读框(ORF),共1 509个碱基,编码503个氨基酸。氨基酸同源性分析表明,SrF3′5′H编码的氨基酸序列与已报道的其他植物的F3′5′H蛋白具有很高的同源性。系统进化树分析显示,鹤望兰SrF3′5′H与非洲紫罗兰蛋白亲缘关系较近。应用半定量PCR分析表明,SrF3′5′H在始花期转录水平达到最高,且在蓝色花瓣中表达最高,在黄色花萼中几乎没有表达。  相似文献   

9.
Abstract

First experimental evidence is herein reported supporting the earlier quantum chemical calculations that 5′-Punne-pyrimiidine-3′ 3′ -Pyrimidine-Punne-5 stack is more stable than 5′-Pyrimiidine-Punne-3′ 3′-Punne-Pyrimidine-5′.  相似文献   

10.
类黄酮3′,5′羟-化酶( flavonoid 3′,5′-hydroxylase, F3′5′H)是植物花青素生物合成途径中的一个关键酶,紫色土豆( Solanum tueb or sum) F3′5′H基因的克隆将为花青素合成调控和花青素代谢工程研究提供优质基因资源。研究采用RACE技术克隆了紫色土豆F3′5′H基因的cDNA全长序列,用生物信息学方法对其核苷酸和蛋白质序列进行了分析,并用半定量PCR 技术分析了F3′5′H基因在不同组织中的表达情况,同时研究了赤霉素和蔗糖处理后F3′5′H基因表达与花青素积累之间的相关性。研究结果表明,克隆的紫色土豆F3′5′H的cDNA全长为1854 bp,包含一个1530 bp的完整ORF,共编码509个氨基酸。生物信息学分析表明,StF3′5′H基因推测编码的氨基酸序列与其它植物的F3′5′H蛋白的相似性很高。 StF3′5′H基因的表达具有组织特异性,在紫色土豆根、茎和叶柄中都有表达,其中在叶柄中表达最强,而在块茎、叶轴和叶片中几乎检测不到StF3′5′H基因的表达。赤霉素和蔗糖能促进紫色土豆StF3′5′H基因的表达,进而促进花青素的积累。  相似文献   

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