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Mesos components (CaCl2, MgSO4, KH2PO4) are critical for improving pear micropropagation

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Abstract

Pear accessions and species show a broad response to tissue culture media due to the wide genetic diversity that exists in the available pear germplasm. An initial study of mineral nutrition using a systematic response surface approach with five Murashige and Skoog medium mineral stock solutions indicated that the mesos factor (CaCl2, MgSO4, and KH2PO4) affected most plant responses and genotypes, suggesting that additional studies were needed to further optimize these three mesos components for a wide range of genotypes. Short stature, leaf spots, edge necrosis, and red or yellow coloration were the main symptoms of poor nutrition in shoot cultures of 10 diverse pear genotypes from six species. A surface response experimental design was used to model the optimal factor and factor levels for responses that included overall quality, leaf character, shoot multiplication, and shoot height. The growth morphology, shoot length, and multiplication of these pear shoots could be manipulated by adjusting the mesos components. The highest quality for the majority of genotypes, including five P. communis cultivars, P. koehnei, P. dimorphophylla, and P. pyrifolia ‘Sion Szu Mi’, required higher concentrations (>1.2× to 2.5×) of all the components than are present in Murashige and Skoog medium. ‘Capital’ (P. calleryana) required high CaCl2 and MgSO4 with low KH2PO4; for ‘Hang Pa Li’ (P. ussuriensis), low CaCl2 and moderate to low MgSO4 and KH2PO4 produced high-quality shoots. Suitable combinations of the meso nutrients produced both optimum shoot number and shoot length in addition to general good plant quality.

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References

  • Adelberg JW, Delgado MP, Tomkins JT (2010) Spent medium analysis for liquid culture micropropagation of Hemerocallis on Murashige and Skoog medium. In Vitro Cell Dev Biol—Plant 46:95–107

    Article  Google Scholar 

  • Aranda-Peres AN, Martinelli AP, Pereira-Peres LE, Higashi EN (2009) Adjustment of mineral elements in the culture medium for the micropropagation of three Vriesea bromeliads from the Brazilian Atlantic Forest: the importance of calcium. HortSci 44:106–112

    Google Scholar 

  • Arrudal SCC, Souza GM, Almeida M, Gonçalves AN (2000) Anatomical and biochemical characterization of the calcium effect on Eucalyptus urophylla callus morphogenesis in vitro. Plant Cell Tissue Organ Cult 63:143–154

    Google Scholar 

  • Bell RL, Reed BM (2002) In vitro tissue culture of pear: advances in techniques for micropropagation and germplasm preservation. Acta Hort 596:412–418

    Google Scholar 

  • Bell RL, Srinivasan C, Lomberk D (2009) Effect of nutrient media on axillary shoot proliferation and preconditioning for adventitious shoot regeneration of pears. In Vitro Cell Dev Biol—Plant 45:708–714

    Article  Google Scholar 

  • Bennett WF (ed) (1993) Nutrient deficiencies and toxicities in crop plants. APS Press, Minneapolis, MN, 202 pp

    Google Scholar 

  • Design-Expert (2010) Design-Expert 8. Stat-Ease, Inc., Minneapolis, MN

    Google Scholar 

  • Evens TJ, Niedz RP (2008) ARS-Media: Ion Solution Calculator Version 1. U.S. Horticultural Research Laboratory, Ft. Pierce, FL. http://www.ars.usda.gov/services/software/download.htm?softwareid=148

  • Greenway MB, Phillips IC, Lloyd MN, Hubstenberger JF, Phillips GC (2012) A nutrient medium for diverse applications and tissue growth of plant species in vitro. In Vitro Cell Dev Biol—Plant 48:403–410

    Article  CAS  Google Scholar 

  • Hermans C, Johnson GN, Strasser RJ, Verbruggen N (2004) Physiological characterisation of magnesium deficiency in sugar beet: acclimation to low magnesium differentially affects photosystems I and II. Planta 220:344–355

    Article  PubMed  CAS  Google Scholar 

  • Hermans C, Vuylsteke M, Coppens F, Cristescu SM, Harren FJ, Inze D, Verbruggen N (2010) Systems analysis of the responses to long-term magnesium deficiency and restoration in Arabidopsis thaliana. New Phytol 187:132–144

