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  • 1
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 257 (1975), S. 253-254 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1 Alkaline sucrose gradient centrifugation patterns of 32P-labelled early replicative intermediates before (a) and after incubation in a cell extract with rifampicin (/?). A portion of sample C (unheated) in Table 1 was centrifuged in an alkaline sucrose gradient (5-20%) at 45,000 r.p.m. for 2 ...
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  • 2
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 270 (1977), S. 78-80 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] The effect of various concentrations of coumermycin on DNA synthesis in coumermycin-sensitive and resistant bacteria during 30 min after infection of phage T7 was examined. T7 DNA synthesis was inhibited by coumermycin, to a greater extent in the sensitive bacteria than in the resistant bacteria ...
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature 253 (1975), S. 652-654 
    ISSN: 1476-4687
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Chemistry and Pharmacology , Medicine , Natural Sciences in General , Physics
    Notes: [Auszug] Fig. 1 Electron micrographs of relaxation complexes that had been treated successively with Pronase, exonuclease III and endonuclease EcoRl. Purified relaxation complexes (34S) were prepared2 from A745 (Col El) thy (ref. 9) grown in a medium containing 3H-thymidine (20mCi mmo!"1). After treatment ...
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 111 (1971), S. 197-201 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Concatenand molecules of lambda DNA were formed even in a recombination dificient system (Int-Red-Rec-) in the late stage of phage growth. No significant difference was observed in the formation of concatemers between recombination deficient and proficient systems. These results suggest that concatemer formation is an intrinsic nature of replication in the late stage. The possibility of concatemer formation by molecular exchanges which do not contribute genetic recombination is not excluded.
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  • 5
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 101 (1968), S. 227-244 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Twenty-four UV sensitive strains which can not carry out the host cell reactivation and two which are deficient in recombination were isolated. By analyzing their properties and genetic locations, 21 UV sensitive strains were classified into the uvrA, B, and C groups and 3 strains into a group which has not been described. Two Rec- strains were classified in the recA group. The UV sensitive mutants of the new group are distinctly different from other mutants in their properties and in the sites of mutation. We named this group the uvrD. These uvrD mutants have the following properties. They have an intermediate sensitivity against UV irradiation and a higher sensitivity against γ-ray irradiation than those of other UV sensitive mutants. The UV damages which are repaired in the participation of the uvrD gene are photoreactivable. In the cells UV irradiated λ phage rapidly loses the susceptibility to photoreactivation during the incubation in broth with chloramphenicol. The DNA of the uvrD mutant is rapidly degraded at a small dose of UV light and to a large extent. The uvrD gene locates very close to the metE gene and uvrD- is dominant over uvrD+. The uvrD cells have the capacity to carry out UV reactivation for UV irradiated λ phage, in contrast to other UV sensitive mutants including the Rec- ones which turned out to have no capacity. A double mutant, uvrB uvrD, is about three times as sensitive as the uvrB mutant against UV irradiation and DNA degradation after UV irradiation takes place at much lower rate than the uvrD mutant. These results show the presence of a functional relation between the uvrB and uvrD genes and suggest that the uvrD gene participate in the repair synthesis at a step following that performed by the uvrB gene.
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  • 6
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 101 (1968), S. 245-256 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary It has been shown that linear DNA molecules of phage λ are converted to the twisted circular structure (species I) by covalent closure of the both strands at the cohesive ends after infection to the immune bacteria and that the twisted circular molecules are transformed to the circular form (species II) by a single-strand break in one of the strands of their DNA. This system offers a very sensitive method to study on the strand breaks or their repair. For characterization of the defects of ultraviolet sensitive strains, the structural changes of ultraviolet irradiated λ DNA in these strains were studied. Ultraviolet irradiation to λ phage greatly reduced the extent of conversion of the molecules to the species I in the uvrD mutant while the irradiation showed little effect on the conversion in the uvrA, B and C mutants. When infected bacteria carrying species I molecules were irradiated, the species I molecules in the uvrD mutant were disrupted while most of the molecules in the uvrA, B and C mutants kept the structure. These results indicate that in the irradiated λ DNA strand breaks are rarely introduced or, if introduced, repaired rapidly in the uvrA, B and C mutants and they are introduced in the uvrD mutant leading to the degradation of the DNA. These results provide a firm evidence that the defect of the uvrD mutant is different from other Her- mutants and in the process of repair synthesis. Ultraviolet irradiation to the uvrD mutants promote the formation of the species I molecules from the infected irradiated λ-DNA. Such effect was not observed with the uvrA mutant. Since the uvrD mutant has UV reactivation capacity and the uvrA mutant has not, the above phenomenon is probably caused by UV reactivation and may provide a more direct method to study the mechanisms of UV reactivation than the plaque assay.
