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在工程醛缩酶中,亚胺反应中间体的结构解释了其对芳基化酮和醛的碳键合活性。

Structure of the iminium reaction intermediate in an engineered aldolase explains the carboligation activity toward arylated ketones and aldehydes.

机构信息

School of Engineering Sciences in Chemistry, Biotechnology and Health, Department of Biomedical Engineering and Health Systems, KTH Royal Institute of Technology, 14152 Huddinge, Sweden.

Department of Chemistry - BMC, Box 576, SE-751 23 Uppsala, Sweden.

出版信息

Structure. 2024 Sep 5;32(9):1322-1326.e4. doi: 10.1016/j.str.2024.06.011. Epub 2024 Jul 15.

Abstract

Two structures of fructose 6-phosphate aldolase, the wild-type and an engineered variant containing five active-site mutations, have been solved by cryoelectron microscopy (cryo-EM). The engineered variant affords production of aldols from aryl substituted ketones and aldehydes. This structure was solved to a resolution of 3.1 Å and contains the critical iminium reaction intermediate trapped in the active site. This provides new information that rationalizes the acquired substrate scope and aids in formulating hypotheses of the chemical mechanism. A Tyr residue (Y131) is positioned for a role as catalytic acid/base during the aldol reaction and the different structures demonstrate mobility of this amino acid residue. Further engineering of this fructose 6-phosphate aldolase (FSA) variant, guided by this new structure, identified additional FSA variants that display improved carboligation activities with 2-hydroxyacetophenone and phenylacetaldehyde.

摘要

两种果糖 6-磷酸醛缩酶结构,野生型和含有五个活性位点突变的工程变体,已通过冷冻电镜(cryo-EM)解决。该工程变体可从芳基取代的酮和醛中生产 aldols。该结构解析至 3.1Å 的分辨率,并包含在活性位点中捕获的关键亚胺反应中间体。这提供了新的信息,合理化了获得的底物范围,并有助于制定化学机制的假设。Tyr 残基(Y131)在 aldol 反应中充当催化酸碱的作用,并且不同的结构证明了该氨基酸残基的可移动性。通过该新结构指导,对该果糖 6-磷酸醛缩酶(FSA)变体进行进一步工程改造,鉴定出具有改进的 2-羟基苯乙酮和苯乙醛的碳连接活性的其他 FSA 变体。

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