Role of phi cells and the endodermis under salt stress in Brassica oleracea

New Phytologist

Volumn 181, Issue 2, 2009, Pages 347-360

  Fernandez Garcia, N ^a   Lopez Perez, L ^a   Hernandez, M ^a   Olmos, E ^a  

^a RESEARCH GROUP ON QUALITY   (Spain)

Author keywords

Apoplast; Broccoli (Brassica oleracea); Endodermis; Phi thickenings; Salt stress

Indexed keywords

ADENOSINE TRIPHOSPHATASE; LANTHANUM; LIGNIN; LIPID; SUBERIN;

DICOTYLEDON; ENVIRONMENTAL STRESS; NINETEENTH CENTURY; SALINITY; SALINITY TOLERANCE; SODIUM; TRACER; TRANSMISSION ELECTRON MICROSCOPY; ULTRASTRUCTURE; X-RAY SPECTROSCOPY;

ARTICLE; BRASSICA; CELL WALL; CHEMISTRY; CYTOLOGY; ENVIRONMENT; ION TRANSPORT; METABOLISM; PHYSIOLOGICAL STRESS; PHYSIOLOGY; PLANT ROOT; PLANT STOMA; SALINITY;

ADENOSINE TRIPHOSPHATASES; BRASSICA; CELL WALL; ENVIRONMENT; ION TRANSPORT; LANTHANUM; LIGNIN; LIPIDS; PLANT ROOTS; PLANT STOMATA; SALINITY; STRESS, PHYSIOLOGICAL;

BRASSICA OLERACEA; BRASSICA OLERACEA VAR. CAPITATA; BRASSICA OLERACEA VAR. ITALICA; BRASSICACEAE;

EID: 57649223954     PISSN: 0028646X     EISSN: 14698137     Source Type: Journal    
DOI: 10.1111/j.1469-8137.2008.02674.x     Document Type: Article

References (44)

