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  • 1
    ISSN: 1432-0983
    Keywords: Key words mtDNA ; Promiscuous DNA ; Maize cmsT ; Organelle genomes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract The DNA sequence of a 7.5-kbp region from the maize cmsT mt genome was determined. Nucleotide-sequence analysis of this region reveals the presence of a ct-like trnI (CAT) gene, orf31 and orf48 which are respectively homologous to the trnI (CAT) gene in the maize and rice chloroplast genomes, and to orf28 and orf64 in the rice chloroplast genome. Northern-blot analysis indicates that the ct-like trnI (CAT) gene is likely to be a pseudo gene in the maize cmsT mt genome because it is not transcribed. A nucleotide-sequence homology search of this 7.5-kbp region reveals several short segments homologous to portions of chloroplast (ct), mitochondrial (mt) and other known genes. These segments range from 17 bp to 187 bp in length with homology from 71 to 100%. These observations also suggest that the transfer of DNA fragments from the ct genome to the mt genome may have occurred at different times during the evolution of the maize mt genome, and that multiple recombination events and rearrangements in both mt and ct genomes have occurred after the transfer of DNA fragments from the ct to the mt genome. A few segments were identified by their homology to be portions of genes from sources other than the ct genome. While it is known that large fragments of ctDNA have been transferred to maize mt genomes, this is the first report of the presence of numerous short ctDNA, or other foreign DNA segments, in the maize cmsT mt genome. These segments may provide valuable information regarding the evolution of plant mt genomes.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] In nuclear transgenic plants, expression of multiple genes requires introduction of individual genes and time-consuming subsequent backcrosses to reconstitute multi-subunit proteins or pathways, a problem that is compounded by variable expression levels. In order to accomplish expression of ...
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature America Inc.
    Nature biotechnology 17 (1999), S. 855-856 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] Environmental concerns have led to a growing public wariness of genetically modified crops around the world. A common concern is the possibility of gene escape through pollen or seed dispersal from crop plants engineered for herbicide resistance to their weedy relatives, possibly creating ...
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Company
    Nature biotechnology 16 (1998), S. 602-602 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] To the editor: It is unfortunate that Stewart and Prakash have missed the point of maternal inheritance of foreign genes in MOST crops, when .they are engineered via the chloroplast genome. Such false and irresponsible statements, solely based on speculation and cursory knowledge or understanding ...
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Company
    Nature biotechnology 16 (1998), S. 345-348 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] Glyphosate is a potent herbicide. It works by competitive inhibition of the enzyme 5-enol-pyruvyl shikimate-3-phosphate synthase (EPSPS), which catalyzes an essential step in the aromatic amino acid biosynthetic pathway. We report the genetic engineering of herbicide resistance by stable ...
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature biotechnology 20 (2002), S. 581-586 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] The potential of genetically modified (GM) crops to transfer foreign genes through pollen to related plant species has been cited as an environmental concern. Until more is known concerning the environmental impact of novel genes on indigenous crops and weeds, practical and ...
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    [s.l.] : Nature Publishing Group
    Nature biotechnology 21 (2003), S. 374-375 
    ISSN: 1546-1696
    Source: Nature Archives 1869 - 2009
    Topics: Biology , Process Engineering, Biotechnology, Nutrition Technology
    Notes: [Auszug] Because chloroplast DNA is usually maternally inherited during seed formation, the engineering of transplastomic crops has been put forward as a promising means of containing transgenes. For this strategy to progress, greater understanding of the process of gene transfer from ...
    Type of Medium: Electronic Resource
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  • 8
    ISSN: 1432-203X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract We report the expression of a protein-based polymer (Gly-Val-Gly-Val-Pro)121, i. e., (GVGVP)121 in transgenic tobacco (Nicotiana tabacum var. Kentucky 17) plants. The plant expression vector pBI121-XZ-120mer which contains the gene (GVGVP)121 with a prokaryotic preferred codon composition driven by the CaMV 35S promoter was introduced into tobacco plants byAgrobacterium-mediated transformation. Stable integration of the (GVGVP)121 polymer gene was confirmed by Southern blot analysis. Northern hybridization showed polymer transcripts in leaves of transgenic plants. The (GVGVP)121 polymer protein was detected in leaves of transgenic plants by Western blot. The (GVGVP)121 protein could be easily purified to a high degree of purity from leaves of transgenic plants by reversible phase transition as revealed by SDS-PAGE gels stained by CuCl2. Transgenic plants grew, flowered, and produced seeds normally.
