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OVERPRODUCTION OF ENCAPSULATED INSECTICIDAL CRYSTAL PROTEINS IN A BACILLUS THURINGIENSIS SPO0A MUTANT

机译:苏云金芽孢杆菌突变体中包封的杀虫晶体蛋白的过量生产

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The spoOA gene of Bacillus subtilis encodes the key factor involved in the initiation of sporulation. It was previously shown that the B. thuringiensis (Bt) cryIIIA gene, encoding a toxin active against coleopteran larvae, is overexpressed in an spoOA mutant of B. subtilis. In this paper we describe the construction of a Bt spoOA mutant strain and its use to produce insecticidal crystal proteins. The spoOA gene of Bt was cloned and identified by its ability to transform a B. subtilis spoOA mutant to prototrophy. Its nucleotide sequence is homologous to the B. subtilis gene. The spoOA gene was replaced in the Bt genome with a disrupted copy to give an Spo(-) strain unable to initiate sporulation. When the cryIIIA gene was cloned in the Bt spoOA mutant, large amounts of toxins were produced and accumulated to form a large crystal inclusion which remained encapsulated within the ghost cell. These encapsulated toxins were highly active against coleopteran larvae. We anticipate that the cryIIIA expression system and the Bt spoOA mutant will provide a convenient process to generate novel formulations of stabilized and environmentally safe Bt-based biopesticides.
机译:枯草芽孢杆菌的spoOA基因编码参与孢子形成的关键因子。以前表明苏云金芽孢杆菌(Bt)cryIIIA基因编码对鞘翅目幼虫有活性的毒素,在枯草芽孢杆菌的spoOA突变体中过表达。在本文中,我们描述了Bt spoOA突变株的构建及其在生产杀虫晶体蛋白中的用途。克隆并通过其将枯草芽孢杆菌spoOA突变体转化为原养型的能力来鉴定Bt的spoOA基因。其核苷酸序列与枯草芽孢杆菌基因同源。 spoOA基因在Bt基因组中被破坏的拷贝所取代,使Spo(-)菌株无法启动孢子形成。当将cryIIIA基因克隆到Bt spoOA突变体中时,会产生并积累大量毒素,形成大的晶体夹杂物,并保留在幽灵细胞内。这些封装的毒素对鞘翅目幼虫具有很高的活性。我们预期cryIIIA表达系统和Bt spoOA突变体将提供一个方便的过程,以生成稳定且对环境安全的基于Bt的生物农药的新型制剂。

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