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  • 7
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 103 (1968), S. 1-10 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The bacterial recA gene participates in the induction by UV irradiation of the clear mutation of phage λ and the Lac- mutation of bacteria. The necessary function is induced by irradiation of Rec+ bacteria and acts upon DNA irradiated with UV light.
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  • 8
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 178 (1980), S. 525-533 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary The dnaA46 cells can grow at high temperature when a high copy number plasmid pKY31, a derivative of pBR322 carrying a segment of the E. coli chromosome, integrates into the bacterial chromosome. In contrast, the dnaA46 polA - cells with the integrated plasmid can not grow at high temperature. Therefore, integration of the plasmid can suppress the dnaA mutation and this suppression requires DNA polymerase I which has been known to be required for plasmid replication. Full reversion of polA or lysogenization of λpolA + is lethal for the dnaA46polA - bacteria that carry the plasmid only in integrated state. Partial reversion of polA allows these cells to grow at both low and high temperatures. Introduction of the plasmid pBR322 into cytoplasm of these bacteria suppresses the lethal effect caused by full reversion of polA or lysogenization of λpolA +. This lethal effect expresses independent of the presence or absence of the dnaA mutation. In partial revertants of polA which have only integrated plasmid, the number of copies of a region near the replication origin of integrated plasmid increases. The number is reduced by the presence of extrachromosomal pBR322. It is suggested that the lethal effect of normal levels of DNA polymerase I in strains that carry only the integrated plasmid is due to excessive initiation of replication of the bacterial chromosome from the plasmid origin and high potential of initiation can be absorbed in many copies of cytoplasmic plasmid, probably, in their replication origins.
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  • 9
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 104 (1969), S. 51-58 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Weak-virulent mutants of temperate coli-phage λ were isolated which can grow on the λCIts lysogen producing a temperature-sensitive repressor but which cannot grow on the wild type λ lysogen producing a normal repressor. Genetic analysis on the mutants shows that their weak-virulence is attributable to two mutations, one (virL) in the region between sus N213 and c 47 and the other (virR) in the region between c 1 and sus O8. Both mutations are located within the region of non-homology between λ and λimm 434 phages. True virulent mutants which can grow on the wild type λ lysogen can be obtained easily from the weak-virulent mutant by an additional mutation, virC in a region very close to virR. The virulent mutants obtained are similar to the classical λvir mutant (Jacob and Wollman, 1954). The virL and virR mutations are probably operator mutations which render the genome insensitive to the λ repressor.
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Molecular genetics and genomics 176 (1979), S. 161-170 
    ISSN: 1617-4623
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Summary Plasmids carrying various portions of colicin E1 plasmid (ColE1) DNA have been isolated in an attempt to determine the regions of ColE1 DNA which are required for maintenance of the plasmid in bacteria. To construct the plasmids, the DNA of a ColE1 derivative that contains a gene which controls ampicillin resistance was cleaved by the restriction endonuclease HaeII. The digestion products were joined by T4 DNA ligase and then used to transform bacteria to ampicillin resistance. The plasmid derivatives obtained in this way were always composed of certain HaeII segments. These contain approximately 10% of the ColE1 genome and include the origin of replication of ColE1. We presume that the region of ColE1 which is common to all these derivatives is required for maintenance of the plasmid. After a description of these results, the nucleotide sequence of this region is presented, and possible roles of the region in plasmid replication and maintenance are discussed.
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