Aluminum (Al) toxicity is a major factor limiting yield production on acid soils (Foy 1983). The initial symptom of Al toxicity in many plants is manifested by the inhibition of root elongation (Ownby and Popham 1990; Llugany et al. 1994; Sasaki et al. 1994; Horst et al. 1997), which occurs during a very short period of time after exposure to Al (Llugany et al. 1994; Staß and Horst 1995). In a large number of recent reports, it was shown that the root apex plays a major role in the Al-sensitivity and response mechanisms (Zhang et al. 1994; Sasaki et al. 1997; Sivaguru and Horst 1998). However, it is interesting to note that stimulatory effects of Al on the growth of plants have also been reported in some studies (Chenery 1955; Konishi et al. 1985; Huang and Bachelard 1993; Osaki et al. 1997). In tea plant (Camellia sinensis L.) a stimulatory effect of Al on the growth was also demonstrated in some experiments, using intact plant (Chenery 1955; Konishi et al. 1985), cultured roots (Tsuji et al. 1994), and pollen tubes (Yokota et al. 1997). The growth of tea roots was typically more stimulated than that of shoots by Al (Konishi et al. 1985). It was assumed that Al effects might be due to the amelioration of phosphorus absorption (Konishi et al. 1985), secretion of malic acid from roots to dissolve aluminum phosphate in the rhizosphere (Jayman and Sivasubramaniam 1975), stimulation of growth of microorganisms on the root surface (Konishi 1990) or replacement of some functions of boron (Konishi 1992; Yokota et al. 1997). However, the stimulatory effects of Al on tea plant growth have not yet been el ucidated. The formation of callose (1,3-β-glucan) has been reported as a common plant response to a variety of stresses, as well as mechanical, biophysical, chemical, and biological injury (Jaffe and Leopold 1984; Zhang et al. 1994). Increased synthesis of callose has been observed upon exposure to excess amounts of some elements, such as boron (McNairn and Currier 1965), cobalt, nickel, zinc (Peterson and Rauser 1979), and manganese (Wissemeier and Horst} 1987, 1992). Callose synthesis was also induced by Al in the roots of Triticum aestivum (Zhang et al. 1994) and Zea mays (Horst et al. 1997; Sivaguru and Horst 1998), suspension-cultured cells of Glycine max (Staß and Horst 1995), and protoplasts of Avena sativa (Schaeffer and Walton 1990) and Zea mays (Wagatsuma et al. 1995). Induction of callose synthesis in roots seems to be a very rapid physiological indicator of Al-induced injury or genotypical differences in Al sensitivity (Wissemeier and Horst 1992; Zhang et al. 1994; Horst et al. 1997). Nevertheless, Al-induced callose synthesis in tea plant, whose growth is stimulated by suitable Al concentrations, has not been described yet. Therefore, to elucidate the physiological basic effects of Al on tea plant, callose synthesis affected by Al in the root tips of intact plants was analyzed in the present study.
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Sep 28, 2005
Papiya Ghosh + 4
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