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利用无细胞蛋白质合成平台进行天然产物咖啡因的生物合成。

Utilizing a cell-free protein synthesis platform for the biosynthesis of a natural product, caffeine.

作者信息

Ditzel Alexander, Zhao Fanglong, Gao Xue, Phillips George N

机构信息

Department of Chemical and Biomolecular Engineering, Rice University, Houston, TX, USA.

Department of Chemistry, Rice University, Houston, TX, USA.

出版信息

Synth Biol (Oxf). 2023 Dec 22;8(1):ysad017. doi: 10.1093/synbio/ysad017. eCollection 2023.

Abstract

Natural products are a valuable source of pharmaceuticals, providing a majority of the small-molecule drugs in use today. However, their production through organic synthesis or in heterologous hosts can be difficult and time-consuming. Therefore, to allow for easier screening and production of natural products, we demonstrated the use of a cell-free protein synthesis system to partially assemble natural products using S-Adenosyl Methionine (SAM)-dependent methyltransferase enzyme reactions. The tea caffeine synthase, TCS1, was utilized to synthesize caffeine within a cell-free protein synthesis system. Cell-free systems also provide the benefit of allowing the use of substrates that would normally be toxic in a cellular environment to synthesize novel products. However, TCS1 is unable to utilize a compound like S-adenosyl ethionine as a cofactor to create ethylated caffeine analogs. The automation and reduced metabolic engineering requirements of cell-free protein synthesis systems, in combination with other synthesis methods, may enable the more efficient generation of new compounds. .

摘要

天然产物是药物的宝贵来源,提供了当今使用的大多数小分子药物。然而,通过有机合成或在异源宿主中生产它们可能既困难又耗时。因此,为了便于更轻松地筛选和生产天然产物,我们展示了使用无细胞蛋白质合成系统,利用依赖S-腺苷甲硫氨酸(SAM)的甲基转移酶反应来部分组装天然产物。茶咖啡因合酶TCS1被用于在无细胞蛋白质合成系统中合成咖啡因。无细胞系统还具有允许使用通常在细胞环境中有毒的底物来合成新产物的优点。然而,TCS1无法利用诸如S-腺苷乙硫氨酸之类的化合物作为辅助因子来生成乙基化咖啡因类似物。无细胞蛋白质合成系统的自动化和降低的代谢工程要求,与其他合成方法相结合,可能使新化合物的生成更加高效。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/636b/10750991/b5e56b46da78/ysad017f1.jpg

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