Cell-Penetrating Peptide-Mediated Transformation of Large Plasmid DNA into Escherichia coli

被引:13
作者
Islam, Md Monirul [1 ,3 ]
Odahara, Masaki [1 ]
Yoshizumi, Takeshi [1 ,4 ]
Oikawa, Kazusato [1 ]
Kimura, Mitsuhiro [1 ,4 ]
Su'etsugu, Masayuki [2 ]
Numata, Keiji [1 ]
机构
[1] RIKEN, Ctr Sustainable Resource Sci, Biomacromol Res Team, 2-1 Hirosawa, Wako, Saitama 3510198, Japan
[2] Rikkyo Univ, Coll Sci, Dept Life Sci, Toshima Ku, 3-34-1 Nishi Ikebukuro, Tokyo 1718501, Japan
[3] Univ Suwon, Dept Biosci & Biotechnol, Hwaseong City 18323, Gyeonggi Do, South Korea
[4] Takasaki Univ Hlth & Welf, 37-1 Nakaorui Machi, Takasaki, Gunma 3700033, Japan
来源
ACS SYNTHETIC BIOLOGY | 2019年 / 8卷 / 05期
关键词
cell-penetrating peptide; Escherichia coli; large-sized plasmid DNA; genetic material transformation; GENE DELIVERY; PLANT-CELLS; PLATFORM; VECTORS; SYSTEM; DEVICE; LYSIS;
D O I
10.1021/acssynbio.9b00055
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
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 industrial purposes.
引用
收藏
页码:1215 / 1218
页数:7
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