Tissue culture and Agrobacterium-mediated transformation of hemp (Cannabis sativa L.)

In Vitro Cellular and Developmental Biology - Plant

Volumn 39, Issue 6, 2003, Pages 578-585

  Feeney, M ^a   Punja, Z K ^a  

^a SIMON FRASER UNIVERSITY   (Canada)

Author keywords

Agrobacterium tumefaciens; Callus; Mannose selection; Phosphomannose isomerase; Regeneration; Suspension culture; Transgenic hemp

Indexed keywords

AGROBACTERIUM; AGROBACTERIUM TUMEFACIENS; CANNABIS; CANNABIS SATIVA; RHIZOBIUM;

EID: 0345802696     PISSN: 10545476     EISSN: None     Source Type: Journal    
DOI: 10.1079/IVP2003454     Document Type: Article

References (31)

1. Braemer, R.; Paris, M. Biotransformation of cannabinoids by a cell suspension culture of Cannabis sativa L. Plant Cell Rep. 6:150-152; 1987.
2. Clarke, R. C. Botany of the genus Cannabis. In: Ranalli, P., ed. Advances in hemp research. New York: Haworth Press; 1999:1-18.
3. Fisse, J.; Braut, F.; Cosson, L.; Paris, M. Étude in vitro des capacités organogénétiques de tissus de Cannabis sativa L. ; effet de différentes substances de croissance. Pl. Méd. Phytoth. 15:217-223; 1981.
4. Forapani, S.; Carboni, A.; Paoletti, C.; Moliterni, V. M. C.; Ranalli, P.; Mandolino, G. Comparison of hemp varieties using random amplified polymorphic DNA markers. Crop Sci. 41:1682-1689; 2001.
5. Gamborg, O. L.; Miller, R. A.; Ojima, K. Nutrient requirements of suspension cultures of soybean root cells. Exp. Cell Res. 50:151-158; 1968.
6. Hartsel, S. C.; Loh, W.H.-T.; Robertson, L. W. Biotransformation of cannabidiol to cannabielsoin by suspension cultures of Cannabis sativa and Saccharum officinarum. Planta Med. 48:17-19; 1983.
7. 1(6)-tetrahydrocannabinol as an isolation artefact of cannabinoid acids formed by callus cultures of Cannabis sativa L. Experientia 38:898-899; 1982.
8. Hemphill, J. K.; Turner, J. C.; Mahlberg, P. G. Studies on growth and cannabinoid composition of callus derived from different strains of Cannabis sativa. Lloydia 41:453-462; 1978.
9. Hood, E. E.; Helmer, G. L.; Fraley, R. T.; Chilton, M.-D. The hypervirulence of Agrobacterium tumefaciens A281 is encoded in a region of pTiBo542 outside of T-DNA. J. Bacteriol. 168:1291-1301; 1986.
10. Itokawa, H.; Takeya, K.; Mihashi, S. Biotransformation of cannabinoid precursors and related alcohols by suspension cultures of callus induced from Cannabis sativa L. Chem. Pharm. Bull. 25:1941-1946; 1977.
11. Jekkel, Z. S.; Hesky, L. E.; Ali, A. H. Effect of different cryoprotectants and transfer temperatures on the survival rate of hemp (Cannabis sativa L.) cell suspension in deep freezing. Acta Biol. Hung. 40:127-136; 1989.
12. Joersbo, M. Advances in the selection of transgenic plants using non-antibiotic marker genes. Physiol. Plant. 111:69-272; 2001.
13. Joersbo, M.; Donaldson, I.; Kreiberg, J.; Petersen, S. G.; Brunstedt, J. ; Okkels, F. T. Analysis of mannose selection used for transformation of sugar beet. Mol. Breed. 4:111-117; 1998.
14. Johnson, P. Industrial hemp: a critical review of claimed potentials for Cannabis sativa. Tappi J. 82:113-123; 1999.
15. Koetsier, P. A.; Schorr, J.; Doerfler, W. A rapid optimized protocol for downward alkaline Southern blotting of DNA. BioTechniques 15:260-262; 1993.
