Lee Mihwa, Maher Megan J, Guss J Mitchell
School of Molecular and Microbial Biosciences (G08), University of Sydney, NSW 2006, Australia.
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2007 Mar 1;63(Pt 3):154-61. doi: 10.1107/S1744309107004009. Epub 2007 Feb 13.
Crystals of a single-point mutant (T109S) of Escherichia coli dihydroorotase (DHOase) with diminished activity grown in the presence of L-dihydroorotate (L-DHO) are tetragonal, with a monomer in the asymmetric unit. These crystals are extremely unstable and disintegrate shortly after formation, which is followed by the growth of orthorhombic crystals from the remnants of the tetragonal crystals or at new nucleation sites. Orthorhombic crystals, for which a structure has previously been reported [Thoden et al. (2001), Biochemistry, 40, 6989-6997; Lee et al. (2005), J. Mol. Biol. 348, 523-533], contain a dimer of DHOase in the asymmetric unit; the active site of one monomer contains the substrate N-carbamyl-L-aspartate (L-CA-asp) and the active site of the other monomer contains the product of the reaction, L-DHO. In the subunit with L-DHO in the active site, a surface loop (residues 105-115) is 'open'. In the other subunit, with L-CA-asp in the active site, the loop folds inwards, forming specific hydrogen bonds from the loop to the L-CA-asp. The tetragonal crystal form can be stabilized by crystallization in the presence of the inhibitor 5-fluoroorotate (FOA), a product (L-DHO) mimic. Crystals of the complex of T109S DHOase with FOA are tetragonal, space group P4(1)2(1)2, with unit-cell parameters a = b = 72.6, c = 176.1 A. The structure has been refined to R and R(free) values of 0.218 and 0.257, despite severe anisotropy of the diffraction. In this structure, the flexible loops are both in the 'open' conformation, which is consistent with FOA, like L-DHO, binding at both sites. The behaviour of the T109S mutant crystals of DHOase in the presence of L-DHO is explained by initial binding of L-DHO to both subunits, followed by slow conversion to L-CA-asp, with consequent movement of the flexible loop and dissolution of the crystals. Orthorhombic crystals are then able to grow in the presence of L-DHO and L-CA-asp.
在L - 二氢乳清酸(L - DHO)存在下生长的、活性降低的大肠杆菌二氢乳清酸酶(DHOase)单点突变体(T109S)晶体为四方晶系,不对称单元中有一个单体。这些晶体极其不稳定,形成后不久就会解体,随后四方晶体的残余部分或在新的成核位点会生长出正交晶体。之前已报道过正交晶体的结构[索登等人(2001年),《生物化学》,40卷,6989 - 6997页;李等人(2005年),《分子生物学杂志》,348卷,523 - 533页],其不对称单元中包含DHOase的二聚体;一个单体的活性位点含有底物N - 氨甲酰 - L - 天冬氨酸(L - CA - asp),另一个单体的活性位点含有反应产物L - DHO。在活性位点含有L - DHO的亚基中,一个表面环(残基105 - 115)是“开放的”。在另一个活性位点含有L - CA - asp的亚基中,该环向内折叠,从环到L - CA - asp形成特定的氢键。四方晶型可以通过在抑制剂5 - 氟乳清酸(FOA,一种产物(L - DHO)模拟物)存在下结晶来稳定。T109S DHOase与FOA复合物的晶体为四方晶系,空间群P4(1)2(1)2,晶胞参数a = b = 72.6,c = 176.1 Å。尽管衍射存在严重的各向异性,但该结构已精修至R和R(自由)值分别为0.218和0.257。在该结构中,柔性环均处于“开放”构象,这与FOA(与L - DHO一样)在两个位点结合是一致的。DHOase的T109S突变体晶体在L - DHO存在下的行为可以解释为L - DHO最初与两个亚基结合,随后缓慢转化为L - CA - asp,从而导致柔性环移动和晶体溶解。然后正交晶体能够在L - DHO和L - CA - asp存在下生长。