    Article  PubMed  CAS  Google Scholar 

  • Jansen MAK, Booij H, Schel JHN, Devries SC (1990) Calcium increases the yield of somatic embryos in carrot embryogenic suspension-cultures. Plant Cell Rep 9:221–223

    Article  CAS  Google Scholar 

  • Kintzios S, Stavropoulou E, Skamneli S (2004) Accumulation of selected macronutrients and carbohydrates in melon tissue cultures: association with pathways of in vitro dedifferentiation and differentiation (organogenesis, somatic embryogenesis). Plant Sci 167:655–664

    Article  CAS  Google Scholar 

  • Leigh RA, Wyn Jones RG (1984) A hypothesis relating critical potassium concentrations for growth to the distribution and functions of this ion in the plant cell. New Phytol 97:1–13

    Article  CAS  Google Scholar 

  • Lloyd G, McCown B (1980) Commercially feasible micropropagation of mountain laurel, Kalmia latifolia, by use of shoot-tip culture. Comb Proceed Int Plant Prop Soc 30:421–427

    Google Scholar 

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

    Article  CAS  Google Scholar 

  • Myers R, Montgomery D (2002) Response surface methodology: process and product optimization using planned experiments. In: Encyclopedia of biopharmaceutical statistics. Wiley, New York, pp 71–73

  • Nakajima I, Ito A, Moriya S, Saito T, Moriguchi T, Yamamoto T (2012) Adventitious shoot regeneration in cotyledons from Japanese pear and related species. In Vitro Cell Dev Biol—Plant 48:396–402

    Google Scholar 

  • Niedz RP, Evens TJ (2006) A solution to the problem of ion confounding in experimental biology. Nat Methods 3:417

    Article  PubMed  CAS  Google Scholar 

  • Niedz RP, Evens TJ (2007) Regulating plant tissue growth by mineral nutrition. In Vitro Cell Dev Biol—Plant 43:370–381

    Article  CAS  Google Scholar 

  • Niedz RP, Hyndman SE, Evens TJ (2007) Using a Gestalt to measure the quality of in vitro responses. Sci Hortic 112:349–359

    Article  Google Scholar 

  • Preece J (1995) Can nutrient salts partially substitute for plant growth regulators? Plant Tissue Cult Biotech 1:26–37

    Google Scholar 

  • Ramage CM, Williams RR (2002) Mineral nutrition and plant morphogenesis. In Vitro Cell Dev Biol—Plant 38:116–124

    Article  CAS  Google Scholar 

  • Reed B, Sarasan V, Kane M, Bunn E, Pence V (2011) Biodiversity conservation and conservation biotechnology tools. In Vitro Cell Dev Biol—Plant 47:1–4

    Article  CAS  Google Scholar 

  • Reed BM, DeNoma JS, Wada S, Postman JD (2012) Micropropagation of pear (Pyrus sp). Chapter 1. In: Lambardi M, Ozudogru EA, Jain SM (eds) Protocols for micropropagation of selected economically-important horticultural plants. Humana, New York, pp 3–18

    Chapter  Google Scholar 

  • Reed BM, Wada S, DeNoma J, Niedz RP (2013) Improving in vitro mineral nutrition for diverse pear germplasm. In Vitro Cell Dev Biol—Plant. doi:10.1007/s11627-013-9504-1

  • Williams RR (1993) Mineral nutrition in vitro—a mechanistic approach. Aust J Bot 41:237–251

    Article  CAS  Google Scholar 

  • Woodhouse PJ, Wild A, Clement CR (1978) Rate of uptake of potassium by three crop species in relation to growth. J Exp Bot 29:885–894

    Article  CAS  Google Scholar 

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Acknowledgments

We thank the NCGR lab personnel for assistance with collection of the data. This project was funded by a grant from the Oregon Association of Nurseries and the Oregon Department of Agriculture and by United States Department of Agriculture, Agricultural Research Service CRIS project 5358-21000-0-38-00D.

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Correspondence to Sugae Wada.

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Editor: Dave Duncan

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Wada, S., Niedz, R.P., DeNoma, J. et al. Mesos components (CaCl2, MgSO4, KH2PO4) are critical for improving pear micropropagation. In Vitro Cell.Dev.Biol.-Plant 49, 356–365 (2013). https://doi.org/10.1007/s11627-013-9508-x

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