| 000 | 01977nam a2200241Ia 4500 | ||
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| 003 | MX-MdCICY | ||
| 005 | 20250625122509.0 | ||
| 040 | _cCICY | ||
| 090 | _aB-5985 | ||
| 245 | 1 | 0 | _aTransgenic plants of coffea canephora from embryogenic callus via agrobacterium tumefaciens-mediated transformation |
| 490 | 0 | _vPlant Cell Reports, 19, p.106-110, 1999 | |
| 520 | 3 | _aAbstract Embryogenic calli were induced from leaf explants of coffee (Coffea canephora)on McCown's woody plant medium (WPM)supplemented with 5 7M N6-(2-isopentenyl)-adenosine (2-iP). These calli were co-cultured with Agrobacterium tumefaciens EHA101 harboring pIG121-Hm, containing #-glucuronidase (GUS), hygromycin phosphotransferase (HPT), and neomycin phosphotransferase II genes. Selection of putative transgenic callus was performed by gradual increase in hygromycin concentration (5, 50, 100 mg/l). The embryogenic calli surviving on medium containing 100 mg/l hygromycin showed a strong GUS-positive reaction with X-Gluc solution. Somatic embryos were formed from these putative transgenic calli and germinated on WPM medium with 5 7M 2-iP. Regenerated small plantlets with shoots and roots were transferred to medium containing both 100 mg/l hygromycin and 100 mg/l kanamycin for final selection of transgenic plants. The selected plantlets exhibited strong GUS activity in leaves and roots as indicated by a deep blue color. GUS and HPT genes were confirmed to be stably integrated into the genome of the coffee plants by the polymerase chain reaction. | |
| 650 | 1 | 4 | _aCOFFEA CANEPHORA |
| 650 | 1 | 4 | _aAGROBACTERIUM TUMEFACIENS |
| 650 | 1 | 4 | _aTRANSFORMATION |
| 700 | 1 | 2 | _aHatanaka, T. |
| 700 | 1 | 2 | _aChoi, Y.E. |
| 700 | 1 | 2 | _aKusano, T. |
| 700 | 1 | 2 | _aSano, H. |
| 856 | 4 | 0 |
_uhttps://drive.google.com/file/d/1oJ4ThleYakSaic7u2MbLHjcc-Wly_VSf/view?usp=drivesdk _zPara ver el documento ingresa a Google con tu cuenta: @cicy.edu.mx |
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