首页> 美国卫生研究院文献>Journal of Bacteriology >Transcriptional regulation of the cryIVD gene operon from Bacillus thuringiensis subsp. israelensis.
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Transcriptional regulation of the cryIVD gene operon from Bacillus thuringiensis subsp. israelensis.

机译:苏云金芽孢杆菌亚种cryIVD基因操纵子的转录调控。以色列。

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摘要

The CryIVD protein is involved in the overall toxicity of the Bacillus thuringiensis subsp. israelensis parasporal inclusions and is one of the four major components of the crystals. Determination of the DNA sequence indicated that the cryIVD gene is the second gene of an operon which includes three genes. The first one encodes a 19-kDa polypeptide and has sequence homology with the orf1 gene of the Bacillus thuringiensis cryIIA and cryIIC operons. The second and third genes have already been identified and encode the CryIVD crystal protein and the P20 polypeptide, respectively. The promoter region was located by deletion analysis, and the 5' end of the mRNA was determined by primer extension mapping. Transcription of the cryIVD gene in B. thuringiensis subsp. israelensis strains is induced 9 h after the beginning of sporulation. Sequence analysis indicated two potential promoters, a strong one and a weak one, recognized respectively by the RNA polymerase associated with the sigma 35 or the sigma 28 factor of B. thuringiensis (sigma E and sigma K of Bacillus subtilis, respectively). Transcriptional lacZ fusion integrated in single copy into the chromosome of various B. subtilis sporulation mutants confirmed the sigma E dependence of cryIVD gene transcription.
机译:CryIVD蛋白与苏云金芽孢杆菌亚种的整体毒性有关。以色列伴孢子夹杂物,是晶体的四个主要成分之一。 DNA序列的确定表明cryIVD基因是操纵子的第二个基因,其包含三个基因。第一个编码19-kDa多肽,并与苏云金芽胞杆菌cryIIA和cryIIC操纵子的orf1基因具有序列同源性。第二个和第三个基因已经被鉴定出并分别编码CryIVD晶体蛋白和P20多肽。通过缺失分析定位启动子区域,并通过引物延伸作图确定mRNA的5'末端。苏云金芽孢杆菌亚种中cryIVD基因的转录孢子形成后9小时诱导出以色列菌株。序列分析表明,两个潜在的启动子,一个强启动子和一个弱启动子,分别被与苏云金芽孢杆菌的σ35或σ28因子相关的RNA聚合酶识别(分别为枯草芽孢杆菌的σE和σK)。转录lacZ融合单拷贝整合到各种枯草芽孢杆菌孢子突变体的染色体中,证实了cryIVD基因转录的σE依赖性。

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