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  • 1970-1974  (8)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 117 (1972), S. 39-44 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Strain 211-1a of the yeast Saccharomyces sp. allows the specific labelling of nuclear and mitochondrial DNA by exogenously supplied radioactive thymidine monophosphate (TMP) during the latter half of log phase growth. Genetic analysis of crosses between derivatives of strain 211-1a and wild-type strains that do not take up TMP showed a 2:2 segregation pattern indicating that a single gene controls the uptake of TMP. The allele allowing the uptake of TMP is recessive in that diploid strains take up TMP only in the homozygous configuration.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 125 (1973), S. 197-216 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary In the simple eucaryote Saccharomyces cerevisiae there are at least three phenotypically distinct classes of mutants sensitive to inactivation by radiations and alkylating agents: class I mutants are sensitive to ultraviolet light and nitrogen mustard (HN2); class II mutants are sensitive to X-rays and methylmethane sulphonate (MMS); and class III mutants are sensitive to all four of these agents. We have constructed doubly mutant strains of types (I, I), (I, II), (I, III), and (II, III) and have measured their sensitivity to UV, X-rays, HN2 and MMS in order to characterize the interactions of the various mutant gene pairs. Class (I, III) double mutants proved to be supersensitive to UV and HN2 and class (II, III) double mutants proved to be supersensitive to X-rays and MMS. All other double mutants showed little or no enhancement of sensitivity over their most sensitive single mutant parents. Mutants of class I are known to be defective in excision repair and our results are consistent with the idea that there exist at least two additional pathways for dark repair in yeast, one capable of repairing X-ray and MMS damage to DNA, and another, possibly analogous to post-replication repair in bacteria, that competes with the other two for damaged regions in DNA.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 120 (1973), S. 171-180 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The irradiation with visible light (Li) of temperate Serratiaphage that is maximally sensitized with either proflavine (PF) or methylene blue (MB) induces—apart from lethal lesions—mutations which are phenotypically expressed as clear (c) or lightly turbid (l) plaques. The mutagenicity of the MB+Li and PF+Li treatment differs in several respects: (i) Up to an inactivation of 6 to 8 lethal hits MB+Li is a much more potent mutagen than PF+Li. (ii) at low levels of survival the dose curve of mutation frequency with MB+Li reaches a peak and then decreases drastically while the mutation frequency after PF+Li continues to increase in proportion to lethal hits induced. (iii) Mapping of 100 MB+Li and 77 PF+Li induced c or l mutants indicates significant difference in the electiveness of the four genomic regions of c or l mutants.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 126 (1973), S. 337-348 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Strain MB1015-5C of Saccharomyces cerevisiae can utilize exogenous thymidine 5′-monophosphate (5′-dTMP) for its DNA synthesis. Studies with either [P32] or [2-C14] labelled 5′-dTMP reveal first that some of the precursor molecules are taken up intact in DNA synthesis and secondly that 3′-digests of highly purified [P32] DNA yield up to 94% of all [P32] as 5′-dTMP [P32]. Under the conditions used in these experiments more than 90% of the exogenously supplied 5′-dTMP is broken down into orthophosphate and thymidine by an acid phosphatase. Only the orthophosphate is utilized by the yeast cells, mainly for RNA synthesis, and thymidine is not taken up. Suppression of the phosphatase activity is possible by addition of inorganic phosphate to the medium; under these conditions breakdown of 5′-dTMP is suppressed but uptake and incorporation of the molecules into the DNA of strain MB1015-5C is still not very effective.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 108 (1970), S. 303-311 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Photodynamically induced DNA damage in Serratiaphase ϰ may be repaired by the host cell. The extent of this host cell reactivation (HCR) depends on the photosensitizing dye used: HCR of proflavine+visible light induced DNA damage appears to be more efficient than the one of DNA damage induced by methylene blue+visible light. This significant difference in HCR is not due to a preferential inhibition of the enzymes of DNA dark repair by either one of the dyes injected into the host cell along with the phage's genome.
    Type of Medium: Electronic Resource
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  • 6
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Although strain 211-1 aM is able to take up 5′-dTMP it cannot overcome growth-inhibition caused by an aminopterin (APT)-sulfanilamide (SAA)-mediated block of thymidylate biosynthesis in the presence of exogenous 5′-dTMP. 11 mutants (T-strains) of strain 211-1 aM were isolated being able to grow under these conditions. Genetical analysis of the T-strains revealed in each case the mutation of a single recessive gene, TYP, to be responsible for this character, and that the mutated genes belong to three complementation groups. One such typ-mutant, strain 211-1 aMT2, studied in detail was found to utilize exogenous 5′-dTMP as poorly as strain 211-1 aM. However, when thymidylate-biosythesis is inhibited by APT plus SAA the utilization of 5′-dTMP is increased by a factor 2.5 as compared to conditions where the antimetabolites are absent. Next we isolated a typ-mutant- derivative (typ tlr- mutant) utilizing exogenous 5′-dTMP better by a factor 2.5 than strain 211-1 aMT2. This typ tlr- mutant was made auxotrophic for 5′-dTMP. The efficiency of utilization of exogenous 5′-dTMP found for these typ tlr tmp-mutants was the same as that of their typ tlr- parental strain in the presence of APT plus SAA.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 131 (1974), S. 57-67 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Strain 211-1aM of Saccharomyces cerevisiae was found to specifically incorporate into its nuclear and mitochondrial DNA exogenous 5′-dTMP when it is incubated in a synthetic medium N rich in inorganic phosphate. 3′-digestions of DNA from cells labelled with 32P-5′-dTMP revealed that the 5′-dTMP molecules pass through cell walls and membranes to the sites of DNA synthesis without being broken down. It is possible in medium N to generate DNA which almost totally derives its thymine-contents from external sources when rather high concentrations of 5′-dTMP (approx. 100 μg/ml) are offered.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 131 (1974), S. 351-358 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Cells of Saccharomyces cerevisiae strain 211-1atmp1-1 which are auxotrophic for 5′-dTMP exhibit “thymineless death” (TLD) when deprived of the nucleotide. After an initial lag of about one generation time cells lose viability in exponential fashion halving their titer every 90 min. Thymine and thymidine (100 μg/ml) cannot prevent TLD in the absence of 5′-dTMP. Although the cell titer is constant during 24 hrs of 5′-dTMP deprivation, the cell mass synthesized increases by a factor of six during this period. Budding is stopped and cells attain a swollen shape. Synthesis of RNA and protein does occur in cells deprived of 5'-dTMP, the rates of synthesis being significantly lower than those in the controls.
    Type of Medium: Electronic Resource
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