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Living Modified Organism (LMO)
The image below identifies the LMO through its unique identifier, trade name and a link to this page of the BCH. Click on it to download a larger image on your computer. For help on how to use it go to the LMO quick-links page.
Liberty Link™ Yieldgard™ maize
EN
T25 x MON810
Yes
ACS-ZMØØ3-2 × MON-ØØ81Ø-6
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Organization:Monsanto ()800 North Lindbergh Blvd.St. Louis, MO
63167, United States of AmericaPhone: + 1 314 694-1000,Fax: +1 314 694-3080,Email:Website: http://www.monsanto.com, -
Organization:Bayer CropScience ()Phone:Fax:Email:Website: http://www.bayercropscience.com,
The stacked maize line ACS-ZMØØ3-2 x MON-ØØ81Ø-6 was obtained through the traditional cross breading of each of the parental organisms to produce a maize that expresses each of PAT and Cry1Ab genes. The expression of these genes are expected to confer resistance to Lepidoptera, and tolerant to glufosinate herbicide.
EN
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-246-6 Organism Zea mays (Maize, Corn, MAIZE)Crops
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BCH-LMO-SCBD-14767-14 Living Modified Organism ACS-ZMØØ3-2 - Liberty Link™ maizeBayer CropScience | Resistance to antibiotics (Ampicillin), Resistance to herbicides (Glufosinate)
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BCH-LMO-SCBD-14750-19 Living Modified Organism MON-ØØ81Ø-6 - YieldGard™ maizeMonsanto | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths), European corn borer (Ostrinia nubilalis))
EN
pDH51, PV-ZMBK07 and PV-ZMGT10
EN
- Cross breeding
0.860 kb
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2.630 kb
|
0.520 kb
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0.530 kb
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0.200 kb
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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-15002-4 Phosphinothricin N-acetyltransferase gene | Streptomyces viridochromogenes (STRVR)Protein coding sequence | Resistance to herbicides (Glufosinate)
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BCH-GENE-SCBD-14975-5 Beta-lactamase gene | Escherichia coli (ECOLX)Protein coding sequence | Resistance to antibiotics (Ampicillin)
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BCH-GENE-SCBD-14985-12 Cry1Ab | Bacillus thuringiensis (Bt, Bacillus, BACTU)Protein coding sequence | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths))
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BCH-GENE-SCBD-100287-7 CaMV 35S promoter | Cauliflower mosaic virus (CaMV)Promoter
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BCH-GENE-SCBD-100290-6 CaMV 35S terminator | Cauliflower mosaic virus (CaMV)Terminator
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BCH-GENE-SCBD-100366-6 CaMV Enhanced 35S promoter | Cauliflower mosaic virus (CaMV)Promoter
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BCH-GENE-SCBD-100359-7 Hsp70 intron | Zea mays (Maize, Corn, MAIZE)Intron
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BCH-GENE-SCBD-101411-3 pUC origin of replicationPlasmid Vector
DNA insert from ACS-ZMØØ3-2 vector pDH51
Glufosinate tolerance in T25 maize due to the enzyme phosphinothricin-N-acetyltransferase (PAT). The PAT enzyme catalyzes the acetylation of phosphinothricin, detoxifying it into an inactive compound. Molecular analyses shows that it has a truncated copy of the bla gene (25% of the 5' end of the bla gene is missing in T25) and an intact Ori-pUC.
DNA insert from MON-ØØ81Ø-6 vector PV-ZMBK07 and PV-ZMGT10
MON810 contains a truncated portion of a synthetic form of the cry1Ab gene from Bacillus thuringiensis subsp. kurstaki. This confers resistance to Lepidoptera pests. Two constructs PV-ZMBK07 and PV-ZMGT10 were used for transformation, but molecular analyses showed no elements from the PV-ZMGT10 construct were integrated and only the elements from construct PV-ZMBK07 have been integrated into its genome. The terminator of the nopaline synthase (nos) gene was lost due to a truncation at the 3' end of the gene cassette during genome integration and is, therefore, not present in MON810.
For additional information on this LMO, please refer to the records of the parental LMOs.
EN
Glufosinate tolerance in T25 maize due to the enzyme phosphinothricin-N-acetyltransferase (PAT). The PAT enzyme catalyzes the acetylation of phosphinothricin, detoxifying it into an inactive compound. Molecular analyses shows that it has a truncated copy of the bla gene (25% of the 5' end of the bla gene is missing in T25) and an intact Ori-pUC.
DNA insert from MON-ØØ81Ø-6 vector PV-ZMBK07 and PV-ZMGT10
MON810 contains a truncated portion of a synthetic form of the cry1Ab gene from Bacillus thuringiensis subsp. kurstaki. This confers resistance to Lepidoptera pests. Two constructs PV-ZMBK07 and PV-ZMGT10 were used for transformation, but molecular analyses showed no elements from the PV-ZMGT10 construct were integrated and only the elements from construct PV-ZMBK07 have been integrated into its genome. The terminator of the nopaline synthase (nos) gene was lost due to a truncation at the 3' end of the gene cassette during genome integration and is, therefore, not present in MON810.
For additional information on this LMO, please refer to the records of the parental LMOs.
EN
- Food
- Feed
- ACS-ZMØØ3-2 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) [ English ]
- MON-ØØ81Ø-6 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) [ English ]
- ACS-ZMØØ3-2 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) ( JRC ) [ English ]
- MON-ØØ81Ø-6 - EU Reference Laboratory for GM Food and Feed (EURL-GMFF) ( JRC ) [ English ]
- ACS-ZMØØ3-2 - CropLife International Detection Methods Database ( CropLife ) [ English ]
- MON-ØØ81Ø-6 - CropLife International Detection Methods Database ( CropLife ) [ English ]
EN
EN
- ACS-ZMØØ3-2 x MON-ØØ81Ø-6 - OECD [ English ]
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