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携带大肠杆菌乳糖区域和鼠伤寒沙门氏菌组氨酸区域的杂种F'因子F42 - 400(F' ts114 lac +,his +)的分离:其在鼠伤寒沙门氏菌中的部分特性及行为

Isolation of a hybrid F' factor-carrying Escherichia coli lactose region and Salmonella typhimurium histidine region, F42-400 (F' ts114 lac+, his+): its partial characterization and behavior in Salmonella typhimurium.

作者信息

Rao R N, Pereira M G

出版信息

J Bacteriol. 1975 Sep;123(3):779-91. doi: 10.1128/jb.123.3.779-791.1975.

Abstract

Episome F' ts114 lac+ (F42-114) was transferred into Salmonella typhimurium carrying an F'his+ (FS400) episome, and fused episome F' ts114 lac+, his+ (F42-400) was obtained. Episome F42-400 could be transferred to S. typhimurium, Escherichia coli and Klebsiella pneumoniae. Identification of the episome was based on: (i) temperature sensitivity of the Lac+ and His+ phenotypes; (ii) the fact that F- segregants, obtained after temperature curing or acridine orange curing, were simultaneously Lac- and His-; and (iii) linkage of lac+ with his+ in episomal transfers to E. coli and S. typhimurium. The frequency of episome transfer was influenced by the genotype of the donor. Plasmid LT2, prevalent in S. typhimurium LT2 strains, was suggested to be responsible for the low fertility of S. typhimurium donors. Episome F42-400 was capable of chromosome mobilization, and the extent of chromosome mobilization was not influenced by the presence or absence of the histidine region on the donor chromosome. Growth in a defined medium with acridine orange was able to cure F42-400. The frequency of curing was increased (the frequency of His+ cells was 0.0001%) if the cells were grown at 40 C in the presence of acridine orange. Selection for temperature-resistant Lac+, His+ derivatives in a strain without histidine deletion yielded Hfr strains. However, similar and stronger selections in strains without the chromosomal histidine region failed to yield Hfr strains. Our inability to obtain Hfr's in strains without the chromosomal histidine region was explained by assuming that the episome F42-400 has lost the F sites involved in integration into the S. typhimurium chromosome.

摘要

游离基因F' ts114 lac+(F42 - 114)被转入携带F'his+(FS400)游离基因的鼠伤寒沙门氏菌中,从而获得了融合游离基因F' ts114 lac+,his+(F42 - 400)。游离基因F42 - 400可转移至鼠伤寒沙门氏菌、大肠杆菌和肺炎克雷伯菌。游离基因的鉴定基于以下几点:(i)Lac+和His+表型的温度敏感性;(ii)经温度处理或吖啶橙处理后获得的F - 分离株同时为Lac - 和His - 这一事实;(iii)在向大肠杆菌和鼠伤寒沙门氏菌进行游离基因转移时,lac+与his+的连锁关系。游离基因转移的频率受供体基因型的影响。在鼠伤寒沙门氏菌LT2菌株中普遍存在的质粒LT2被认为是鼠伤寒沙门氏菌供体育性低的原因。游离基因F42 - 400能够进行染色体转移,且染色体转移的程度不受供体染色体上组氨酸区域存在与否的影响。在含有吖啶橙的限定培养基中生长能够消除F42 - 400。如果细胞在40℃、存在吖啶橙的条件下生长,消除频率会增加(His+细胞的频率为0.0001%)。在没有组氨酸缺失的菌株中选择耐温的Lac+、His+衍生物可产生高频重组(Hfr)菌株。然而,在没有染色体组氨酸区域的菌株中进行类似且更强的选择未能产生Hfr菌株。我们无法在没有染色体组氨酸区域的菌株中获得Hfr菌株,这一现象可通过假设游离基因F42 - 400已失去参与整合到鼠伤寒沙门氏菌染色体中的F位点来解释。

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