Aschern Moritz, Braad Jochem, Milito Alfonsina, Alzuria David, Yang Jae-Seong
Centre for Research in Agricultural Genomics (CRAG), CSIC-IRTA-UAB-UB, Barcelona, Spain.
Doctoral Program of Biotechnology, Faculty of Pharmacy and Food Sciences, Universitat de Barcelona, Barcelona, Spain.
Front Plant Sci. 2025 Mar 7;16:1544873. doi: 10.3389/fpls.2025.1544873. eCollection 2025.
The Modular Cloning (MoClo) toolkit allows for straightforward and flexible construction of genetic modules for gene expression in the microalgal model species, fostering developments in algal biotechnology. Efficiently expressing transgenes from the nuclear genome of requires the proper insertion of introns throughout the respective gene, as it can substantially enhance the gene expression. To facilitate synthetic biology approaches in this microalga, we developed a novel strategy for intron insertion into synthetic DNA fragments. Our method aligns with current MoClo standards, and its feasibility is demonstrated by assembling genes of various lengths and successfully expressing them in . Examples include enhanced expression with increased intron numbers, a fungal luciferase enabling bioluminescence in , and a fungal tryptophan decarboxylase.
模块化克隆(MoClo)工具包能够直接且灵活地构建用于微藻模式物种基因表达的遗传模块,推动藻类生物技术的发展。要从核基因组高效表达转基因,需要在各个基因中适当插入内含子,因为这可显著增强基因表达。为促进在这种微藻中开展合成生物学方法,我们开发了一种将内含子插入合成DNA片段的新策略。我们的方法符合当前MoClo标准,通过组装不同长度的基因并在[具体微藻名称]中成功表达来证明其可行性。实例包括随着内含子数量增加增强[具体基因名称]表达、一种能使[具体微藻名称]产生生物发光的真菌荧光素酶以及一种真菌色氨酸脱羧酶。