Peoples T R, Koch D W
Department of Plant Science, University of New Hampshire, Durham, New Hampshire 03824.
Plant Physiol. 1979 May;63(5):878-81. doi: 10.1104/pp.63.5.878.
Alfalfa was grown hydroponically in 0, 0.6, and 4.8 millimolar K in order to determine the influence of tissue level of K on photosynthesis, dark respiration, photorespiration, stomatal and mesophyll resistance to CO(2), photosystem I and II activity, and synthesis and activity of ribulose 1,5-bisphosphate carboxylase (RuBPc).A severe (0.0 millimolar) and mild (0.6 millimolar) K deficiency, compared to plants grown at 4.8 millimolar K, produced a significant decrease in photosynthesis and photorespiration, but an increase in dark respiration. Both deficient K levels increased hydrophyllic resistance to CO(2), but only the severe deficiency increased stomatal resistance.Photosystem I and II activity of isolated chloroplasts was not affected by K deficiency. The apparent activity of a crude RuBPc preparation was significantly reduced in severely deficient plants. Activity of the enzyme could not be restored to normal rates by the addition of K to the reaction medium.The specific activity of RuBPc isolated from severely K-deficient and K-sufficient leaflets was not significantly different, suggesting that K does not function in RuBPc activity. Incorporation of [(14)C]leucine into RuBPc, as a measure of synthesis, by K-deficient leaflets was reduced to 15% of K-sufficient leaflets. The addition of K to the reaction medium stimulated [(14)C]leucine incorporation into RuBPc and 10 millimolar KNO(3) increased incorporation to 80% of K-sufficient leaflets. Actinomycin D and cycloheximide suppressed the K-stimulated incorporation of [(14)C]leucine into RuBPc, suggesting that the K-stimulated synthesis of RuBPc most likely represents de novo synthesis.
紫花苜蓿在钾浓度分别为0、0.6和4.8毫摩尔的水培条件下生长,以确定组织中钾水平对光合作用、暗呼吸、光呼吸、气孔和叶肉对二氧化碳的阻力、光系统I和II活性以及1,5-二磷酸核酮糖羧化酶(RuBPc)的合成与活性的影响。与在4.8毫摩尔钾条件下生长的植株相比,严重(0.0毫摩尔)和轻度(0.6毫摩尔)钾缺乏导致光合作用和光呼吸显著降低,但暗呼吸增加。两种钾缺乏水平均增加了对二氧化碳的亲水性阻力,但只有严重缺乏增加了气孔阻力。分离叶绿体的光系统I和II活性不受钾缺乏的影响。在严重缺乏的植株中,粗制RuBPc制剂的表观活性显著降低。向反应介质中添加钾不能使该酶的活性恢复到正常水平。从严重缺钾和钾充足的小叶中分离出的RuBPc的比活性没有显著差异,表明钾在RuBPc活性中不起作用。作为合成量度,缺钾小叶中[(14)C]亮氨酸掺入RuBPc的量降至钾充足小叶的15%。向反应介质中添加钾刺激了[(14)C]亮氨酸掺入RuBPc,10毫摩尔硝酸钾将掺入量提高到钾充足小叶的80%。放线菌素D和环己酰亚胺抑制了钾刺激的[(14)C]亮氨酸掺入RuBPc,表明钾刺激的RuBPc合成很可能代表从头合成。