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Osmotic Adjustment of Cultured Tobacco Cells (Nicotiana tabacum var. Samsum) Grown on Sodium Chloride

机译:氯化钠上培养的烟草细胞的渗透调节

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摘要

Tobacco cell cultures (var. Samsum) were grown on increasing levels of NaCl to select variants for increased salt tolerance. The osmotic adjustment of NaCl-adapted and nonadapted cell lines was studied. Both cell lines were grown on modified Linsmaier and Skoog medium with or without NaCl. Few differences were found in the response of adapted and nonadapted lines to NaCl.The concentrations of sugars, Na+, Cl, and NO3 were identical in the cells and medium. Potassium and amino acids were accumulated by the cells. All of the above solutes accounted for 80 to 90% of the osmotic potential for both cell lines when grown on basal medium with or without NaCl. The osmotic potential of growing cells was always 1 to 3 bars more negative than that of the medium. During the first 10 days culture, the cells hydrolyzed the 117 millimolar sucrose present in the fresh media, and the media became more negative by 3 bars. Growing cells absorbed and metabolized the sugars, NH4+, and NO3 during the next 25 days, and the osmotic potential of the media and cells became less negative. The addition of 130 millimolar NaCl made the media and cells osmotically more negative by 6 bars throughout the growth cycle, as compared with cells growing on basal medium.The efflux of cellular solutes during distilled H2O washes was resolved into two components. The fast component (0.6 to 1.7 minutes half-time) included solutes of the free space and cytoplasm, whereas the slow component (1.6 to 4.9 hours half-time) represented the vacuolar solutes. Sodium and Cl were present in the vacuole. No differences were observed in the solute efflux between the adapted and nonadapted cell lines.
机译:烟草细胞培养物(Samsum变种)在NaCl含量增加的条件下生长,以选择变异体以提高耐盐性。研究了NaCl适应和非适应细胞系的渗透调节。两种细胞系均在含有或不含NaCl的改良Linsmaier和Skoog培养基上生长。适应和非适应品系对NaCl的反应几乎没有差异。糖,Na + ,Cl -和NO3 -的浓度在细胞和培养基中是相同的钾和氨基酸被细胞积累。在含有或不含NaCl的基础培养基上生长时,所有上述溶质均占两种细胞系渗透势的80%至90%。生长中的细胞的渗透势总是比培养基的负势高1至3 bar。在培养的前10天中,细胞水解了新鲜培养基中存在的117毫摩尔蔗糖,培养基的负压降低了3 bar。在接下来的25天中,生长中的细胞吸收并代谢了糖,NH4 + 和NO3 -,并且培养基和细胞的渗透势变得更弱。与在基础培养基上生长的细胞相比,添加130毫摩尔NaCl使培养基和细胞在整个生长周期中渗透压降低了6 bar。在蒸馏水洗涤过程中,细胞溶质的流出被分解为两个部分。快速成分(半场时间为0.6至1.7分钟)包括自由空间和细胞质的溶质,而慢速成分(半场时间为1.6至4.9小时)代表液泡溶质。液泡中存在钠和Cl -。在适应细胞系和非适应细胞系之间的溶质流出没有观察到差异。

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