Identification and characterization of a second NMN adenylyltransferase gene in Saccharomyces cerevisiae

被引:32
作者
Emanuelli, M
Amici, A
Carnevali, F
Pierella, F
Raffaelli, N
Magni, G
机构
[1] Univ Ancona, Ist Biochim, Fac Med, I-60100 Ancona, Italy
[2] Univ Ancona, Dipartimento Biotecnol Agrarie & Ambientali, I-60100 Ancona, Italy
关键词
NMN adenylyltransferase; NAD(+) biosynthesis; cloning; yeast;
D O I
10.1016/S1046-5928(02)00645-9
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The enzyme nicotinamide mononucleotide (NMN) adenylyltransferase (NMNAT) (EC 2.7.7.1) catalyzes the transfer of the adenylyl moiety of ATP to NMN to form NAD(+). On the basis of a remarkable structural similarity with previously described Saccharomyces cerevisiae NMNAT (yNMNAT-1), the YGR010-encoded protein was identified as a second isoform of yeast NMNAT (yNMNAT-2). The YGR010 gene was isolated, cloned into a T7-based vector, and successfully expressed in Escherichia coli BL21 cells, yielding high level of NMN adenylyltransferase activity. The purification procedure reported in this paper, consisting of two chromatographic steps, allowed the isolation of 3 mg of electrophoretically homogeneous yNMNAT-2 from 1 liter of E coli culture. Under SDS/PAGE, the recombinant protein resulted in a single polypeptide of 46 kDa, in agreement with the molecular mass of the hypothetical protein encoded by YGR010 gene. The N-terminal sequence of the purified recombinant yNMNAT-2 exactly corresponds to the predicted sequence. Molecular and kinetic properties of recombinant yNMNAT-2 are reported and compared with those already known for yNMNAT-1. (C) 2002 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:357 / 364
页数:8
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