Genetic Engineering of Escherichia coli BL21 (DE3) with a codon-optimized insecticidal toxin complex gene tccZ.

Mosibudi Thabiki Malomane, Kulsum Kondiah, Mahloro Hope Serepa-Dlamini
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Abstract

A toxin complex consists of a high-molecular-weight group of toxins that exhibits insecticidal activity against insect pests. These toxins are a promising alternative to Bacillus thuringiensis (Bt) toxins that have been extensively utilized in insect pest control. Herein, a codon-optimized insecticidal gene (tccZ) (381 bp) identified in Pantoea ananatis strain MHSD5 (a bacterial endophyte previously isolated from Pellaea calomelanos) was ligated into the pET SUMO expression vector and expressed in Escherichia coli BL21 (DE3). We report the success of cloning the tccZ gene into the pET SUMO vector and ultimately the transformation into E. coli BL21 (DE3) competent cells. However, despite conducting a time course of expression as well as isopropyl β-d-1-thiogalactopyranoside (IPTG) dosage optimization to determine optimal conditions for expression, TccZ protein expression could not be detected on Stain-Free and Coomassie-stained SDS-PAGE gels.

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Abstract Image

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密码子优化杀虫毒素复合基因tccZ的大肠杆菌BL21 (DE3)基因工程研究
毒素复合物由高分子量的毒素组成,对害虫具有杀虫活性。这些毒素是苏云金芽孢杆菌(Bacillus thuringiensis, Bt)毒素的一种很有前途的替代品,Bt毒素已被广泛用于害虫防治。本研究将原分离自褐皮霉内生菌Pantoea ananatis菌株MHSD5的密码子优化杀虫基因(tccZ) (381 bp)连接到pET SUMO表达载体上,并在大肠杆菌BL21 (DE3)中表达。我们成功地将tccZ基因克隆到pET SUMO载体中,并最终转化到大肠杆菌BL21 (DE3)感态细胞中。然而,尽管进行了表达时间过程和异丙基β-d-1-巯基半乳糖苷(IPTG)剂量优化以确定最佳表达条件,但在stainfree和comasassie染色的SDS-PAGE凝胶上均未检测到TccZ蛋白的表达。
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