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Sequence expression and function of the gene for the nonphosphorylating NADP-dependent glyceraldehyde-3-phosphate dehydrogenase of Streptococcus mutans.

机译:变形链球菌的非磷酸化NADP依赖性甘油醛-3-磷酸甘油醛脱氢酶基因的序列表达和功能。

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摘要

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.
机译:我们报告了变形链球菌NG5基因组的2,019-bp区域的测序,该序列包含1,428-bp的开放阅读框(ORF),其推定翻译产物与非磷酸化,NADP依赖性甘油醛-的氨基酸序列具有50%的同一性。玉米和豌豆的3-磷酸脱氢酶(GAPN)。该ORF位于编码磷酸烯醇丙酮酸:糖磷酸转移酶转运系统的酶I的ptsI基因的下游约200bp处。假定的gapN基因已被灭活的突变体BCH150缺乏野生型菌株中存在的GAPN活性,因此可以肯定地将ORF鉴定为变形链球菌gapN基因。变形链球菌的另一种菌株DC10仍具有GAPN活性,该菌株含有插入失活的ptsI基因,而唾液链球菌ATCC 25975仍具有GAPN活性,其在ptsI和gapN基因之间含有插入元件。由于野生型变形链球菌NG5既缺乏葡萄糖6-磷酸脱氢酶又缺乏NADH:NADP氧化还原酶活性,因此依赖NADP的3-磷酸甘油醛脱氢酶作为产生NADPH用于生物合成反应的手段是重要的。

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