Quaternary ammonium salt containing soybean oil: An efficient nanosize gene delivery carrier for halophile green microalgal transformation

被引:6
作者
Akbari, Fariba [1 ,2 ]
Khosroushahi, Ahmad Yari [3 ,4 ]
Yeganeh, Hamid [5 ]
机构
[1] Tabriz Univ Med Sci, Fac Pharm, Res Ctr Pharmaceut Nanotechnol, Tabriz, Iran
[2] Tabriz Univ Med Sci, Fac Pharm, Student Res Comm, Tabriz, Iran
[3] Tabriz Univ Med Sci, Fac Pharm, Drug Appl Res Ctr, Tabriz, Iran
[4] Tabriz Univ Med Sci, Fac Pharm, Dept Pharmacognosy, Tabriz, Iran
[5] IPPI, Tehran, Iran
关键词
Dunaliella salina; Green fluorescent protein; Nanolipoplex; Soybean oil; ANTIBACTERIAL POLYURETHANE COATINGS; PYRIDINIUM CATIONIC LIPIDS; TRANSFECTION EFFICIENCY; IN-VITRO; GOLD NANOPARTICLES; POLYAMIDOAMINE DENDRIMERS; FLOW-CYTOMETRY; SINGLE PRIMARY; DNA COMPLEXES; VERNONIA OIL;
D O I
10.1016/j.cbi.2014.10.006
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Dunaliella salina, a halophile green microalga, is considered a robust photobioreactor and a remarkable cost beneficial system for the production of therapeutic recombinant proteins. In this study, with low overall cost, a proper cationic lipid was synthesized from renewable soybean oil as an efficient gene delivery carrier for D. salina cells to create appropriate protein-producing transformed cell lines. To obtain an effective carrier, quaternary ammonium salt containing soybean oil (QASSO) was synthesized through the ring opening reaction of the epoxy groups of epoxidized soybean oil with diethylamine. QASSO was characterized using nuclear magnetic resonance and Fourier-transform infrared instruments. QASSO was used to prepare nanolipoplex construct using plasmid DNA molecules containing green fluorescent protein (GFP) as reporter gene. These nanolipoplexes (QASSO-pGFP, N/P = 3) and QASSO had diameter of 63.62 and 110.63 nm, and zeta potential of -68.89 and 48.25 mV at pH 7.0, respectively. Results indicated the GFP gene expression and cytoplasmic accumulation of GFP protein in the transformants after incubation under desirable conditions for 48 h and 1 week. The transformation efficiency was quantitatively assayed by flow cytometry, which yielded transformations of 58.87% and 48.34% for QASSO and 38.32% and a negligible percentage for Polyfect(R) after 48 h and 1 week incubation, respectively. (C) 2014 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:80 / 89
页数:10
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