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解析乳酸脱氢酶的进化轨迹为变构作用提供了新的见解。

Deciphering Evolutionary Trajectories of Lactate Dehydrogenases Provides New Insights into Allostery.

机构信息

Université Grenoble Alpes, CNRS, CEA, IBS, F-38000 Grenoble, France.

Laboratoire de Biométrie et Biologie Évolutive, Université Claude Bernard Lyon 1, CNRS, UMR5558, Villeurbanne F-69622, France.

出版信息

Mol Biol Evol. 2023 Oct 4;40(10). doi: 10.1093/molbev/msad223.

Abstract

Lactate dehydrogenase (LDH, EC.1.1.127) is an important enzyme engaged in the anaerobic metabolism of cells, catalyzing the conversion of pyruvate to lactate and NADH to NAD+. LDH is a relevant enzyme to investigate structure-function relationships. The present work provides the missing link in our understanding of the evolution of LDHs. This allows to explain (i) the various evolutionary origins of LDHs in eukaryotic cells and their further diversification and (ii) subtle phenotypic modifications with respect to their regulation capacity. We identified a group of cyanobacterial LDHs displaying eukaryotic-like LDH sequence features. The biochemical and structural characterization of Cyanobacterium aponinum LDH, taken as representative, unexpectedly revealed that it displays homotropic and heterotropic activation, typical of an allosteric enzyme, whereas it harbors a long N-terminal extension, a structural feature considered responsible for the lack of allosteric capacity in eukaryotic LDHs. Its crystallographic structure was solved in 2 different configurations typical of the R-active and T-inactive states encountered in allosteric LDHs. Structural comparisons coupled with our evolutionary analyses helped to identify 2 amino acid positions that could have had a major role in the attenuation and extinction of the allosteric activation in eukaryotic LDHs rather than the presence of the N-terminal extension. We tested this hypothesis by site-directed mutagenesis. The resulting C. aponinum LDH mutants displayed reduced allosteric capacity mimicking those encountered in plants and human LDHs. This study provides a new evolutionary scenario of LDHs that unifies descriptions of regulatory properties with structural and mutational patterns of these important enzymes.

摘要

乳酸脱氢酶(LDH,EC.1.1.127)是一种参与细胞无氧代谢的重要酶,催化丙酮酸转化为乳酸和 NADH 转化为 NAD+。LDH 是研究结构-功能关系的相关酶。本研究提供了我们理解 LDH 进化的缺失环节。这使得能够解释(i)LDH 在真核细胞中的各种进化起源及其进一步多样化,以及(ii)与调节能力有关的细微表型修饰。我们鉴定了一组显示出真核样 LDH 序列特征的蓝细菌 LDH。以蓝细菌 Aponinum LDH 为代表的生化和结构特征表明,它显示出同促和异促激活,这是一种变构酶的典型特征,而它具有长的 N 端延伸,这一结构特征被认为是真核 LDH 缺乏变构能力的原因。它的晶体结构以两种不同的构象得到解决,这两种构象分别代表了变构 LDH 中遇到的 R 活性和 T 无活性状态。结构比较结合我们的进化分析有助于确定 2 个氨基酸位置,这些位置可能在真核 LDH 中变构激活的衰减和消失中起主要作用,而不是 N 端延伸的存在。我们通过定点突变测试了这一假设。所得的蓝细菌 Aponinum LDH 突变体显示出变构能力降低,类似于植物和人 LDH 中遇到的情况。本研究提供了 LDH 的新进化情景,将调节特性的描述与这些重要酶的结构和突变模式统一起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/980f/10583557/58de4121a686/msad223f1.jpg

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