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枯草芽孢杆菌中琥珀酸脱氢酶的生物合成与膜结合

Biosynthesis and membrane binding of succinate dehydrogenase in Bacillus subtilis.

作者信息

Hederstedt L, Rutberg L

出版信息

J Bacteriol. 1980 Dec;144(3):941-51. doi: 10.1128/jb.144.3.941-951.1980.

Abstract

Antibodies specific for the Mr 65,000 (flavoprotein) and the Mr 28,000 subunits of the succinic dehydrogenase (SDH) of Bacillus subtilis were obtained. By using these antibodies it was shown that both subunits accumulated in the cytoplasm during 5-aminolevulinic acid starvation of a 5-aminolevulinic acid auxotroph. In the cytoplasm the subunits were not associated since they precipitated essentially independently of each other with subunit-specific antibody. In sodium dodecyl sulfate-polyacrylamide gel electrophoresis the cytoplasmic subunits migrated identically with the corresponding subunits from the purified membrane-bound SDH complex. Cytoplasmic subunits were pulse-labeled with L-[35S]methionine during 5-aminolevulinic acid starvation. The labeled subunits bound to the membrane when heme synthesis was resumed and also when protein synthesis was blocked by chloramphenicol before readdition of 5-aminolevulinic acid. The experiments thus demonstrated a precursor relationship between cytoplasmic subunits and the subunits of the membrane-bound SDH complex. All SDH-negative mutants isolated so far carry mutations in the citF locus. None of the mutants was found to have either the Mr 65,000 or the Mr 28,000 SDH subunits in the membrane. Four citF mutants, however, contained both subunits in the cytoplasm. Three of these mutants lacked spectrally detectable cytochrome b558. The respective mutations mapped at one end of the citF locus. These results strongly support our previous suggestion that cytochrome b558 is (part of) a membrane binding site for SDH in B. subtilis.

摘要

获得了对枯草芽孢杆菌琥珀酸脱氢酶(SDH)的65,000 Mr(黄素蛋白)和28,000 Mr亚基具有特异性的抗体。通过使用这些抗体表明,在5-氨基乙酰丙酸营养缺陷型菌株的5-氨基乙酰丙酸饥饿期间,这两个亚基都在细胞质中积累。在细胞质中,这些亚基没有结合,因为它们基本上能与亚基特异性抗体独立沉淀。在十二烷基硫酸钠-聚丙烯酰胺凝胶电泳中,细胞质亚基的迁移情况与纯化的膜结合SDH复合物中的相应亚基相同。在5-氨基乙酰丙酸饥饿期间,用L-[35S]甲硫氨酸对细胞质亚基进行脉冲标记。当血红素合成恢复时,以及在重新添加5-氨基乙酰丙酸之前用氯霉素阻断蛋白质合成时,标记的亚基都能与膜结合。因此,这些实验证明了细胞质亚基与膜结合SDH复合物的亚基之间存在前体关系。到目前为止分离出的所有SDH阴性突变体在citF基因座上都携带突变。没有发现任何一个突变体的膜中有65,000 Mr或28,000 Mr的SDH亚基。然而,四个citF突变体在细胞质中都含有这两个亚基。其中三个突变体缺乏光谱可检测的细胞色素b558。相应的突变位于citF基因座的一端。这些结果有力地支持了我们之前的推测,即细胞色素b558是枯草芽孢杆菌中SDH的膜结合位点(的一部分)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cb98/294756/8e9ce7194c8a/jbacter00573-0085-a.jpg

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