Control of expression by the cellulose synthase ( bcsA) promoter region from Acetobacter xylinum BPR 2001

• Published in: Gene 1998-06, Vol.213 (1), p.93-100
• Main Authors: Nakai, T., Moriya, A., Tonouchi, N., Tsuchida, T., Yoshinaga, F., Horinouchi, S., Sone, Y., Mori, H., Sakai, F., Hayashi, T.
• Format: Article
• Language: English
• Subjects: Amino Acid Sequence; Arabidopsis Proteins; Base Sequence; bcs operon; Cloning, Molecular; DNA, Complementary - genetics; Enzyme Induction; Escherichia coli - genetics; Gene Expression Regulation, Bacterial; Gene regulation; Genes, Bacterial; Genes, Reporter; Gluconacetobacter xylinus - genetics; Glucosyltransferases - biosynthesis; Glucosyltransferases - genetics; Molecular Sequence Data; Operon; Promoter Regions, Genetic - physiology; Recombinant Fusion Proteins - biosynthesis; Recombinant Fusion Proteins - genetics; Ribosome-binding site; RNA, Bacterial - metabolism; RNA, Messenger - metabolism; RNA, Ribosomal, 16S - metabolism; Sequence Alignment; Sequence Homology, Amino Acid; Sequencing; Species Specificity; Transcription, Genetic
• ISSN: 0378-1119; 1879-0038
• DOI: 10.1016/S0378-1119(98)00191-7

The 5′ upstream region (about 3.1 kb) of the cellulose synthase operon ( bcs operon) has been isolated by cloning from Acetobacter xylinum strain BPR 2001. The expression level of the upstream region was determined using sucrose synthase cDNA as a reporter gene in the shuttle vector pSA19. The expression occurred with the 1.1-kb upstream sequence from the ATG start codon of the bcs operon but not with the 241-bp upstream sequence in A. xylinum, although neither the 1.1-kb nor the 241-bp upstream sequence caused any expression as a promoter in Escherichia coli. The level of expression with the 1.1-kb upstream sequence in A. aceti was 75% of that in A. xylinum. These results suggest that the upstream region functions as a specific promoter for the Acetobacter genus. The expression was reduced by the introduction of the 241-bp upstream region between the lac promoter and the reporter gene in E. coli and was not detected in A. xylinum. This suggests that the short upstream region composed of 241 bp contains the site(s) which causes a negative regulation on the transcription for bcs operon. The production of recombinant protein with the ribosome-binding site (RBS) of A. xylinum obtained from the bcs operon, was reduced to about half in E. coli, and that with the site of the lac promoter was also reduced to about half in A. xylinum. This shows that a species-specific predominance occurs during interaction between mRNA and 16S rRNA in the RBS between A. xylinum and E. coli.