Literature DB >> 17183485

Transcriptional regulation of catabolic pathways for aromatic compounds in Corynebacterium glutamicum.

K Brinkrolf1, I Brune, A Tauch.   

Abstract

Corynebacterium glutamicum is a gram-positive soil microorganism able to utilize a large variety of aromatic compounds as the sole carbon source. The corresponding catabolic routes are associated with multiple ring-fission dioxygenases and among other channeling reactions, include the gentisate pathway, the protocatechuate and catechol branches of the beta-ketoadipate pathway and two potential hydroxyquinol pathways. Genes encoding the enzymatic machinery for the bioconversion of aromatic compounds are organized in several clusters in the C. glutamicum genome. Expression of the gene clusters is under specific transcriptional control, apparently including eight DNA-binding proteins belonging to the AraC, IclR, LuxR, PadR, and TetR families of transcriptional regulators. Expression of the gentisate pathway involved in the utilization of 3-hydroxybenzoate and gentisate is positively regulated by an IclR-type activator. The metabolic channeling of ferulate, vanillin and vanillate into the protocatechuate branch of the beta-ketoadipate pathway is controlled by a PadR-like repressor. Regulatory proteins of the IclR and LuxR families participate in transcriptional regulation of the branches of the beta-ketoadipate pathway that are involved in the utilization of benzoate, 4-hydroxybenzoate and protocatechuate. The channeling of phenol into this pathway may be under positive transcriptional control by an AraC-type activator. One of the potential hydroxyquinol pathways of C. glutamicum is apparently repressed by a TetR-type regulator. This global analysis revealed that transcriptional regulation of aromatic compound utilization is mainly controlled by single regulatory proteins sensing the presence of aromatic compounds, thus representing single input motifs within the transcriptional regulatory network of C. glutamicum.

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Year:  2006        PMID: 17183485

Source DB:  PubMed          Journal:  Genet Mol Res        ISSN: 1676-5680


  28 in total

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2.  KdgR, an IClR family transcriptional regulator, inhibits virulence mainly by repression of hrp genes in Xanthomonas oryzae pv. oryzae.

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Journal:  J Bacteriol       Date:  2015-01-12       Impact factor: 3.490

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5.  Phenylacetic acid catabolism and its transcriptional regulation in Corynebacterium glutamicum.

Authors:  Xi Chen; Thomas A Kohl; Christian Rückert; Dmitry A Rodionov; Ling-Hao Li; Jiu-Yuan Ding; Jörn Kalinowski; Shuang-Jiang Liu
Journal:  Appl Environ Microbiol       Date:  2012-06-08       Impact factor: 4.792

6.  Transcriptional regulation of the vanillate utilization genes (vanABK Operon) of Corynebacterium glutamicum by VanR, a PadR-like repressor.

Authors:  Kambiz Morabbi Heravi; Julian Lange; Hildegard Watzlawick; Jörn Kalinowski; Josef Altenbuchner
Journal:  J Bacteriol       Date:  2014-12-22       Impact factor: 3.490

7.  Comparative Analysis of the IclR-Family of Bacterial Transcription Factors and Their DNA-Binding Motifs: Structure, Positioning, Co-Evolution, Regulon Content.

Authors:  Inna A Suvorova; Mikhail S Gelfand
Journal:  Front Microbiol       Date:  2021-06-10       Impact factor: 5.640

8.  PcaO positively regulates pcaHG of the beta-ketoadipate pathway in Corynebacterium glutamicum.

Authors:  Ke-Xin Zhao; Yan Huang; Xi Chen; Nan-Xi Wang; Shuang-Jiang Liu
Journal:  J Bacteriol       Date:  2010-01-15       Impact factor: 3.490

9.  Identification and genomic analysis of transcription factors in archaeal genomes exemplifies their functional architecture and evolutionary origin.

Authors:  Ernesto Pérez-Rueda; Sarath Chandra Janga
Journal:  Mol Biol Evol       Date:  2010-02-01       Impact factor: 16.240

10.  Regulation of expression of genes involved in quinate and shikimate utilization in Corynebacterium glutamicum.

Authors:  Haruhiko Teramoto; Masayuki Inui; Hideaki Yukawa
Journal:  Appl Environ Microbiol       Date:  2009-04-17       Impact factor: 4.792

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