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Living Modified Organism (LMO)
  |  
Decisions on the LMO Risk Assessments  
published: 24 Apr 2026 last updated: 16 Jul 2026
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.
Nematode-resistant and herbicide-tolerant soybean
EN
GMB151 x DAS44406
Yes
BCS-GM151-6 x DAS-444Ø6-6
The soybean (Glycine max) was produced through cross breeding of modified parental varieties BCS-GM151-6 x DAS-444Ø6-6.
Soybean BCS-GM151-6 was modified for resistance to plant-parasitic nematode and for tolerance to 4-hydroxyphenylpyruvate dioxygenase (HPPD)-inhibiting herbicides. To achieve resistance to nematodes, the soybean expresses Bacillus thuringiensis Cry14Ab1, an insecticidal crystal protein that is active against susceptible nematodes, including soybean cyst nematode. The protein is considered to act through disruption of intestinal cells following ingestion. To achieve tolerance to (HPPD)-inhibiting herbicides, the soybean expresses a modified Pseudomonas fluorescens HPPD, containing amino acid substitutions that reduce sensitivity to herbicides such as isoxaflutole and mesotrione.
Soybean DAS-444Ø6-6 was modified for glyphosate, 2,4-Dichlorophenoxyacetic acid (2,4-D) and glufosinate herbicide tolerance. To achieve glyphosate tolerance, the soybean expresses modified Zea mays enzyme 5-enolpyruvylshikimate-3-phosphate synthase, which has reduced binding affinity for glyphosate and allows continued synthesis of aromatic amino acids through the shikimate pathway in the presence of the herbicide. To achieve tolerance to aryloxyalkanoate herbicides, including 2,4-dichlorophenoxyacetic acid, the soybean expresses aryloxyalkanoate dioxygenase (AAD-12), which degrades these herbicides into non-herbicidal compounds. To achieve tolerance to glufosinate, the soybean expresses the gene from Streptomyces viridochromogenes encoding phosphinothricin N-acetyltransferase encoding gene, which inactivates the active compound L-phosphinothricin through acetylation of the primary amino group. 
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.
  • BCH-LMO-SCBD-115763-2 Living Modified Organism BCS-GM151-6 - Plant-Parasitic Nematode-Protected and Herbicide Tolerant Soybean
    BASF Plant Science GmbH | Resistance to diseases and pests (Nematodes), Resistance to herbicides, Tolerance to isoxaflutole, Tolerance to mesotrione
  • BCH-ORGA-SCBD-10453-8 Organism Glycine max (Soybean, Soya bean, Soya / soja /соя, SOYBN)
    Crops
  • BCH-LMO-SCBD-105041-4 Living Modified Organism DAS-444Ø6-6 - Enlist E3™ Soybean
    Dow AgroSciences | Resistance to 2,4-Dichlorophenoxyacetic acid, Resistance to herbicides (Glufosinate, Glyphosate)
Soybean variety Throne (for event GMB151)
EN
  • DAS-68416-4 - Enlist™ Soybeans
    | Dow AgroSciences GmbH | Resistance to herbicides (Glufosinate), Tolerance to 2,4-Dichlorophenoxyacetic acid
  • DAS-81419-2 × DAS-444Ø6-6 - Conkesta Enlist E3™ Soybean
    | Resistance to diseases and pests (Insects, Lepidoptera (butterflies and moths)), Resistance to herbicides (Glufosinate, Glyphosate), Tolerance to 2,4-Dichlorophenoxyacetic acid
Characteristics of the modification process
pSZ8832 and pDAB8264
EN
  • Cross breeding
Some of these genetic elements may be present as fragments or truncated forms. Please see notes below, where applicable.
