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Journal of Bacteriology, April 2003, p. 2520-2527, Vol. 185, No. 8
0021-9193/03/$08.00+0 DOI: 10.1128/JB.185.8.2520-2527.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
Transcription of Clostridium cellulovorans Cellulosomal Cellulase and Hemicellulase Genes
Sung Ok Han,1 Hideaki Yukawa,2 Masayuki Inui,2 and Roy H. Doi1*
Section of Molecular and Cellular Biology, University of California, Davis, California 95616,1
Molecular Microbiology and Genetics Lab, RITE Institute, Kyoto 619-0292, Japan2
Received 10 January 2003/
Accepted 3 February 2003
Transcription of the cellulosomal cellulase/hemicellulase genes of Clostridium cellulovorans has been investigated by Northern blot, reverse transcriptase PCR (RT-PCR), primer extension, and S1 nuclease analysis. Northern hybridizations revealed that the cellulosomal cbpA gene cluster is transcribed as polycistronic mRNAs of 8 and 12 kb. The 8-kb mRNA coded for cbpA and exgS, and the 12-kb mRNA coded for cbpA, exgS, engH, and engK. The sizes of the mRNAs were about 3 kb for engE, 1.8 kb for manA, 2.7 kb for xynA, and 4 kb for pelA, indicating monocistronic transcription of these genes. Primer extension and S1 nuclease analysis of C. cellulovorans RNA showed that the transcriptional start sites of cbpA, engE, manA, and hbpA were located 233, 97, 64, and 61 bp upstream from the first nucleotide of each of the respective translation initiation codons. Alignment of the cbpA, engE, manA, and hbpA promoter regions provided evidence for highly conserved sequences that exhibited strong similarity to the
A consensus promoter sequences of gram-positive bacteria.
* Corresponding author. Mailing address: Section of Molecular and Cellular Biology, University of California, Davis, CA 95616. Phone: (530) 752-3191. Fax: (530) 752-3085. E-mail:
rhdoi{at}ucdavis.edu.
Journal of Bacteriology, April 2003, p. 2520-2527, Vol. 185, No. 8
0021-9193/03/$08.00+0 DOI: 10.1128/JB.185.8.2520-2527.2003
Copyright © 2003, American Society for Microbiology. All Rights Reserved.
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