Engineering of a Malonyl-CoA Ligase for Production of Fluorinated Polyketide Extender Units.

IF 2.6 4区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY ChemBioChem Pub Date : 2024-07-22 DOI:10.1002/cbic.202400532
Thaddeus Q Paulsel, Gavin John Williams
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Abstract

Enzymatic platforms for producing malonyl-CoA-based extender units required for polyketide biosynthesis are often based on malonyl-CoA ligases such as MatB from Rhizobium trifolii and Rhodopseudomonas palustris. However, despite broad interest in the fluorination of polyketides and prior success with engineering MatB homologs, the suitability of MatB for accessing the tertiary substituted fluoromethylmalonyl-CoA needed to produce flurithromycin and solithromycin has not yet been reported. Herein, we report the structure-guided engineering of a MatB homolog to optimize the production of fluoromethylmalonyl-CoA, resulting in a variant with increased conversion and providing a platform to produce a suitable building block mixture for fluorinated macrolide production. Additionally, the mutant demonstrated broad utility for various substituted malonyl-CoAs. The MatB mutant sets the stage to access fluorinated macrolides by coupling it with altered PKS machinery to install fluorinated malonyl-CoA into macrolide scaffolds.

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工程化丙二酰-CoA 连接酶用于生产含氟多酮扩展单元。
生产多酮生物合成所需的丙二酰-CoA 延伸单元的酶平台通常基于丙二酰-CoA 连接酶,如来自三叶根瘤菌(Rhizobium trifolii)和棕榈假单胞菌(Rhodopseudomonas palustris)的 MatB。然而,尽管人们对多酮苷的氟化反应有着广泛的兴趣,而且之前在 MatB 同源物的工程化方面也取得了成功,但 MatB 是否适合获取生产氟霉素和索利霉素所需的三级取代氟甲基丙二酰-CoA 还未见报道。在此,我们报告了对 MatB 同源物进行结构指导工程化以优化氟甲基丙二酰基-CoA 的生产,从而产生了一种转化率更高的变体,并为生产含氟大环内酯的合适构件混合物提供了一个平台。此外,该突变体还显示出对各种取代丙二酰-CoAs 的广泛用途。MatB 突变体为获得含氟大环内酯奠定了基础,通过将其与改变的 PKS 机制耦合,将含氟丙二酰-CoA 安装到大环内酯支架中。
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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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