EC Number   |
|---|
    2.7.7.27 | - |
| 2.7.7.27 | ADG1 encodes the small subunit, ADG2 encodes the large subunit |
| 2.7.7.27 | altered AGP large subunit (Sh2r6hs) from maize containing two alterations relative to the wild-type maize Sh2 sequence is introduced into wheat. The rev6 alteration confers reduced phosphate inhibition and decreased heat stability in maize and the hs alteration increases AGP subunit interactions and enzyme stability in Escherichia coli. Low-level expression of Sh2r6hs under control of the maize Sh2 promoter increases yield in wheat |
| 2.7.7.27 | apl1, DNA and amino acid determination and analysis, expression in Escherichia coli |
| 2.7.7.27 | apl2, DNA and amino acid determination and analysis, expression in Escherichia coli |
| 2.7.7.27 | apl3, DNA and amino acid determination and analysis, expression in Escherichia coli |
| 2.7.7.27 | apl4, DNA and amino acid determination and analysis, expression in Escherichia coli |
| 2.7.7.27 | aps1, DNA and amino acid determination and analysis, expression in Escherichia coli |
| 2.7.7.27 | bacterial glgC-TM gene, which codes for catalytically active, allosteric-insensitive enzyme, is introduced into seeds of Oryza sativa using an Agrobacterium tumefaciens-mediated transformation. The TM enzyme is expressed in the cytoplasm or amyloplast in Oryza sativa endosperm. Starch synthesis and consequently seed weight can be increased by manipulation of the cytoplasmic AGPase catalytic activity in transgenic rice |
| 2.7.7.27 | C-terminal truncated enzyme forms, expression in Escherichia coli |