  • BCH-GENE-SCBD-100290-6 CaMV 35S terminator | Cauliflower mosaic virus (CaMV)
    Terminator
  • BCH-GENE-SCBD-115761-1 Cry14Ab1 | Bacillus thuringiensis (Bt, Bacillus, BACTU)
    Protein coding sequence | Resistance to diseases and pests (Nematodes)
  • BCH-GENE-SCBD-104802-5 Polyubiquitin10 gene promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoter
  • BCH-GENE-SCBD-104793-3 4-hydroxyphenylpyruvate dioxygenase | Pseudomonas fluorescens (PSEFL)
    Protein coding sequence | Resistance to herbicides
  • BCH-GENE-SCBD-101419-5 Optimized chloroplast transit peptide | Zea mays (Maize, Corn, MAIZE) | Helianthus annuus (Sunflower, HELAN)
    Transit signal
  • BCH-GENE-SCBD-115762-1 Leader sequence | Tobacco etch virus (TEV)
    Leader sequence
  • BCH-GENE-SCBD-100366-6 CaMV Enhanced 35S promoter | Cauliflower mosaic virus (CaMV)
    Promoter
  • BCH-GENE-SCBD-104795-4 RB7 matrix attachment region | Nicotiana tabacum (Tobacco, TOBAC )
    Enhancer
  • BCH-GENE-SCBD-104646-4 Histone H4 gene 3' UTR | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Terminator
  • BCH-GENE-SCBD-46333-8 5-enolpyruvylshikimate-3-phosphate synthase | Zea mays (Maize, Corn, MAIZE)
    Protein coding sequence | Resistance to herbicides (Glyphosate)
  • BCH-GENE-SCBD-104648-2 Histone H3 Gene II intron 1 | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Intron
  • BCH-GENE-SCBD-104647-3 Histone H4 gene Promoter | Arabidopsis thaliana (Thale cress, Mouse-ear cress, Arabidopsis, ARATH)
    Promoter
  • BCH-GENE-SCBD-104805-2 Aryloxyalkanoate dioxygenase gene | Delftia acidovorans (DELAC)
    Protein coding sequence | Resistance to herbicides
  • BCH-GENE-SCBD-104806-3 ORF23 3' Untranslated region | Agrobacterium tumefaciens (Agrobacterium)
    Terminator
  • BCH-GENE-SCBD-101900-6 CsVMV promoter | Cassava vein mosaic virus (Cassava vein mosaic virus, CVMV, CsVMV)
    Promoter
  • BCH-GENE-SCBD-15002-5 Phosphinothricin N-acetyltransferase | Streptomyces viridochromogenes (STRVR)
    Protein coding sequence | Resistance to herbicides (Glufosinate)
  • BCH-GENE-SCBD-104807-2 ORF1 3' Untranslated region | Agrobacterium tumefaciens (Agrobacterium)
    Terminator
DNA insert from BCS-GM151-6 (vector pSZ8832)
The transforming plasmid pSZ8832 contained a transfer DNA (T-DNA) region comprising two gene cassettes expressing the nematode resistance protein Cry14Ab-1, derived from Bacillus thuringiensis, and the herbicide tolerance protein HPPD-4, a modified 4-hydroxyphenylpyruvate dioxygenase derived from Pseudomonas fluorescens. Transformation of the soybean was achieved through Agrobacterium tumefaciens-mediated transformation. 
(1) Transcription of the cry14Ab-1 coding sequence is directed by the promoter of the ubiquitin 10 gene from Arabidopsis thaliana, which is expected to promote constitutive expression in plant tissues. Transcription is terminated by the 3′ untranslated region of the 35S terminator from Cauliflower mosaic virus. Expression of this cassette results in production of the Cry14Ab-1 protein, which confers resistance to plant parasitic nematodes.
(2) Transcription of the hppdPf-4Pa coding sequence is directed by an enhanced 35S promoter from Cauliflower mosaic virus containing duplicated enhancer regions to promote high levels of transcription. A leader sequence from Tobacco etch virus is present to enhance translation efficiency. The coding region includes a synthetic chloroplast transit peptide derived from Zea mays and Helianthus annuus sequences to direct the expressed protein to the chloroplast. Transcription is terminated by the 3′ untranslated region of the 35S transcript from Cauliflower mosaic virus. Expression of this cassette results in production of the modified HPPD-4 protein containing amino acid substitutions associated with reduced sensitivity to HPPD-inhibiting herbicides, thereby conferring tolerance to herbicides such as isoxaflutole and mesotrione.
