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Genetic suppression analysis of non-antibiotic-producing mutants of the Streptomyces coelicolor absA locus

机译:遗传抑制分析中霉菌突变体的突变体突变体

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摘要

The absA locus in Streptomyces coelicolor A3(2) was identified because mutations in it uncoupled sporulation from antibiotic synthesis: absA mutants failed to produce any of the four antibiotics characteristic of S. coelicolor. These mutants are now shown to contain point mutations in the absA1 gene which encodes the histidine kinase sensor-transmitter protein of a two-component signalling system. The absA1 non-antibiotic-producing mutants, which are unpigmented, spontaneously acquire pigmented colony sectors. Genetic analysis established that the pigmented sectors contain second-site suppressive mutations, sab (for suppressor of abs). Phenotypic characterization showed that sab strains produce all four antibiotics; some overproduce antibiotics and are designated Pha, for precocious hyperproduction of antibiotics. A set of sab mutations responsible for suppression was localized by plasmid-mediated and protoplast fusion mapping techniques to the vicinity of the absA locus. DNA cloned from this region was used to construct phage that could transduce sab mutations. Sequence analysis of sab strains defined sab mutations in both the absA1 gene and the absA2 gene; the latter encodes the two-component system’s response regulator.
机译:鉴定了链霉菌菌溶胶A3(2)中的ABSA基因座,因为它在抗生素合成的突变中突变:ABSA突变体未能产生S.共射出的四种抗生素特征。现在显示这些突变体在ABSA1基因中含有点突变,其编码双组分信号系统的组分激酶传感器 - 发射蛋白。 ABSA1非抗生素的突变体,其是未珍明的,自发地获得着色素菌落部门。遗传分析确定着色的扇区含有第二位点抑制突变,SAB(用于ABS的抑制剂)。表型表征显示SAB菌株产生所有四种抗生素;一些过度产量的抗生素并被指定为PHA,用于抗生素的早熟超级化。负责抑制的一组SAB突变通过质粒介导的和原生质体融合映射技术定位于ABSA基因座附近。从该区域克隆的DNA用于构建可以转化SAB突变的噬菌体。 SAB菌株的序列分析在ABSA1基因和ABSα2基因中定义了SAB突变;后者编码双组分系统的响应调节器。

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