Daugherty M, Vonstein V, Overbeek R, Osterman A
Integrated Genomics Inc., Chicago, Illinois 60612, USA.
J Bacteriol. 2001 Jan;183(1):292-300. doi: 10.1128/JB.183.1.292-300.2001.
Shikimate kinase (EC 2.7.1.71) is a committed enzyme in the seven-step biosynthesis of chorismate, a major precursor of aromatic amino acids and many other aromatic compounds. Genes for all enzymes of the chorismate pathway except shikimate kinase are found in archaeal genomes by sequence homology to their bacterial counterparts. In this study, a conserved archaeal gene (gi1500322 in Methanococcus jannaschii) was identified as the best candidate for the missing shikimate kinase gene by the analysis of chromosomal clustering of chorismate biosynthetic genes. The encoded hypothetical protein, with no sequence similarity to bacterial and eukaryotic shikimate kinases, is distantly related to homoserine kinases (EC 2.7.1.39) of the GHMP-kinase superfamily. The latter functionality in M. jannaschii is assigned to another gene (gi591748), in agreement with sequence similarity and chromosomal clustering analysis. Both archaeal proteins, overexpressed in Escherichia coli and purified to homogeneity, displayed activity of the predicted type, with steady-state kinetic parameters similar to those of the corresponding bacterial kinases: K(m,shikimate) = 414 +/- 33 microM, K(m,ATP) = 48 +/- 4 microM, and k(cat) = 57 +/- 2 s(-1) for the predicted shikimate kinase and K(m,homoserine) = 188 +/- 37 microM, K(m,ATP) = 101 +/- 7 microM, and k(cat) = 28 +/- 1 s(-1) for the homoserine kinase. No overlapping activity could be detected between shikimate kinase and homoserine kinase, both revealing a >1,000-fold preference for their own specific substrates. The case of archaeal shikimate kinase illustrates the efficacy of techniques based on reconstruction of metabolism from genomic data and analysis of gene clustering on chromosomes in finding missing genes.
莽草酸激酶(EC 2.7.1.71)是分支酸七步生物合成途径中的一种关键酶,分支酸是芳香族氨基酸和许多其他芳香族化合物的主要前体。除莽草酸激酶外,分支酸途径中所有酶的基因都可通过与细菌对应基因的序列同源性在古细菌基因组中找到。在本研究中,通过对分支酸生物合成基因的染色体聚类分析,一个保守的古细菌基因(詹氏甲烷球菌中的gi1500322)被确定为缺失的莽草酸激酶基因的最佳候选基因。编码的假定蛋白与细菌和真核生物的莽草酸激酶没有序列相似性,但与GHMP激酶超家族的高丝氨酸激酶(EC 2.7.1.39)有较远的亲缘关系。詹氏甲烷球菌中的后一种功能被指定给另一个基因(gi591748),这与序列相似性和染色体聚类分析结果一致。这两种在大肠杆菌中过表达并纯化至均一的古细菌蛋白都表现出预测类型的活性,其稳态动力学参数与相应细菌激酶的相似:预测的莽草酸激酶的K(m,莽草酸)=414±33μM,K(m,ATP)=48±4μM,k(cat)=57±2 s(-1);高丝氨酸激酶的K(m,高丝氨酸)=188±37μM,K(m,ATP)=101±7μM,k(cat)=28±1 s(-1)。在莽草酸激酶和高丝氨酸激酶之间未检测到重叠活性,两者都显示出对其自身特定底物有>1000倍的偏好。古细菌莽草酸激酶的例子说明了基于从基因组数据重建代谢和分析染色体上的基因聚类来寻找缺失基因的技术的有效性。