Recent Advances in Biocatalytic and Chemoenzymatic Synthesis of Oligonucleotides

IF 2.8 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY ChemBioChem Pub Date : 2025-01-24 DOI:10.1002/cbic.202400987
Pierre Nicolas Bizat, Nazarii Sabat, Marcel Hollenstein
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Abstract

Access to synthetic oligonucleotides is crucial for applications in diagnostics, therapeutics, synthetic biology, and nanotechnology. Traditional solid phase synthesis is limited by sequence length and complexities, low yields, high costs and poor sustainability. Similarly, polymerase-based approaches such as in vitro transcription and primer extension reactions do not permit any control on the positioning of modifications and display poor substrate tolerance. In response, biocatalytic and chemoenzymatic strategies have emerged as promising alternatives, offering selective and efficient pathways for oligonucleotide synthesis. These methods leverage the precision and efficiency of enzymes to construct oligonucleotides with high fidelity. Recent advancements have focused on optimized systems and/or engineered enzymes enabling the incorporation of chemically modified nucleotides. Biocatalytic approaches, particularly those using DNA/RNA polymerases provide advantages in milder reaction conditions and enhanced sustainability. Chemoenzymatic methods, combining chemical synthesis and enzymes, have proven to be effective in overcoming limitations of traditional solid phase synthesis. This review summarizes recent developments in biocatalytic and chemoenzymatic strategies to construct oligonucleotides, highlighting innovations in enzyme engineering, substrate and reaction condition optimization for various applications. We address crucial details of the methods, their advantages, and limitations as well as important insights for future research directions in oligonucleotide production.

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生物催化和化学酶合成寡核苷酸的研究进展。
获得合成寡核苷酸对于诊断、治疗、合成生物学和纳米技术的应用至关重要。传统的固相合成技术受到序列长度和复杂性、收率低、成本高和可持续性差的限制。同样,基于聚合酶的方法,如体外转录和引物延伸反应,不允许对修饰的定位进行任何控制,并且显示出较差的底物耐受性。因此,生物催化和化学酶的策略已经成为有希望的替代方案,为寡核苷酸合成提供了选择性和高效的途径。这些方法利用酶的精度和效率来构建高保真度的寡核苷酸。最近的进展集中在优化系统和/或工程酶上,使化学修饰的核苷酸能够结合。生物催化方法,特别是那些使用DNA/RNA聚合酶的方法,在温和的反应条件和增强的可持续性方面具有优势。化学酶法是化学合成与酶相结合的方法,已被证明能有效地克服传统固相合成的局限性。本文综述了生物催化和化学酶技术在构建寡核苷酸方面的最新进展,重点介绍了酶工程、底物和反应条件优化等方面的创新。我们讨论了这些方法的关键细节,它们的优点和局限性,以及对未来寡核苷酸生产研究方向的重要见解。
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来源期刊
ChemBioChem
ChemBioChem 生物-生化与分子生物学
CiteScore
6.10
自引率
3.10%
发文量
407
审稿时长
1 months
期刊介绍: ChemBioChem (Impact Factor 2018: 2.641) publishes important breakthroughs across all areas at the interface of chemistry and biology, including the fields of chemical biology, bioorganic chemistry, bioinorganic chemistry, synthetic biology, biocatalysis, bionanotechnology, and biomaterials. It is published on behalf of Chemistry Europe, an association of 16 European chemical societies, and supported by the Asian Chemical Editorial Society (ACES).
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