Pope M K, Green B, Westpheling J
Genetics Department, University of Georgia, Athens 30302, USA.
J Bacteriol. 1998 Mar;180(6):1556-62. doi: 10.1128/JB.180.6.1556-1562.1998.
Mutants blocked at the earliest stage of morphological development in Streptomyces species are called bld mutants. These mutants are pleiotropically defective in the initiation of development, the ability to produce antibiotics, the ability to regulate carbon utilization, and the ability to send and/or respond to extracellular signals. Here we report the identification and partial characterization of a 99-amino-acid open reading frame (ORF99) that is capable of restoring morphogenesis, antibiotic production, and catabolite control to all of the bldB mutants. Of the existing bld mutants, bldB is of special interest because the phenotype of this mutant is the most pleiotropic. DNA sequence analysis of ORF99 from each of the existing bldB mutants identified base changes either within the coding region of the predicted protein or in the regulatory region of the gene. Primer extension analysis identified an apparent transcription start site. A promoter fusion to the xylE reporter gene showed that expression of bldB is apparently temporally regulated and that the bldB gene product is involved in the regulation of its own expression.
在链霉菌属物种中,在形态发育最早阶段受阻的突变体被称为bld突变体。这些突变体在发育起始、产生抗生素的能力、调节碳利用的能力以及发送和/或响应细胞外信号的能力方面存在多效性缺陷。在此,我们报告了一个99个氨基酸的开放阅读框(ORF99)的鉴定和部分特征,该阅读框能够恢复所有bldB突变体的形态发生、抗生素产生和分解代谢控制。在现有的bld突变体中,bldB特别引人关注,因为该突变体的表型具有最强的多效性。对每个现有bldB突变体的ORF99进行DNA序列分析,确定了预测蛋白质编码区域内或基因调控区域的碱基变化。引物延伸分析确定了一个明显的转录起始位点。与xylE报告基因的启动子融合表明,bldB的表达明显受到时间调控,并且bldB基因产物参与其自身表达的调控。