Literature DB >> 2194094

Linkage map of Escherichia coli K-12, edition 8.

B J Bachmann1.   

Abstract

The linkage map of Escherichia coli K-12 depicts the arrangement of genes on the circular chromosome of this organism. The basic units of the map are minutes, determined by the time-of-entry of markers from Hfr into F- strains in interrupted-conjugation experiments. The time-of-entry distances have been refined over the years by determination of the frequency of cotransduction of loci in transduction experiments utilizing bacteriophage P1, which transduces segments of DNA approximately 2 min in length. In recent years, the relative positions of many genes have been determined even more precisely by physical techniques, including the mapping of restriction fragments and the sequencing of many small regions of the chromosome. On the whole, the agreement between results obtained by genetic and physical methods has been remarkably good considering the different levels of accuracy to be expected of the methods used. There are now few regions of the map whose length is still in some doubt. In some regions, genetic experiments utilizing different mutant strains give different map distances. In other regions, the genetic markers available have not been close enough to give accurate cotransduction data. The chromosome is now known to contain several inserted elements apparently derived from lambdoid phages and other sources. The nature of the region in which the termination of replication of the chromosome occurs is now known to be much more complex than the picture given in the previous map. The present map is based upon the published literature through June of 1988. There are now 1,403 loci placed on the linkage group, which may represent between one-third and one-half of the genes in this organism.

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Year:  1990        PMID: 2194094      PMCID: PMC372767          DOI: 10.1128/mr.54.2.130-197.1990

Source DB:  PubMed          Journal:  Microbiol Rev        ISSN: 0146-0749


  1176 in total

1.  The recQ gene of Escherichia coli K12: molecular cloning and isolation of insertion mutants.

Authors:  K Nakayama; N Irino; H Nakayama
Journal:  Mol Gen Genet       Date:  1985

2.  Nucleotide sequence of the iron regulatory gene fur.

Authors:  S Schäffer; K Hantke; V Braun
Journal:  Mol Gen Genet       Date:  1985

3.  Molecular cloning and functional analysis of the cysG and nirB genes of Escherichia coli K12, two closely-linked genes required for NADH-dependent nitrite reductase activity.

Authors:  H Macdonald; J Cole
Journal:  Mol Gen Genet       Date:  1985

4.  Gene fusions to the ptsM/pel locus of Escherichia coli.

Authors:  E T Palva; P Saris; T J Silhavy
Journal:  Mol Gen Genet       Date:  1985

5.  Characterization of a mutation conferring radiation sensitivity, ior, located close to the gene coding for deoxycytidine deaminase in Escherichia coli.

Authors:  A M Estevenon; B Martin; N Sicard
Journal:  Mol Gen Genet       Date:  1985

6.  Transcription analysis of the sucAB, aceEF and lpd genes of Escherichia coli.

Authors:  M E Spencer; J R Guest
Journal:  Mol Gen Genet       Date:  1985

7.  Site-specific mutagenesis of Escherichia coli gltT yields a weak, glutamic acid-inserting ochre suppressor.

Authors:  L A Raftery; M Yarus
Journal:  J Mol Biol       Date:  1985-07-20       Impact factor: 5.469

8.  The effect of the locus pstB on phosphate binding in the phosphate specific transport (PST) system of Escherichia coli.

Authors:  R Levitz; I Friedberg; R Brucker; A Fux; E Yagil
Journal:  Mol Gen Genet       Date:  1985

9.  The fim genes responsible for synthesis of type 1 fimbriae in Escherichia coli, cloning and genetic organization.

Authors:  P Klemm; B J Jørgensen; I van Die; H de Ree; H Bergmans
Journal:  Mol Gen Genet       Date:  1985

10.  Identification of the gene appA for the acid phosphatase (pH optimum 2.5) of Escherichia coli.

Authors:  E Dassa; P L Boquet
Journal:  Mol Gen Genet       Date:  1985
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  457 in total

1.  A study of AroP-PheP chimeric proteins and identification of a residue involved in tryptophan transport.

Authors:  A J Cosgriff; G Brasier; J Pi; C Dogovski; J P Sarsero; A J Pittard
Journal:  J Bacteriol       Date:  2000-04       Impact factor: 3.490

2.  Escherichia coli outer membrane protein TolC is involved in production of the peptide antibiotic microcin J25.

Authors:  M A Delgado; J O Solbiati; M J Chiuchiolo; R N Farías; R A Salomón
Journal:  J Bacteriol       Date:  1999-03       Impact factor: 3.490

3.  Effect of different concentrations of H-NS protein on chromosome replication and the cell cycle in Escherichia coli.

Authors:  T Atlung; F G Hansen
Journal:  J Bacteriol       Date:  2002-04       Impact factor: 3.490

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

Authors:  Vladislav A Lanzov; Irina V Bakhlanova; Alvin J Clark
Journal:  Genetics       Date:  2003-04       Impact factor: 4.562

5.  Characterization of a second lysine decarboxylase isolated from Escherichia coli.

Authors:  Y Kikuchi; H Kojima; T Tanaka; Y Takatsuka; Y Kamio
Journal:  J Bacteriol       Date:  1997-07       Impact factor: 3.490

6.  Cloning and characterization of the region III flagellar operons of the four Shigella subgroups: genetic defects that cause loss of flagella of Shigella boydii and Shigella sonnei.

Authors:  A A Al Mamun; A Tominaga; M Enomoto
Journal:  J Bacteriol       Date:  1997-07       Impact factor: 3.490

7.  Sequence analysis of the gyrA and parC homologues of a wild-type strain of Vibrio parahaemolyticus and its fluoroquinolone-resistant mutants.

Authors:  J Okuda; E Hayakawa; M Nishibuchi; T Nishino
Journal:  Antimicrob Agents Chemother       Date:  1999-05       Impact factor: 5.191

8.  FNR-mediated oxygen-responsive regulation of the nrdDG operon of Escherichia coli.

Authors:  T Boston; T Atlung
Journal:  J Bacteriol       Date:  2003-09       Impact factor: 3.490

9.  Effect of cell growth rate on expression of the anaerobic respiratory pathway operons frdABCD, dmsABC, and narGHJI of Escherichia coli.

Authors:  C P Tseng; A K Hansen; P Cotter; R P Gunsalus
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

10.  Escherichia coli possesses two homologous anaerobic C4-dicarboxylate membrane transporters (DcuA and DcuB) distinct from the aerobic dicarboxylate transport system (Dct).

Authors:  S Six; S C Andrews; G Unden; J R Guest
Journal:  J Bacteriol       Date:  1994-11       Impact factor: 3.490

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