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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Theoretical and applied genetics 95 (1997), S. 424-430 
    ISSN: 1432-2242
    Keywords: Key words Lr19 translocation ; Thinopyrum ; Ph-induced recombinants ; Physical mapping
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract  Following the induction of allosyndetic pairing between the Thinopyrum-derived Lr19 translocation in ‘Indis’ wheat and homoeologous wheat chromatin, eight suspected recombinants for the Lr19 region were recovered. These selections were characterised for marker loci that were previously used to construct a physical map of the Lr19 segment. At the same time near-isogenic lines were developed for some of the selected segments and tested for seedling leaf-rust resistance in order to confirm the presence of Lr19. It appeared that three of the four white-endosperm selections do not possess Lr19 and only one, 88M22-149, is a true Lr19 recombinant. The resistance gene in the three non-Lr19 selections resides on chromosome 6B, appears to derive from ‘Indis’, and was selected unintentionally during backcrossing. The pedigree of ‘Indis’ is suspect and it is believed that the Lr19 translocation in ‘Indis’ is in reality the Th. ponticum-derived (T4) segment rather than being of Th. distichum origin as was believed earlier. The white-endosperm recombinant, 88M22-149, retained the complete Lr19 resistance and was apparently re-located to chromosome arm 7BL in a double-crossover event. 88M22-149 has lost the Sd1 gene and often shows strong self-elimination in translocation heterozygotes. This effect may result from additional gametocidal loci or from an altered chromosome structure following re-location of the segment. 88M22-149 in fact contains a duplicated region involving the Wsp-B1 locus. Three selections had partially white endosperms and expressed Lr19 and other Thinopyrum marker alleles. Polymorphisms for the available markers confirmed that the translocated segment in at least one of them had been shortened through recombination with chromosome arm 7DL. Further markers need to be studied in order to determine whether the translocation in the remaining two partially white recombinants had also undergone recombination with wheat. The eighth selection has yellow endosperm and appears to self-eliminate in certain translocation heterozygotes. No evidence of recombination could be found with the markers used. If the latter selections are in fact recombinants they may prove useful in attempts to unravel the complex segregation distortion mechanism.
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  • 2
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract A recombinant strain of Saccharomyces cerevisiae was constructed that contained the genes encoding a bacterial α-amylase (AMY1), a yeast glucoamylase (STA2) and a bacterial pullulanase (pulA). The Bacillus amyloliquefaciens α-amylase and S. cerevisiae var. diastaticus glucoamylase genes were expressed in S. cerevisiae using their native promoters and the encoded enzymes secreted under direction of their native leader sequences. In contrast, the Klebsiella pneumoniae pullulanase gene was placed under the control of the yeast alcohol dehydrogenase gene promoter (ADC1 P ) and secreted using the yeast mating pheromone α-factor secretion signal (MFα1 S ). Transcription termination of the pullulanase gene was affected by the yeast tryptophan synthase gene terminator (TRP5 T), whereas termination of the glucoamylase and α-amylase genes was directed by their native terminators. Pullulanase (PUL1) produced by recombinant yeasts containing ADC1 P MFα1 S pulA TRP5T (designated PUL1) was further characterized and compared to its bacterial counterpart (PulA). The different genes were introduced into S. cerevisiae in different combinations and the various amylolytic Saccharomyces transformants compared to Schwanniomyces occidentalis. Introduction of PUL1 into a S. cerevisiae strain containing both STA2 and AMY1, resulted in 99% assimilation of starch
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  • 3
    ISSN: 1432-0614
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: Abstract  A recombinant strain of Saccharomyces cerevisiae was constructed that contained the genes encoding a bacterial α-amylase (AMY1), a yeast glucoamylase (STA2) and a bacterial pullulanase (pulA). The Bacillus amyloliquefaciensα-amylase and S. cerevisiae var. diastaticus glucoamylase genes were expressed in S. cerevisiae using their native promoters and the encoded enzymes secreted under direction of their native leader sequences. In contrast, the Klebsiella pneumoniae pullulanase gene was placed under the control of the yeast alcohol dehydrogenase gene promoter (ADC1 P ) and secreted using the yeast mating pheromone α-factor secretion signal (MF α 1 S ). Transcription termination of the pullulanase gene was effected by the yeast tryptophan synthase gene terminator (TRP5 T ), whereas termination of the glucoamylase and α-amylase genes was directed by their native terminators. Pullulanase (PUL1) produced by recombinant yeasts containing ADC1 P MF α 1 S pulA TRP5 T (designated PUL1) was further characterized and compared to its bacterial counterpart (PulA). The different genes were introduced into S. cerevisiae in different combinations and the various amylolytic Saccharomyces transformants compared to Schwanniomyces occidentalis. Introduction of PUL1 into a S. cerevisiae strain containing both STA2 and AMY1, resulted in 99% assimilation of starch
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  • 4
    Publication Date: 1995-03-01
    Print ISSN: 0175-7598
    Electronic ISSN: 1432-0614
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Published by Springer
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  • 5
    Publication Date: 1995-03-01
    Print ISSN: 0175-7598
    Electronic ISSN: 1432-0614
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Published by Springer
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