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  • Chromatographie, Dünnschicht  (1)
  • Glucose derepression  (1)
  • INO2  (1)
  • Chemistry
  • Deutschland
  • Lactobacillus delbrueckii subsp. lactis
  • Springer  (4)
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Keywords
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  • 1
    Electronic Resource
    Electronic Resource
    Influence of gene dosage and autoregulation of the regulatory genes INO2 and INO4 on inositol/choline-repressible gene transcription in the yeast Saccharomyces cerevisiae (1997)
    Springer
    Current genetics 31 (1997), S. 462-468 
    Details
    ISSN: 1432-0983
    Keywords: Key words Transcriptional regulation ; Phospholipid biosynthesis ; Saccharomyces cerevisiae ; INO2
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Expression of structural genes of phospholipid biosynthesis in yeast is mediated by the inositol/choline-responsive element (ICRE). ICRE-dependent gene activation, requiring the regulatory genes INO2 and INO4, is repressed in the presence of the phospholipid precursors inositol and choline. INO2 and, to a less extent, INO4 are positively autoregulated by functional ICRE sequences in the respective upstream regions. However, an INO2 allele devoid of its ICRE functionally complemented an ino2 mutation and completely restored inositol/choline regulation of Ino2p-dependent reporter genes. Low-level expression of INO2 and INO4 genes, each under control of the heterologous MET25 promoter, did not alter the regulatory pattern of target genes. Thus, upstream regions of INO2 and INO4 are not crucial for transcriptional control of ICRE-dependent genes by inositol and choline. Interestingly, over-expression of INO2, but not of INO4, counteracted repression by phospholipid precursors. Possibly, a functional antagonism between INO2 and a negative regulator is the key event responsible for repression or de-repression.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/s002940050231
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  • 2
    Electronic Resource
    Electronic Resource
    Cloning and DNA sequence analysis of pepQ, a prolidase gene from Lactobacillus delbrueckii subsp. lactis DSM7290 and partial characterization of its product (1995)
    Springer
    Molecular genetics and genomics 247 (1995), S. 494-500 
    Details
    ISSN: 1617-4623
    Keywords: Prolidase ; Metalloprotease ; Lactobacillus delbrueckii subsp. lactis ; Nucleotide sequence analysis
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract From a genomic library of Lactobacillus delbrueckii subsp. lactis (DSM7290) DNA, in the low-copy-number vector pLG339, a recombinant clone was selected, which complemented a mutation in the prolidase gene (pepQ) of Escherichia coli UK173. Nucleotide sequence analysis revealed an open reading frame of 1104 nucleotides corresponding to a protein of 368 amino acids with a calculated pI of 4.64 and a molecular mass of 41087 Da. The start site of pepQ transcription was determined by primer extension analysis with mRNA prepared from L. delbrueckii. Based on homology of the gene product to various peptidases and on the substrate specificity determined, the peptidase was designated PepQ. The influence of various protease inhibitors and cations on peptidase activity indicated that PepQ is a metalloprotease. The absence of a membrane-spanning domain and a signal peptide sequence argues for a cytoplasmic localization of the enzyme.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00293152
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  • 3
    Electronic Resource
    Electronic Resource
    Isolation and expression analysis of two yeast regulatory genes involved in the derepression of glucose-repressible enzymes (1987)
    Springer
    Molecular genetics and genomics 209 (1987), S. 366-373 
    Details
    ISSN: 1617-4623
    Keywords: Glucose repression ; Glucose derepression ; Regulatory genes ; Expression analysis ; Saccharomyces cerevisiae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Yeast strains carrying one of the two regulatory mutations cat1 and cat3 are defectve in derepression of several glucose-repressible enzymes that are necessary for utilizing non-fermentable carbon sources. Hence, these strains fail to grow on ethanol, glycerol or acetate. The synthesis of isocitrate lyase, malate synthase, malate dehydrogenase and fructose-1,6-bisphosphatase is strongly affected in cat1 and cat3 strains. Genes CAT1 and CAT3 have been isolated by complementation of the cognate, mutations after transformation with an episomal plasmid gene library. The restriction map of CAT1 proved its allelism to the earlier isolated SNF1 gene. Both genes appear to exist as single-copy genes per haploid genome as indicated by Southern hybridization. Northern analysis has shown that the 1.35 kb CAT3 mRNA is constitutively expressed, independent of the carbon source in the medium. Derepression studies with CAT3 transformants using a multi-copy plasmid showed over-expression of glyoxylate cycle enzymes. This result would be consistent with a direct effector function for the CAT3 gene product.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00329667
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  • 4
    Electronic Resource
    Electronic Resource
    Trennung und Identifizierung von 12 antimikrobiellen Verbindungen mittels Dünnschicht-Chromatographie (1979)
    Springer
    Fresenius' Zeitschrift für analytische Chemie 294 (1979), S. 36-41 
    Details
    ISSN: 1618-2650
    Keywords: Trenn. von Antimikrobiellen Verbindungen ; Chromatographie, Dünnschicht
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenfassung Die Trennung und Identifizierung von halogenierten, vorwiegend aliphatischen antimikrobiellen Verbindungen, von Formaldehyd abgebenden Substanzen und von Sulfonsäure-Derivaten auf dünnschicht-chromatographischem Wege wird beschrieben. Die Trennung erfolgt auf einer Kieselgel-Cellulose-Mischschicht mit Äthylacetat/Methanol/10% Ammoniak (65+30+5) als Laufmittel. Zur Sichtbarmachung und zur Identifizierung sind mehrere Sprühmittel notwendig: äthanolischeMethylgelb-Lösung mit anschließender UV-Bestrahlung, Phenylhydrazinsulfonat und Natronlauge sowie Hydroxylamin/Eisen(III)-chlorid und Nitroprussidnatrium-Kaliumhexacyanoferrat (III) u. a. Anhand der verschiedenen Rf-Werte und der Anfärbungen lassen sich die antimikrobiellen Verbindungen rasch und einfach identifizieren.
    Notes: Summary The analysis of halogenated, mainly aliphatic compounds, of formaldehyde donors and of derivatives of sulphonic acid is described. The separation is carried out on plates coated with a mixed layer of silica gel and cellulose and a solvent mixture of ethylacetate/methanol/10% ammonia (65+30+5), whereas for the detection and identification several spray reagents have to be used: ethanolic solution of Methyl Yellow with subsequent UV irradiation, phenylhydrazine-4-sulphonic acid and sodium hydroxide, hydroxylamine/iron(III) chloride, sodium nitroprusside/potassium hexacyanoferrate(III) and others. The Rf-values and the colourations of the spots allow to identify the examined compounds rapidly and without further chemical procedures.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1007/BF00694659
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