Affiliation:
1. Department of Microbiology, University of Massachusetts, Amherst, Massachusetts 01003
Abstract
ABSTRACT
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.
Publisher
American Society for Microbiology
Subject
Molecular Biology,Microbiology
Cited by
35 articles.
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