Department of Chemical Engineering, Texas A&M University, College Station, Texas 77843, United States.
Department of Biology, Texas A&M University, College Station, Texas 77843, United States.
ACS Synth Biol. 2021 Sep 17;10(9):2151-2158. doi: 10.1021/acssynbio.1c00228. Epub 2021 Aug 16.
Benzoxazoles are frequently found in synthetic pharmaceuticals and medicinally active natural products. To facilitate benzoxazole-based drug development, an eco-friendly and rapid platform for benzoxazole production is required. In this study, we have completed the biosynthesis of benzoxazoles in by coexpressing the minimal set of enzymes required for their biosynthesis. Moreover, by coupling this -based platform with precursor-directed biosynthesis, we have shown that the benzoxazole biosynthetic system is highly promiscuous in incorporating fluorine, chlorine, nitrile, picolinic, and alkyne functionalities into the scaffold. Our -based system thus paves the way for straightforward generation of novel benzoxazole analogues through future protein engineering and combinatorial biosynthesis.
苯并恶唑类化合物广泛存在于合成药物和药用活性天然产物中。为了促进基于苯并恶唑的药物开发,需要一个环保且快速的苯并恶唑生产平台。在这项研究中,我们通过共表达苯并恶唑生物合成所需的最小酶组,完成了 中苯并恶唑的生物合成。此外,通过将基于 的平台与前体定向生物合成相耦合,我们表明苯并恶唑生物合成系统在将氟、氯、腈、吡啶甲酸和炔烃官能团掺入支架中具有很高的混杂性。因此,我们的 系统为通过未来的蛋白质工程和组合生物合成直接生成新型苯并恶唑类似物铺平了道路。