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Living Modified Organism (LMO)
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Potato modified for reduced sucrose synthesis
EN
5 independent lines
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OrganizationInstitut für Pflanzengenetik und Kulturpflanzenforschung ()Corrensstrasse 3Gatersleben,
06466 , GermanyPhone: +49 (0)39482 5-0 ,Fax: +49 (0) 39482 5139,Email: info@ipk-gatersleben.de,Website: http://www.ipk-gatersleben.de,
The genetically modified plants constitutively express the coding region of the cytosolic fructose-1,6-bisphosphatase in an antisense orientation.
Fructose-1,6-bisphosphatase is involved in the sucrose biosynthesis. As a result of the genetic modification endogenous FBPase is inhibited which leads to a reduced sucrose content in the modified potato plants.
Fructose-1,6-bisphosphatase is involved in the sucrose biosynthesis. As a result of the genetic modification endogenous FBPase is inhibited which leads to a reduced sucrose content in the modified potato plants.
The term “Recipient organism” refers to an organism (either already modified or non-modified) that was subjected to genetic modification, whereas “Parental organisms” refers to those that were involved in cross breeding or cell fusion.
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BCH-ORGA-SCBD-12106-6 Organism Solanum tuberosum (Potato, SOLTU)Crops
Dervative of pBIN19
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- Agrobacterium-mediated DNA transfer
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Some of these genetic elements may be present as fragments or truncated
forms. Please see notes below, where applicable.
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BCH-GENE-SCBD-100287-7 CaMV 35S promoterPromoter
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BCH-GENE-SCBD-111545-2 Fructose-1,6-bisphosphatase gene | (Potato)Protein coding sequence | Changes in quality and/or metabolite content (Carbohydrates)
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BCH-GENE-SCBD-100271-5 Octopine Synthase Gene TerminatorTerminator
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BCH-GENE-SCBD-15001-5 Neomycin Phosphotransferase II | (Bacteria)Protein coding sequence | Resistance to antibiotics (Kanamycin)
The neomycin phosphotransferase II of the Tn5 transposon (CS-nptII-ECOLX) is used as a selection marker.
- Research
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