Expression of the β-D-Glucosidase 1 Gene in Bifidobacterium breve 203 during Acclimation to Cellobiose
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- 資料種別
- 記事
- 著者・編者
- Naoki NunouraKohji OhdanKenji 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
- 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.
- DOI
- 10.1016/s0922-338x(97)80134-1
- 関連情報(URI)
- 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 siteSingle-step method of RNA isolation by acid guanidinium thiocyanate-phenol-chloroform extractionRapid and sensitive detection of point mutations and DNA polymorphisms using the polymerase chain reactionPhosphoproteins and the phosphoenolpyruvate: sugar phosphotransferase system of <i>Streptococcus salivarius</i>. Detection of two different ATP-dependent phosphorylations of the phosphocarrier protein HPrProtein kinase‐dependent HPr/CcpA interaction links glycolytic activity to carbon catabolite repression in Gram‐positive bacteriaLac 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 T4Silencing 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 sourceGenetic regulatory mechanisms in the synthesis of proteinsCompilation of<i>E.coli</i>mRNA promoter sequencesDNAase footprinting a simple method for the detection of protein-DNA binding specificityPROTEIN MEASUREMENT WITH THE FOLIN PHENOL REAGENTRegulation of the bgl operon of Escherichia coli by transcriptional antitermination.The interaction of RNA polymerase and lac repressor with the lac control regionInducible System for the Utilization of β-Glucosides in <i>Escherichia coli</i> I. Active Transport and Utilization of β-GlucosidesProtein phosphorylation and regulation of carbon metabolism in gram-negative versus gram-positive bacteriaElectrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applicationsVergleichende untersuchungen über die Bifidobakterien aus dem Verdauungstrakt von Menschen und TierenGenomic sequencingDNA sequencing with chain-terminating inhibitorsThe 3′-terminal sequence of Escherichia coli 16s ribosomal RNA: complementarity to nonsense triplets and ribosome binding sitesSite-directed mutagenesis of a catabolite repression operator sequence in Bacillus subtilisStructure of the DNA-binding region of lac repressor inferred from its homology with cro repressorStudies on glucosaminidaseIncrease in β-d-glucoside-assimilating ability of Bifidobacterium breve 203 due to acclimation to β-d-glucosidePurification 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 401Cloning 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CrossrefCiNii Articles
- 書誌ID(NDLBibID)
- 4209651
- NII論文ID
- 110002682500