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PMID: 6325394 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Direct evidence for specific binding of the replicative origin of the Escherichia coli chromosome to the membrane.

Journal of bacteriology ·Vol. 158 ·No. 1 ·1984-04-00 ·Pages 313-6

Kusano T, Steinmetz D, Hendrickson WG, Murchie J, King M, Benson A, Schaechter M

Abstract

The origin of replication of the Escherichia coli chromosomal DNA binds with high affinity to outer membrane preparations. This specific binding requires a 463-base-pair region of origin DNA between positions -45 and +417 of the oriC map. We show that binding does not require the presence of adjacent regions. From further analysis, we conclude that more than one binding site resides within the 325-base-pair fragment between positions +38 (BamHI) and +417 (XhoI). When this fragment is cut, two pieces bind with high affinity and one binds with lesser affinity. The binding ability of one of the high affinity sites is abolished by cutting it at position +92 with BamHI.

MeSH Terms
Binding Sites Cell Membrane/metabolism Chromosomes, Bacterial/metabolism DNA Replication DNA Restriction Enzymes DNA, Bacterial/analysis,metabolism Escherichia coli/metabolism,ultrastructure
Chemicals
DNA, Bacterial DNA Restriction Enzymes
Authors & Affiliations
7 authors, click to expand affiliations / ORCID
Kusano T
Steinmetz D
Hendrickson W G
Murchie J
King M
Benson A
Schaechter M
References (11)
11 references, click to expand
  1. Detection of two restriction endonuclease activities in Haemophilus parainfluenzae using analytical agarose--ethidium bromide electrophoresis.
    Biochemistry. 1973 Jul 31;12(16):3055-63 PMID: 4354250
  2. A rapid alkaline extraction procedure for screening recombinant plasmid DNA.
    Nucleic Acids Res. 1979 Nov 24;7(6):1513-23 PMID: 388356
  3. Isolation of a replication origin complex from Escherichia coli.
    Proc Natl Acad Sci U S A. 1980 Jan;77(1):262-6 PMID: 6244549
  4. A general method for defining restriction enzyme cleavage and recognition sites.
    Methods Enzymol. 1980;65(1):391-404 PMID: 6246360
  5. Replication origin of the Escherichia coli K-12 chromosome: the size and structure of the minimum DNA segment carrying the information for autonomous replication.
    Mol Gen Genet. 1980 Apr;178(1):9-20 PMID: 6991883
  6. Binding of the origin of replication of Escherichia coli to the outer membrane.
    Cell. 1982 Oct;30(3):915-23 PMID: 6754093
  7. Chromosomal replication origin from the marine bacterium Vibrio harveyi functions in Escherichia coli: oriC consensus sequence.
    Proc Natl Acad Sci U S A. 1983 Mar;80(5):1164-8 PMID: 6338499
  8. Specific in vitro binding of a plasmid to a membrane fraction of Bacillus subtilis.
    Proc Natl Acad Sci U S A. 1983 Jan;80(2):574-8 PMID: 6300855
  9. Purified dnaA protein in initiation of replication at the Escherichia coli chromosomal origin of replication.
    Proc Natl Acad Sci U S A. 1983 Oct;80(19):5817-21 PMID: 6310593
  10. Recognition sites for a membrane-derived DNA binding protein preparation in the E. coli replication origin.
    Mol Gen Genet. 1983;191(3):460-5 PMID: 6355768
  11. Purification of the E. coli dnaA gene product.
    EMBO J. 1982;1(12):1545-9 PMID: 6327277
Article Info
Journal
Journal of bacteriology
Abbr.
J Bacteriol
ISSN
0021-9193
Published
1984-04-00
Pages
313-6
Language
English
Region
United States
NLM ID
2985120R
PMCID
PMC215414
Subset
IM
Grants
NIAID NIH HHS · R01 AI 09465 · United States
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