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Title of Journal: Appl Microbiol Biotechnol

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Abbravation: Applied Microbiology and Biotechnology

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Springer Berlin Heidelberg

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DOI

10.1016/0009-2614(89)87131-3

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1432-0614

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Induction and carbon catabolite repression of phen

Authors: Juraj Szőköl Lenka Rucká Michaela Šimčíková Petr Halada Jan Nešvera Miroslav Pátek
Publish Date: 2014/06/18
Volume: 98, Issue: 19, Pages: 8267-8279
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Abstract

Rhodococcus erythropolis CCM2595 is able to efficiently utilize phenol and other aromatic compounds We cloned and sequenced its complete gene cluster — catA catB catC catR pheR pheA2 pheA1 — involved in the orthocleavage pathway of phenol The activity of the key enzyme of the phenol degradation pathway twocomponent phenol hydroxylase was found to be induced by phenol When both phenol and succinate were present in the medium phenol hydroxylase activity decreased substantially To analyze the regulation of phenol degradation at the transcriptional level the transcriptional fusions of the divergently oriented promoters PpheA2 and PpheR with the gfpuv reporter gene were constructed The promoters driving expression of the genes of the pheR–pheA2pheA1 cluster were localized by determining the respective transcriptional start points Measurements of GFP fluorescence as well as quantitative RTPCR revealed that expression of the phe genes is induced by phenol at the transcriptional level The transcription of pheA2A1 and pheR was repressed by succinate whereas no repression by glucose or glycerol was observed Activation of the R erythropolis CCM2595 pheA2 promoter by PheR an AraCtype transcriptional regulator was demonstrated by overexpression of the pheR gene Analysis of the transcriptional regulation of two similar phe clusters from R jostii RHA1 by various substrates showed that the type of carbon catabolite repression and the temporal transcriptional pattern during cultivation are different in each of the three phe clusters analyzed

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