本文へ移動

Expression of the β-D-Glucosidase 1 Gene in Bifidobacterium breve 203 during Acclimation to Cellobiose

記事を表すアイコン

Expression of the β-D-Glucosidase 1 Gene in Bifidobacterium breve 203 during Acclimation to Cellobiose

国立国会図書館請求記号
Z53-S65
国立国会図書館書誌ID
4209651
資料種別
記事
著者
Naoki Nunouraほか
出版者
Suita : Society of Fermentation and Bioengineering
出版年
1997-04
資料形態
掲載誌名
Journal of Fermentation and Bioengineering 83(4) 1997.04
掲載ページ
p.309~314
詳細を見る

全国の図書館の所蔵

国立国会図書館以外の全国の図書館の所蔵状況を表示します。

所蔵のある図書館から取寄せることが可能かなど、資料の利用方法は、ご自身が利用されるお近くの図書館へご相談ください

その他

  • CiNii Research

    検索サービス
    デジタル
    連携先のサイトで、CiNii Researchが連携している機関・データベースの所蔵状況を確認できます。

書誌情報

この資料の詳細や典拠(同じ主題の資料を指すキーワード、著者名)等を確認できます。

資料種別
記事
著者・編者
Naoki Nunoura
Kohji Ohdan
Kenji Yamamoto 他
タイトル(掲載誌)
Journal of Fermentation and Bioengineering
巻号年月日等(掲載誌)
83(4) 1997.04
掲載巻
83
掲載号
4
掲載ページ
309~314
掲載年月日(W3CDTF)
1997-04
ISSN(掲載誌)
0922-338X
出版事項(掲載誌)
Suita : Society of Fermentation and Bioengineering
出版地(国名コード)
JP
本文の言語コード
eng
NDLC
対象利用者
一般
所蔵機関
国立国会図書館
請求記号
Z53-S65
連携機関・データベース
国立国会図書館 : 国立国会図書館雑誌記事索引
書誌ID(NDLBibID)
4209651
整理区分コード
632

デジタル

要約等
Abstract The β- d -glucosidase I (EC 3.2.1.21) activity of Bifidobacterium breve 203 isolated from feces of adult humans was found to be very low, but when B. breve 203 was acclimated to cellobiose, the activity of the enzyme increased in the acclimated cell, B. breve 203 clb. With the aim of elucidating the mechanism, responsible for this increased activity the translation and transcription of the β- d -glucosidase I gene were investigated using an antibody against β- d -glucosidase I and a probe specific to the gene, respectively. Western and Northern blots showed marked differences in the expression of the enzyme and the level of its mRNA between B. breve 203 and B. breve 203 clb. However, genomic Southern blots revealed only insignificant differences in the copy numbers of the open reading frames in the two strains. The 5′ flanking regions of the β- d -glucosidase I gene of B. breve 203 and that of B. breve 203 clb were therefore analyzed. The transcriptional start point, located 94 bp upstream from the first methionine codon, was identified by primer extension. A sequence, -TTGGAA-(15 bp)-TAATCT-, located 8 bp upstream from the transcriptional start point, was assigned as the promoter of the gene. A sequence highly homologous to the lac operator region of Escherichia coli was found downstream of the transcriptional start point.
参照
Sequence and characteristics of the Bifidobacterium longum gene encoding l-lactate dehydrogenase and the primary structure of the enzyme: a new feature of the allosteric site
Single-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extraction
Rapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reaction
Phosphoproteins and the phosphoenolpyruvate: sugar phosphotransferase system of <i>Streptococcus salivarius</i>. Detection of two different ATP-dependent phosphorylations of the phosphocarrier protein HPr
Protein kinase‐dependent HPr/CcpA interaction links glycolytic activity to carbon catabolite repression in Gram‐positive bacteria
Lac repressor with the helix-turn-helix motif of lambda cro binds to lac operator.
Cleavage of Structural Proteins during the Assembly of the Head of Bacteriophage T4
Silencing of Escherichia coli bgl promoter by flanking sequence elements.
Growth, enzyme levels, and some metabolic properties of an Escherichia coli mutant grown on L-threonine as the sole carbon source
Genetic regulatory mechanisms in the synthesis of proteins
Compilation of<i>E.coli</i>mRNA promoter sequences
DNAase footprinting a simple method for the detection of protein-DNA binding specificity
PROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENT
Regulation of the bgl operon of Escherichia coli by transcriptional antitermination.
The interaction of RNA polymerase and lac repressor with the lac control region
Inducible System for the Utilization of β-Glucosides in <i>Escherichia coli</i> I. Active Transport and Utilization of β-Glucosides
Protein phosphorylation and regulation of carbon metabolism in gram-negative versus gram-positive bacteria
Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications
Vergleichende untersuchungen über die Bifidobakterien aus dem Verdauungstrakt von Menschen und Tieren
Genomic sequencing
DNA sequencing with chain-terminating inhibitors
The 3′-terminal sequence of Escherichia coli 16s ribosomal RNA: complementarity to nonsense triplets and ribosome binding sites
Site-directed mutagenesis of a catabolite repression operator sequence in Bacillus subtilis
Structure of the DNA-binding region of lac repressor inferred from its homology with cro repressor
Studies on glucosaminidase
Increase in β-d-glucoside-assimilating ability of Bifidobacterium breve 203 due to acclimation to β-d-glucoside
Purification and characterization of β-D-glucosidase (β-D-fucosidase) from Bifidobacterium breve clb acclimated to cellobiose.
Structural Analysis of Disaccharides Synthesized by<i>β</i>-<scp>d</scp>-Glucosidase of<i>Bifidobacterium hreve</i>clb and Their Assimilation by<i>Bifidobacteria</i>
p-Nitrophenyl glycoside-hydrolyzing activities in Bifidobacteria and characterization of β-d-galactosidase of Bifidobacterium longum 401
Cloning and nucleotide sequence of the β-D-glucosidase gene from Bifidobacterium breve clb, and expression of β-D-glucosidase activity in Escherichia coli.
連携機関・データベース
国立情報学研究所 : CiNii Research
提供元機関・データベース
雑誌記事索引データベース
Crossref
CiNii Articles
書誌ID(NDLBibID)
4209651
NII論文ID
110002682500