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活性位点环中残基 42 的赖氨酸类似物侧链修饰可恢复铜绿假单胞菌 PchB 中的异分支酸-丙酮酸裂解酶活性。

Modification of residue 42 of the active site loop with a lysine-mimetic side chain rescues isochorismate-pyruvate lyase activity in Pseudomonas aeruginosa PchB.

机构信息

Department of Molecular Biosciences, University of Kansas, Lawrence, KS 66045, USA.

出版信息

Biochemistry. 2012 Sep 25;51(38):7525-32. doi: 10.1021/bi300472n. Epub 2012 Sep 12.

Abstract

PchB is an isochorismate-pyruvate lyase from Pseudomonas aeruginosa. A positively charged lysine residue is located in a flexible loop that behaves as a lid to the active site, and the lysine residue is required for efficient production of salicylate. A variant of PchB that lacks the lysine at residue 42 has a reduced catalytic free energy of activation of up to 4.4 kcal/mol. Construction of a lysine isosteric residue bearing a positive charge at the appropriate position leads to the recovery of 2.5-2.7 kcal/mol (about 60%) of the 4.4 kcal/mol by chemical rescue. Exogenous addition of ethylamine to the K42A variant leads to a neglible recovery of activity (0.180 kcal/mol, roughly 7% rescue), whereas addition of propylamine caused an additional modest loss in catalytic power (0.056 kcal/mol, or 2% loss). This is consistent with the view that (a) the lysine-42 residue is required in a specific conformation to stabilize the transition state and (b) the correct conformation is achieved for a lysine-mimetic side chain at site 42 in the course of loop closure, as expected for transition-state stabilization by the side chain ammonio function. That the positive charge is the main effector of transition state stabilization is shown by the construction of a lysine-isosteric residue capable of exerting steric effects and hydrogen bonding but not electrostatic effects, leading to a modest increase of catalytic power (0.267-0.505 kcal/mol of catalytic free energy, or roughly 6-11% rescue).

摘要

PchB 是铜绿假单胞菌中的一种异分支酸-丙酮酸裂解酶。一个带正电荷的赖氨酸残基位于一个灵活的环中,充当活性部位的盖子,赖氨酸残基对于水杨酸的高效生产是必需的。缺乏残基 42 处赖氨酸的 PchB 变体的催化自由能激活降低了多达 4.4 kcal/mol。在适当位置带有正电荷的赖氨酸类似物的构建导致通过化学拯救恢复了 4.4 kcal/mol 的 2.5-2.7 kcal/mol(约 60%)。向 K42A 变体中外源添加乙胺导致活性可忽略不计的恢复(0.180 kcal/mol,约 7%的挽救),而添加丙胺导致催化能力的额外适度损失(0.056 kcal/mol,或 2%的损失)。这与以下观点一致:(a)赖氨酸 42 残基需要在特定构象中以稳定过渡态,并且(b)在环闭合过程中,在 42 位上实现了赖氨酸类似物侧链的正确构象,这与侧链氨功能稳定过渡态相一致。正电荷是稳定过渡态的主要效应物,这可以通过构建能够发挥空间效应和氢键但不能发挥静电效应的赖氨酸类似物残基来证明,这导致催化能力适度增加(催化自由能的 0.267-0.505 kcal/mol,或约 6-11%的挽救)。

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