Literature DB >> 6232260

Facile and gentle method for quantitative lysis of Escherichia coli and Salmonella typhimurium.

S Crabtree, J E Cronan.   

Abstract

Garrett et al. (Mol. Gen. Genet. 182:326-331, 1981) constructed strains of Escherichia coli harboring derivatives of plasmid pBR322 that carry the lysis genes (S, R, and Rz) of phage lambda. The plasmid construction placed the genes under control of the lactose operon operator-promotor (and thus of lac repressor). Induction of E. coli strains carrying these plasmids resulted in rapid lysis of the culture unless the S gene was defective, in which case the cells grew normally. A freeze-thaw treatment of induced cells carrying an S- plasmid gave quantitative lysis of either E. coli or Salmonella typhimurium cells under exceptionally gentle conditions. The method was equally effective on exponential phase cells and stationary phase cells and was readily extended to a large number of independent cultures.

Entities:  

Mesh:

Substances:

Year:  1984        PMID: 6232260      PMCID: PMC215424          DOI: 10.1128/jb.158.1.354-356.1984

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  21 in total

1.  Complications in the simplest cellular enzyme assay: lysis of Escherichia coli for the assay of beta-galactosidase.

Authors:  S L Putnam; A L Koch
Journal:  Anal Biochem       Date:  1975-02       Impact factor: 3.365

2.  Maximizing gene expression on a plasmid using recombination in vitro.

Authors:  T M Roberts; G D Lauer
Journal:  Methods Enzymol       Date:  1979       Impact factor: 1.600

3.  Lysis defective mutants of bacteriophage lambda: on the role of the S function in lysis.

Authors:  R W Reader; L Siminovitch
Journal:  Virology       Date:  1971-03       Impact factor: 3.616

4.  Interaction of ribosomes and the cell envelope of Escherichia coli mediated by lysozyme.

Authors:  D Patterson; M Weinstein; R Nixon; D Gillespie
Journal:  J Bacteriol       Date:  1970-02       Impact factor: 3.490

5.  Convenient method for detecting 14CO2 in multiple samples: application to rapid screening for mutants.

Authors:  H Tabor; C W Tabor; E W Hafner
Journal:  J Bacteriol       Date:  1976-10       Impact factor: 3.490

6.  An efficient and reproducible procedure for the formation of spheroplasts from variously grown Escherichia coli.

Authors:  B Witholt; M Boekhout; M Brock; J Kingma; H V Heerikhuizen; L D Leij
Journal:  Anal Biochem       Date:  1976-07       Impact factor: 3.365

7.  Unsaturated fatty acid synthesis is not required for induction of lactose transport in Escherichia coli.

Authors:  W D Nunn; J E Cronan
Journal:  J Biol Chem       Date:  1974-02-10       Impact factor: 5.157

8.  Characterization of amber and ochre suppressors in Salmonella typhimurium.

Authors:  F Winston; D Botstein; J H Miller
Journal:  J Bacteriol       Date:  1979-01       Impact factor: 3.490

9.  Selective release of enzymes from bacteria.

Authors:  L A Heppel
Journal:  Science       Date:  1967-06-16       Impact factor: 47.728

10.  Glucose and gluconate metabolism in an Escherichia coli mutant lacking phosphoglucose isomerase.

Authors:  D G Fraenkel; S R Levisohn
Journal:  J Bacteriol       Date:  1967-05       Impact factor: 3.490

View more
  4 in total

1.  Scavenging of cytosolic octanoic acid by mutant LplA lipoate ligases allows growth of Escherichia coli strains lacking the LipB octanoyltransferase of lipoic acid synthesis.

Authors:  Fatemah A M Hermes; John E Cronan
Journal:  J Bacteriol       Date:  2009-08-14       Impact factor: 3.490

2.  Rapid and Scalable Preparation of Bacterial Lysates for Cell-Free Gene Expression.

Authors:  Andriy Didovyk; Taishi Tonooka; Lev Tsimring; Jeff Hasty
Journal:  ACS Synth Biol       Date:  2017-08-21       Impact factor: 5.110

3.  Genetic and biochemical characterization of an Escherichia coli K-12 mutant deficient in acyl-coenzyme A thioesterase II.

Authors:  M L Narasimhan; J L Lampi; J E Cronan
Journal:  J Bacteriol       Date:  1986-03       Impact factor: 3.490

4.  A bifunctional vector system for controlled expression and subsequent release of the cloned gene product by phi X174 lysis protein-E.

Authors:  U Bläsi; S Kalousek; W Lubitz
Journal:  Appl Microbiol Biotechnol       Date:  1990-08       Impact factor: 4.813

  4 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.