Plaxton W C
Department of Biology, Queen's University, Kingston, Ontario K7L 3N6, Canada.
Plant Physiol. 1991 Dec;97(4):1334-8. doi: 10.1104/pp.97.4.1334.
Leucoplast pyruvate kinase (PK(p); EC 2.7.1.40) from endosperm of developing castor oil seeds (Ricinus communis L. cv Baker 296) appears to be highly susceptible to limited degradation by a cysteine endopeptidase during the purification of the enzyme or incubation of clarified homogenates at 4 degrees C. Purified castor seed PK(p) was previously reported to consist of immunologically related 57.5 and 44 kilodalton subunits (Plaxton WC, Dennis DT, Knowles VL [1990] Plant Physiol 94: 1528-1534). By contrast, immunoreactive polypeptides of about 63.5 and 54 kilodaltons were observed when a western blot of an extract prepared under denaturing conditions was probed with affinity purified rabbit anti-(castor seed PK(p)) immunoglobulin G. Proteolytic activity against PK(p) was estimated by the disappearance of the 63.5 and 54 kilodalton subunits and the concomitant appearance of lower molecular mass immunoreactive degradation products during the incubation of clarified homogenates at 4 degrees C. The presence of 2 millimolar dithiothreitol accelerated the degradation of PK(p). The conservation of the 63.5 and 54 kilodalton subunits was observed after extraction of the enzyme in the presence of 1 millimolar p-hydroxymecuribenzoate, or 1 millimolar Nalpha-p-tosyl-l-lysine chloromethyl ketone, or 10 millimolar iodoacetate. These results reveal that a cysteine endopeptidase was responsible for the in vitro proteolysis of PK(p). This endopeptidase is present throughout all stages of endosperm development. Its PK(p)-degrading activity, however, appears to be most pronounced in preparations from older endosperm. When lysates of purified leucoplasts were incubated at 4 degrees C for up to 21 hours, no degradation of PK(p) was observed; this indicated an extra-leucoplastic localization for the cysteine endopeptidase. Although the in vivo subunit structure of PK(p) remains uniform throughout all stages of endosperm development, the large decrease in PK activity that accompanies castor seed maturation coincides with a marked reduction in the concentration of PK(p).
发育中的蓖麻种子(Ricinus communis L. cv Baker 296)胚乳中的质体丙酮酸激酶(PK(p);EC 2.7.1.40)在酶的纯化过程中或澄清匀浆于4℃孵育时,似乎极易受到一种半胱氨酸内肽酶的有限降解作用。先前报道纯化的蓖麻种子PK(p)由免疫相关的57.5 kDa和44 kDa亚基组成(Plaxton WC,Dennis DT,Knowles VL [1990] Plant Physiol 94: 1528 - 1534)。相比之下,当用亲和纯化的兔抗(蓖麻种子PK(p))免疫球蛋白G探测变性条件下制备的提取物的蛋白质印迹时,观察到了约63.5 kDa和54 kDa的免疫反应性多肽。通过在4℃孵育澄清匀浆过程中63.5 kDa和54 kDa亚基的消失以及伴随出现的较低分子量免疫反应性降解产物,来估计针对PK(p)的蛋白水解活性。2 mM二硫苏糖醇的存在加速了PK(p)的降解。在1 mM对羟基汞苯甲酸、1 mM Nα - 对甲苯磺酰 - L - 赖氨酸氯甲基酮或10 mM碘乙酸存在下提取酶后,观察到63.5 kDa和54 kDa亚基得以保留。这些结果表明,一种半胱氨酸内肽酶负责PK(p)的体外蛋白水解。这种内肽酶在胚乳发育的所有阶段均存在。然而,其PK(p)降解活性在来自较老胚乳的制剂中似乎最为明显。当纯化的质体裂解物在4℃孵育长达21小时时,未观察到PK(p)的降解;这表明半胱氨酸内肽酶定位于质体外。尽管PK(p)在胚乳发育的所有阶段的体内亚基结构保持一致,但蓖麻种子成熟过程中PK活性的大幅下降与PK(p)浓度的显著降低相吻合。