Shatzman A R, Kosman D J
J Bacteriol. 1979 Jan;137(1):313-20. doi: 10.1128/jb.137.1.313-320.1979.
The synthesis and subcellular localization of the two superoxide dismutases of Dactylium dendroides were studied in relation to changes in copper and manganese availability. Cultures grew normally at all medium copper concentrations used (10 nM to 1 mM). In the presence of high (10 muM) copper, manganese was poorly absorbed in comparison to the other metals in the medium. However, cells grown at 10 nM copper exhibited a 3.5-fold increase in manganese content, while the concentration of the other metals remained constant. Cultures grown at 10 nM copper or more had 80% Cu/Zn enzyme and 20% mangani enzyme; the former was entirely in the cytosol, and the latter was mitochondrial. Removal of copper from the medium resulted in decreased Cu/Zn superoxide dismutase synthesis with a concomitant increase in the mangani enzyme such that total cellular superoxide dismutase activity remained constant. The mangani enzyme in excess of the 20% was present in the non-mitochondrial fraction. The mitochondria, therefore, show no variability with respect to superoxide dismutase content, whereas the soluble fraction varies from 100 to 13% Cu/Zn superoxide dismutase. Copper-starved cells that were synthesizing predominantly mangani superoxide dismutase could be switched over to mostly Cu/Zn superoxide dismutase synthesis by supplementing the medium with copper during growth. Immunoprecipitation experiments suggest that the decrease in Cu/Zn activity at low copper concentration is a result of decreased synthesis of that protein rather than the production of an inactive apoprotein.
研究了树状指霉两种超氧化物歧化酶的合成及亚细胞定位与铜和锰可利用性变化的关系。在所用的所有培养基铜浓度(10 nM至1 mM)下,培养物均正常生长。在高铜(10 μM)存在的情况下,与培养基中的其他金属相比,锰的吸收较差。然而,在10 nM铜浓度下生长的细胞锰含量增加了3.5倍,而其他金属的浓度保持不变。在10 nM铜或更高浓度下生长的培养物中,Cu/Zn酶占80%,锰酶占20%;前者完全位于细胞质中,后者位于线粒体中。从培养基中去除铜会导致Cu/Zn超氧化物歧化酶合成减少,同时锰酶增加,从而使细胞总超氧化物歧化酶活性保持不变。超过20%的锰酶存在于非线粒体部分。因此,线粒体的超氧化物歧化酶含量没有变化,而可溶性部分的Cu/Zn超氧化物歧化酶含量从100%变化到13%。在生长过程中通过向培养基中补充铜,主要合成锰超氧化物歧化酶的缺铜细胞可以转变为主要合成Cu/Zn超氧化物歧化酶。免疫沉淀实验表明,低铜浓度下Cu/Zn活性的降低是该蛋白质合成减少的结果,而不是无活性脱辅基蛋白的产生。