Library

feed icon rss

Your email was sent successfully. Check your inbox.

An error occurred while sending the email. Please try again.

Proceed reservation?

Export
  • 1
    ISSN: 1399-3054
    Source: Blackwell Publishing Journal Backfiles 1879-2005
    Topics: Biology
    Notes: Degenerate oligonucleotide primers based on the amino acid sequences of gibberellin (GA) 20-oxidases from pumpkin and Arabidopsis were used in nested polymerase chain reactions to generate an internal cDNA fragment from rice (Oryza satiya L.) seedlings. Using this fragment as a probe, a full-length cDNA (pOs20ox) was isolated from a cDNA library constructed from rice seedlings. The deduced amino acid sequence of Os20ox showed good identity (42–55%) with the GA 20-oxidases from pumpkin and Arabidopsis. Recombinant Os20ox protein, produced in Escherichia coli, catalyzed the conversion of GA12 and GA53 to GA9 and GA20, respectively. In contrast to the enzyme from immature pumpkin seeds, the recombinant rice GA 20-oxidase did not produce the tricarboxylic acids GA25 and GA17 from GA12 and GA53, respectively. The conversion rate of GA53 was higher than that of GA12. which is consistent with the relatively high abundance of 13-hydroxylated GAs in rice seedlings. Os20ox mRNA accumulated at higher levels in seedlings of two GA-deficient dwarf mutants than in normal plants. Treatment with uniconazole-P. an inhibitor of GA biosynthesis, increased abundance of the mRNA, while exogenously applied GA3 decreased it. These results suggest that the expression of the Os20ox gene is regulated by the level of physiologically active GA.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
  • 2
    ISSN: 1432-0983
    Keywords: Key wordsGibberella fujikuroi ; Gibberellin biosynthesis ; Copalyl diphosphate synthase gene ; ent-kaurene synthase gene
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The gene coding for copalyl diphosphate synthase (CPS), which represents the first gene of the gibberellin pathway, was isolated from the rice pathogen Gibberella fujikuroi. This fungus is used commercially for the production of gibberellic acid and related gibberellins. CPS is a terpene cyclase which catalyzes the first specific step of the gibberellin (GA) pathway as it branches off from the general isoprenoid (biosynthetic) pathway at geranylgeranyl disphosphate (GGDP). A cDNA fragment of the cps gene from the fungus G. fujikuroi was amplified by RT-PCR using oligonucleotides based on amino-acid sequences which were conserved between the plant CPSs and the bifunctional CPS/KS of the fungus Phaeosphaeria sp. L487. A 588-bp fragment obtained with nested PCR was used to isolate the corresponding genomic clone of the cps gene from the wild-type λ-library. This gene consists of three exons and two introns. The three exons are 2877 bp long and encode 959 amino-acid residues. The protein shares 48% identity with the bifunctional Phaeosphaeria sp. L487 FCPS and between 16% and 18% identity to the corresponding plant CPSs. Expression of the G. fujikuroi cps gene is strongly enhanced under conditions optimized for gibberellin biosynthesis and is reduced when high amounts of ammonium are present in the medium. Gene disruption, followed by gibberellin assays and Southern-blot analysis of the transformants, demonstrated clearly that the cloned gene has the expected function in the biosynthesis of fungal gibberellins.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
    BibTip Others were also interested in ...
Close ⊗
This website uses cookies and the analysis tool Matomo. More information can be found here...