Biosynthesis of Tetracyclines. I. The Halide Metabolism of Streptomyces aureofaciens Mutants. The Preparation and Characterization of Tetracycline, 7-Chloro36-tetracycline and 7-Bromotetracycline

1959 ◽  
Vol 81 (12) ◽  
pp. 3069-3075 ◽  
Author(s):  
Albert P. Doerschuk ◽  
J. R. D. McCormick ◽  
Joseph J. Goodman ◽  
Stephen A. Szumski ◽  
John A. Growich ◽  
...  
1988 ◽  
Vol 150 (5) ◽  
pp. 438-440 ◽  
Author(s):  
Ivana Vančurová ◽  
Aleš Vančura ◽  
Jindřich Volc ◽  
Jiří Neužzil ◽  
Miroslav Flieger ◽  
...  

1988 ◽  
Vol 170 (11) ◽  
pp. 5192-5196 ◽  
Author(s):  
I Vancurová ◽  
A Vancura ◽  
J Volc ◽  
J Neuzil ◽  
M Flieger ◽  
...  

Microbiology ◽  
2011 ◽  
Vol 157 (6) ◽  
pp. 1629-1639 ◽  
Author(s):  
Renata Novakova ◽  
Alena Rehakova ◽  
Peter Kutas ◽  
Lubomira Feckova ◽  
Jan Kormanec

Two regulators, Aur1P and Aur1R, have been previously found to control expression of the aur1 polyketide gene cluster involved in biosynthesis of the angucycline-like antibiotic auricin in Streptomyces aureofaciens CCM 3239 in a cascade mechanism. Here, we describe the characterization of two additional regulatory genes, aur1PR2 and aur1PR3, encoding homologues of the SARP family of transcriptional activators that were identified in the upstream part of the aur1 cluster. Expression of both genes is directed by a single promoter, aur1PR2p and aur1Pr3p, respectively, induced in late exponential phase. Disruption of aur1PR2 in S. aureofaciens CCM 3239 had no effect on auricin production. However, the disruption of aur1PR3 dramatically reduced auricin compared with its parental wild-type strain. Transcription from the aur1Ap promoter, directing expression of the first biosynthetic gene in the auricin gene cluster, was similarly decreased in the S. aureofaciens CCM 3239 aur1PR3 mutant. Transcription from the aur1PR3p promoter increased in the S. aureofaciens CCM 3239 aur1R mutant strain, and the TetR family negative regulator Aur1R was shown to specifically bind the aur1PR3p promoter. These results indicate a complex regulation of the auricin cluster by the additional SARP family transcriptional activator Aur1PR3.


IUBMB Life ◽  
1998 ◽  
Vol 46 (4) ◽  
pp. 657-665
Author(s):  
Tatiana Horecká ◽  
Dusan Perecko ◽  
Eva Kutejová ◽  
Darina Mikulásová ◽  
Marta Kollárová

Microbiology ◽  
2010 ◽  
Vol 156 (8) ◽  
pp. 2374-2383 ◽  
Author(s):  
Renata Novakova ◽  
Peter Kutas ◽  
Lubomira Feckova ◽  
Jan Kormanec

Two regulatory genes, aur1P and aur1R, have been previously identified upstream of the aur1 polyketide gene cluster involved in biosynthesis of the angucycline-like antibiotic auricin in Streptomyces aureofaciens CCM 3239. The aur1P gene encodes a protein similar to the response regulators of bacterial two-component signal transduction systems and has been shown to specifically activate expression of the auricin biosynthetic genes. The aur1R gene encodes a protein homologous to transcriptional repressors of the TetR family. Here we describe the characterization of the aur1R gene. Expression of the gene is directed by a single promoter, aur1Rp, which is induced just before stationary phase. Disruption of aur1R in S. aureofaciens CCM 3239 had no effect on growth and differentiation. However, the disrupted strain produced more auricin than its parental wild-type S. aureofaciens CCM 3239 strain. Transcription from the aur1Ap and aur1Pp promoters, directing expression of the first biosynthetic gene in the auricin gene cluster and the pathway-specific transcriptional activator, respectively, was increased in the S. aureofaciens CCM 3239 aur1R mutant strain. However, Aur1R was shown to bind specifically only to the aur1Pp promoter in vitro. This binding was abolished by the addition of auricin and/or its intermediates. The results indicate that the Aur1R regulator specifically represses expression of the aur1P gene, which encodes a pathway-specific activator of the auricin biosynthetic gene cluster in S. aureofaciens CCM 3239, and that this repression is relieved by auricin or its intermediates.


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