Notes
  • The inserted cassettes are present in the counter-clockwise orientation.
  • Molecular characterization by sequencing analysis indicated the presence of a single, intact copy of the intended T-DNA insertion without rearrangements. 
  • A 21 base pair sequence corresponding to the ORIpVS1 vector backbone was detected in the soybean genome; this sequence does not contain any antibiotic resistance coding region. 
  • The insertion event also resulted in a 63 base pair deletion of host genomic DNA. Bioinformatic analysis indicated that the insert is located within the 3′ untranslated region of a putative BON1-associated protein 1 (BAP1)-like gene on chromosome 7 which has a function in a signal transduction cascade in Arabidopsis thaliana but is uncharacterized in Glycine max. No evidence of instability of the inserted genetic material was reported.

DNA insert from DAS-444Ø6-6 (vectors pDAB8264)
The transforming plasmid pDAB8264 contained a transfer DNA region comprising three gene cassettes expressing the proteins 2mEPSPS (modified 5-enolpyruvylshikimate-3-phosphate synthase gene) derived from Zea mays, aryloxyalkanoate dioxygenase (AAD-12) from Delftia acidovorans, and phosphinothricin N-acetyltransferase (PAT) from Streptomyces viridochromogenes.
(1) Transcription of the 2mepsps coding sequence is directed by H4 histone (H4A748) promoter together with the 5′ untranslated region and an intron from the histone 3 gene from Arabidopsis thaliana. The coding region includes an optimized chloroplast transit peptide derived from Zea mays and Helianthus annuus RuBisCO sequences to direct the expressed protein to the chloroplast. Transcription is terminated by the 3′ untranslated region of the H4A748 gene from Arabidopsis thaliana. A matrix attachment region from the Nicotiana tabacum rb7 gene is also present to increase gene expression. Expression of this cassette results in production of the 2mEPSPS protein containing two amino acid substitutions that confer reduced sensitivity to glyphosate, thereby allowing continued synthesis of aromatic amino acids through the shikimate pathway in the presence of the herbicide.
(2) Transcription of the aad-12 coding sequence is directed by the promoter together with the 5′ untranslated region and intron from the polyubiquitin 10 gene from Arabidopsis thaliana. Transcription is terminated by the 3' untranslated region (3' UTR) of open reading frame 23 (ORF23) of plasmid pTi15955 from Agrobacterium tumefaciens. Expression of this cassette results in production of the AAD-12 protein, an alpha-ketoglutarate-dependent dioxygenase that metabolically inactivates herbicides of the aryloxyalkanoate family, including 2,4-dichlorophenoxyacetic acid (2,4-D).
(3) Transcription of the pat coding sequence is directed by the promoter together with the 5′ untranslated region from the Cassava Vein Mosaic virus. Transcription is terminated by the 3' UTR of the ORF1 of plasmid pTi15955 from Agrobacterium tumefaciens. Expression of this cassette results in production of the PAT protein, a phosphinothricin acetyltransferase that inactivates glufosinate through acetylation.
Note
  • Molecular characterization by Southern blot analysis indicated that a single, intact copy of the intended T-DNA insertion containing the aad-12, 2mepsps and pat expression cassettes was integrated into the soybean genome.
  • Southern blot analysis confirmed the absence of integrated plasmid backbone DNA.
  • The integrity of the inserted DNA was demonstrated over five breeding generations. Segregation analyses confirmed the expected Mendelian inheritance pattern, indicating stable inheritance during conventional breeding.
  • No evidence of rearrangement or instability of the inserted genetic material was reported.

For additional information on this LMO, please refer to the records of the parental LMOs.
EN
LMO characteristics
EN
  • Feed
  • Food
Additional Information
EN
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Record type Field Record(s)
Risk Assessment generated by a regulatory process Living modified organism(s) 1