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霍乱弧菌独立分离的无毒突变体中突变的遗传图谱分析。

Genetic mapping of mutations in independently isolated nontoxinogenic mutants of Vibrio cholerae.

作者信息

Baine W B, Vasil M L, Holmes R K

出版信息

Infect Immun. 1978 Jul;21(1):194-200. doi: 10.1128/iai.21.1.194-200.1978.

Abstract

Conjugal mating experiments were performed between donor strains of Vibrio cholerae carrying the vibrio sex plasmid P and recipient strains lacking the P plasmid. Donor and recipient genotypes differed with respect to toxinogenicity (tox), nutritional requirements, and antibiotic susceptibilities. Recombinants carrying selected donor and recipient markers were produced at low frequencies in conjugal matings. Mapping of tox markers was accomplished by scoring for the frequency of coinheritance of the donor tox allele with selected and unselected donor markers. Four independently isolated tox markers were analyzed. Each of these four tox markers was shown to be linked to the his-1 site in linkage group I on the genetic map of V. cholerae. In matings between a recipient strain carrying the tox-1 marker and donor strains carrying either tox-2, tox-3, or tox-4, all selected his+ recombinants remained nontoxinogenic. Matings between multiply marked strains demonstrated that the position of tox-1 with respect to other genetic loci in linkage group I is as follows: met-2--trp-1--asp-1--nal-1--his-1--tox-1. These findings demonstrate that a chromosomal determinant linked to his-1 in linkage group I on the genetic map of V. cholerae is essential for toxinogenesis and suggest that tox-1,tox-2, tox-3, and tox-4 may be alleles of a single tox gene.

摘要

对携带霍乱弧菌性菌毛质粒P的霍乱弧菌供体菌株与缺乏P质粒的受体菌株进行了接合交配实验。供体和受体的基因型在产毒性(tox)、营养需求和抗生素敏感性方面存在差异。在接合交配中,携带选定的供体和受体标记的重组体以低频率产生。通过对供体tox等位基因与选定和未选定的供体标记的共遗传频率进行评分,完成了tox标记的定位。分析了四个独立分离的tox标记。这四个tox标记中的每一个都被证明与霍乱弧菌遗传图谱上连锁群I中的his-1位点相连。在携带tox-1标记的受体菌株与携带tox-2、tox-3或tox-4的供体菌株之间的交配中,所有选定的his+重组体仍无毒性。多重标记菌株之间的交配表明,tox-1在连锁群I中相对于其他基因座的位置如下:met-2--trp-1--asp-1--nal-1--his-1--tox-1。这些发现表明,在霍乱弧菌遗传图谱上连锁群I中与his-1相连的一个染色体决定因素对于产毒至关重要,并表明tox-1、tox-2、tox-3和tox-4可能是单个tox基因的等位基因。

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