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In vitro growth and single-leaf photosynthetic response of Cymbidium plantlets to super-elevated CO2 under cold cathode fluorescent lamps

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Abstract

To examine the effectiveness of super-elevated (10,000 µmol mol−1) CO2 enrichment under cold cathode fluorescent lamps (CCFL) for the clonal propagation of Cymbidium, plantlets were cultured on modified Vacin and Went (VW) medium under 0, 3,000 and 10,000 µmol mol−1 CO2 enrichment and two levels of photosynthetic photon flux density (PPFD, 45 and 75 µmol m−2 s−1). Under high PPFD, 10,000 µmol mol−1 CO2 increased root dry weight and promoted shoot growth. In addition, a decrease in photosynthetic capacity and chlorosis at leaf tips were observed. Rubisco activity and stomatal conductance of these plantlets were lower than those of plantlets at 3,000 µmol mol−1 CO2 under high PPFD, which had a higher photosynthetic capacity. On the other hand, plantlets on Kyoto medium grown in 10,000 µmol mol−1 CO2 under high PPFD had a higher photosynthetic rate than those on modified VW medium; no chlorosis was observed. Furthermore, growth of plantlets, in particular the roots, was remarkably enhanced. This result indicates that a negative response to super-elevated CO2 under high PPFD could be improved by altering medium components. Super-elevated CO2 enrichment of in vitro-cultured Cymbidium could positively affect the efficiency and quality of commercial production of clonal orchid plantlets.

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Abbreviations

CCFL:

Cold cathode fluorescent lamps

VW:

Vacin and Went

PPFD:

Photosynthetic photon flux density

References

  • Arnon DI (1949) Copper enzymes in isolated chloroplasts. Polyphenoloxidase in Beta vulgaris. Plant Physiol 24:1–15

    Article  CAS  PubMed  Google Scholar 

  • Bowes G (1991) Growth at elevated CO2: photosynthetic responses mediated through Rubisco. Plant Cell Environ 14:795–806

    Article  CAS  Google Scholar 

  • Cook AC, Tissue DT, Roberts SW, Oechel WC (1998) Effects of long-term elevated CO2 from natural CO2 springs on Nardus stricta: photosynthesis, biochemistry, growth and phenology. Plant Cell Environ 21:417–425

    Article  CAS  Google Scholar 

  • Croonenborghs S, Ceusters J, Londers E, De Proft MP (2009) Effects of elevated CO2 on growth and morphological characteristics of ornamental bromeliads. Sci Hortic 121:192–198

    Article  CAS  Google Scholar 

  • Drake BG, Gonzàlez-Meler MA, Long SP (1997) More efficient plants: a consequence of rising atmospheric CO2? Annu Rev Plant Physiol Plant Mol Biol 48:609–639

    Article  CAS  PubMed  Google Scholar 

  • Evans JR (1983) Nitrogen and photosynthesis in the flag leaf of wheat (Triticum aestivum L.). Plant Physiol 72:297–302

    Article  CAS  PubMed  Google Scholar 

  • Evans JR (1986) The relationship between carbon-dioxide-limited photosynthetic rate and ribulose-1,5-bisphosphate-carboxylase content in two nuclear-cytoplasm substitution lines of wheat, and the coordination of ribulose-bisphosphate-carboxylation and electron-transport capacities. Planta 167:351–358

    Article  CAS  Google Scholar 

  • Evans JR (1989) Photosynthesis and nitrogen relationships in leaves of C3 plants. Oecologia 78:9–19

    Article  Google Scholar 

  • Farrar JF, Williams ML (1991) The effects of increased atmospheric carbon dioxide and temperature on carbon partitioning, source-sink relations and respiration. Plant Cell Environ 14:819–830

    Article  CAS  Google Scholar 

  • Gouk SS, Yong JWH, Hew CS (1997) Effects of super-elevated CO2 on the growth and carboxylating enzymes in an epiphytic CAM orchid plantlet. J Plant Physiol 151:129–136

    CAS  Google Scholar 

  • Gouk SS, He J, Hew CS (1999) Changes in photosynthetic capability and carbohydrate production in an epiphytic CAM orchid plantlet exposed to super-elevated CO2. Environ Exp Bot 41:219–230

    Article  Google Scholar 

  • Gunderson CA, Wullschleger SD (1994) Photosynthetic acclimation in trees to rising atmospheric CO2: a broader perspective. Photosynth Res 39:369–388

    Article  CAS  Google Scholar 

  • Harmens H, Stirling CM, Marshall C, Farrar JF (2000) Does down-regulation of photosynthetic capacity by elevated CO2 depend on N supply in Dactylis glomerata? Physiol Plant 108:43–50

    CAS  Google Scholar 

  • Hew CS, Ye QS, Pan RC (1989) Pathways of carbon fixation in some thin leaved orchids. Lindleyana 4:154–157

