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A colicin-tolerant Escherichia coli mutant that confers Hfl phenotype carries two mutations in the region coding for the C-terminal domain of FtsH (HflB)

机译：赋予HFL表型的耐凝聚型大肠杆菌突变体在编码FTSH（HFLB）的C末端结构域的区域中携带两个突变

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1. A colicin-tolerant Escherichia coli mutant that confers Hfl phenotype carries two mutations in the region coding for the C-terminal domain of FtsH (HflB) [J] . Teff D., Shotland Y., Ogura T., FEMS Microbiology Letters . 2000,第1期

机译：赋予Hfl表型的耐大肠埃希菌的大肠杆菌突变体在编码FtsH（HflB）C端结构域的区域携带两个突变
2. Characterization of a conserved alpha-helical, coiled-coil motif at the C-terminal domain of the ATP-dependent FtsH (HflB) protease of Escherichia coli. [J] . Shotland Y, Teff D, Koby S, Journal of Molecular Biology . 2000,第4期

机译：大肠杆菌ATP依赖的FtsH（HflB）蛋白酶的C末端结构域的保守α-螺旋，卷曲螺旋基序的表征。
3. Characterization of mutants of the Escherichia coli AAA protease, FtsH, carrying a mutation in the central pore region [J] . Okuno T, Yamanaka K, Ogura T Journal of Structural Biology . 2006,第1期

机译：大肠杆菌AAA蛋白酶FtsH突变体的表征，该突变体在中央孔区域携带突变
4. Genetic engineering of two Escherichia coli strains designed to bioaccumulate copper and cadmium: Construction, characterization, and mutational analysis of key regions involved in high affinity metal binding. [D] . Zagorski, Nicholas. 2003

机译：设计用于生物积累铜和镉的两种大肠杆菌菌株的基因工程：涉及高亲和力金属结合的关键区域的构建，表征和突变分析。
5. Escherichia coli mutant Y16 is a double mutant carrying thermosensitive ftsH and ftsI mutations. [O] . K J Begg, T Tomoyasu, W D Donachie, 1992

机译：大肠杆菌突变体Y16是带有热敏ftsH和ftsI突变的双重突变体。
6. Escherichia coli mutant Y16 is a double mutant carrying thermosensitive ftsH and ftsI mutations. [O] . Begg, K J, Tomoyasu, T, Donachie, W D, 1992

机译：大肠杆菌突变体Y16是带有热敏ftsH和ftsI突变的双重突变体。
7. Identification and Characterization of Mutations in 'Escherichia coli' That Selectively Influence the Growth of Hybrid Lambda Bacteriophages Carrying the Immunity Region of Bacteriophage P22 [R] . Strauch, M. A., Baumann, M., Friedman, D. I., 1986

机译：“大肠杆菌”突变的鉴定和表征，选择性地影响携带噬菌体p22免疫区的杂种λ噬菌体的生长

A colicin-tolerant Escherichia coli mutant that confers Hfl phenotype carries two mutations in the region coding for the C-terminal domain of FtsH (HflB)

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