Sugarbeet modified for herbicide and fungus resistance | BCH-LMO-SCBD-111881 | Living Modified Organism | Biosafety Clearing-House

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BCH-LMO-SCBD-111881-2   |   PDF   |   Print   |  

Living Modified Organism (LMO)

Decisions on the LMO Risk Assessments  
published: 22 Mar 2017 last updated: 18 May 2017
Living Modified Organism identity
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.
Sugarbeet modified for herbicide and fungus resistance
EN
TAD13, TAD 18, TAD28, TAD33 and TAD44.
No
Sugarbeets were modified to constitutively express phosphinothricin acetyltransferase (pat) gene. As a result of the genetic modification the resulting sugarbeet is tolerant to L-phosphinothricin-containing herbicides.

Furthermore, the plants were also modified to constitutively express the defensin-like protein 1 gene (AMP1) of Dahlia merckii. Defensins have antimicrobial properties, therefore the introduction of the AMP1 gene confers a resistance to pathogenic fungi to the plants.
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.
EN
Characteristics of the modification process
pIG35SDM
EN
  • Direct DNA transfer
Some of these genetic elements may be present as fragments or truncated forms. Please see notes below, where applicable.
The pIG35SDM plasmid was transferred into the plants as naked DNA via protoplast transformation. As a result, some of the transformation events have the entire transformation vector integrated into their genome while others only contain parts thereof.

In addition to the genetic elements listed above, the pIG35SDM plasmid also contained the following sequences which were also transferred into the modified sugarbeet but are non-functional in plants:

* The imidazoleglycerol phosphate dehydratase (his3) gene from Saccharomyces cerevisiae which is expressed as a selection marker in bacteria under the control of its native promoter and terminator sequences. Furthermore, due to the close proximity of these genes within the yeast genome, the transcription initiation site of the yeast ATP-dependent RNA helicase (ded1) gene and the first 6 bp of the ded1 coding sequence are included with of the 3‘ sequence of the his3 gene.

* Portions of the Lac operon from Escherichia coli, specifically: a 12 bp sequence of the N terminus of the lacZ  gene, the promoter/operator region of the lacZ gene and 88 bp of the sequence of the C terminus of the lacI gene.

* The origin of replication of the  pMB1 plasmid from E. coli.

Each of the transformation events contain up to three copies of the genes integrated into their respective genomes. There is no extrachromosomal replication of the genetic material.
EN
LMO characteristics
EN
  • Research
Detection method(s)
EN
Additional Information
EN
Records referencing this document Show in search
Record type Field Record(s)
Country's Decision or any other Communication Living modified organism(s) 1
Risk Assessment generated by a regulatory process Living modified organism(s) 1