识别催化三键键和环氧群形成的非血红二铁蛋白
概括
研究人员确定了植物酶和克隆基因,这些基因负责制造乙酸和环氧脂肪酸. 在Arabidopsis thaliana种子中表达这些基因显著增加了这些有价值化合物的产生.
科学领域:
- 生物化学 生物化学
- 植物分子生物学 植物分子生物学
- 有机化学 有机化学
背景情况:
- 在600多种天然化合物中发现了乙烯键.
- 了解这些化合物的生物合成对于各种应用至关重要.
研究的目的:
- 描述参与形成乙酸和环氧脂肪酸的植物酶.
- 为了克隆编码这些酶的基因.
- 为了研究这些基因在模型植物中的功能表达.
主要方法:
- 脂肪酸修饰路径的酶特性.
- 编码乙酸和环氧脂肪酸合成序列的基因克隆.
- 用克隆cDNAs进行Arabidopsis thaliana的遗传转化.
- 对转基因种子中的脂肪酸概况的分析.
主要成果:
- 确定了两种催化Delta12乙烯基和Delta12环氧基组形成的植物酶.
- 编码这些酶的基因被克隆,并显示其序列相似.
- 这些基因在Arabidopsis thaliana种子中的表达导致乙酸脂肪酸 (高达25%) 和环氧化脂肪酸 (高达15%) 的显著增加.
- 描述的酶与含有非血红素铁的膜蛋白与含有氨酸丰富的基因具有相似之处.
结论:
- 这项研究成功地确定并克隆了乙酸和环氧脂肪酸生物合成中的关键酶的基因.
- 阿拉比多普西斯 (Arabidopsis thaliana) 的基因工程可以增强这些有价值的脂肪酸的产生.
- 这些酶具有特征,表明它们在与膜相关的催化过程中发挥作用.
相关概念视频
Oxidation of Alkenes: Syn Dihydroxylation with Osmium Tetraoxide
Alkenes are converted to 1,2-diols or glycols through a process called dihydroxylation. It involves the addition of two hydroxyl groups across the double bond with two different stereochemical approaches, namely anti and syn. Dihydroxylation using osmium tetroxide progresses with syn stereochemistry.
Oxidation of Alkenes: Anti Dihydroxylation with Peroxy Acids
Diols are compounds with two hydroxyl groups. In addition to syn dihydroxylation, diols can also be synthesized through the process of anti dihydroxylation. The process involves treating an alkene with a peroxycarboxylic acid to form an epoxide. Epoxides are highly strained three-membered rings with oxygen and two carbons occupying the corners of an equilateral triangle. This step is followed by ring-opening of the epoxide in the presence of an aqueous acid to give a trans diol.
Preparation of Diols and Pinacol Rearrangement
Compounds bearing two hydroxyl groups are known as diols. When the hydroxyl groups are located on adjacent carbon atoms, the diols are called vicinal diols or glycols. Under acidic conditions, vicinal diols undergo a specific reaction called pinacol rearrangement.
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
The reaction begins with transferring a proton from the acid catalyst to one of the hydroxyl groups, producing an oxonium ion.
Preparation of Epoxides
Overview
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Epoxides result from alkene oxidation, which can be achieved by a) air, b) peroxy acids, c) hypochlorous acids, and d) halohydrin cyclization.
Epoxidation with Peroxy Acids
Epoxidation of alkenes via oxidation with peroxy acids involves the conversion of a carbon–carbon double bond to an epoxide using the oxidizing agent meta-chloroperoxybenzoic acid, commonly known as MCPBA. Since the O–O bond of peroxy acids is very weak, the addition of electrophilic oxygen of peroxy acids to...
Protein Modifications in the RER
Modification of secretory and transmembrane proteins entering the rough ER begins in the ER lumen. These modifications aid in protein folding and stabilize the acquired tertiary structure. Protein modifications in the rough ER co-occur at different stages of protein folding.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal sequences.
Broadly, these modifications can be categorized into four main categories — glycosylation, formation of disulfide bonds, assembly of protein subunits, and specific proteolytic cleavages like removal of signal sequences.
Oxidation of Phenols to Quinones
In the presence of oxidizing agents, phenols are oxidized to quinones. Quinones can be easily reduced back to phenols using mild reducing agents. The electron-donating hydroxyl group enhances the reactivity of the aromatic ring, enabling oxidation of the ring even in the absence of an α hydrogen.
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...
o-hydroxy phenols are oxidized to o-quinones and p-hydroxy phenols to p-quinones. Such redox reactions involve the transfer of two electrons and two protons. The reversible redox property is crucial in...


