Hyperhydricity

The Aloe polyphylla plant on the left is a healthy plant taken from tissue culture, while the plant on the right exhibits hyperhydric symptoms

Hyperhydricity (previously known as vitrification) is a physiological malformation that results in excessive hydration, low lignification, impaired stomatal function and reduced mechanical strength of tissue culture-generated plants. The consequence is poor regeneration of such plants without intensive greenhouse acclimation for outdoor growth.[1] Additionally, it may also lead to leaf-tip and bud necrosis in some cases, which often leads to loss of apical dominance in the shoots.[2] In general, the main symptom of hyperhydricity is translucent characteristics signified by a shortage of chlorophyll and high water content. Specifically, the presence of a thin or absent cuticular layer, reduced number of palisade cells, irregular stomata, less developed cell wall and large intracellular spaces in the mesophyll cell layer have been described as some of the anatomic changes associated with hyperhydricity.[3]

Causes

The main causes of hyperhydricity in plant tissue culture are those factors triggering oxidative stresses such as high salt concentration, high relative humidity, low light intensity, gas accumulation in the atmosphere of the jar, length of time intervals between subcultures; number of subcultures, concentration and type of gelling agent, the type of explants used, the concentrations of microelement and hormonal imbalances.[4] Hyperhydricity is commonly apparent in liquid culture-grown plants or when there is low concentration of gelling agent. High ammonium concentration also contributes to hyperhydricity.[5]

Control

Hyperhydricity can be monitored by modifying the atmosphere of the culture vessels. Adjusting the relative humidity in the vessel is one of the most important parameters to be controlled. Use of gas-permeable membranes may help in this regard as this allows increased exchange of water vapor and other gases such as ethylene with the surrounding environment. Using higher concentration of a gelling agent, on top of the use of a higher-strength gelling agent may reduce the risk from hyperhydricity. Hyperhydricity can also be controlled by bottom cooling, which allows water to condense on the medium,[6] the use of cytokinin-meta-topolin (6-(3-Hydroxybenzylamino)purine), the combination of lower cytokinin and ammonium nitrate in the medium, use of nitrate or glutamine as the sole nitrogen source and decreasing the ratio of NH4+:NO3- in the medium.[7] In studies on calcium deficiency in tissue cultures of Lavandula angustifolia, it was shown that an increase in calcium in the medium reduced hyperhydricity.[8]

See also

Notes and references

  1. ↑ Kei-ichiro U, Susan C and Kalidas S (1998). Reduced hyperhydricity and enhanced growth of tissue culture-generated raspberry (Rubus sp.) clonal lines by Pseudomonas sp. isolated from oregano. Process Biochemistry 33(4): 441-445.
  2. ↑ Cassells A and Curry R (2001). Oxidative stress and physiological, epigenetic and genetic variability in plant tissue culture: implications for micropropagators and genetic engineers. Plant Cell Tissue And Organ Culture. 64(2-3):145-157
  3. ↑ Franck T, Kevers C, Gaspar T, Dommes J, Deby C, Greimers R, Serteyn D and Deby-Dupont G (2004). Hyperhydricity of Prunus avium shoots cultured on gelrite: a controlled stress response. Plant Physiology and Biochemistry, 42: 519-527
  4. ↑ 2
  5. ↑ Franck T, Kevers C, Gaspar T, Dommes J, Deby C, Greimers R, Serteyn D and Deby-Dupont G (2004). Hyperhydricity of Prunus avium shoots cultured on gelrite: a controlled stress response. Plant Physiology and Biochemistry, 42: 519-527
  6. ↑ Pérez-Tornero O, Egea J, Olmos E and Burgos L (2001). Control of Hyperhydricity in Micropropagated Apricot Cultivars. In Vitro Cellular & Developmental Biology. Plant. 37(2): 250-254
  7. ↑ Bairu M, Stirk W, Dolezal K, Van Staden J (2007). Optimizing the micropropagation protocol for the endangered Aloe polyphylla: can meta-topolin and its derivatives serve as replacement for benzyladenine and zeatin? Plant Cell Tissue Organ Cult 90:15–23
  8. ↑ Machado, M.P., A.L.L. Silva, L.A. Biasi, C. Deschamps, J.C. Bespalhok Filho and F. Zanette. (2014). "Influence of calcium content of tissue on hyperhydricity and shoot-tip necrosis of in vitro regenerated shoots of Lavandula angustifolia Mill.". Brazilian Archives of Biology and Technology. 57 (5): 636-643.

External links

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