1. + recirculation by the phloem is crucial for salt tolerance. The EMBO Journal 22 : 2004 2014.
2. Christodoulakis NS, Psaras GK. 1987. Stomata on the primary root of Ceratonia siliqua. Annals of Botany 60 : 295 297.
3. Degenhardt B, Gimmler H. 2000. Cell wall adaptations to multiple environmental stresses in maize roots. Journal of Experimental Botany 51 : 595 603.
4. Enstone DE, Peterson CA, Ma F. 2003. Root endodermis and exodermis: structure, function, and responses to the environment. Journal of Plant Growth Regulation 21 : 335 351.
5. Esau K. 1943. Vascular differentiation in the pear root. Hilgardia 15 : 299 324.
6. Fernández-García N, Carvajal M, Olmos E. 2004. Graft union formation in tomato plants: Peroxidase and catalase involvement. Annals of Botany 93 : 53 60.
7. Franke R, Schreiber L. 2007. Suberin - a biopolyester forming apoplastic plant interfaces. Current Opinion in Plant Biology 10 : 252 259.
8. Gaxiola R, Larrinoa IF, Villalba JM, Serrano RG. 1992. A novel and conserved salt-induced protein is an important determinant of salt tolerance in yeast. The EMBO Journal 11 : 3157 3164.
9. Gerrath JM, Covington L, Doubt J, Larson DW. 2002. Occurrence of phi thickenings is correlated with gymnosperm systematics. Canadian Journal of Botany 80 : 852 860.
10. Gerrath JM, Matthes U, Purich M, Larson DW. 2005. Root environmental effects on phi thickening production and root morphology in three gymnosperms. Canadian Journal of Botany 83 : 379 385.
11. Haas DL, Carothers ZB, Robbins RR. 1976. Observations on the Phi-thickenings and casparian strips in Pelargonium roots. American Journal of Botany 63 : 863 867.
12. Hose E, Clarkson DT, Steudle E, Schreiber L, Hartung W. 2001. The exodermis: a variable apoplastic barrier. Journal of Experimental Botany 52 : 2245 2264.
13. Krishnamurthy KV. 1999. Light microscopic cytochemistry. In : Krishnamurthy KV, ed. Methods in cell wall cytochemistry. Boca Raton, FL, USA : CRC Pres LLC, 29 150.
14. Lehmann H, Stelzer R, Holzamer S, Kunz U, Gierth M. 2000. Analytical electron microscopical investigations on the apoplastic pathways of lanthanum transport in barley roots. Planta 211 : 816 822.
15. Lopez-Perez L, Fernandez-Garcia N, Olmos E, Carvajal M. 2007. The Phi thickening in roots of broccoli plants: an acclimation mechanism to salinity. International Journal of Plant Science 168 : 1141 1149.
16. Ma F, Peterson CA. 2001. Frequencies of plasmodesmata in Allium cepa L. roots: implications for solute transport pathways. Journal of Experimental Botany 52 : 1051 1061.
17. Mackenzie KAD. 1979. The development of the endodermis and Phi layer of apple roots. Protoplasma 100 : 21 32.
18. Niu X, Bressan RA, Hasegawa P, Pardo J. 1995. Íon homeostasis in NaCl stress environments. Plant Physiology 109 : 735 742.
19. +-ATPase gene expresión in a glycophyte and halophyte. Plant Physiology 103 : 713 718.
20. Olmos E, Hellin E. 1997. Cytochemical localization of ATPase plasma membrane and acid phosphatase by cerium-based method in a s alt-adapted cell line of Pisum sativum. Journal of Experimental Botany 48 : 1529 1535.
21. Olmos E, Hellin E. 1998. Ultrastructural differences of hyperhydric and normal leaves from regenerated carnation plants. Scientia Horticulturae 75 : 91 101.
22. Olmos E, Kiddle G, Pellny TK, Kumar S, Foyer CH. 2006. Modulation of plant morphology, root architecture, and cell structure by low vitamin C in Arabidopsis thaliana. Journal of Experimental Botany 57 : 1645 1655.
23. Pan CX, Nakao Y, Nii N. 2006. Anatomical development of Phi thickening and the casparian strip in loquat roots. Journal of the Japanese Society of Horticultural Science 75 : 445 449.
24. +. Journal of Experimental Botany 55 : 939 949.
25. Peterson CA, Emanuel ME, Weerdenburg CA. 1981. The permeability of phi thickenings in apple (Pyrus malus) and geranium (Pelargonium hortorum) roots to an apoplastic fluorescent dye tracer. Canadian Journal of Botany 59 : 1107 1110.
26. Peterson CA, Enstone DE. 1996. Functions of passage cells in the endodermis and exodermis of roots. Physiologia Plantarum 97 : 592 598.
27. Peterson TA, Swanson ES, Hull RJ. 1986. Use of lanthanum to trace apoplastic solute transport in intact plants. Journal of Experimental Botany 37 : 807 822.
28. Peyrano G, Taleisnik E, Quiroga M, deForchetti SM, Tigier H. 1997. Salinity effects on hydraulic conductance, lignin content and peroxidase activity in tomato roots. Plant Physiology and Biochemistry 35 : 387 393.
29. Pratikakis E, Rhizopoulou S, Psaras GK. 1998. A phi layer in roots of Ceratonia siliqua L. Botanica Acta 111 : 93 98.
30. Reinhardt DH, Rost TL. 1995. Salinity accelerates endodermal development and induces an exodermis in cotton seedling roots. Environmental and Experimental Botany 35 : 563 574.
31. Robards AW, Robb ME. 1974. Entry of ions and molecules into roots: investigation using electron-opaque tracers. Planta 120 : 1 12.
32. Russow E. 1875. Betrachtungen uber das Leitbundel und Grundgewebe aus vergleichend morphologishem und phylogentischem Gesischstpunkt. Dorpat, Estonia : Schnakenburg's Anstalt.
33. 3 deficiency and NaCl stress on suberin deposition in rhizo- and hypodermal (RHCW) and endodermal cell walls (ECW) of castor bean (Ricinus communis L.) roots. Plant and Soil 269 : 333 339.
34. Schröder M, Kunz U, Lehmann H. 2002. On the evidence of a diffusion barrier in the outer cortex apoplast of cress-roots (Lepidium sativum), demonstrated by analytical electron microscopy. Journal of Plant Physiology 159 : 1197 1204.
35. +-pump activity by 14-3-3 proteins in barley (Hordeum disticum) roots under salt stress. Russian Journal of Plant Physiology 49 : 754 760.
36. Soukup A, Malá J, Hrubcová M, Kálal J, Votrubová O. 2004. Differences in anatomical structure and lignin content of roots of pedunculate oak and wild cherry-tree plantlets during acclimation. Biologia Plantarum 48 : 481 489.
37. Van Tieghem P. 1871. Mémoire sur la racine. Annals des Science Naturelles (Paris) 13 : 187 195.
38. Van Tieghem P. 1888. Le réseau de soutien de l'ecorce de la racine. Annals des Science Naturelles. Botanique Series 7/8 : 375 378.
39. +-ATPase in the root endodermis. Plant Journal 27 : 191 201.
40. Walker RR, Sedgley M, Blesing MA, Douglas TJ. 1984. Anatomy, ultrastructure and assimilate concentrations of roots of citrus genotypes differing in ability for salt exclusion. Journal of Experimental Botany 35 : 1481 1494.
41. Weerdenburg CA, Peterson CA. 1983. Structural changes in phi thickenings during primary and secondary growth in roots. 1. Apple (Pyrus malus) Rosaceae. Canadian Journal of Botany 61 : 2570 2577.
42. Wilcox H. 1962. Growth studies of the root of incense cedar, Libocedrus decurrens. I. The origin and development of primary tissues. American Journal of Botany 49 : 221 236.
43. +-ATPase in root plasma membrane of two wheat cultivars. Plant Science 166 : 913 918.
44. Zimmermann HM, Hartmann K, Schreiber L, Steudle E. 2000. Chemical composition of apoplastic transport barriers in relation to radial hydraulic conductivity of corn roots (Zea mays L.). Planta 210 : 302 311.