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用于水解蛋白质和肽而不引起消旋化并用于测定其真实D-氨基酸含量的改进方法。

Improved method for hydrolyzing proteins and peptides without inducing racemization and for determining their true D-amino acid content.

作者信息

D'Aniello A, Petrucelli L, Gardner C, Fisher G

机构信息

Department of Biochemistry and Molecular Biology, Zoological Station A Dohrn, Naples, Italy.

出版信息

Anal Biochem. 1993 Sep;213(2):290-5. doi: 10.1006/abio.1993.1423.

Abstract

A new method of hydrolyzing proteins and peptides without racemizing the amino acids has been developed. This method consists of performing a brief partial chemical hydrolysis for 15 min in 6 M HCl at 80-90 degrees C, followed by an enzymatic hydrolysis with pronase for 12-16 h at 50 degrees C, and finally an enzymatic hydrolysis with leucine aminopeptidase and peptidyl-D-amino acid hydrolase for 24 h. Using this new method the time required for complete hydrolysis of proteins is less than 3 days. The total hydrolysis averages 97-100%, and the amount of racemization of the amino acids is less than 0.002%. This method may then be used as a tool to easily determine the intrinsic D-amino acid content of peptides or proteins from animal or vegetable tissues.

摘要

一种在不使氨基酸消旋的情况下水解蛋白质和肽的新方法已经开发出来。该方法包括在80 - 90摄氏度的6M盐酸中进行15分钟的短暂部分化学水解,然后在50摄氏度下用链霉蛋白酶进行12 - 16小时的酶水解,最后用亮氨酸氨肽酶和肽基-D-氨基酸水解酶进行24小时的酶水解。使用这种新方法,蛋白质完全水解所需的时间少于3天。总水解率平均为97 - 100%,氨基酸的消旋量小于0.002%。然后,这种方法可以用作一种工具,轻松测定来自动物或植物组织的肽或蛋白质的固有D-氨基酸含量。

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