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首页> 外文期刊>Journal of applied microbiology >Cloning and study of the expression of a novel cry1 la-type gene from Bacillus thuringiensis subsp. kurstaki
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Cloning and study of the expression of a novel cry1 la-type gene from Bacillus thuringiensis subsp. kurstaki

机译:苏云金芽孢杆菌亚种cry11a新型基因的克隆与表达研究。库尔斯塔基

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Aims: Cloning and expression of a new ciy1 Ia-type gene of Bacillus thuringiensis. Methods and Results: PCR amplification, using gene cry1 I-specific primers revealed the presence of such a gene in the strain BNS3 of Bacillus thuringiensis subsp. kurstaki. The cloning and sequencing from BNS3 of the cry1 Ia-type gene, called crybns3-3, showed an open reading frame of 2160-bp, encoding a protein of 719 amino acid residues. Both nucleotide and amino acid sequences similarity analysis revealed that the crybns3-3 is a new cry1 Ia-type gene, presenting several differences from the cry1 Ia-type genes. The study of the expression of crybns3-3 by Northern blot and RT-PCR showed that it was transcribed. The expression of crybns3-3 under the control of BtI and BtII promoters revealed that Crybns3-3 would co-crystallize with the endogenous delta-endotoxins. Conclusions: crybns3-3 is a novel oylla gene isolated from B. thuringiensis subsp. kurstaki strain BNS3. Significance and Impact of the Study: The characteristics of crybns3-3 indicate that it is a new cry1 Ia-type gene. Amino acid residue substitutions presented in Crybns3-3 could be exploited for both toxicity and specificity studies. Crybns3-3 would interact and co-crystallize at least partially with the endogenous delta-endotoxins of BNS3, and then participate in the formation of the parasporal crystal inclusions.
机译:目的:苏云金芽孢杆菌新的ciy1 Ia型基因的克隆和表达。方法与结果:使用基因cry11 I特异性引物进行PCR扩增,发现该基因在苏云金芽孢杆菌Bsp3菌株中存在。库尔斯塔基。从BNS3的cry1 Ia型基因crybns3-3的克隆和测序显示2160 bp的开放阅读框,编码719个氨基酸残基的蛋白质。核苷酸和氨基酸序列相似性分析均表明,crybns3-3是一个新的cry1 Ia型基因,与cry1 Ia型基因存在若干差异。通过Northern印迹和RT-PCR对crybns3-3表达的研究表明它是被转录的。在BtI和BtII启动子的控制下,crybns3-3的表达表明Crybns3-3与内源性δ-内毒素共结晶。结论:crybns3-3是从苏云金芽孢杆菌亚种中分离得到的一种新的oylla基因。库尔斯塔基菌株BNS3。研究的意义和影响:crybns3-3的特征表明它是一个新的cry1 Ia型基因。 Crybns3-3中提出的氨基酸残基取代可用于毒性和特异性研究。 Crybns3-3将与BNS3的内源性δ-内毒素相互作用并至少部分共结晶,然后参与孢子旁晶体包裹体的形成。

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