Rapoza M P, Webster R E
Department of Biochemistry, Duke University Medical Center, Durham, North Carolina 27710.
J Bacteriol. 1993 Mar;175(6):1856-9. doi: 10.1128/jb.175.6.1856-1859.1993.
The noncapsid assembly proteins pI and pI of the filamentous bacteriophage f1 are inserted into the inner membrane of Escherichia coli via an internal signal sequence. Inhibition of the activity of SecA with low concentrations of sodium azide results in rapid accumulation of pI and pI proteins in the cytoplasm. However, both proteins are inserted into the membrane under the same conditions when synthesized in bacteria containing a secA azide resistance mutation. The other noncapsid assembly protein, pIV, is an outer membrane protein synthesized with a cleavable signal sequence. Wild-type bacteria accumulate the precursor to pIV when protein synthesis is in the presence of low concentrations of sodium azide. These results suggest that the f1 bacteriophage assembly proteins require SecA and consequently the bacterial Sec system to reach their proper membrane location.
丝状噬菌体f1的非衣壳组装蛋白pI和pII通过内部信号序列插入大肠杆菌的内膜。用低浓度叠氮化钠抑制SecA的活性会导致pI和pII蛋白在细胞质中迅速积累。然而,当在含有secA叠氮化钠抗性突变的细菌中合成时,这两种蛋白在相同条件下都能插入膜中。另一种非衣壳组装蛋白pIV是一种带有可裂解信号序列合成的外膜蛋白。当蛋白质合成在低浓度叠氮化钠存在的情况下进行时,野生型细菌会积累pIV的前体。这些结果表明,f1噬菌体组装蛋白需要SecA,因此需要细菌的Sec系统才能到达其正确的膜定位。