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铜绿假单胞菌染色体图谱上hisI基因和pru(脯氨酸利用)基因的修订位置。

Revised locations of the hisI and pru (proline utilization) genes on the Pseudomonas aeruginosa chromosome map.

作者信息

Soldati L, Crockett R, Carrigan J M, Leisinger T, Holloway B W, Haas D

出版信息

Mol Gen Genet. 1984;193(3):431-6. doi: 10.1007/BF00382080.

Abstract

The location of genes in the vicinity of the major FP2 origin on the chromosome of Pseudomonas aeruginosa PAO has been revised. The markers hisI (a transduction group of histidine biosynthetic genes) and pru (a gene cluster encoding proline utilization functions) were located in the 90 to 95/0 min chromosome region by a series of plate matings mediated by R68.45. Three-factor-crosses using this plasmid established the following marker order: pur-67 pru hisI/cys-59 proB ilvB/C. Genetic evidence is presented to confirm the previous observations that FP2 can mobilize the chromosome from at least two origins near proB and in both directions. Thus, when markers in this chromosome region are analyzed by FP2 crosses only, the mapping data may be difficult to interpret. This complication can be overcome by the use of R68.45 and Tfr (transposon-facilitated recombination) or Hfr donors.

摘要

铜绿假单胞菌PAO染色体上主要FP2起源附近基因的定位已被修正。通过由R68.45介导的一系列平板交配,标记物hisI(组氨酸生物合成基因的一个转导组)和pru(编码脯氨酸利用功能的一个基因簇)被定位在90至95/0分钟的染色体区域。使用该质粒进行的三因子杂交确定了以下标记顺序:pur-67 pru hisI/cys-59 proB ilvB/C。提供了遗传证据以证实先前的观察结果,即FP2可以从proB附近的至少两个起源并双向动员染色体。因此,当仅通过FP2杂交分析该染色体区域中的标记时,图谱数据可能难以解释。通过使用R68.45和Tfr(转座子促进的重组)或Hfr供体可以克服这种复杂性。

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