    Google Scholar 

  • Hew CS, Hin SE, Yong JWH, Gouk SS, Tanaka M (1995) In vitro CO2 enrichment of CAM orchid plantlets. J Hortic Sci 70:721–736

    Google Scholar 

  • Kanemoto K, Yamashita Y, Ozawa T, Imanishi N, Nguyen NT, Suwa R, Mohapatra PK, Kanai S, Moghaieb RE, Ito J, Shemy HEI, Fujita K (2009) Photosynthetic acclimation to elevated CO2 is dependent on N partitioning and transpiration in soybean. Plant Sci 177:398–403

    Article  CAS  Google Scholar 

  • Kozai T (1991) Photoautotrophic micropropagation. In Vitro Cell Dev Biol Plant 27:47–51

    Google Scholar 

  • Kozai T, Oki H, Fujiwara K (1987) Effects of CO2 enrichment and sucrose concentration under high photosynthetic photon fluxes on growth of tissue-cultured Cymbidium plantlets during the preparation stage: symposium on plant micropropagation in horticultural industries. Arlon, Belgium, pp 135–141

    Google Scholar 

  • Kozai T, Kubota C, Watabebe I (1988) Effects of basal medium composition of the growth on carnation plantlets in auto- and mixo-trophic tissue culture. Acta Hortic 230:159–166

    Google Scholar 

  • Long SP, Drake BG (1992) Photosynthetic CO2 assimilation and rising atmospheric CO2 concentrations. In: Baker NR, Thomas H (eds) Crop photosynthesis: spatial and temporal determinants. Elsevier, Amsterdam, pp 69–95

    Google Scholar 

  • Ludewig F, Sonnewald U (2000) High CO2-mediated down-regulation of photosynthetic gene transcripts is caused by accelerated leaf senescence rather than sugar accumulation. FEBS Lett 479:19–24

    Article  CAS  PubMed  Google Scholar 

  • Mackowiak CL, Wheeler RM (1996) Growth and stomatal behavior of hydroponically cultured potato (Solanum tuberosum L.) at elevated and super-elevated CO2. J Plant Physiol 149:205–210

    CAS  Google Scholar 

  • Makino A (1994) Biochemistry of C3-photosynthesis in high CO2. J Plant Res 107:79–84

    Article  CAS  Google Scholar 

  • Makino A, Mae T, Ohira K (1985) Photosynthesis and ribulose-1,5-bisphosphate carboxylase/oxygenase in rice leaves from emergence through senescence. Quantitative analysis by carboxylation/oxygenation and regeneration of ribulose 1,5-bisphosphate. Planta 166:414–420

    Article  CAS  Google Scholar 

  • McDonald EP, Erickson JE, Kruger EL (2002) Can decreased transpiration limit plant nitrogen acquisition in elevated CO2? Funct Plant Biol 29:1115–1120

    Article  Google Scholar 

  • Moore BD, Cheng SH, Sims D, Seemann JR (1999) The biochemical and molecular basis for photosynthetic acclimation to elevated atmospheric CO2. Plant Cell Environ 22:567–582

    Article  CAS  Google Scholar 

  • Morel GM (1960) Producing virus-free Cymbidium. Am Orchid Soc Bull 29:495–497

    Google Scholar 

  • Mortensen LM (1987) Review: CO2 enrichment in greenhouse. Crop responses. Sci Hortic 33:1–25

    Article  Google Scholar 

  • Murashige T, Skoog F (1962) A revised medium for rapid growth and bio assays with tobacco tissue culture. Physiol Plant 15:473–497

    Article  CAS  Google Scholar 

  • Neales TF, Incoll LD (1968) The control of leaf photosynthesis rate by the level of assimilate concentration in the leaf: a review of the hypothesis. Bot Rev 34:107–125

    Article  Google Scholar 

  • Nitsch C, Nitsch JP (1967) The induction of flowering in vitro in stem segment of Plumbago indica L. II. The production of reproductive buds. Planta 72:371–384

    Article  CAS  Google Scholar 

  • Paul MJ, Foyer CH (2001) Sink regulation of photosynthesis. J Exp Bot 52:1383–1400

    Article  CAS  PubMed  Google Scholar 

  • Pettersson R, McDonald AJS (1994) Effects of nitrogen supply on the acclimation of photosynthesis to elevated CO2. Photosynth Res 39:389–400

    Article  CAS  Google Scholar 

  • Rolland F, Moore B, Sheen J (2002) Sugar sensing and signaling in plants. Plant Cell 14:185–205

    Google Scholar 

  • Sage RF (1994) Acclimation of photosynthesis to increasing atmospheric CO2: the gas exchange perspective. Photosynth Res 39:351–368

