Wubbolts M G, Terpstra P, van Beilen J B, Kingma J, Meesters H A, Witholt B
Department of Chemistry, University of Groningen, The Netherlands.
J Biol Chem. 1990 Oct 15;265(29):17665-72.
The pncB gene from Escherichia coli, which encodes nicotinic acid phosphoribosyltransferase (EC 2.4.2.11), was cloned on a 1.5-kilobase TaqI-EcoRI fragment. Its position on the E. coli chromosome was determined at 20.8 min between the asnS and pepN loci. The nucleotide sequence of the gene and the transcription and translation initiation sites were determined. Expression of pncB on a multicopy plasmid leads to a 25-fold increase in nicotinic acid phosphoribosyltransferase activity. Growth of E. coli in the presence of nicotinic acid leads to strong repression of nicotinic acid phosphoribosyltransferase activity, indicating that the cloned pncB sequence contains its own control sequences. It is shown that increased nicotinic acid phosphoribosyltransferase activity effects a 5-fold increase in the intracellular concentration of NAD. The cloned pncB gene can therefore be used as a tool to raise intracellular cofactor levels.
来自大肠杆菌的pncB基因编码烟酸磷酸核糖基转移酶(EC 2.4.2.11),该基因被克隆在一个1.5千碱基的TaqI-EcoRI片段上。它在大肠杆菌染色体上的位置被确定在asnS和pepN基因座之间的20.8分钟处。测定了该基因的核苷酸序列以及转录和翻译起始位点。pncB在多拷贝质粒上的表达导致烟酸磷酸核糖基转移酶活性增加25倍。在烟酸存在的情况下大肠杆菌的生长导致烟酸磷酸核糖基转移酶活性受到强烈抑制,这表明克隆的pncB序列包含其自身的控制序列。结果表明,烟酸磷酸核糖基转移酶活性的增加使细胞内NAD浓度提高了5倍。因此,克隆的pncB基因可作为提高细胞内辅因子水平的工具。