Islam Md Monirul, Odahara Masaki, Yoshizumi Takeshi, Oikawa Kazusato, Kimura Mitsuhiro, Su'etsugu Masayuki, Numata Keiji
Biomacromolecules Research Team , RIKEN Center for Sustainable Resource Science , 2-1 Hirosawa , Wako-shi , Saitama 351-0198 , Japan.
Department of Life Science, College of Science , Rikkyo University , 3-34-1 Nishi-Ikebukuro , Toshima-ku, Tokyo , 171-8501 , Japan.
ACS Synth Biol. 2019 May 17;8(5):1215-1218. doi: 10.1021/acssynbio.9b00055. Epub 2019 Apr 22.
The highly efficient genetic transformation of cells is essential for synthetic biology procedures, especially for the transformation of large gene clusters. In this technical note, we present a novel cell-penetrating peptide (CPP)-mediated large-sized plasmid DNA transformation system for Escherichia coli. A large plasmid (pMSR227, 205 kb) was complexed with cationic peptides containing a CPP motif and was successfully transformed into E. coli cells. The transformants containing the plasmid DNA exhibited expression of a reporter gene encoding a red fluorescent protein. The transformation efficiency was significantly higher than that obtained using the heat-shock method and was similar to that of electroporation. This technique can be used as a platform for the simple and highly efficient transformation of large DNA molecules under mild conditions without causing significant damage to DNA, accelerating synthetic biology investigations for the design of genetically engineered microorganisms for industrial purposes.
细胞的高效遗传转化对于合成生物学程序至关重要,特别是对于大基因簇的转化。在本技术说明中,我们提出了一种用于大肠杆菌的新型细胞穿透肽(CPP)介导的大尺寸质粒DNA转化系统。一个大质粒(pMSR227,205 kb)与含有CPP基序的阳离子肽复合,并成功转化到大肠杆菌细胞中。含有质粒DNA的转化子表现出编码红色荧光蛋白的报告基因的表达。转化效率显著高于热休克法,与电穿孔法相似。该技术可作为一个平台,在温和条件下对大DNA分子进行简单高效的转化,而不会对DNA造成重大损伤,从而加速用于工业目的的基因工程微生物设计的合成生物学研究。