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Yasuhiko Miwa

Researcher at Fukuyama University

Publications -  18
Citations -  1200

Yasuhiko Miwa is an academic researcher from Fukuyama University. The author has contributed to research in topics: Catabolite repression & Operon. The author has an hindex of 13, co-authored 18 publications receiving 1183 citations.

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Combined transcriptome and proteome analysis as a powerful approach to study genes under glucose repression in Bacillus subtilis

TL;DR: It is found that CcpA and IolR, a repressor of the iol divergon, were involved in the glucose repression of the synthesis of inositol dehydrogenase encoded by iolG included in the above list.
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Evaluation and characterization of catabolite-responsive elements (cre) of Bacillus subtilis

TL;DR: Examination of catabolite repression of beta-galactosidase synthesis in the integrants led to the following conclusions: (i) lower mismatching of cre sequences to the query sequence is required for their function; (ii) although cre sequences are partially palindromic, low mismatching in the same direction as that of transcription of the target genes is more critical for their functions than that in the inverse direction.
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Specific recognition of the Bacillus subtilis gnt cis‐acting catabolite‐responsive element by a protein complex formed between CcpA and seryl‐phosphorylated HPr

TL;DR: A molecular mechanism underlying catabolite repression in B. subtilis mediated by CcpA and P‐ser‐HPr is proposed and specific protection of the gnt CRE against DNase I digestion is confirmed.
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Catabolite repression of the Bacillus subtilis gnt operon exerted by two catabolite‐responsive elements

TL;DR: In vivo results implied that catabolite repression exerted by creup was probably independent of catabolites exerted by credown; both creup and credown catabolITE repression involved CcpA.
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Possible function and some properties of the CcpA protein of Bacillus subtilis.

TL;DR: Analysis of revertants from the alsA1 mutant by direct sequencing indicated that this mutation comprises a base substitution of guanine atucleotide -14 to adenine within the Shine-Dalgarno sequence of the ccpA gene (ccpA translation starts at nucleotide +1).