Chang K, Roberts J K
Department of Biochemistry, University of California, Riverside, California 92521.
Plant Physiol. 1992 May;99(1):291-7. doi: 10.1104/pp.99.1.291.
Our aim was to determine whether fixation of inorganic carbon (C(i)), due to phosphoenolpyruvate carboxylase activity, is limited by the availability of C(i) in the cytoplasm of maize (Zea mays L.) root tips. Rates of C(i) uptake and metabolism were measured during K(2)SO(4) treatment, which stimulates dark C(i) fixation. (13)C(i) uptake was followed by (13)C-nuclear magnetic resonance (NMR); 5 millimolar K(2)SO(4) had no significant effect on (13)C(i) influx. The contribution of respiratory CO(2) production to cytoplasmic HCO(3) (-) was measured using in vivo(13)C-NMR and (1)H-NMR of cell extracts; K(2)SO(4) treatment had no effect on respiratory CO(2) production. The concentration of cytoplasmic HCO(3) (-) was estimated to be approximately 11 millimolar, again with K(2)SO(4) having no significant effect. These experiments allowed us to determine the extent to which extracellularly supplied (14)C(i) was diluted in the cytoplasm by respiratory CO(2) and thereby measure phosphoenolpyruvate (PEP) carboxylase activity in vivo using (14)C(i). PEP carboxylase activity in root tips was enhanced approximately 70% over controls within 12 minutes of the addition of 5 millimolar K(2)SO(4). The activity of carbonic anhydrase, which provides PEP carboxylase with C(i), was determined by saturation transfer (13)C-NMR to be more than 200 times that of PEP carboxylase in vivo. The regulation of PEP carboxylase in K(2)SO(4)-treated roots is discussed.
我们的目的是确定由于磷酸烯醇式丙酮酸羧化酶的活性,无机碳(C(i))的固定是否受到玉米(Zea mays L.)根尖细胞质中C(i)可用性的限制。在K(2)SO(4)处理期间测量C(i)的吸收和代谢速率,K(2)SO(4)处理可刺激暗C(i)固定。通过(13)C核磁共振(NMR)跟踪(13)C(i)的吸收;5毫摩尔的K(2)SO(4)对(13)C(i)流入没有显著影响。使用细胞提取物的体内(13)C-NMR和(1)H-NMR测量呼吸作用产生的CO(2)对细胞质HCO(3)(-)的贡献;K(2)SO(4)处理对呼吸作用产生的CO(2)没有影响。估计细胞质HCO(3)(-)的浓度约为11毫摩尔,同样K(2)SO(4)没有显著影响。这些实验使我们能够确定细胞外供应的(14)C(i)在细胞质中被呼吸作用产生的CO(2)稀释的程度,从而使用(14)C(i)在体内测量磷酸烯醇式丙酮酸(PEP)羧化酶的活性。在添加5毫摩尔K(2)SO(4)后的12分钟内,根尖中的PEP羧化酶活性比对照提高了约70%。通过饱和转移(13)C-NMR测定,为PEP羧化酶提供C(i)的碳酸酐酶的活性在体内比PEP羧化酶的活性高200多倍。讨论了K(2)SO(4)处理的根中PEP羧化酶的调节。