摘要:本试验以红色荧光蛋白mRuby2(重组表达质粒pBMR和表达宿主细胞KRX)为供试材料,研究了在不同培养温度及不同诱导表达方法对红色荧光蛋白mRuby2表达的影响,扫描了表达细胞激发波谱和发射波谱,同时在峰值位置进行了单点荧光强度的测定。实验结果表明荧光蛋白mRuby2的激发波长的峰值为561nm,发射波长的峰值为598nm,和文献中的mRuby2纯蛋白质的激发和发射峰略有差异;激发光谱和发射光谱则和文献中的相似,在扫描范围内是单峰的光谱。在比较了24℃和37℃培养温度下三种接种诱导表达方法的差异后,在37℃培养温度下详细地比较了三种接种诱导表达方法关差异,不同的接种诱导表达方法间的荧光强度差异显著。总的说来,单菌落直接接种诱导表达荧光强度显著地高于其它二种接种诱导表达方法。表达细胞经过4℃冰箱保存后荧光强度能显著地增加。25541 毕业论文关键词:红色荧光蛋白;mRuby2;接种培养方法;优化表达。
Optimal expression of red fluorescent protein mRuby2
Abstract: Using the red fluorescent protein mRuby2 (recombinant expression plasmid pBMR in host cell KRX),the effects of culturing temperature and inoculation method on the expression of recombinant mRuby2 were investigated by scanning the excitation spectrum and emission spectrum, and measuring their peak fluorescent brightness. The results showed that the excitation peak of the recombined fluorescent protein mRuby2 was 561 nm, while the emission peak was 598 nm, slightly different from their values of pure protein. Its excitation spectrum and emission spectrum, similar to those of pure protein, were single peak spectrum. After comparing its expressions at 24℃ and 37℃, detailed comparison of three inoculation methods was carried out with 37℃ culturing temperature. Generally, single colony inoculation expression method was significantly better than both ordinary two-step inoculation expression method and one-ring inoculation expression method. The fluorescent brightness could be significantly increased by storing the expression cells in 4℃ refrigerator.
Key words: red fluorescent protein; mRuby2; inoculation method; optimized expression.
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