Literature DB >> 788869

Influence of temperature on growth of lipopolysaccharide-deficient (rough) mutants of Salmonella typhimurium and Salmonella minnesota.

A K Chatterjee, K E Sanderson, H Ross.   

Abstract

Smooth strains of Salmonella typhimurium and S. minnesota, and chemotypes Ra, Rb, and Rc, which are deficient in lipopolysaccharide components of the somatic side chains and outer core region, grow normally on nutrient agar and nutrient broth up to 45 degrees C. However, most mutants with defects in the heptose region of the LPS (chemotypes Rd2 and Re) do not grow on this medium at 42 degrees C or above; a few grow at 42 degrees C but not at 45 degrees C. In liquid medium (nutrient broth, or phosphate minimal medium), growth, measured as turbidity or as colony-forming units, stops 60 to 90 min after shift from 30 to 42 degrees C; DNA and protein synthesis cease at the same time. Growth does not reoccur at 42 degrees C; protein synthesis and growth reinitiate upon shift to 30 or 37 degrees C. Growth cessation does not alter cell morphology in the phase-contrast microscope. Growth of heptose-deficient strains at 42 degrees C in nutrient broth is restored by MgCl2 (0.5 mM), NaCl (50 mM), or sucrose (100 mM). Sensitivity to smooth-specific and rough-specific phages, and analysis of LPS composition, indicate that heptose-deficient mutants grown at temperatures from 30 to 45 degrees C, and in the presence or absence of high salt, do not contain heptose or O-specific sugars in their LPS.

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Year:  1976        PMID: 788869     DOI: 10.1139/m76-226

Source DB:  PubMed          Journal:  Can J Microbiol        ISSN: 0008-4166            Impact factor:   2.419


  12 in total

1.  The polysaccharide portion of lipopolysaccharide regulates antigen-specific T-cell activation via effects on macrophage-mediated antigen processing.

Authors:  N M Zirk; S F Hashmi; H K Ziegler
Journal:  Infect Immun       Date:  1999-01       Impact factor: 3.441

2.  Unusual susceptibility of Erwinia amylovora to antibacterial agents in relation to the barrier function of its cell envelope.

Authors:  A K Chatterjee; R F Buss; M P Starr
Journal:  Antimicrob Agents Chemother       Date:  1977-05       Impact factor: 5.191

3.  Isolation and characterization of two genes, waaC (rfaC) and waaF (rfaF), involved in Pseudomonas aeruginosa serotype O5 inner-core biosynthesis.

Authors:  T R de Kievit; J S Lam
Journal:  J Bacteriol       Date:  1997-06       Impact factor: 3.490

4.  Molecular cloning and characterization of the nontypeable Haemophilus influenzae 2019 rfaE gene required for lipopolysaccharide biosynthesis.

Authors:  N G Lee; M G Sunshine; M A Apicella
Journal:  Infect Immun       Date:  1995-03       Impact factor: 3.441

5.  Spontaneous release of lipopolysaccharide by Pseudomonas aeruginosa.

Authors:  J E Cadieux; J Kuzio; F H Milazzo; A M Kropinski
Journal:  J Bacteriol       Date:  1983-08       Impact factor: 3.490

6.  Interactions of cations with membrane fractions of smooth and rough strains of Salmonella typhimurium and other Gram-negative bacteria.

Authors:  H Stan-Lotter; K E Sanderson
Journal:  J Bacteriol       Date:  1981-05       Impact factor: 3.490

7.  OpsX from Haemophilus influenzae represents a novel type of heptosyltransferase I in lipopolysaccharide biosynthesis.

Authors:  Sabine Gronow; Werner Brabetz; Buko Lindner; Helmut Brade
Journal:  J Bacteriol       Date:  2005-09       Impact factor: 3.490

8.  Molecular cloning and functional expression of the rfaE gene required for lipopolysaccharide biosynthesis in Salmonella typhimurium.

Authors:  U H Jin; T W Chung; Y C Lee; S D Ha; C H Kim
Journal:  Glycoconj J       Date:  2001-10       Impact factor: 2.916

9.  Molecular analysis of the rfaD gene, for heptose synthesis, and the rfaF gene, for heptose transfer, in lipopolysaccharide synthesis in Salmonella typhimurium.

Authors:  D M Sirisena; P R MacLachlan; S L Liu; A Hessel; K E Sanderson
Journal:  J Bacteriol       Date:  1994-04       Impact factor: 3.490

10.  Cloning and characterization of the Escherichia coli K-12 rfa-2 (rfaC) gene, a gene required for lipopolysaccharide inner core synthesis.

Authors:  L Chen; W G Coleman
Journal:  J Bacteriol       Date:  1993-05       Impact factor: 3.490

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