Naliwajski Marcin R, Skłodowska Maria
Department of Plant Physiology and Biochemistry, Faculty of Biology and Environmental Protection, University of Lodz, Banacha 12/16, 90-237, Lodz, Poland,
Protoplasma. 2014 Jan;251(1):201-9. doi: 10.1007/s00709-013-0538-3. Epub 2013 Aug 29.
Proline is an important osmolyte appearing as the result of salt stress response of plants. In the present study, we measured the proline concentration, activities of pyrroline-5-carboxylate synthetase (P5CS), pyrroline-5-carboxylate reductase (P5CR), and proline dehydrogenase (PDH) key regulatory enzymes in the biosynthesis and degradation of proline in the acclimated (AC20) and the non-acclimated (NAC) cucumber cell suspension cultures subjected to moderate (150 mM NaCl; AC20-150, NAC-150, respectively) and severe (200 mM NaCl; AC20-200, NAC-200, respectively) salt stress. The data showed that salt stress brought about a linear increase in proline content in both types of cultures. However, in the acclimated culture proline accumulation was observed earlier, in third hour after stress. Only in the acclimated culture moderate and severe stresses up-regulated P5CS activity throughout the experiment, whereas the activity of P5CR grew in response to both NaCl concentrations only in 24th and 48th hour. The severe salt stress resulted in decrease in P5CR in NAC-200 cultures. In response to salt stress, both types of cell suspension cultures reacted with decline in PDH activity below the spectrophotometrically detected level. Cell cultures vigor correlated with salt concentration and time of exposure to the stress factor. Both NaCl concentrations caused linear decline in vigor of the non-acclimated culture up to 80-90 % at the end of the experiment, whereas in the acclimated culture significant decrease by about 30-40 % was reached in 24th hour after stress. The presented data suggest that acclimation to salt stress up-regulated proline synthesis enzyme activity and caused intensive accumulations of proline by inhibiting its oxidation.
脯氨酸是植物盐胁迫响应产生的一种重要渗透调节物质。在本研究中,我们测定了经驯化(AC20)和未经驯化(NAC)的黄瓜细胞悬浮培养物中脯氨酸的浓度,以及脯氨酸生物合成和降解过程中的关键调节酶——吡咯啉 - 5 - 羧酸合成酶(P5CS)、吡咯啉 - 5 - 羧酸还原酶(P5CR)和脯氨酸脱氢酶(PDH)的活性。这些细胞悬浮培养物分别经受中度(150 mM NaCl;分别为AC20 - 150、NAC - 150)和重度(200 mM NaCl;分别为AC20 - 200、NAC - 200)盐胁迫。数据表明,盐胁迫使两种培养物中的脯氨酸含量呈线性增加。然而,在驯化培养物中,脯氨酸积累在胁迫后第3小时就较早出现。仅在驯化培养物中,中度和重度胁迫在整个实验过程中上调了P5CS活性,而P5CR的活性仅在第24小时和第48小时对两种NaCl浓度有响应而增加。重度盐胁迫导致NAC - 200培养物中P5CR活性下降。响应盐胁迫,两种类型的细胞悬浮培养物的PDH活性均下降至低于分光光度法检测水平。细胞培养物活力与盐浓度和胁迫因子暴露时间相关。两种NaCl浓度均使未经驯化培养物的活力在实验结束时线性下降至80 - 90%,而在驯化培养物中,胁迫后第24小时活力显著下降约30 - 40%。所呈现的数据表明,对盐胁迫的驯化上调了脯氨酸合成酶活性,并通过抑制脯氨酸氧化导致其大量积累。