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生物受体立体选择性的发现:阿纳尔多·皮乌蒂与天门冬酰胺对映体的味道——125 周年纪念的历史和分析。

The discovery of stereoselectivity at biological receptors: Arnaldo Piutti and the taste of the asparagine enantiomers--history and analysis on the 125th anniversary.

机构信息

Department of Medicine, University of Colorado School of Medicine, Aurora, USA.

出版信息

Chirality. 2012 Dec;24(12):959-76. doi: 10.1002/chir.22071. Epub 2012 Oct 3.

Abstract

In 1886, Italian chemist Arnaldo Piutti isolated, for the first time, d-asparagine, the enantiomer of the known l-asparagine. He obtained 100 g of D-asparagine from 6500 kg of vetches. Using an ingenious synthetic scheme, Piutti established the chemical structure of asparagine and demonstrated that his isolation of D-asparagine from plants was not the result of the racemization of L-asparagine during the extraction procedure. He found a striking difference in the taste of asparagine: L-asparagine was without taste, while D-asparagine was intensely sweet. This was the first example of enantioselectivity in a receptor-mediated biological activity. Receptors constitute one of the most important and most intensively studied phenomena in biology, and enantioselectivity in receptor-mediated activity, including at the sweetness receptor, is today an important and commonly seen aspect of receptor function. Therefore, Piutti's discovery, although made ca. 15 years before the emergence of the receptor concept, was a milestone. The publication of Piutti's asparagine work prompted several eminent scientists, including Louis Pasteur and Arthur Cushny, a leading pharmacologist of the time, to remark on the importance of the discovery. Piutti also carried out investigations in many other fields, e.g., other organic compounds and reactions, pharmaceuticals, alimentary products, radioactivity, noble gases, and spectroscopy. Considerable progress has been made in recent decades concerning the biology and chemistry of sweet taste, but the details of the interactions of chiral molecules with the sweetness receptor remain poorly understood. Piutti and his discovery are largely forgotten today; they deserve the attention of the chirality and receptor "communities."

摘要

1886 年,意大利化学家阿纳尔多·皮乌蒂(Arnaldo Piutti)首次分离出 d-天冬酰胺,这是已知 l-天冬酰胺的对映异构体。他从 6500 公斤野豌豆中提取到 100 克 D-天冬酰胺。皮乌蒂采用巧妙的合成方案,确定了天冬酰胺的化学结构,并证明他从植物中分离出 D-天冬酰胺并非是由于提取过程中天冬酰胺的外消旋化。他发现天冬酰胺的味道有显著差异:l-天冬酰胺没有味道,而 D-天冬酰胺则非常甜。这是首例在受体介导的生物活性中表现出对映体选择性的例子。受体是生物学中最重要和研究最深入的现象之一,而在受体介导的活性中对映体选择性,包括甜味受体,是当今受体功能的一个重要且常见的方面。因此,尽管皮乌蒂的发现比受体概念的出现早了大约 15 年,但却是一个里程碑。皮乌蒂的天冬酰胺研究结果发表后,引起了几位杰出科学家的关注,包括路易斯·巴斯德(Louis Pasteur)和当时的著名药理学家亚瑟·库什尼(Arthur Cushny)。皮乌蒂还在许多其他领域进行了研究,例如其他有机化合物和反应、药物、食品、放射性、稀有气体和光谱学。近年来,有关甜味的生物学和化学方面取得了相当大的进展,但手性分子与甜味受体相互作用的细节仍知之甚少。皮乌蒂及其发现今天在很大程度上被遗忘了;他们值得手性和受体“社区”的关注。

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