Jove
Visualize
联系我们
JoVE
x logofacebook logolinkedin logoyoutube logo
关于 JoVE
概览领导团队博客JoVE 帮助中心
作者
出版流程编辑委员会范围与政策同行评审常见问题投稿
图书馆员
用户评价订阅访问资源图书馆顾问委员会常见问题
研究
JoVE JournalMethods CollectionsJoVE Encyclopedia of Experiments存档
教育
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab Manual教师资源中心教师网站
使用条款与条件
隐私政策
政策

相关概念视频

Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis01:13

Esters to Carboxylic Acids: Acid-Catalyzed Hydrolysis

2.8K
Hydrolysis of esters under acidic conditions proceeds through a nucleophilic acyl substitution. In the presence of excess water, the reaction proceeds in a reversible manner, forming carboxylic acids and alcohols.
During hydrolysis, the ester is first activated towards nucleophilic attack through the protonation of the carboxyl oxygen atom by the acid catalyst. The protonation makes the ester carbonyl carbon more electrophilic. In the next step, water acts as a nucleophile and adds to the...
2.8K
Esters to Carboxylic Acids: Saponification01:25

Esters to Carboxylic Acids: Saponification

4.4K
Esters can be hydrolyzed to carboxylic acids under acidic or basic conditions. Base-promoted hydrolysis of esters is a nucleophilic acyl substitution reaction in which esters react with an aqueous base, followed by an acid to give carboxylic acids. This reaction is also known as saponification because it forms the basis for making soaps from fats.
The reaction requires a base in stoichiometric amounts, which participates in the reaction and is not regenerated later. So, the base acts as a...
4.4K
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism01:13

Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Mechanism

7.8K
Carboxylic acids react with alcohols to yield esters via an acid-catalyzed condensation reaction called Fischer esterification. This is a nucleophilic acyl substitution reaction that proceeds via a tetrahedral intermediate, where a water molecule is eliminated as the leaving group.
7.8K
Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview01:20

Carboxylic Acids to Esters: Acid-Catalyzed (Fischer) Esterification Overview

17.9K
The Fischer esterification reaction was developed by the German chemist Emil Fischer in 1895. It is a condensation reaction between carboxylic acids and alcohols in an acidic medium to give esters and water.
17.9K
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation02:17

Reduction of Alkenes: Asymmetric Catalytic Hydrogenation

3.3K
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
3.3K
Catalysis02:50

Catalysis

26.8K
The presence of a catalyst affects the rate of a chemical reaction. A catalyst is a substance that can increase the reaction rate without being consumed during the process. A basic comprehension of a catalysts’ role during chemical reactions can be understood from the concept of reaction mechanisms and energy diagrams.
26.8K

您也可能阅读

相关文章

通过共同作者、期刊和引用图与本文相关的文章。

排序
Same author

A Dynamic NMR Lineshape Simulation Framework for Lipid Diffusion and Membrane Thinning in Bicelles and Nanodiscs.

The journal of physical chemistry. B·2026
Same author

Primary Health Conditions Among Medical Crowdfunding Campaigns in the United States: Natural Language Processing Study.

JMIR AI·2026
Same author

Molecular Mechanisms Governing Peptide Nanodisc Assembly and Stability.

bioRxiv : the preprint server for biology·2026
Same author

Gangliosides GM3 And GD3 Modulate Insulin Aggregation Pathways and Reduce Cytotoxicity Through Structural Remodeling.

bioRxiv : the preprint server for biology·2026
Same author

Unraveling design principles of protein landscapes in photosynthetic membranes in plant chloroplasts.

Science advances·2026
Same author

Functional Amyloids as Multifunctional Platforms for Targeted Drug Delivery and Immunotherapy.

Langmuir : the ACS journal of surfaces and colloids·2025

相关实验视频

Updated: Jun 15, 2025

Defining Substrate Specificities for Lipase and Phospholipase Candidates
08:59

Defining Substrate Specificities for Lipase and Phospholipase Candidates

Published on: November 23, 2016

14.9K

基于脂质的催化被证明是由双器启用的质水解.

Shu Liu1,2, Kiran Kumar3,4, Tracey Bell1

  • 1Department of Biological Science and Integrative Nanoscience Institute, Florida State University, Tallahassee, FL 32306, USA.

Membranes
|August 28, 2024
PubMed
概括

脂质聚合物可以在它们的疏水性区域内催化化学反应,模仿生物催化. 这项研究表明,脂质可以加速水解,开辟生物化学和合成生物学的新途径.

关键词:
生物化学 生物化学催化剂是一种催化剂.异质的异质的异质的脂肪液滴滴滴滴滴滴滴滴滴滴滴滴滴滴滴滴分区分区分区分区分区分区分药理学 药理学 药理学 药理学 药理学合成生物学 合成生物学一个小泡.

更多相关视频

Biomembrane Fabrication by the Solvent-assisted Lipid Bilayer SALB Method
09:38

Biomembrane Fabrication by the Solvent-assisted Lipid Bilayer SALB Method

Published on: December 1, 2015

14.9K
Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions
12:18

Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions

Published on: August 3, 2021

3.5K

相关实验视频

Last Updated: Jun 15, 2025

Defining Substrate Specificities for Lipase and Phospholipase Candidates
08:59

Defining Substrate Specificities for Lipase and Phospholipase Candidates

Published on: November 23, 2016

14.9K
Biomembrane Fabrication by the Solvent-assisted Lipid Bilayer SALB Method
09:38

Biomembrane Fabrication by the Solvent-assisted Lipid Bilayer SALB Method

Published on: December 1, 2015

14.9K
Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions
12:18

Assembly of Cell Mimicking Supported and Suspended Lipid Bilayer Models for the Study of Molecular Interactions

Published on: August 3, 2021

3.5K

科学领域:

  • 生物化学 生化学
  • 有机化学 有机化学
  • 合成生物学 合成生物学

背景情况:

  • 脂质通常不被视为生物系统中的催化剂.
  • 聚合物中的两性化合物在合成化学中表现出催化活性.
  • 脂质双层提供适合化学反应的疏水环境.

研究的目的:

  • 为了证明脂质聚合物可以为化学反应提供催化环境.
  • 探索脂质双层在加速生化过程中的潜力.
  • 用基于脂质的系统研究素-AM的水解.

主要方法:

  • 采用了双相八醇水系统,其中含有阴性两性 (CTAB,八基胺).
  • 在水环境中用脂囊泡取代了八醇.
  • 使用定量光监测反应动力学,并用1H-NMR对产品进行表征.

主要成果:

  • 脂质聚合物和脂囊泡成功催化了素-AM的水解.
  • 观察到的催化周转数在10^-7到10^-8s^-1的范围内.
  • 1H-NMR证实了产品与水解相一致.

结论:

  • 脂质聚合物可以通过在疏水微环境中隔离反应物来起到催化剂的作用.
  • 这一发现对理解生物化学,药理学和合成生物学中的脂质作用有重要意义.
  • 脂质代表了一个潜在的催化剂类别,超出了传统的酶作用.