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拟南芥中的超氧化物歧化酶:一个具有不同调控和蛋白质定位的多样化酶家族。

Superoxide dismutase in Arabidopsis: an eclectic enzyme family with disparate regulation and protein localization.

作者信息

Kliebenstein D J, Monde R A, Last R L

机构信息

Boyce Thompson Institute for Plant Research, and Section of Genetics and Development, Cornell University, Ithaca, NY 14853-1901, USA.

出版信息

Plant Physiol. 1998 Oct;118(2):637-50. doi: 10.1104/pp.118.2.637.

Abstract

A number of environmental stresses can lead to enhanced production of superoxide within plant tissues, and plants are believed to rely on the enzyme superoxide dismutase (SOD) to detoxify this reactive oxygen species. We have identified seven cDNAs and genes for SOD in Arabidopsis. These consist of three CuZnSODs (CSD1, CSD2, and CSD3), three FeSODs (FSD1, FSD2, and FSD3), and one MnSOD (MSD1). The chromosomal location of these seven SOD genes has been established. To study this enzyme family, antibodies were generated against five proteins: CSD1, CSD2, CSD3, FSD1, and MSD1. Using these antisera and nondenaturing-polyacrylamide gel electrophoresis enzyme assays, we identified protein and activity for two CuZnSODs and for FeSOD and MnSOD in Arabidopsis rosette tissue. Additionally, subcellular fractionation studies revealed the presence of CSD2 and FeSOD protein within Arabidopsis chloroplasts. The seven SOD mRNAs and the four proteins identified were differentially regulated in response to various light regimes, ozone fumigation, and ultraviolet-B irradiation. To our knowledge, this is the first report of a large-scale analysis of the regulation of multiple SOD proteins in a plant species.

摘要

许多环境胁迫可导致植物组织内超氧化物生成增加,人们认为植物依靠超氧化物歧化酶(SOD)来清除这种活性氧。我们已在拟南芥中鉴定出7个SOD的cDNA和基因。它们包括3个铜锌超氧化物歧化酶(CSD1、CSD2和CSD3)、3个铁超氧化物歧化酶(FSD1、FSD2和FSD3)以及1个锰超氧化物歧化酶(MSD1)。这7个SOD基因的染色体定位已确定。为研究这个酶家族,我们制备了针对5种蛋白质(CSD1、CSD2、CSD3、FSD1和MSD1)的抗体。利用这些抗血清和非变性聚丙烯酰胺凝胶电泳酶分析,我们在拟南芥莲座叶组织中鉴定出了两种铜锌超氧化物歧化酶、铁超氧化物歧化酶和锰超氧化物歧化酶的蛋白质及活性。此外,亚细胞分级分离研究揭示了拟南芥叶绿体中存在CSD2和铁超氧化物歧化酶蛋白。所鉴定出的7种SOD mRNA和4种蛋白质在响应不同光照条件、臭氧熏蒸和紫外线B照射时受到不同程度的调控。据我们所知,这是关于植物物种中多种SOD蛋白调控的大规模分析的首次报道。

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