Normark S, Edlund T, Grundström T, Bergström S, Wolf-Watz H
J Bacteriol. 1977 Dec;132(3):912-22. doi: 10.1128/jb.132.3.912-922.1977.
Escherichia coli K-12 ampicillin-resistant mutants hyperproducing chromosomal beta-lactamase arose spontaneously from strains carrying ampA1 ampC(+). Such mutants were found even in a recA background. Two Amp(r)-100 strains were analyzed genetically. The Amp(r)-100 resistance level of both strains could be transduced by direct selection for ampicillin resistance. Several classes of ampicillin-resistant transductants were found that differed from one another in the beta-lactamase activity and the ampicillin resistance mediated by an ampA1 ampC(+)-carrying strain. The data suggested that beta-lactamase hyperproduction was due to repetitions of the chromosomal amp genes. The size of the repeated region was calculated from cotransduction estimates, using the formula of Wu (Genetics 54:405-410, 1966), and was found to be about 1 min in one strain and 1.5 min in the other. Second-step Amp(r)-400 mutants were isolated from an Amp(r)-100 strain. The resistance of these mutants was apparently also due to repetitions, each mediating a resistance to about 10 mug/ml. Mutants of wild-type strains that were moderately resistant to ampicillin also gave rise to intermediate-resistance classes, suggesting repetitions of the wild-type amp alleles. F' factors hyperproducing chromosomal beta-lactamase by gene repetitions were constructed. They mediated levels of ampicillin resistance comparable to that of naturally occurring resistance plasmids. The expression of beta-lactamase hyperproduction was not affected by the presence of ampA and ampC alleles in trans and did not act in trans on the other alleles.
携带ampA1 ampC(+)的大肠杆菌K - 12氨苄青霉素抗性突变体自发产生了超量产生染色体β - 内酰胺酶的突变体。甚至在recA背景的菌株中也发现了此类突变体。对两个Amp(r)-100菌株进行了遗传分析。通过直接选择氨苄青霉素抗性,可以转导这两个菌株的Amp(r)-100抗性水平。发现了几类氨苄青霉素抗性转导子,它们在β - 内酰胺酶活性以及由携带ampA1 ampC(+)的菌株介导的氨苄青霉素抗性方面彼此不同。数据表明β - 内酰胺酶的超量产生是由于染色体amp基因的重复。利用Wu(《遗传学》54:405 - 410,1966)的公式,根据共转导估计计算出重复区域的大小,发现一个菌株中约为1分钟,另一个菌株中约为1.5分钟。从一个Amp(r)-100菌株中分离出了第二步的Amp(r)-400突变体。这些突变体的抗性显然也是由于重复,每个重复介导对约10μg/ml的抗性。对氨苄青霉素具有中度抗性的野生型菌株的突变体也产生了中等抗性类别,表明野生型amp等位基因的重复。构建了通过基因重复超量产生染色体β - 内酰胺酶的F'因子。它们介导的氨苄青霉素抗性水平与天然存在的抗性质粒相当。β - 内酰胺酶超量产生的表达不受反式存在的ampA和ampC等位基因的影响,并且对其他等位基因不具有反式作用。