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软体动物血细胞中的一氧化氮合酶活性。

Nitric oxide synthase activity in molluscan hemocytes.

作者信息

Conte A, Ottaviani E

机构信息

Department of Animal Biology, University of Modena, Italy.

出版信息

FEBS Lett. 1995 May 29;365(2-3):120-4. doi: 10.1016/0014-5793(95)00439-g.

Abstract

The hemocytes of the freshwater snail Viviparus ater have nitric oxide synthase (NOS) activity, as demonstrated by [3H]citrulline and nitrite + nitrate formation. The enzyme is NADPH dependent and is competitively inhibited by the mammalian NOS inhibitor NG-monomethyl-L-arginine (Ki = 4.7 microM). The Km for L-arginine is 2.5 microM. 70% of the total activity is observed at very low free Ca2+ concentration (3 nM). LPS treatment increased total NOS activity 2.4 fold. The activity is partly present in the non-soluble fraction of hemocytes (24% and 8% in non-stimulated and LPS-stimulated snails, respectively). An antiserum to the C-terminal synthetic pentadecapeptide of the rat cerebellar NOS inhibited the enzyme activity in a concentration-dependent manner. This is the first biochemical demonstration of the existence of NOS activity in molluscan hemocytes, the cells responsible for defence mechanisms.

摘要

通过[3H]瓜氨酸以及亚硝酸盐和硝酸盐的生成证明,淡水螺类——黑瓶螺的血细胞具有一氧化氮合酶(NOS)活性。该酶依赖于NADPH,并受到哺乳动物NOS抑制剂NG-单甲基-L-精氨酸的竞争性抑制(Ki = 4.7 microM)。L-精氨酸的Km为2.5 microM。在极低的游离Ca2+浓度(3 nM)下可观察到总活性的70%。脂多糖(LPS)处理使总NOS活性增加了2.4倍。该活性部分存在于血细胞的不溶性部分(未刺激和LPS刺激的蜗牛中分别为24%和8%)。针对大鼠小脑NOS C端合成十五肽的抗血清以浓度依赖的方式抑制了该酶的活性。这是首次在软体动物血细胞(负责防御机制的细胞)中进行的关于NOS活性存在的生化证明。

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