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  • Arabidopsis thaliana  (1)
  • β-Lactamase  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Archives of microbiology 152 (1989), S. 437-440 
    ISSN: 1432-072X
    Keywords: Genetic transformation ; Plasmid ; Recombination ; pBR322 ; Chromosomal integration ; β-Lactamase ; Azotobacter vinelandii
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The soil bacterium Azotobacter vinelandii was genetically transformed by chromosomal integration to ampicillin and/or tetracycline resistance using restriction endonuclease-linearized plasmids. Polyacrylamide gel electrophoresis of protein extracts from three independently isolated ampicillin resistant transformants showed the presence of a 28 Kd band which is the approximate size of the ampicillin resistance gene product (i.e., β-lactamase). Moreover, with nitrocefin, a chromogenic cephalosporin, as a substrate, it was shown that all of the ampicillin resistant transformants produced functional β-lactamase. DNA hybridization showed that the chromosomal DNA from transformed cells contained plasmid DNA sequences at discrete sites. Growth experiments indicated that stable A. vinelandii transformants that carry functional integrated DNA were physiologically impaired.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1573-5028
    Keywords: adenine phosphoribosyltransferase ; Arabidopsis thaliana ; purine metabolism ; selectable marker
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract An intact cDNA fromArabidopsis thaliana for adenine phosphoribosyltransferase (APRT) was isolated and sequenced. The cDNA is 729 nucleotides in length and predicts a protein ofM r 27140. The deduced amino acid sequence has been compared with those of other APRTs and shown to be most similar to theEscherichia coli protein. Construction of a molecular tree of the known APRT amino acid sequences indicates theA. thaliana andE. coli APRT sequences form one cluster and the currently available vertebrate and invertebrate sequences form a separate grouping. Since it is possible to select either for or against the expression of APRT, the isolation of this APRT cDNA clone will allow these selection schemes to be used in plant genetic experiments.
    Type of Medium: Electronic Resource
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