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  • 1
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    FEBS Letters 333 (1993), S. 238-242 
    ISSN: 0014-5793
    Keywords: Glyoxylate pathway ; Isocitrate lyase ; Promoter element ; Regulation ; Yeast
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    FEBS Letters 320 (1993), S. 271-275 
    ISSN: 0014-5793
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology , Chemistry and Pharmacology , Physics
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Amsterdam : Elsevier
    Gene 125 (1993), S. 125-133 
    ISSN: 0378-1119
    Keywords: GCR1 ; GPM1 ; Saccharomyces cerevisiae ; gene expression ; glycolysis ; regulation ; repressor/activator
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 0378-1119
    Keywords: Saccharomyces cerevisiae ; chromosomal locations ; homology to mammals ; nucleotide sequences ; sequence comparisons
    Source: Elsevier Journal Backfiles on ScienceDirect 1907 - 2002
    Topics: Biology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 10 (1985), S. 103-110 
    ISSN: 1432-0983
    Keywords: Yeast taxonomy ; DNA homologies ; Southern analysis ; Glycolytic gene probes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The genePDC1 ofSaccharomyces cerevisiae coding for pyruvate decarboxylase (E.C. 4.1.1.1.) was used as a hybridization probe to detect gene sequence homologies in different strains ofSaccharomyces cerevisiae and in other yeast species. Additionally six other genes coding for glycolytic enzymes as well as the genesURA3 of the pyrimidine synthetic andTRP1 of the tryptophan synthetic pathways were used. A restriction polymorphism for the BamH1 fragments carrying thePDC1 gene was evident within the speciesSaccharomyces cerevisiae. All strains definitely declared asSaccharomyces cerevisiae showed the same restriction patterns. Hybridizations of different intensities were observed only with species in the familySaccharomycetaceae. Hybridizations with different genes showed different degrees of conservation for certain DNA sequences.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 9 (1985), S. 547-551 
    ISSN: 1432-0983
    Keywords: MAL regulatory loci ; Segregation analysis ; Saccharomyces cerevisiae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary By hybridization with a putative MAL2p regulatory sequence we have identified a 19 kb long BamH1 DNA fragment to contain the MALp sequence in a MAL4 strain. A mixture of recombinant plasmids was prepared by ligation of purified 19 kb BamH1 fragments partially digested with Sau3A into the multicopy vector YEp1357. The source of DNA was a strain carrying the MAL4 locus. Yeast maltose non-fermenting strains were transformed with the plasmid mixture. A recombinant plasmid, pRM-4, containing the MAL4p regulatory gene was isolated that complements the maltose-negative phenotype. The plasmid was shown to confer the ability to synthesize maltase to recipient strains grown under inducing as well as under repressing conditions. The MAL4p regulatory sequence cloned was used as a probe in hybridization experiments to study the degrees of homology between the different MAL regulatory genes. The results showed that the sequence from MAL4 strains is strongly homologous to that of MAL3 strains whereas it shows significant differences to the ones of MAL1 and MAL2 strains. Southern analysis of the segregants of crosses between maltose-positive strains and ma10 strains allowed us to localize the maltase regulatory sequence of each MAL locus within a characteristic BamH1 fragment of genomic DNA hybridizing to the isolated sequence.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Current genetics 9 (1985), S. 539-545 
    ISSN: 1432-0983
    Keywords: Maltose fermentation ; Regulatory sequence ; Saccharomyces cerevisiae
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Yeast genomic libraries containing the MAL1, MAL2-8 c and MAL3 loci were used to transform Ma10 strains to a maltose-positive phenotype. A plasmid called pRM-2 was isolated. mal0 strains synthesized alpha-glucosidase when transformed with this plasmid. Specific activities in the range of 500–1,000 mU/mg protein were detected. An increase of 2–3fold could be observed when the isolated sequence was subcloned in the yeast multicopy vector YEp 1357. Plasmid pRM-2 contains a maltase regulatory sequence as demonstrated by its ability to transform a maltose-negative regulatory mutant to a maltose-positive phenotype. That result also indicated that the mal0 recipient strains are defective in the regulatory gene. Hybridization experiments of genomic EcoRl digests to the isolated plasmid pRM-2 showed characteristic EcoRl fragments in all maltose fermenting strains. Some of the fragments are lacking in the ma10 strains suggesting that the regulatory sequence is located in these fragments. BamHl genomic fragments hybridizing to pRM-2 had different sizes for strains containing different MAL loci. Stable transformants which had integrated pRM-2 either in the TRP1 locus or in the MAL2 locus were obtained. The isolation of the latter type indicates that the cloned sequence is homologous to that present at the MAL2 locus.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 137 (1984), S. 10-13 
    ISSN: 1432-072X
    Keywords: L-Arabinose ; D-Xylose ; Gratuitous inducer ; α-Galactosidase
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract L-Arabinose has been described as a gratuitous inducer of the yeast α-galactosidase. This has been found to be an artefact resulting from galactose contamination of commercial samples of L-arabinose. The inactivation produced on UDP-glucose 4-epimerase by the pentose does not amplify the inducer activity of contaminating D-galactose.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Yeast DNA pools were prepared by ligating partial Sau3A genomic digests from strains carrying various MAL genes into the BamHI site of the yeast-Escherichia coli shuttle vector YRp7. They were used to transform recipient yeast strains that could not utilize maltose since they lacked a classical MAL gene. Transformants were obtained that could use maltose and also formed normal levels of maltase. They were unstable. They would lose the selective marker TRP1 of YRp7 alone, together with the ability to utilize maltose or only the ability to utilize maltose. The insertion of one of the plasmids was used as a hybridization probe for the others and found to share homologous sequences with all. They were then shown to contain the replication origin of the yeast 2 μm circle plasmid and additional genomic digests of total yeast DNA. They hybridized at various degrees of efficiency with several bands, indicating that they were part of a family of repeated sequences. Apparently, it was the combination of the replication origin of the 2 μm circles with the additional sequences that promoted maltose utilization.
    Type of Medium: Electronic Resource
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