In vitro production of potato microtubers in liquid medium using temporary immersion

SummaryCIRAD developed a new apparatus for plant tissue culture, using temporary immersion in a liquid medium. This apparatus was adapted to the microtuber production in potato. The procedure is as follows: single node cultivation on MS medium containing 30 g/l sucrose in the light for 2 weeks, induction of microtuberisation with 80 g/l sucrose over a 2 week period in the light, followed by a further 6 weeks in the dark. All experiments were performed at 20 °C. The basic vessel had a capacity of approximately 11;30 nodes were cultivated per vessel. Depending on the cultivars tested (Bintje, Ostara and Désirée) 47 to 115 microtubers were harvested per vessel. Between 30 and 60% of the microtubers weighted over 0.5 g and between 10 and 40% over 0.8 g. Sprouting is still under investigation. Preliminary results indicate that the dormancy period was relatively short and several stems were obtained per microtuber. These results seem to be better than those usually reported. Only one simple protocol has been tested and further improvements are probably easy to obtain.

[1]  M. Lartaud,et al.  Improvement of somatic embryogenesis in Hevea brasiliensis (Müll. Arg.) using the temporary immersion technique , 1997, In Vitro Cellular & Developmental Biology - Plant.

[2]  T. Kozai,et al.  Multiplication of potato plantlets in vitro with sugar free medium under high photosynthetic photon flux. , 1988 .

[3]  M. Akita,et al.  Stimulation of potato (Solanum tuberosum L.) tuberization by semicontinuous liquid medium surface level control , 2004, Plant Cell Reports.

[4]  P. Debergh Effects of agar brand and concentration on the tissue culture medium , 1983 .

[5]  P. Struik,et al.  An integrated view of the hormonal regulation of tuber formation in potato (Solanum tuberosum) , 1989 .

[6]  P. Weathers,et al.  Regeneration of plants using nutrient mist culture , 1988, In Vitro Cellular & Developmental Biology.

[7]  R. H. Zimmerman,et al.  Micropropagation: technology and application. , 1990 .

[8]  R. Langille,et al.  Stable, position-related responses to retinoic acid by chick limb-bud mesenchymal cells in serum-free cultures , 1994, In Vitro Cellular & Developmental Biology - Animal.

[9]  F. Côté,et al.  Comparison of methods of liquid medium culture for banana micropropagation , 2004, Plant Cell, Tissue and Organ Culture.

[10]  V. Alchanatis,et al.  Morphological control and mensuration of potato plantlets from tissue cultures for automated micropropagation , 1994, Plant Cell, Tissue and Organ Culture.

[11]  C. Teisson,et al.  Amplified somatic embryogenesis from male flowers of triploid banana and plantain cultivars (Musa spp.) , 1994, In Vitro – Plant.

[12]  P. Debergh,et al.  Liquid medium additions to established tissue cultures to improve elongation and rooting in vivo , 2004, Plant Cell, Tissue and Organ Culture.

[13]  C. Teisson,et al.  A New Concept of Plant In Vitro Cultivation Liquid Medium: Temporary Immersion , 1995 .

[14]  J. Seabrook,et al.  Microtuberization of layered shoots and nodal cuttings of potato: The influence of growth regulators and incubation periods , 1994, Plant Cell, Tissue and Organ Culture.

[15]  H. Etienne,et al.  Culture in vitro par immersion temporaire : un nouveau récipient , 1995 .

[16]  D. Newman,et al.  THE DISTRIBUTION OF RANGE IN SAMPLES FROM A NORMAL POPULATION, EXPRESSED IN TERMS OF AN INDEPENDENT ESTIMATE OF STANDARD DEVIATION , 1939 .

[17]  Jenny Aitken-Christie,et al.  DEVELOPMENT OF A SEMI-AUTOMATED MICROPROPAGATION SYSTEM , 1988 .

[18]  P. Ollitrault,et al.  Improvement of Citrus somatic embryo development by temporary immersion , 1997, Plant Cell, Tissue and Organ Culture.