    Type of Medium: Electronic Resource
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  • 9
    ISSN: 1432-203X
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: ABSTRACT We report the expression of a protein-based polymer (Gly-Val-Cly-Val-Pro)121, i.c., (GVGVP)121 in transgenic tobacco (Nicotiana tabacum var. Kentucky 17) plants. The plant expression vector pBI121-XT-120mer which contains the gene (GVGVP)121 with a prokaryotic preferred codon composition driven by the CaMV 35S promoter was introduced into tobacco plants by Agrobacterium-mediated transformation. Stable integration of the (GVGVP)121 polymer gene was cofirmed by Southern blot analysis. Northern hybridization showed polymer transcripts in leaves of transgenic plants. The (GVGVP)121 polymer protein was detected in leaves of transgenic plants by Western blot. The (GVGVP)121 protein could be easily purified to a high degree of purity from leaves of transgenic plants by reversible phase transition as revealed by SDS-PAGE gels stained by CuCl2. Transgenic plants grew, flowered, and produced seeds normally.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Springer
    Photosynthesis research 19 (1988), S. 23-37 
    ISSN: 1573-5079
    Keywords: binding ; uptake ; transformation ; DNA ; cyanobacteria ; etioplasts
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract Discoveries of the uptake and expression of various Escherichia coli plasmids by the cyanobacterium Anacystis nidulans and isolated cumber etioplasts are reviewed. In particular, the binding and uptake of nick-translated 32P-labeled plasmids and the expression of genes in the native plasmids are considered. Permeaplasts of A. nidulans 6301 and isolated EDTA-washed cucumber etioplasts exhibit binding and uptake of DNA that is unaffected by uncouplers of photophosphorylation or by dissipators of transmembrane proton graident. ATP inhibits both binding and udptake by permeaplasts or EDTA-washed etioplasts but the analog AMP-PNP (non-hydrolzable) is noninhibitory. With permeaplasts there is no effect of 20 mM Mg2+ (in the light) upon intake, whereas with EDTA-washed etioplasts, Mg2+ at the same concentration inhibits uptake as does 20 mM Ca2+. The transformation of A. nidulans 6301 to ampicillin-resistance by the plasmid pBR322 is much enhanced in permeaplasts. Indeed extracts of transformed cells catalyze the hydrolosis of the β-lactam nitrocefin. Transfromation of A. nidulans to antibiotic resistance may also be achieved with the plasmids pHUB4 and pCH1. The effect of light on transformation of A. nidulans 6301 differs with different plasmids. In pBR322 transformants the expression of ribulose bisphosphate carboxylase-oxygenase (RuBisCO) is markedly elevated. In these transformants, the foreign plasmid replicates by a pathway involving chromosomal integration and dissociation. The plasmid pCS75, a derivative of pUC9 (and therefore of pBR322) containing a Pst1 insert carrying genes for the large and small (S) subunits of RuBisCO from A. nidulans, is taken up and expressed in EDTA-washed cucumber cotyledon etioplasts. Expression is evidenced by the hydrolysis of nitrocefin and immunoprecipitation of labeled S subunits of RuBisCO (utilizing etioplasts which have been labeled with 35S-methionine after incubation with pCS75). The plasmid pUC9-CM carrying a cat gene is also expressed in cucumber etioplasts in a manner that demonstrates dependence both on the duration of etioplast washing by EDTA and plasmid concentration. Translation (as measured by 35S-methionine incorporation) by EDTA-washed etioplasts increases with cotyledon greening. However the enhancement of translation by prior incubation of EDTA-washed plastids with pCS75 decreases to zero during 24hr of cotyledon greening. Results suggest that the expression of foreign DNA in plastids may depend critically upon their developmental state.
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