Use of high acyl donor concentrations leads to penicillin acylase inactivation in the course of peptide synthesis

被引:5
作者
Shcherbakova, TA
Korennykh, AV
van Langen, LM
Sheldon, RA
Svedas, VK [1 ]
机构
[1] Moscow MV Lomonosov State Univ, Fac Bioengn & Bioinformat, Moscow 119992, Russia
[2] Moscow MV Lomonosov State Univ, Belozersky Inst Physicochem Biol, Moscow 119992, Russia
[3] Delft Univ Technol, Organ Chem Lab, NL-2628 BL Delft, Netherlands
基金
俄罗斯基础研究基金会;
关键词
penicillin acylase; enzyme stability; inactivation by substrate;
D O I
10.1016/j.molcatb.2004.07.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Enzyme inactivation has been observed in the course of penicillin acylase-catalyzed hydrolysis and aminolysis of D-phenylglycine amide. Inactivation was very sensitive to the D-phenylglycine amide concentration: at pH 9.5, 25degreesC and 400 mM substrate, penicillin acylase lost more than 90% of its initial catalytic activity in half an hour, in the presence of 100 mM substrate, 50% of the initial activity in two hours, whereas in the absence of substrate, no significant enzyme inactivation was observed in three hours. Observed enzyme inactivation limits use of high acyl donor concentrations at penicillin acylase-catalyzed peptide synthesis. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:63 / 65
页数:3
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