Dergiler / Turkish Journal of Biology / 2012 / Cilt: 36 - Sayı: 2

Apoplastic and symplastic solute concentrations contribute to osmotic adjustment in bean genotypes during drought stress

Sayfa
151–160
Yayın Tarihi
2012-02-01
DOI
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In addition, the drought-tolerant cultivar showed a much higher capacity to maintain osmotic adjustment between the symplast and the apoplast.

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Amaç & Hipotez:The present study investigates changes in the inorganic ions, proline, and endogenous abscisic acid (ABA) contents of the apoplastic and symplastic compartments of leaves from drought-tolerant (Yakutiye) and drought-sensitive (Zulbiye) cultivars of the common bean (Phaseolus vulgaris L.).
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Temel Bulgular & Veri:Drought stress caused a decrease in leaf water potential and stomatal conductance in both cultivars.
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Sonuç & Katkı:In addition, the drought-tolerant cultivar showed a much higher capacity to maintain osmotic adjustment between the symplast and the apoplast.
🔬Tür:Araştırma Makalesi
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Key words: Apoplast · symplast · drought stress

Özet

The present study investigates changes in the inorganic ions, proline, and endogenous abscisic acid (ABA) contents of the apoplastic and symplastic compartments of leaves from drought-tolerant (Yakutiye) and drought-sensitive (Zulbiye) cultivars of the common bean (Phaseolus vulgaris L.). Drought stress caused a decrease in leaf water potential and stomatal conductance in both cultivars. Concentrations of proline in the drought-tolerant and drought-sensitive cultivars increased in response to drought stress in both compartments. The symplastic K+ concentration decreased in both cultivars. However, the opposite trend was observed concerning K+ concentrations in the apoplastic areas. While the symplastic Na+ concentrations significantly decreased in the drought-tolerant cultivar, the apoplastic Na+ concentrations increased during drought stress. However, Na+ concentrations did not significantly change in either of the compartments in the drought-sensitive cultivar. The Ca2+ concentrations in the sensitive cultivar significantly decreased in both compartments during drought stress. In the tolerant cultivar, the Ca2+ concentration significantly increased in the symplast but decreased in the apoplast. Cl- concentrations in the tolerant cultivar did not significantly change in either compartment. In the sensitive cultivar, the Cl- concentration increased in the apoplastic area but decreased in the symplastic area. In addition, while the symplastic sap of the leaves exhibited a constant pH value, it diminished in the apoplast during drought stress. Symplastic and apoplastic ABA concentrations significantly increased in both cultivars. It might be said that inorganic ions (especially Na+, K+, and Ca2+) and ABA concentrations changed between the apoplastic and symplastic spaces to contribute to osmotic adjustment under drought stress. In addition, the drought-tolerant cultivar showed a much higher capacity to maintain osmotic adjustment between the symplast and the apoplast.

Abstract

The present study investigates changes in the inorganic ions, proline, and endogenous abscisic acid (ABA) contents of the apoplastic and symplastic compartments of leaves from drought-tolerant (Yakutiye) and drought-sensitive (Zulbiye) cultivars of the common bean (Phaseolus vulgaris L.). Drought stress caused a decrease in leaf water potential and stomatal conductance in both cultivars. Concentrations of proline in the drought-tolerant and drought-sensitive cultivars increased in response to drought stress in both compartments. The symplastic K+ concentration decreased in both cultivars. However, the opposite trend was observed concerning K+ concentrations in the apoplastic areas. While the symplastic Na+ concentrations significantly decreased in the drought-tolerant cultivar, the apoplastic Na+ concentrations increased during drought stress. However, Na+ concentrations did not significantly change in either of the compartments in the drought-sensitive cultivar. The Ca2+ concentrations in the sensitive cultivar significantly decreased in both compartments during drought stress. In the tolerant cultivar, the Ca2+ concentration significantly increased in the symplast but decreased in the apoplast. Cl- concentrations in the tolerant cultivar did not significantly change in either compartment. In the sensitive cultivar, the Cl- concentration increased in the apoplastic area but decreased in the symplastic area. In addition, while the symplastic sap of the leaves exhibited a constant pH value, it diminished in the apoplast during drought stress. Symplastic and apoplastic ABA concentrations significantly increased in both cultivars. It might be said that inorganic ions (especially Na+, K+, and Ca2+) and ABA concentrations changed between the apoplastic and symplastic spaces to contribute to osmotic adjustment under drought stress. In addition, the drought-tolerant cultivar showed a much higher capacity to maintain osmotic adjustment between the symplast and the apoplast.

