首页> 外文会议>International Conference on Bioinformatics and Biomedical Engineering >Cloning and expression of a thermostable pullulanase gene from Thermotoga maritima MSB8 in Bacillus subtilis WB600
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Cloning and expression of a thermostable pullulanase gene from Thermotoga maritima MSB8 in Bacillus subtilis WB600

机译:来自枯草芽孢杆菌WB600的Thermotoga Maritima MSB8克隆和表达HotiToolaba Maritima MSB8

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The pulA gene enconding a thermostable pullulanase of 844 amino acids was cloned by PCR amplification from the genomic DNA of Thermotoga maritima MSB8. We successfully expressed the pulA gene in a protease-deficient strain Bacillus subtilis WB600, and the expressed pullulanase was secreted into the culture broth. Preliminary results showed that the pullulanase exhibited optimal activity at 90°C, and was stable at the temperature range from 30 to 80°C for 30 min. The stable pH range for this pullulanase was from 5.5 to 7.0, with an optimum at pH6.0.
机译:通过来自Thermotoga Maritima MSB8的基因组DNA的PCR扩增克隆了与844个氨基酸的热稳定胶酶的普拉基因克隆。我们在蛋白酶缺陷菌株枯草芽孢杆菌WB600中成功地表达了普拉基因,并且表达的淀粉酶分泌到培养液中。初步结果表明,淀粉酶在90℃下表现出最佳活性,并在30至80℃的温度范围内稳定30分钟。该淀粉酶的稳定pH范围为5.5至7.0,在pH6.0处最佳。

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