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Journal of Bacteriology, October 2002, p. 5330-5338, Vol. 184, No. 19
0021-9193/02/$04.00+0     DOI: 10.1128/JB.184.19.5330-5338.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

Interdependent Expression of the ccoNOQP-rdxBHIS Loci in Rhodobacter sphaeroides 2.4.1

Jung Hyeob Roh and Samuel Kaplan^*

Department of Microbiology and Molecular Genetics, The University of Texas Health Science Center Medical School, Houston, Texas 77030

Received 19 April 2002/ Accepted 30 June 2002

The rdxBHIS gene cluster of Rhodobacter sphaeroides 2.4.1, located downstream of the ccoNOQP operon encoding the cbb₃ cytochrome c oxidase, is required for the posttranscriptional modification of the cbb₃ cytochrome c oxidase. The cbb₃ cytochrome c oxidase is the main terminal oxidase under microaerobic conditions, as well as a component of the signal transduction pathway controlling photosynthesis gene expression. Because of the intimate functional and positional relationships of the ccoNOQP operon and the rdxBHIS gene cluster, we have examined the transcriptional activities of this DNA region in order to understand their expression and regulation. Northern blot analysis and reverse transcription-PCR, together with earlier complementation analysis, suggested that the ccoNOQP-rdxBHIS cluster is transcribed as ccoNOQP-, ccoNOQP-rdxBH-, rdxBH-, and rdxIS-specific transcripts. Multiple transcriptional start sites have been identified by primer extension analyses: five for ccoN, four for rdxB, and one for rdxI. Transcription from P1_N of ccoN and P1_B of rdxB is dependent on the presence of FnrL. LacZ fusion analysis support the above-described studies, especially the importance of FnrL. Expression of the cco-rdx cluster is closely related to photosynthesis gene expression, suggesting that transcript stoichiometry and presumably the stoichiometry of the gene products are critical factors in controlling photosynthesis gene expression.

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* Corresponding author. Mailing address: Department of Microbiology and Molecular Genetics, The University of Texas Health Science Center Medical School, 6431 Fannin St., Houston, TX 77030. Phone: (713) 500-5502. Fax: (713) 500-5499. E-mail: samuel.kaplan{at}uth.tmc.edu.

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Journal of Bacteriology, October 2002, p. 5330-5338, Vol. 184, No. 19
0021-9193/02/$04.00+0     DOI: 10.1128/JB.184.19.5330-5338.2002
Copyright © 2002, American Society for Microbiology. All Rights Reserved.

This article has been cited by other articles:

• Bruscella, P., Eraso, J. M., Roh, J. H., Kaplan, S. (2008). The Use of Chromatin Immunoprecipitation to Define PpsR Binding Activity in Rhodobacter sphaeroides 2.4.1. J. Bacteriol. 190: 6817-6828 [Abstract] [Full Text]  
• Ouchane, S., Picaud, M., Therizols, P., Reiss-Husson, F., Astier, C. (2007). Global Regulation of Photosynthesis and Respiration by FnrL: THE FIRST TWO TARGETS IN THE TETRAPYRROLE PATHWAY. J. Biol. Chem. 282: 7690-7699 [Abstract] [Full Text]  
• Roh, J. H., Smith, W. E., Kaplan, S. (2004). Effects of Oxygen and Light Intensity on Transcriptome Expression in Rhodobacter sphaeroides 2.4.1: REDOX ACTIVE GENE EXPRESSION PROFILE. J. Biol. Chem. 279: 9146-9155 [Abstract] [Full Text]