Sun Warren, Shahinas Dea, Bonvin Julie, Hou Wenjuan, Kimber Matthew S, Turnbull Joanne, Christendat Dinesh
Department of Cell and Systems Biology, University of Toronto, Ontario, Canada.
J Biol Chem. 2009 May 8;284(19):13223-32. doi: 10.1074/jbc.M806272200. Epub 2009 Mar 10.
TyrA proteins belong to a family of dehydrogenases that are dedicated to l-tyrosine biosynthesis. The three TyrA subclasses are distinguished by their substrate specificities, namely the prephenate dehydrogenases, the arogenate dehydrogenases, and the cyclohexadienyl dehydrogenases, which utilize prephenate, l-arogenate, or both substrates, respectively. The molecular mechanism responsible for TyrA substrate selectivity and regulation is unknown. To further our understanding of TyrA-catalyzed reactions, we have determined the crystal structures of Aquifex aeolicus prephenate dehydrogenase bound with NAD(+) plus either 4-hydroxyphenylpyuvate, 4-hydroxyphenylpropionate, or l-tyrosine and have used these structures as guides to target active site residues for site-directed mutagenesis. From a combination of mutational and structural analyses, we have demonstrated that His-147 and Arg-250 are key catalytic and binding groups, respectively, and Ser-126 participates in both catalysis and substrate binding through the ligand 4-hydroxyl group. The crystal structure revealed that tyrosine, a known inhibitor, binds directly to the active site of the enzyme and not to an allosteric site. The most interesting finding though, is that mutating His-217 relieved the inhibitory effect of tyrosine on A. aeolicus prephenate dehydrogenase. The identification of a tyrosine-insensitive mutant provides a novel avenue for designing an unregulated enzyme for application in metabolic engineering.
酪氨酸A(TyrA)蛋白属于一类专门用于L-酪氨酸生物合成的脱氢酶家族。TyrA的三个亚类通过其底物特异性来区分,即预苯酸脱氢酶、莽草酸脱氢酶和环己二烯基脱氢酶,它们分别利用预苯酸、L-莽草酸或两种底物。负责TyrA底物选择性和调节的分子机制尚不清楚。为了进一步了解TyrA催化的反应,我们测定了嗜热栖热菌预苯酸脱氢酶与NAD(+)加上4-羟基苯丙酮酸、4-羟基苯丙酸或L-酪氨酸结合的晶体结构,并将这些结构作为指导,针对活性位点残基进行定点诱变。通过突变和结构分析相结合,我们证明了His-147和Arg-250分别是关键的催化基团和结合基团,Ser-126通过配体的4-羟基参与催化和底物结合。晶体结构表明,已知的抑制剂酪氨酸直接结合到酶的活性位点,而不是变构位点。然而,最有趣的发现是,His-217的突变消除了酪氨酸对嗜热栖热菌预苯酸脱氢酶的抑制作用。酪氨酸不敏感突变体的鉴定为设计一种用于代谢工程的无调控酶提供了一条新途径。