Mojica T
Mol Gen Genet. 1975;138(2):113-26. doi: 10.1007/BF02428116.
Phage P1 does not adsorb to S. typhinurium wild type cells. It does adsorb to rough derivatives including strains with mutations in the galE gene. Phage strain P1CM clr-100 can be efficiently propagated in S. typhimurium derivatives, either by induction of a lysogene, or by lytic infection. Phage P1 lysates are able to mobilize genetic markers in a generalized fashion. The transduction system is essentially identical to that in Escherichia coli, except that CaCl2 is not required for efficient adsorption. Two regions of the S. typhimurium chromosome were mapped by P1-mediated transduction. Several examples of genes linked by P1, and unlinked by P22, are presented. The relative efficiency of P1 over P22 in transduction was not determined, however. Data presented indicate unambigously that the gene order for the trp region is: his ... dad A-hem A-trp-pyrF ... pyrC but known markers in between were not used. The gene order for the cys A region was determined to be as follows: pheA ... purC-cys A-trz A-pts-dsd-aro D-purF ... his, and special mapping problems for this region are discussed.
噬菌体P1不吸附鼠伤寒沙门氏菌野生型细胞。它能吸附粗糙衍生物,包括galE基因突变的菌株。噬菌体菌株P1CM clr-100可以通过诱导溶原菌或溶菌感染在鼠伤寒沙门氏菌衍生物中高效繁殖。噬菌体P1裂解物能够以广义方式转移遗传标记。转导系统与大肠杆菌中的基本相同,只是高效吸附不需要CaCl2。通过P1介导的转导绘制了鼠伤寒沙门氏菌染色体的两个区域。给出了一些由P1连锁但不由P22连锁的基因实例。然而,未确定P1相对于P22在转导中的相对效率。所呈现的数据明确表明,trp区域的基因顺序为:his... dad A-hem A-trp-pyrF... pyrC,但未使用其间的已知标记。确定cys A区域的基因顺序如下:pheA... purC-cys A-trz A-pts-dsd-aro D-purF... his,并讨论了该区域的特殊作图问题。