在大肠杆菌的接合过程中，靠近原点的标记的重组频率较低。 - Suppr

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超能文献

Low recombination frequency for markers very near the origin in conjugation in E. coli.

作者信息

Low B

出版信息

Genet Res. 1965 Nov;6(3):469-73. doi: 10.1017/s0016672300004341.

DOI:10.1017/s0016672300004341

PMID:5321521

Abstract

摘要

相似文献

Low recombination frequency for markers very near the origin in conjugation in E. coli.

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引用本文的文献

Conjugational hyperrecombination achieved by derepressing the LexA regulon, altering the properties of RecA protein and inactivating mismatch repair in Escherichia coli K-12.

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Mapping of two transcription mutations (tlnI and tlnII) conferring thiolutin resistance, adjacent to dnaZ and rho in Escherichia coli.

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Site-specific recombination following conjugation in Escherichia coli K-12.

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Convenient construction of recA deletion derivatives of Escherichia coli.

J Bacteriol. 1983 Oct;156(1):458-9. doi: 10.1128/jb.156.1.458-459.1983.

Use of a known plasmid and transposon as tracers for the incompatibility classification of a cryptic plasmid.

Mol Gen Genet. 1982;186(2):282-8. doi: 10.1007/BF00331863.

Conjugal transfer of bacterial chromosomes mediated by the RK2 plasmid transfer origin cloned into transposon Tn5.

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Pseudoinversions in the chromosome of Escherichia coli K-12.

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Inversion of transfer modes and sex factor-chromosome interactions in conjugation in Escherichia coli.

J Bacteriol. 1967 Jan;93(1):98-106. doi: 10.1128/jb.93.1.98-106.1967.

The tolC locus in Escherichia coli K12.

Genetics. 1971 Jan;67(1):39-53. doi: 10.1093/genetics/67.1.39.

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