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Literature summary for 2.7.1.163 extracted from

  • Zernova, O.; Zhong, W.; Zhang, X.H.; Widholm, J.
    Tissue culture specificity of the tobacco ASA2 promoter driving hpt as a selectable marker for soybean transformation selection (2008), Plant Cell Rep., 27, 1705-1711.
    View publication on PubMed

Application

Application Comment Organism
biotechnology resistance against hyromycin B mediated by transformation of the hph gene Escherichia coli
molecular biology gene is used as selectable marker, mediates hygromycin resistence Escherichia coli

Cloned(Commentary)

Cloned (Comment) Organism
The hpt coding region is obtained by a XhoI digestion of the vector pCAMBIA1380 and is cloned into the SalI-cut pBluescript KSII. The EcoRV-XhoI fragment of the hpt coding sequence is ligated with the SmaI-XhoI fragment of pHAG to obtain the intermediate plasmid pHyII, so that the hpt coding region is flanked by the 2.3 kb ASA2 promoter at the 5'end and the Arabidopsis actin2 terminator at the 3'end. Finally, the SacI-SacII fragment of pHyII is ligated into the SacI-SacII-cut pBluescript KSII to complete the transformation vector pXZIII-8. Escherichia coli

Organism

Organism UniProt Comment Textmining
Escherichia coli
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Protein sequence is used (vector pCAMBIA1380) for a selectable marker for soybean transformation selection.
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Synonyms

Synonyms Comment Organism
HPT
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Escherichia coli
hygromycin phosphotransferase
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Escherichia coli