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Comparison of the Tu elongation factors from Staphylococcus aureus and Escherichia coli: possible basis for elfamycin insensitivity.

机译:金黄色葡萄球菌和大肠杆菌的Tu延伸因子的比较:依法霉素不敏感的可能依据。

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摘要

In a previous study (C. C. Hall, J. D. Watkins, and N. H. Georgopapadakou, Antimicrob. Agents Chemother. 33:322-325, 1989), the elongation factor Tu (EF-Tu) from Staphylococcus aureus was found to be insensitive to a series of kirromycin analogs which were inhibitory to the EF-Tu from Escherichia coli. In the present study, the EF-Tu from S. aureus was partially purified and characterized. Its apparent molecular mass was approximately 41,000 Da, and the enzyme copurified with EF-Ts (molecular mass, 34,000 Da). S. aureus EF-Tu differed from its E. coli counterpart in that it bound negligible amounts of [3H]GDP, in addition to being insensitive to pulvomycin and aurodox (50% inhibitory concentrations, approximately 100 and 1,000 microM, respectively, versus 2 and 0.2 microM, respectively, for E. coli). The results are consistent with the formation of a stable EF-Tu.EF-Ts complex that affects the interaction of EF-Tu with guanine nucleotides and inhibitors.
机译:在先前的研究中(CC Hall,JD Watkins和NH Georgopapadakou,Antimicrob。Agents Chemother。33:322-325,1989),发现金黄色葡萄球菌的延伸因子Tu(EF-Tu)对一系列对大肠杆菌的EF-Tu具有抑制作用的奇异霉素类似物。在本研究中,来自金黄色葡萄球菌的EF-Tu已部分纯化和表征。它的表观分子量约为41,000 Da,该酶与EF-Ts共纯化(分子量34,000 Da)。金黄色葡萄球菌EF-Tu与大肠埃希菌的不同之处在于,除了对pulvomycin和aurodox不敏感外,其结合的[3H] GDP量可忽略不计(50%抑制浓度,分别约为100和1,000 microM,而2对于大肠杆菌,分别为0.2和0.2 microM)。该结果与稳定的EF-Tu.EF-Ts复合物的形成相一致,该复合物影响EF-Tu与鸟嘌呤核苷酸和抑制剂的相互作用。

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