Development of Casparian strip in rice cultivars

References

• Perumalla CJ, Peterson CA, Enstone DE. A survey of angiosperm species to detect hypodermal Casparian bands. I. Roots with a uniserate hypodermis and epidermis. Bot J Linn Soc 1990; 103:93 - 112
   Web of Science ®Google Scholar
• Enstone DE, Peterson CA, Ma F. Root endodermis and exodermis: structure, function and responses to the environment. J Plant Growth Regul 2003; 21:335 - 351
   Web of Science ®Google Scholar
• Ma F, Peterson CA. Current insights into the development, structure and chemistry of the endodermis and exodermis of roots. Can J Bot 2003; 81:405 - 421
   Google Scholar
• Clark LH, Harris WH. Observations of the root anatomy of rice (Oryza sativa L.). Amer J Bot 1981; 68:154 - 161
   Web of Science ®Google Scholar
• Peterson CA. Exodermal Casparian bands: their significance for ion uptake by roots. Physiol Plant 1988; 72:204 - 208
   Web of Science ®Google Scholar
• Ranathunge K, Kotula L, Steudle E, Lafitte R. Water permeability and reflection coefficient of the outer part of young rice roots are differently affected by closure of water channels (aquaporins) or blockage of apoplastic pores. J Exp Bot 2004; 55:433 - 447
   PubMed Web of Science ®Google Scholar
• Wu XQ, Zhu JM, Wang QL, Hu YX, Lin JX. Advances in studies on Casparian strips. Chin Bull Bot 2002; 19:302 - 309
   Google Scholar
• Wu XQ, Zhu JM, Huang RZ, Wang QL, Zheng WJ, Hu YX, et al. Evidence of Casparian Strip in the foliar endodermis of Pinus bungeana. Acta Bot Sin 2001; 43:1081 - 1084
   Google Scholar
• Wu XQ, Lin JX, Lin QQ, Wang J, Schreiber L. Casparian strips in needles are more solute permeable than endodermal transport barriers in roots of Pinus bungeana. Plant Cell Physiol 2005; 46:1799 - 1808
   PubMed Web of Science ®Google Scholar
• Schreiber L, Breiner HW, Riederer M, Duggelin M, Guggenheim R. The Casparian band of Clivia miniata Reg. roots: isolation, fine structure and chemical nature. Bot Acta 1994; 107:353 - 361
   Google Scholar
• Zeier J, Schreiber L. Comparative investigation of primary and tertiary endodermal cell walls isolated from the roots of five monocotyledonous species: chemical composition in relation to fine structure. Planta 1998; 206:349 - 361
   Web of Science ®Google Scholar
• Hartmann K, Peiter E, Koch K, Schubert S, Schreiber L. Chemical composition and ultrastructure of broad bean (Vicia faba L.) nodule endodermis in comparison to the root endodermis. Planta 2002; 215:14 - 25
   PubMed Web of Science ®Google Scholar
• Nagahashi G, Thompson WW, Leonard RT. The Casparian strip as a barrier to the movement of lanthanum in maize roots. Science 1974; 183:670 - 671
   PubMed Web of Science ®Google Scholar
• Steudle E, Peterson CA. How does water get through roots?. J Expl Bot 1998; 49:775 - 788
   Web of Science ®Google Scholar
• Stasovsky E, Peterson CA. Effects of drought and subsequent rehydration on the structure, vitality and permeability of Allium cepa adventitious root. Can J Bot 1993; 71:700 - 707
   Google Scholar
• Yokoyama M, Karahara I. Radial widening of the Casparian strip follows induced radial expansion of endodermal cells. Planta 2001; 213:474 - 477
   PubMed Web of Science ®Google Scholar
• Karahara I, Ikeda A, Kondo T, Uetake Y. Development of the Casparian strip in primary roots of maize under salt stress. Planta 2004; 219:41 - 47
   PubMed Web of Science ®Google Scholar
• Krishnamurthy P, Ranathunge K, Franke R, Prakash HS, Schreiber L, Mathew MK. The role of root apoplastic transport barriers in salt tolerance of rice (Oryza sativa L.). Planta 2009; 230:119 - 134
   PubMed Web of Science ®Google Scholar
• Kotula L, Ranathunge K, Schreiber L, Steudle E. Functional and chemical comparison of apoplastic barriers to radial oxygen loss in roots of rice (Oryza sativa L.) grown in aerated or deoxygenated solution. J Exp Bot 2009; 60:2155 - 2167
