Michaelis S, Inouye H, Oliver D, Beckwith J
J Bacteriol. 1983 Apr;154(1):366-74. doi: 10.1128/jb.154.1.366-374.1983.
A phoA-lacZ gene fusion was used to isolate mutants altered in the alkaline phosphatase signal sequence. This was done by selecting Lac+ mutants from a phoA-lacZ fusion strain that produces a membrane-bound hybrid protein and is unable to grow on lactose. Two such mutant derivatives were characterized. The mutations lie within the phoA portion of the fused gene and cause internalization of the hybrid protein. When the mutations were genetically recombined into an otherwise wild-type phoA gene, they interfered with export of alkaline phosphatase to the periplasm. The mutant alkaline phosphatase protein was found instead in the cytoplasm in precursor form. DNA sequence analysis demonstrated that both mutations lead to amino acid alterations in the signal sequence of alkaline phosphatase.
利用phoA-lacZ基因融合来分离碱性磷酸酶信号序列发生改变的突变体。这是通过从产生膜结合杂合蛋白且无法在乳糖上生长的phoA-lacZ融合菌株中筛选Lac+突变体来实现的。对两个这样的突变衍生物进行了表征。这些突变位于融合基因的phoA部分内,并导致杂合蛋白的内化。当这些突变通过基因重组导入到其他方面为野生型的phoA基因中时,它们会干扰碱性磷酸酶向周质的输出。相反,突变的碱性磷酸酶蛋白以前体形式存在于细胞质中。DNA序列分析表明,这两个突变均导致碱性磷酸酶信号序列中的氨基酸改变。