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一种与大肠杆菌σ因子同源的枯草芽孢杆菌发育基因产物。

A developmental gene product of Bacillus subtilis homologous to the sigma factor of Escherichia coli.

作者信息

Stragier P, Bouvier J, Bonamy C, Szulmajster J

出版信息

Nature. 1984;312(5992):376-8. doi: 10.1038/312376a0.

Abstract

Sporulation of Bacillus subtilis involves sequential morphological and biochemical changes and is regulated by specific genes (spo genes) estimated to occupy more than 30 loci. A mutation in any one of these genes blocks the sporulation process at the corresponding developmental stage. Despite intensive genetic studies, the nature and function of the spo gene products remain unknown. Vegetative B. subtilis RNA polymerase core enzyme may interact with several sigma factors and discriminate among different classes of promoters. During sporulation, new polypeptides are associated with the core enzyme which may have a central role in modifying its promoter recognition specificity. As a first step to understanding their function in the switch from vegetative to sporulation mode, several early sporulation genes have been cloned and analysed. Here we report the cloning and nucleotide sequence of the spoIIG gene of B. subtilis. This gene encodes a polypeptide with a predicted relative molecular mass of 27,652 which contains a 65-amino acid region highly homologous to an internal part of the Escherichia coli sigma factor.

摘要

枯草芽孢杆菌的孢子形成涉及一系列形态和生化变化,并受估计占据30多个位点的特定基因(spo基因)调控。这些基因中任何一个发生突变都会在相应发育阶段阻断孢子形成过程。尽管进行了深入的遗传学研究,但spo基因产物的性质和功能仍然未知。营养型枯草芽孢杆菌RNA聚合酶核心酶可能与几种σ因子相互作用,并区分不同类别的启动子。在孢子形成过程中,新的多肽与核心酶结合,这可能在改变其启动子识别特异性方面起核心作用。作为了解它们在从营养型向孢子形成模式转变中功能的第一步,几个早期孢子形成基因已被克隆和分析。在此,我们报告枯草芽孢杆菌spoIIG基因的克隆及核苷酸序列。该基因编码一种预测相对分子质量为27,652的多肽,其中包含一个与大肠杆菌σ因子内部部分高度同源的65个氨基酸区域。

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