   PubMed Web of Science ®Google Scholar
• Ranathunge K, Steudle E, Lafitte R. Control of water uptake by rice (Oryza sativa L.): role of the outer part of the root. Planta 2003; 217:193 - 205
   PubMed Web of Science ®Google Scholar
• Brundrett MC, Enstone DE, Peterson CA. A berberine-aniline blue fluorescent staining procedure for suberin, lignin and callose in plant tissues. Protoplasma 1988; 146:133 - 142
   Web of Science ®Google Scholar
• Lux A, Morita S, Abe J, Ito K. An improved method for clearing and staining free-hand sections and whole-mount samples. Ann Bot 2005; 96:989 - 996
   PubMed Web of Science ®Google Scholar
• Xie JX, Chang JB, Wang XM. Applications of infrared spectra in organic chemistry and pharmaceutical chemist 2001; Beijing Science Press
   Google Scholar
• Lopes MH, Neto P, Barros AS, Rutledge D, Delgadillo I, Gil AM. Quantitation of aliphatic suberin in Quercus suber L. cork by FTIR spectroscopy and solid-state 13C-NMR spectroscopy. Biopolymers 2000; 57:344 - 351
   PubMed Web of Science ®Google Scholar
• Peterson CA, Perumalla CJ. A survey of angiosperm species to detect hypodermal casparian bands. II. Roots with a multiseriate hypodermis or epidermis. Bot J Linn Soc 1990; 103:113 - 125
   Web of Science ®Google Scholar
• Clarkson DT. Waisel Y, Eshel A, Kafkafi U. Root structure and sites of ion uptake. Plant Roots: the Hidden Half 1996; 2nd ed New York, NY Marcel Dekker 483 - 510
   Google Scholar
• Damus M, Peterson RL, Enstone DE, Peterson CA. Modifications of cortical cell walls in roots of seedless vascular plants. Bot Acta 1997; 110:190 - 195
   Google Scholar
• Meyer CJ, Seago JL Jr, Peterson CA. Environmental effects on the maturation of the endodermis and exodermis of Iris germanica roots. Ann Bot 2009; 103:687 - 702
   PubMed Web of Science ®Google Scholar
• Schreiber L, Hartmann K, Skrabs M, Zeier J. Apoplastic barriers in roots: chemical composition of endodermal and hypodermal cell walls. J Exp Bot 1999; 50:1267 - 1280
   Web of Science ®Google Scholar
• Bernards MA. Demystifying suberin. Can J Bot 2002; 80:227 - 240
   Google Scholar
• Zeier J, Schreiber L. Chemical composition of hypodermal and endodermal cell walls and xylem vessels isolated from Clivia miniata (identification of the biopolymers lignin and suberin). Plant Physiol 1997; 113:1223 - 1231
   PubMed Web of Science ®Google Scholar
• Kolattukudy PE. Polyesters in higher plants. Adv Biochem Eng Biot 2001; 71:1 - 49
   PubMedGoogle Scholar
• Zimmermann HM, Steudle E. Apoplastic transport across young maize roots: effect of the exodermis. Planta 1998; 206:7 - 19
   Web of Science ®Google Scholar
• Wu XQ, Zhang DX, Hu YX, Lin JX. The function of Pinus bungeana foliar endodermis as apoplastic barrier under salt stress. J Trop Subtrop Bot 2007; 15:203 - 208
   Google Scholar
• Armstrong W, Cousins D, Armstrong J, Turner DW, Beckett PM. Oxygen distribution in wetland plant roots and permeability barriers to gas-exchange with the rhizosphere: a microelectrode and modelling study with Phragmites australis. Ann Bot 2000; 86:687 - 703
   Web of Science ®Google Scholar
• Soukup A, Armstrong W, Schreiber L, Franke R, Votrubová O. Apoplastic barriers to radial oxygen loss and solute penetration: a chemical and functional comparison of the exodermis of two wetland species, Phragmites australis and Glyceria maxima. New Phytol 2007; 173:264 - 278
   PubMed Web of Science ®Google Scholar
• Cruz RT, Jordan WR, Drew MC. Structural changes and associated reduction of hydraulic conductance in roots of Sorghum bicolor L. following exposure to water deficit. Plant Physiol 1992; 99:203 - 212
   PubMed Web of Science ®Google Scholar