1996
DOI: 10.1271/bbb.60.1776
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Sequence-specific Binding Sites in the Taka-amylase A G2 Promoter for the CreA Repressor Mediating Carbon Catabolite Repression

Abstract: The N-terminal part of the CreA protein encompassing two zinc fingers was expressed in Escherichia coli as a fusion protein with the maltose binding protein (MalE) of E. coli. Our results show that CreA binds to the promoter of the Taa-G2 gene encoding Taka-amylase A of Aspergillus oryzae. DNase I footprinting experiments showed that CreA bound to three sites with high affinity and to one site with low affinity within the first 401-bp region upstream of the transcription initiation site. All of the sites conta… Show more

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Cited by 36 publications
(27 citation statements)
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“…5). The biosynthesis of α-amylase in most species of the genus Bacillus is repressed by readily metabolizable substrates, especially glucose, by a mechanism of catabolite repression, mediated by the protein encoded by the CreA gene [31]- [32]. Among the organic nitrogen sources, peptone (24.64 U/ml) proved to be the most suitable followed by tryptone (21.66 U/ml) as compared to the inorganic N 2 sources i.e.…”
Section: Bacillus Subtilismentioning
confidence: 99%
“…5). The biosynthesis of α-amylase in most species of the genus Bacillus is repressed by readily metabolizable substrates, especially glucose, by a mechanism of catabolite repression, mediated by the protein encoded by the CreA gene [31]- [32]. Among the organic nitrogen sources, peptone (24.64 U/ml) proved to be the most suitable followed by tryptone (21.66 U/ml) as compared to the inorganic N 2 sources i.e.…”
Section: Bacillus Subtilismentioning
confidence: 99%
“…The regulation of taaG2 is characterized by a high expression level, carbon repression, and induction by various a-glucosides described above. Three transcription factors, Hap complex, CreA, and AmyR, are involved in this characteristic expression (Kato et al, 1996(Kato et al, , 1997(Kato et al, , 1998Nagata et al, 1993;Tanaka et al, 2000;Tani et al, 2000Tani et al, , 2001.…”
Section: Regulation Of the Amylase Gene Expressionmentioning
confidence: 99%
“…Our previous promoter analyses of the taaG2 gene, which encodes Taka-amylase A of A. oryzae, have indicated functional binding sequences for the Hap complex and CreA involved in transcriptional enhancement and carbon catabolite repression respectively. [1][2][3][4] The ciselement required for the induction, SRE (starch responsive element), has also been identified on the taaG2 promoter. 5) SRE was found to overlap with Region IIIa, which is highly conserved in the promoter regions of the amylolytic genes in various Aspergillus species.…”
mentioning
confidence: 99%