    Article  CAS  Google Scholar 

  • Sage RF, Sharkey TD, Seemann JR (1989) Acclimation of photosynthesis to elevated CO2 in five C3 species. Plant Physiol 89:590–596

    Article  CAS  PubMed  Google Scholar 

  • Sicher RC (1998) Yellowing and photosynthetic decline of barley primary leaves in response to atmospheric CO2 enrichment. Physiol Plant 103:193–200

    Article  CAS  Google Scholar 

  • Sicher RC (2008) Effects of CO2 enrichment on soluble amino acids and organic acids in barley primary leaves as a function of age, photoperiod and chlorosis. Plant Sci 174:576–582

    Article  CAS  Google Scholar 

  • Stitt M, Krapp A (1999) The interaction between elevated carbon dioxide and nitrogen nutrition: the physiological and molecular background. Plant Cell Environ 22:583–621

    Article  CAS  Google Scholar 

  • Tanaka M, Nagae S, Goi M (1992) Growth of tissue cultured Spathiphyllum on rockwool in a novel film culture vessel under high CO2. Acta Hortic 314:139–146

    Google Scholar 

  • Tanaka M, Yap DCH, Ng CKY, Hew CS (1999) The physiology of Cymbidium plantlets cultured in vitro under conditions of high carbon dioxide and low photosynthetic photon flux density. J Hortic Sci Biotech 74:632–638

    Google Scholar 

  • Tanaka M, Norikane A, Watanabe T (2009) Cold cathode fluorescent lamps (CCFL): revolutionary light source for plant micropropagation. Biotech Biotechnol Equip 23:1497–1503

    Article  Google Scholar 

  • Taub DR, Wang X (2008) Why are nitrogen concentrations in plant tissues lower under elevated CO2? A critical examination of the hypotheses. J Integr Plant Biol 50:1365–1374

    CAS  PubMed  Google Scholar 

  • Teixeira da Silva JA, Yam T, Fukai S, Nayak N, Tanaka M (2005) Establishment of optimum nutrient media for in vitro propagation of Cymbidium Sw. (Orchidaceae) using protocorm-like body segments. Prop Ornamental Plants 5:129–136

    Google Scholar 

  • Tsukamoto Y, Kano K, Katsuura T (1963) Instant media for orchid seed germination. Am Orchid Soc Bull 32:354–355

    Google Scholar 

  • Ueno O, Sentoku N (2006) Comparison of leaf structure and photosynthetic characteristics of C3 and C4 Alloteropsis semialata subspecies. Plant Cell Environ 29:257–268

    Article  CAS  PubMed  Google Scholar 

  • Usuda H, Shimogawara K (1998) The effects of increased atmospheric carbon dioxide on growth, carbohydrates, and photosynthesis in radish, Raphanus sativus. Plant Cell Physiol 39:1–7

    CAS  Google Scholar 

  • Vacin EF, Went FW (1949) Some pH changes in nutrient solutions. Bor Gaze 110:605–613

    Article  CAS  Google Scholar 

  • Van Oosten JJ, Besford RT (1996) Acclimation of photosynthesis to elevated CO2 through feedback regulation of gene expression: climate of opinion. Photosynth Res 48:353–365

    Article  Google Scholar 

  • Wheeler RM, Mackowiak CL, Siegriest LM, Sager JC (1993) Supraoptimal carbon dioxide effects on growth of soybean [Glycine max (L.) Merr.]. J Plant Physiol 142:173–178

    CAS  PubMed  Google Scholar 

  • Wimber DE (1963) Clonal multiplication of cymbidiums through tissue culture of the shoot meristem. Am Orchid Soc Bull 32:105–107

    Google Scholar 

  • Yang CS, Kozai T, Jeong BR (1995) Ionic composition and strength of culture medium affect photoautotrophic growth, transpiration and net photosynthetic rates of strawberry plantlets in vitro. Acta Hortic 393:219–226

    Google Scholar 

  • Zhao ZR, Li GR, Huang GQ (1991) Promotive effect of potassium on adventitious root formation in some plants. Plant Sci 79:47–50

    Article  CAS  Google Scholar 

Download references

Acknowledgments

The authors thank Prof. T. Araki and Mr. Y Suidu, Department of Plant Resources, Faculty of Agriculture, Kyusyu University for their generous assistance and advice on the analysis of total Rubisco activity. The authors also thank Dr. J. A. Teixeira da Silva, Department of Applied Biological Science, Faculty of Agriculture, Kagawa University for critical reading and editing of the manuscript.

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Correspondence to Michio Tanaka.

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Communicated by P. Kumar.

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Norikane, A., Takamura, T., Morokuma, M. et al. In vitro growth and single-leaf photosynthetic response of Cymbidium plantlets to super-elevated CO2 under cold cathode fluorescent lamps. Plant Cell Rep 29, 273–283 (2010). https://doi.org/10.1007/s00299-010-0820-1

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