Journal of Bacteriology, April 1999, p. 2513-2518, Vol. 181, No. 8
0021-9193/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
Department of Microbiology, University of Massachusetts, Amherst, Massachusetts 01003
Received 26 August 1998/Accepted 4 February 1999
Degenerate oligonucleotides were used to randomize 21 bp of the
53-bp minimal bop promoter in three 7-bp segments,
including the putative TATA box and the upstream activator sequence
(UAS). The mutagenized bop promoter and the wild-type
structural gene and transcriptional terminator were inserted into a
shuttle plasmid capable of replication in the halophilic archaeon
Halobacterium sp. strain S9. Active promoters were isolated
by screening transformants of an orange (Pum
bop) Halobacterium mutant for purple
(Pum+ bop+) colonies on agar plates
and analyzed for bop mRNA and/or bacteriorhodopsin content.
Sequence analysis yielded the consensus sequence 5'-tyT(T/a)Ta-3', corresponding to the promoter TATA box element 30 to 25 bp 5' of the
transcription start site. A putative UAS, 5'-ACCcnactagTTnG-3', located
52 to 39 bp 5' of the transcription start site was found to be
conserved in active promoters. This study provides direct evidence for
the requirement of the TATA box and UAS for bop promoter activity.
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