Harnessing the Power of SMART Single-Molecule Display for Enzyme Evolution: A Focus on Oxidase

IF 4.5 2区 生物学 Q1 BIOCHEMICAL RESEARCH METHODS
ACS Synthetic Biology Pub Date : 2026-08-21 Epub Date: 2026-02-23 DOI:10.1021/acssynbio.5c00968
Kalhari Munaweera, Nana Odake, Hannah Patricia Halim, Kakeru Ikeda, Bo Zhu, Maurizio Camagna, Tomokazu Ito, Tetsuya Kitaguchi, Naoto Nemoto, Hideo Nakano, Jasmina Damnjanović
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引用次数: 0

Abstract

For a rapid and cost-effective evolution of tailor-made enzymes, we established a high-throughput in vitro selection platform named SMART (Single-Molecule Assay on Ribonucleic acid by Translated product), integrating mRNA display, next-generation sequencing, and bioinformatics. SMART represents a versatile system where a module termed an auxiliary unit allows enzyme-specific selection under various experimental conditions. Here, we report on the establishment of SMART for oxidases using a model enzyme, Schizosaccharomyces pombed-amino acid oxidase (SpDAAO), and ascorbate peroxidase 2 as the auxiliary enzyme to detect hydrogen peroxide produced by the oxidase, and mediate biotinylation of active single-molecule display complexes. As a proof-of-concept, a library including site-saturation mutagenesis at the catalytic residue Y232 of SpDAAO was subjected to a single SMART selection round, yielding enrichment of the active enzyme variant. The results demonstrate the utility of SMART as a fast, robust, and efficient platform with the potential of customization for other enzyme chemistries through appropriate modifications of the auxiliary unit. Using SMART, desired enzyme variants can be selected in just a few hours by a single person without the need for costly equipment or any bias or limitations.

利用SMART单分子显示的力量促进酶的进化:以氧化酶为重点。
为了快速、低成本地进化定制酶,我们建立了一个高通量的体外选择平台SMART (Single-Molecule Assay on ribonucicacid by translingproduct),整合了mRNA展示、下一代测序和生物信息学。SMART代表了一个多功能系统,其中一个模块称为辅助单元,允许在各种实验条件下进行酶特异性选择。在这里,我们报道了用一种模式酶——裂糖酵母d-氨基酸氧化酶(SpDAAO)和抗坏血酸过氧化物酶2作为辅助酶来检测氧化酶产生的过氧化氢,并介导活性单分子显示复合物的生物素化,从而建立氧化酶SMART。作为概念验证,一个包含SpDAAO催化残基Y232位点饱和突变的文库进行了一次SMART选择,产生了活性酶变体的富集。结果表明,SMART是一个快速、稳健、高效的平台,通过适当修改辅助单元,具有定制其他酶化学的潜力。使用SMART,一个人可以在短短几个小时内选择所需的酶变体,而不需要昂贵的设备或任何偏见或限制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
8.00
自引率
10.60%
发文量
380
审稿时长
6-12 weeks
期刊介绍: The journal is particularly interested in studies on the design and synthesis of new genetic circuits and gene products; computational methods in the design of systems; and integrative applied approaches to understanding disease and metabolism. Topics may include, but are not limited to: Design and optimization of genetic systems Genetic circuit design and their principles for their organization into programs Computational methods to aid the design of genetic systems Experimental methods to quantify genetic parts, circuits, and metabolic fluxes Genetic parts libraries: their creation, analysis, and ontological representation Protein engineering including computational design Metabolic engineering and cellular manufacturing, including biomass conversion Natural product access, engineering, and production Creative and innovative applications of cellular programming Medical applications, tissue engineering, and the programming of therapeutic cells Minimal cell design and construction Genomics and genome replacement strategies Viral engineering Automated and robotic assembly platforms for synthetic biology DNA synthesis methodologies Metagenomics and synthetic metagenomic analysis Bioinformatics applied to gene discovery, chemoinformatics, and pathway construction Gene optimization Methods for genome-scale measurements of transcription and metabolomics Systems biology and methods to integrate multiple data sources in vitro and cell-free synthetic biology and molecular programming Nucleic acid engineering.
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