ENZYMATIC-SYNTHESIS OF GUANINE-NUCLEOTIDES LABELED WITH N-15 AT THE 2-AMINO GROUP OF THE PURINE RING

被引:7
作者
BOUHSS, A
SAKAMOTO, H
PALIBRODA, N
CHIRIAC, M
SARFATI, R
SMITH, JM
CRAESCU, CT
BARZU, O
机构
[1] INST PASTEUR,UNITE CHIM ORGAN,F-75724 PARIS 15,FRANCE
[2] INST CURIE,INSERM,U350,BIOL SECT,F-91405 ORSAY,FRANCE
[3] INST ISOTOPE & MOLEC TECHNOL INST,R-3400 CLUJ NAPOCA,ROMANIA
[4] R&D SYST INC,MINNEAPOLIS,MN 55413
关键词
D O I
10.1006/abio.1995.1101
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
GMP and dGMP labeled with N-15 at the 2-amino group of the purine ring was obtained enzymatically from NH4Cl (>99 at.% N-15) and from IMP or (ZIMP, respectively, by several reactions involving IMP-dehydrogenase, GMP-synthetase, adenylate kinase, and creatine kinase, The first three enzymes were obtained by overexpression in Escherichia coli of the corresponding genes, The isotope content of the primary amino group of guanine determined by mass spectrometry after acid hydrolysis of nucleotides was found higher than 98 at.% N-15, The proton NMR spectrum of [N-15]GMP in solution in the absence of nitrogen decoupling showed a doublet with a coupling constant of 92 Hz, When nitrogen decoupling was used during the acquisition time, the doublet was replaced by a single peak at 6.47 ppm, indicating that the corresponding proton is bound to N-15. (C) 1995 Academic Press,Inc.
引用
收藏
页码:18 / 23
页数:6
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