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首页> 外文期刊>The biochemical journal >Water- and solute-accessible spaces of purified peroxisomes. Evidence that peroxisomes are permeable to NAD+
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Water- and solute-accessible spaces of purified peroxisomes. Evidence that peroxisomes are permeable to NAD+

机译:纯化过氧化物酶体的水和溶质可及空间。过氧化物酶体可渗透NAD +的证据

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pPeroxisomes were purified from liver homogenates from rats, treated with the peroxisome proliferator clofibrate, by a combination of differential centrifugation and isopycnic centrifugation in iso-osmotic self-generating Percoll gradients. Structural integrity of the peroxisomes appeared to be preserved as evidenced by a high degree of catalase latency, the absence of catalase release during purification and the exclusion of inulin (mol.wt. +/- 5000). Spaces for water and solutes were measured after incubation of the peroxisomes in iso-osmotic sucrose with radioactive water or solutes and separation of the organelles from their media by centrifugation through an organic layer. Extraperoxisomal water was corrected for by the use of radioactive dextran or inulin. The sucrose, glucose, urea, methanol and acetate-accessible spaces were identical, suggesting that these spaces represent the volume in which molecules that can cross the membrane distribute. This volume equalled 50-65% of the water space. Urate and NAD+, a cofactor of peroxisomal beta-oxidation of fatty acids, also distributed in this volume, but were also partly bound. Urate and NAD+ binding was not abolished by sonication, which released the bulk of matrix catalase activity, but NAD+ binding was seriously diminished. The peroxisomal water and sucrose spaces were estimated to be 107 microliters and 55 microliters per g of liver tissue from a clofibrate-treated rat. From quantitative morphometric data [Anthony, Schmucker, Mooney & Jones (1978) J. Lipid Res. 19, 154-165] and our marker enzyme analyses, as well as from our experimentally determined water spaces of mitochondrial and microsomal fractions, it could be calculated that the volume contamination by lysosomes, mitochondria and microsomes did not exceed 1, 8 and 6% respectively. Our data indicate that apparently intact peroxisomes are permeable to a number of small molecules, including NAD+. Whether the NAD+-binding sites in sonicated peroxisomes mirror the likely existence of a membrane carrier requires further investigation./p
机译:通过过分离心和等渗离心在等渗自生Percoll梯度中的组合,从大鼠肝脏匀浆中纯化过氧化物酶体,用过氧化物酶体增殖物氯贝特酶处理。过氧化氢酶的结构完整性似乎得到了保留,这可以通过高度的过氧化氢酶潜伏期,纯化过程中不存在过氧化氢酶释放以及菊粉排除(摩尔重量+/- 5000)来证明。在等渗蔗糖中的过氧化物酶体与放射性水或溶质一起孵育,并通过离心通过有机层将细胞器从其介质中分离出来之后,测量水和溶质的空间。通过使用放射性右旋糖酐或菊粉校正过氧化物酶体外水。蔗糖,葡萄糖,尿素,甲醇和乙酸盐可及的空间是相同的,这表明这些空间代表了可以穿过膜的分子分布的体积。这个体积等于水空间的50-65%。尿酸盐和脂肪酸过氧化物酶体β-氧化的辅助因子NAD +也分布在该体积中,但也部分结合。超声处理并没有消除尿酸盐和NAD +的结合,从而释放了大量的基质过氧化氢酶活性,但NAD +的结合却被严重削弱。据估计,每克来自clofibrate处理的大鼠肝脏组织的过氧化物酶体水和蔗糖空间分别为107微升和55微升。根据定量形态计量数据[Anthony,Schmucker,Mooney& Jones(1978)J. Lipid Res。 19,154-165]和我们的标记酶分析,以及我们根据实验确定的线粒体和微粒体级分的水空间,可以计算出溶酶体,线粒体和微粒体的体积污染不超过1、8和6%分别。我们的数据表明,看起来完整的过氧化物酶体可渗透包括NAD +在内的许多小分子。超声过氧化物酶体中的NAD +结合位点是否反映了膜载体的可能存在,需要进一步研究。

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