Sequence-specific Binding Sites in the Taka-amylase A G2 Promoter for the CreA Repressor Mediating Carbon Catabolite Repression

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概要

• 論文の詳細を見る

• 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 contained sequences related to the CreA consensus binding site (5'-SYGGRG-3'), and are suggested to participate in repression of the Taa-G2 gene in response to glucose.

• 社団法人日本農芸化学会の論文
• 1996-11-23

著者

• Kato Masashi

  Department Of Bioenvironmental Medicine Graduate School Of Medicine Chiba University

• Sekine Kotaro

  Department Of Applied Biological Sciences Faculty Of Agriculture Nagoya University

• Tsukagoshi Norihiro

  Department Of Applied Biological Sciences Faculty Of Agriculture Nagoya University

• Kato Masashi

  Department Of Applied Biological Chemistry Fuculty Of Agriculture Meijo University

• Kato Masashi

  Department Of Applied Biological Sciences Faculty Of Agriculture Nagoya University

• Kato Masashi

  Department Of Applied Biological Chemistry Faculty Of Agriculture Meijo University

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