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The SnRK2.1 protein was expressed in a cell-free expression system based on an E. coli ribosomal extract (S30 extract). S30 extract was prepared as previously reported [18] with some modifications. Briefly, in order to bypass the exogenous addition of commercial creatine kinase (CK) and T7 RNA polymerase (T7 RNAP) into the cell-free reaction mixtures, two types of S30 extracts (CK-T7 extract and BL21 extract) were prepared. The CK-T7 extract was prepared from the E. coli strain BL21 Star (DE3) (Life Technologies) harboring a CK and T7 RNAP expression vector pETDuet-CK-T7 (Figure 1). CK and T7 RNAP were expressed during the cultivation of E. coli via IPTG induction (1.0 mM) at 0.5 OD600. |
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Protocol tips |
The SnRK2.1 protein was expressed in a cell-free expression system based on an E. coli ribosomal extract (S30 extract). S30 extract was prepared as previously reported [18] with some modifications. Briefly, in order to bypass the exogenous addition of commercial creatine kinase (CK) and T7 RNA polymerase (T7 RNAP) into the cell-free reaction mixtures, two types of S30 extracts (CK-T7 extract and BL21 extract) were prepared. The CK-T7 extract was prepared from the E. coli strain BL21 Star (DE3) (Life Technologies) harboring a CK and T7 RNAP expression vector pETDuet-CK-T7 (Figure 1). CK and T7 RNAP were expressed during the cultivation of E. coli via IPTG induction (1.0 mM) at 0.5 OD600. |
Publication protocol
The SnRK2.1 protein was expressed in a cell-free expression system based on an E. coli ribosomal extract (S30 extract). S30 extract was prepared as previously reported [18] with some modifications. Briefly, in order to bypass the exogenous addition of commercial creatine kinase (CK) and T7 RNA polymerase (T7 RNAP) into the cell-free reaction mixtures, two types of S30 extracts (CK-T7 extract and BL21 extract) were prepared. The CK-T7 extract was prepared from the E. coli strain BL21 Star (DE3) (Life Technologies) harboring a CK and T7 RNAP expression vector pETDuet-CK-T7 (Figure 1). CK and T7 RNAP were expressed during the cultivation of E. coli via IPTG induction (1.0 mM) at 0.5 OD600. The cells were harvested 2 h after induction and used for preparing the CK-T7 extract. The standard BL21 S30 extract was prepared from the E. coli strain BL21 Star (DE3) as previously reported [18].
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