EC Number   |
|---|
   1.23.1.1 | - |
| 1.23.1.1 | expressed in BL21 (DE3)-RIL cells |
| 1.23.1.1 | expressed in Escherichia coli BL21 (DE3) cells |
| 1.23.1.1 | expressed in Escherichia coli BL21(DE3) cells |
| 1.23.1.1 | expressed in Escherichia coli BL21(DE3)pLysS cells |
| 1.23.1.1 | expressed in Escherichia coli Nova Blue cells |
| 1.23.1.1 | expressed in Escherichia coli Nova-Blue cells |
| 1.23.1.1 | expressed in Triticum aestivum cultivars Bobwhite, Madison, and Fielder |
| 1.23.1.1 | gene pinZ, recombinant expression in Arabidopsis thaliana under the control of the cauliflower mosaic virus 35S promoter, pinZ expression causes dynamic metabolic changes in stems, but not in roots and leaves. Accumulation of the glucoside of secoisolariciresinol appears to be elevated in the transgenic plant. Expression of pinZ influenced the metabolisms of lignan and glucosinolates but not so much of neolignans such as guaiacylglycerol-8-O-4'-feruloyl ethers, recombinant enzyme tissue expression pattern in plant seedlings |
| 1.23.1.1 | gene PLR2, recombinant expression of N-terminal and C-terminal fusions of LuPLR2 with EGFP or GUS in transgenic tobacco mesophyll cells, and LuPLR2 overexpression in transgenic flax plants, via transformation by Agrobacterium tumefaciens strain GV3101, quantitative RT-PCR expression analysis of LuPLR1 and LuPLR2 expressions in leaves and seeds, subcloning in Escherichia coli strain HB101. cis-Elements, responsible for gene expression in response to stress, are located in separate portions of the LuPLR2 promoter, presence of two MYB-binding sites. Quantitative RT-PCR expression analysis of LuPLR2 in transgenic seedlings, analysis of transcriptional regulation of the LuPLR2 gene |
