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首页> 外文期刊>Russian journal of genetics >Construction of the new Escherichia coli K-12 MG 1655 novel strain with improved growth characteristics for application in metabolic engineering
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Construction of the new Escherichia coli K-12 MG 1655 novel strain with improved growth characteristics for application in metabolic engineering

机译:具有改善的生长特性的新大肠杆菌K-12 MG 1655新型菌株的构建,用于代谢工程

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MG1655 of Escherichia coli K-12 is frequently used in metabolic engineering as the wild-type strain. However, its two mutations, ilvG and rph-1 provide a negative effect on culture growth. The "polar effect" of rph-1 decreases the level of pyrE expression, causing partial auxotrophy for pyrimidines. Mutation ilvG leading to the appearance of Val(S) phenotype causes retardation of cell growth rate on media containing amino acids. In this work, the substitution of two loci in the genome of MG1655 with the recovery of the wild-type phenotype was accomplished. Gene rph (wt) from the chromosome of E. coli TG1 was marked via Red-dependent integration of DNA fragment carrying lambda attL-Cm-R-lambda attR and transduced with phage P1 into MG1655; later, the Cm-R marker was removed with the use of lambda Xis/Int recombinase. Parallel to this procedure, a spontaneous Val(R) mutant of E. coli MG1655 yielding colonies of maximal size on M9 medium with glucose in the presence of L-Val (50 mu g/ml) was isolated. It was shown that a nucleotide deletion in the isolated Val(R) strain had been generated in the region of the identified ilvG mutation, which led to the recovery of the reading frame and active protein synthesis. This mutation named ilvG-15, which is the only reason for the Val(R) phenotype in the obtained strain, was transferred to MG1655-rph (wt) using cotransduction, by analogy to the transfer of rph (wt). Evaluation of rates of aerobically growing cells (mu, hour-1) on M9 medium with glucose produced the following values: 0.56, 0.69, and 0.73 for strains MG1655,MG1655-rph (wt), and MG1655-(rph (wt), ilvG-15), respectively.
机译:大肠杆菌K-12的MG1655通常作为野生型菌株用于代谢工程中。但是,它的两个突变ilvG和rph-1对培养物的生长产生负面影响。 rph-1的“极性效应”降低了pyrE表达的水平,引起嘧啶的部分营养缺陷。导致Val(S)表型出现的突变ilvG导致细胞在含有氨基酸的培养基上的生长速度减慢。在这项工作中,通过恢复野生型表型完成了MG1655基因组中两个基因座的替换。大肠杆菌TG1染色体的rph(wt)基因通过Red依赖性整合携带lambda attL-Cm-R-lambda attR的DNA片段进行标记,并通过噬菌体P1转入MG1655。之后,使用λXis / Int重组酶去除Cm-R标记。与此方法平行,分离出自产MG9655的大肠杆菌MG1655的自发Val突变体,该突变体在存在L-Val(50μg/ ml)的葡萄糖的M9培养基上产生最大大小的菌落。结果表明,在已鉴定的ilvG突变区域中已产生分离的Val(R)菌株中的核苷酸缺失,这导致阅读框的恢复和活性蛋白的合成。通过共转导,类似于rph(wt)的转移,将该突变命名为ilvG-15,这是获得的菌株中Val(R)表型的唯一原因,该突变通过共转导被转移至MG1655-rph(wt)。在含葡萄糖的M9培养基上评估需氧生长细胞的速度(mu,hour-1)产生以下值:菌株MG1655,MG1655-rph(wt)和MG1655-(rph(wt),分别为0.56、0.69和0.73, ilvG-15)。

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