Boyd D A, Cvitkovitch D G, Hamilton I R
Department of Oral Biology, University of Manitoba, Winnipeg, Canada.
J Bacteriol. 1995 May;177(10):2622-7. doi: 10.1128/jb.177.10.2622-2627.1995.
We report the sequencing of a 2,019-bp region of the Streptococcus mutans NG5 genome which contains a 1,428-bp open reading frame (ORF) whose putative translation product had 50% identity to the amino acid sequences of the nonphosphorylating, NADP-dependent glyceraldehyde-3-phosphate dehydrogenases (GAPN) from maize and pea. This ORF is located approximately 200 bp downstream of the ptsI gene coding for enzyme I of the phosphoenolpyruvate:sugar phosphotransferase transport system. Mutant BCH150, in which the putative gapN gene had been inactivated, lacked GAPN activity that was present in the wild-type strain, thus positively identifying the ORF as the S. mutans gapN gene. Another strain of S. mutans, DC10, which contains an insertionally inactivated ptsI gene, still possessed GAPN activity, as did S. salivarius ATCC 25975, which contains an insertion element between the ptsI and gapN genes. Since the wild-type S. mutans NG5 lacks both glucose-6-phosphate dehydrogenase and NADH:NADP oxidoreductase activities, the NADP-dependent glyceraldehyde-3-phosphate dehydrogenase is important as a means of generating NADPH for biosynthetic reactions.
我们报道了变形链球菌NG5基因组一个2019 bp区域的测序结果,该区域包含一个1428 bp的开放阅读框(ORF),其推定的翻译产物与玉米和豌豆中不依赖磷酸化、依赖NADP的甘油醛-3-磷酸脱氢酶(GAPN)的氨基酸序列有50%的同一性。这个ORF位于编码磷酸烯醇丙酮酸:糖磷酸转移酶转运系统中酶I的ptsI基因下游约200 bp处。突变体BCH150中推定的gapN基因已失活,缺乏野生型菌株中存在的GAPN活性,从而明确鉴定该ORF为变形链球菌gapN基因。变形链球菌的另一个菌株DC10含有一个插入失活的ptsI基因,仍具有GAPN活性,唾液链球菌ATCC 25975也一样,它在ptsI和gapN基因之间含有一个插入元件。由于野生型变形链球菌NG5缺乏葡萄糖-6-磷酸脱氢酶和NADH:NADP氧化还原酶活性,依赖NADP的甘油醛-3-磷酸脱氢酶作为为生物合成反应生成NADPH的一种方式很重要。