Novakova Renata, Homerova Dagmar, Feckova Lubomira, Kormanec Jan
Institute of Molecular Biology, Centre of Excellence for Molecular Medicine, Slovak Academy of Sciences, Dubravska cesta 21, 845 51 Bratislava, Slovak Republic.
Microbiology (Reading). 2005 Aug;151(Pt 8):2693-2706. doi: 10.1099/mic.0.28019-0.
A gene, aur1P, encoding a protein similar to the response regulators of bacterial two-component signal transduction systems, was identified upstream of the aur1 polyketide gene cluster involved in biosynthesis of the angucycline-like antibiotic auricin in Streptomyces aureofaciens CCM 3239. Expression of the gene was directed by a single promoter, aur1Pp, which was transcribed at low levels during the exponential phase and induced just before the stationary phase. A divergently transcribed gene, aur1R, has been identified upstream of aur1P, encoding a protein homologous to transcriptional repressors of the TetR family. The aur1P gene was disrupted in the S. aureofaciens CCM 3239 chromosome by homologous recombination. The mutation in the aur1P gene had no effect on growth and differentiation. However, biochromatographic analysis of culture extracts from the S. aureofaciens aur1P-disrupted strain revealed that auricin was not produced in the mutant. This indicated that aur1P is essential for auricin production. Transcription from the previously characterized aur1Ap promoter, directing expression of the first gene, aur1A, in the auricin gene cluster, was dramatically decreased in the S. aureofaciens CCM 3239 aur1P mutant strain. Moreover, the Aur1P protein, overproduced in Escherichia coli, was shown to bind specifically upstream of the aur1Ap promoter region. The results indicated that the Aur1P regulator activates expression of the auricin biosynthesis genes.
在金色链霉菌CCM 3239中,参与类蒽环类抗生素奥里星生物合成的奥里星聚酮基因簇上游,鉴定出了一个名为aur1P的基因,该基因编码一种与细菌双组分信号转导系统的应答调节因子相似的蛋白质。该基因的表达由单一启动子aur1Pp指导,在指数生长期转录水平较低,在稳定期前被诱导。在aur1P上游已鉴定出一个反向转录的基因aur1R,它编码一种与TetR家族转录抑制因子同源的蛋白质。通过同源重组,aur1P基因在金色链霉菌CCM 3239染色体中被破坏。aur1P基因的突变对生长和分化没有影响。然而,对金色链霉菌aur1P破坏菌株的培养提取物进行生物色谱分析发现,突变体中不产生奥里星。这表明aur1P对奥里星的产生至关重要。在金色链霉菌CCM 3239 aur1P突变菌株中,先前鉴定的指导奥里星基因簇中第一个基因aur1A表达的aur1Ap启动子的转录显著降低。此外,在大肠杆菌中过量产生的Aur1P蛋白被证明能特异性结合在aur1Ap启动子区域的上游。结果表明,Aur1P调节因子激活奥里星生物合成基因的表达。