State Key Laboratory of Bioreactor Engineering, School of Biotechnology, East China University of Science and Technology, Shanghai 200237, China.
Department of Bioproducts and Biosystems Engineering, University of Minnesota, Twin cities, Saint Paul, MN 55108, USA.
J Biotechnol. 2024 Sep 20;393:91-99. doi: 10.1016/j.jbiotec.2024.07.018. Epub 2024 Jul 25.
Genetic code expansion technology allows the incorporation of unnatural amino acids (UAAs) into proteins, which is useful in protein engineering, synthetic biology, and gene therapy. Despite its potential applications in various species, filamentous fungi remain unexplored. This study aims to address this gap by developing these techniques in Aspergillus nidulans. We introduced an amber stop codon into a specific sequence within the reporter gene expressed in A. nidulans and replaced the anticodon of the fungal tRNA with CUA. This resulted in the synthesis of the target protein, confirming the occurrence of amber suppression in the fungus. When exogenous E. coli tRNA (Ec. tRNA) and E. coli tyrosyl-tRNA (Ec.TyrRS) were introduced into A. nidulans, they successfully synthesized the target protein via amber suppression and were shown to be orthogonal to the fungal translation system. By replacing the wild-type Ec.TyrRS with a mutant with a higher affinity for the UAA O-methyl-L-tyrosine, the fungal system was able to initiate the synthesis of the UAA-labeled protein (UAA-protein). We further increased the expression level of the UAA-protein through several rational modifications. The successful development of a genetic code expansion technique for A. nidulans has introduced a potentially valuable approach to the study of fungal protein structure and function.
遗传密码扩展技术允许将非天然氨基酸(UAAs)掺入蛋白质中,这在蛋白质工程、合成生物学和基因治疗中非常有用。尽管该技术在各种物种中有潜在的应用,但丝状真菌仍未被探索。本研究旨在通过在构巢曲霉中开发这些技术来填补这一空白。我们在构巢曲霉中表达的报告基因的特定序列中引入了一个琥珀终止密码子,并将真菌 tRNA 的反密码子替换为 CUA。这导致目标蛋白的合成,证实了真菌中琥珀抑制的发生。当外源性大肠杆菌 tRNA(Ec. tRNA)和大肠杆菌酪氨酸 tRNA(Ec.TyrRS)被引入构巢曲霉时,它们通过琥珀抑制成功合成了目标蛋白,并被证明与真菌翻译系统正交。通过用对 UAA O-甲基-L-酪氨酸具有更高亲和力的突变体取代野生型 Ec.TyrRS,真菌系统能够启动 UAA 标记蛋白(UAA-蛋白)的合成。我们通过几种合理的修饰进一步提高了 UAA-蛋白的表达水平。构巢曲霉遗传密码扩展技术的成功开发为研究真菌蛋白质结构和功能引入了一种潜在有价值的方法。