Mendz G L, Jimenez B M, Hazell S L, Gero A M, O'Sullivan W J
School of Biochemistry and Molecular Genetics, University of New South Wales, Kensington, Australia.
J Appl Bacteriol. 1994 Jul;77(1):1-8. doi: 10.1111/j.1365-2672.1994.tb03036.x.
The incorporation of pyrimidine nucleotide precursors into Helicobacter pylori and the activities of enzymes involved in their synthetic pathways were investigated by radioactive tracer analysis and 31P nuclear magnetic resonance spectroscopy. The bacterium was found to take up aspartate and bicarbonate and to incorporate carbon atoms from these precursors into its genomic DNA. Orotate, an intermediate of de novo pyrimidine biosynthesis, and uracil and uridine, precursors for pyrimidine pathways, were also incorporated by the micro-organism. Radiolabelled substrates were used to assess the activities of aspartate transcarbamoylase, orotate phosphoribosyltransferase, orotidylate decarboxylase, CTP synthetase, uracil phosphoribosyltransferase, thymidine kinase and deoxycytidine kinase in bacterial lysates. The study provided evidence for the presence in H. pylori of an operational de novo pathway, and a less active salvage pathway for the biosynthesis of pyrimidine nucleotides.
通过放射性示踪分析和³¹P核磁共振光谱法,研究了嘧啶核苷酸前体掺入幽门螺杆菌的情况以及参与其合成途径的酶的活性。发现该细菌能够摄取天冬氨酸和碳酸氢盐,并将这些前体中的碳原子掺入其基因组DNA中。微生物还能掺入嘧啶从头生物合成的中间体乳清酸以及嘧啶途径的前体尿嘧啶和尿苷。使用放射性标记的底物来评估细菌裂解物中天冬氨酸转氨甲酰酶、乳清酸磷酸核糖基转移酶、乳清酸核苷酸脱羧酶、CTP合成酶、尿嘧啶磷酸核糖基转移酶、胸苷激酶和脱氧胞苷激酶的活性。该研究为幽门螺杆菌中存在有效的嘧啶核苷酸从头合成途径以及活性较低的补救途径提供了证据。