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Biochemistry & Molecular Biology (Note)

Enhanced poly(3-hydroxybutyrate) production in transgenic tobacco BY-2 cells using engineered acetoacetyl-CoA reductase

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Pages 986-988 | Received 29 Aug 2014, Accepted 11 Dec 2014, Published online: 03 Feb 2015

Figures & data

Fig. 1. The plasmids used in this study.

Notes: phaC: PHA synthase gene, phaB: acetoacetyl-CoA reductase gene (wild type and TS mutant), 35S: 35S cauliflower mosaic virus promoter, NOS: nopaline synthase terminator, Kmr: kanamycin resistance gene, T-LB and T-RB: left and right borders of T-DNA, respectively.

Fig. 1. The plasmids used in this study.Notes: phaC: PHA synthase gene, phaB: acetoacetyl-CoA reductase gene (wild type and TS mutant), 35S: 35S cauliflower mosaic virus promoter, NOS: nopaline synthase terminator, Kmr: kanamycin resistance gene, T-LB and T-RB: left and right borders of T-DNA, respectively.

Fig. 2. RT-PCR of transgenic tobacco harboring phaB and phaC genes.

Notes: 1-3: transformants of pRIphaC-phaB(WT), 4-6: transformants of pRIphaC-phaB(TS), 7: wild-type BY2, and 8: positive control (plasmid).

Fig. 2. RT-PCR of transgenic tobacco harboring phaB and phaC genes.Notes: 1-3: transformants of pRIphaC-phaB(WT), 4-6: transformants of pRIphaC-phaB(TS), 7: wild-type BY2, and 8: positive control (plasmid).

Fig. 3. P(3HB) content in transgenic tobacco BY-2 cells.

Notes: WT: transformants of pRIphaC-phaB(WT), TS: transformants of pRIphaC-phaB(TS).

Fig. 3. P(3HB) content in transgenic tobacco BY-2 cells.Notes: WT: transformants of pRIphaC-phaB(WT), TS: transformants of pRIphaC-phaB(TS).

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