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Bu Makaleye Atıf Yap

GÜLER, N. S., SAĞLAM, A., DEMİRALAY, M., KADIOĞLU, A. (2012). Apoplastic and symplastic solute concentrations contribute to osmotic adjustment in bean genotypes during drought stress. Turkish Journal of Biology, Cilt: 36 - Sayı: 2, 151–160. https://ajindex.com/articles/181842

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Kaynakça (12)

  1. Hernández JA, Ferrer MA, Jimenez A et al. Antioxidant system and O2·-/H2O2 production in the apoplast of pea leaves. Its relation with salt-induced necrotic lesions in minor veins. Plant Physiol 127: 817-831, 2001.
  2. Patakas A, Noitsakis B. Mechanisms involved in diurnal changes of osmotic potential in grapevines under drought conditions. J Plant Physiol 154: 767-774, 1999.
  3. Hasegawa PM, Bressa RA, Zhu JK et al. Plant cellular and molecular responses to high salinity. Annu Rev Plant Physiol Plant Mol Biol 51: 463-499, 2000.
  4. Rhodes D, Samaras Y. Genetic control of osmoregulation in plant. In: Strange K. ed. Cellular and Molecular Physiology of Cell Volume Regulation. CRC Press; 1994: pp. 347-361.
  5. Kavi Kishor PB, Sangam S, Amrutha RN et al. Regulation of proline biosynthesis, degradation, uptake and transport in higher plants: its implication in plant growth and abiotic stress tolerance. Current Sci 88: 424-438, 2005. Tanner JJ. Structural biology of proline catabolism. Amino Acids 35: 719-730, 2008.
  6. Hoque MA, Okuma E, Banu MNA et al. Exogenous proline mitigates the detrimental eff ects of salt stress more than exogenous betaine by increasing antioxidant enzyme activities. J Plant Physiol 164: 553-561, 2007.
  7. LaRosa PC, Hasegawa PM, Rhodes D et al. Abscisic acid stimulated osmotic adjustment and its involvement in adaptation of tobacco cells to NaCl. Plant Physiol 85: 174-181, 1987. Dietz KJ. Functions and responses of the leaf apoplast under stress. Prog Bot 58: 221-225, 1997.
  8. Gao G, Knight MR, Trewavas AJ et al. Self-reporting Arabidopsis expressing pH and Ca2+ indicators unveil ion dynamics in the cytoplasm and in the apoplast under abiotic stress. Plant Physiol 134: 898-908, 2004.
  9. Almeida DPF, Huber DJ. Apoplastic pH and inorganic ion levels in tomato fruit: a potential means for regulation of cell wall metabolism during ripening. Physiol Plantarum 105: 506- 512, 1999.
  10. Rayle DL, Cleland RE. Th e acid growth theory of auxin- induced cell elongation is alive and well. Plant Physiol 99: 1271-1274, 1992. Richards RA. Variation between and within species of rapeseed (Brassica campestris and B. napus) in response to drought stress. II. Physiological and biochemistry characters. Aust J Agric Res 29: 495-501, 1978.
  11. Subbarao GV, Johansen C, Slinkard AE. Strategies for improving drought resistance in grain legumes. Crit Rev Plant Sci 14: 469-523, 1995.
  12. Blum A, Ebercon A. Cell membrane stability as a measure of drought and heat tolerance in wheat. Crop Sci 21: 43-47, 1