Subramaniam P S, Xie G, Xia T, Jensen R A
Department of Microbiology and Cell Science, University of Florida, Gainesville 32611, USA.
J Bacteriol. 1998 Jan;180(1):119-27. doi: 10.1128/JB.180.1.119-127.1998.
3-Deoxy-D-manno-octulosonate 8-phosphate (KDOP) synthase and 3-deoxy-D-arabino-heptulosonate 7-phosphate (DAHP) synthase catalyze similar phosphoenolpyruvate-utilizing reactions. The genome of Neisseria gonorrhoeae contains one gene encoding KDOP synthase and one gene encoding DAHP synthase. Of the two nonhomologous DAHP synthase families known, the N. gonorrhoeae protein belongs to the family I assemblage. KDOP synthase exhibited an ability to replace arabinose-5-P with either erythrose-4-P or ribose-5-P as alternative substrates. The results of periodate oxidation studies suggested that the product formed by KDOP synthase with erythrose-4-P as the substrate was 3-deoxy-D-ribo-heptulosonate 7-P, an isomer of DAHP. As expected, this product was not utilized as a substrate by dehydroquinate synthase. The significance of the ability of KDOP synthase to substitute erythrose-4-P for arabinose-5-P is (i) recognition of the possibility that the KDOP synthase might otherwise be mistaken for a species of DAHP synthase and (ii) the possibility that the broad-specificity type of KDOP synthase might be a relatively vulnerable target for antimicrobial agents which mimic the normal substrates. An analysis of sequences in the database indicates that the family I group of DAHP synthase has a previously unrecognized membership which includes the KDOP synthases. The KDOP synthases fall into a subfamily grouping which includes a small group of DAHP synthases. Thus, family I DAHP synthases separate into two subfamilies, one of which includes the KDOP synthases. The two subfamilies appear to have diverged prior to the acquisition of allosteric-control mechanisms for DAHP synthases. These allosteric control specificities are highly diverse and correlate with the presence of N-terminal extensions which lack homology with one another.
3-脱氧-D-甘露辛酮糖酸8-磷酸(KDOP)合酶和3-脱氧-D-阿拉伯庚酮糖酸7-磷酸(DAHP)合酶催化相似的利用磷酸烯醇丙酮酸的反应。淋病奈瑟菌的基因组包含一个编码KDOP合酶的基因和一个编码DAHP合酶的基因。在已知的两个非同源DAHP合酶家族中,淋病奈瑟菌蛋白属于家族I类群。KDOP合酶表现出能用赤藓糖-4-磷酸或核糖-5-磷酸替代阿拉伯糖-5-磷酸作为替代底物的能力。高碘酸盐氧化研究结果表明,KDOP合酶以赤藓糖-4-磷酸为底物形成的产物是3-脱氧-D-核糖庚酮糖酸7-磷酸,它是DAHP的一种异构体。不出所料,脱氢奎尼酸合酶不能利用该产物作为底物。KDOP合酶能用赤藓糖-4-磷酸替代阿拉伯糖-5-磷酸的意义在于:(i)认识到KDOP合酶可能会被误认为是某种DAHP合酶的可能性;(ii)KDOP合酶的广泛特异性类型可能是模仿正常底物的抗菌剂相对易攻击的靶点。数据库序列分析表明,DAHP合酶的家族I类群有一个先前未被识别的成员,其中包括KDOP合酶。KDOP合酶属于一个亚家族群,该亚家族群包括一小部分DAHP合酶。因此,家族I类DAHP合酶分为两个亚家族,其中一个亚家族包括KDOP合酶。这两个亚家族似乎在获得DAHP合酶的变构调节机制之前就已经分化。这些变构调节特异性高度多样,并且与彼此缺乏同源性的N端延伸的存在相关。