16. Kramer, C.; DiMaio, J.; Carswell, G. K.; Shillito, R. D. Selection of transformed protoplast-derived Zea mays colonies with phosphinothricin and a novel assay using the pH indicator chlorophenol red. Planta 190:454-458; 1993.
17. Loh, W.H.-T.; Hartsel, S. C.; Robertson, L. W. Tissue culture of Cannabis sativa L. and in vitro biotransformation of phenolics. Z. Pflanzenphysiol. 111:S.395-400; 1983.
18. Lucca, P.; Ye, X.; Potrykus, I. Effective selection and regeneration of transgenic rice plants with mannose as selective agent. Mol. Breed. 7:43-49; 2001.
19. MacKinnon, L.; McDougall, G.; Aziz, N.; Millam, S. Progress towards transformation of fibre hemp. Scottish Crop Research Institute Annual Report 2000/2001. Invergowrie, Dundee: Scottish Crop Research Institute; 2000:84-86.
20. Mandolino, G.; Ranalli, P. Advances in biotechnological approaches for hemp breeding and industry. In: Ranalli, P., ed. Advances in hemp research. New York: Haworth Press; 1999:185-208.
21. Miles, J. S.; Guest, J. R. Nucleotide sequence and transcriptional start point of the phosphomannose isomerase gene (man A) of Escherichia coli. Gene 32:41-48; 1984.
22. Murashige, T.; Skoog, F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol. Plant. 15:473-497; 1962.
23. Negrotto, D.; Jolley, M.; Beer, S.; Wenck, A. R.; Hansen, G. The use of phosphomannose-isomerase as a selectable marker to recover transgenic maize plants (Zea mays L.) via Agrobacterium transformation. Plant Cell Rep. 19:798-803; 2000.
24. Reed, J.; Privalle, L.; Powell, M. L.; Meghji, M.; Dawson, J.; Dunder, E.; Suttie, J.; Wenck, A.; Launis, K.; Kramer, C.; Chang, Y.-F.; Hansen, G.; Wright, M. Phosphomannose isomerase: an efficient selectable marker for plant transformation. In Vitro Cell. Dev. Biol. Plant 37:127-132; 2001.
25. Richez-Dumanois, C.; Braut-Boucher, F.; Cosson, L.; Paris, M. Multiplication végétative in vitro du chanvre (Cannabis sativa L.). Application à la conservation des clones sélectionnés. Agronomie 6:487-495; 1986.
26. Sambrook, J.; Fritsch, E. F.; Maniatis, T. Molecular cloning: a laboratory manual, 2nd edn. Cold Spring Harbor, NY: Cold Spring Harbor Laboratory Press; 1989.
27. Schluter, C.; Punja, Z. K. Genetic diversity among natural and cultivated field populations and seed lots of American ginseng (Panax quinquefolius L.) in Canada. Int. J. Plant Sci. 163:427-439; 2002.
28. Turner, C. E.; Elsohly, M. A.; Boeren, E. G. Constituents of Cannabis sativa L. XVII. A review of the natural constituents. J. Nat. Prod. 43:169-237; 1980.
29. Veliky, I. A.; Genest, K. Growth and metabolites of Cannabis sativa cell suspension cultures. Lloydia 35:450-456; 1972.
30. Wright, M.; Dawson, J.; Dunder, E.; Suttie, J.; Reed, J.; Kramer, C.; Chang, Y.; Novitzky, R.; Wang, H.; Artim-Moore, L. Efficient biolistic transformation of maize (Zea mays L.) and wheat (Triticum aestivum L.) using the phosphomannose isomerase gene, pmi, as the selectable marker. Plant Cell Rep. 20:429-436; 2001.
31. Zhang, P.; Potrykus, I.; Puonti-Kaerlas, J. Efficient production of transgenic cassava using negative and positive selection. Trans. Res. 9: 405-415; 2000.