Literature DB >> 6782085

Morphological effect of cerulenin treatment on Streptococcus faecalis as studied by ultrastructure reconstruction.

M L Higgins, D D Carson, L Daneo-Moore.   

Abstract

Exponential-phase cells of Streptococcus faecalis ATCC 9790 were treated with a concentration of cerulenin (5 micrograms/ml) that has been shown to block both lipoteichoic acid and lipid synthesis and cell division within 10 min. The morphological effect of this treatment was studied by making three-dimensional reconstructions of cells based on measurements taken from axial thin sections. This analysis indicated that cerulenin interferes with cell division by inhibiting normal constriction of the division furrow and centripetal growth of the cross wall in envelope growth sites. Rather than dividing, many of the sites in treated cells apparently continue to elongate and produce abnormally large amounts of peripheral wall surface. These observations were interpreted in terms of a previously proposed model in which cerulenin would prevent the synthesis of a lipid-containing inhibitor of autolytic enzyme activity needed for division. In addition, measurements showed that the average number of envelope growth sites per cell increased during treatment, suggesting that although cerulenin treatment blocks division, it does not interfere with the formation of new envelope growth sites. It was also observed that the size and frequency of mesosomes did not decline during the 60-min period of drug treatment. This tends to decrease the likelihood that mesosomes are formed from a pool of intracellular membrane precursors that would be depleted during a period of restricted lipid biosynthesis.

Entities:  

Mesh:

Substances:

Year:  1980        PMID: 6782085      PMCID: PMC294404          DOI: 10.1128/jb.143.2.989-994.1980

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


  16 in total

Review 1.  Problems of cell wall and membrane growth, enlargement, and division.

Authors:  G D Shockman; L Daneo-Moore; M L Higgins
Journal:  Ann N Y Acad Sci       Date:  1974-05-10       Impact factor: 5.691

2.  Effect of inhibition of deoxyribonucleic acid and protein synthesis on the direction of cell wall growth in Streptococcus faecalis.

Authors:  M L Higgins; L Daneo-Moore; D Boothby; G D Shockman
Journal:  J Bacteriol       Date:  1974-05       Impact factor: 3.490

3.  Reinitiation of cell wall growth after threonine starvation of Streptococcus faecalis.

Authors:  M L Higgins; H M Pooley; G D Shockman
Journal:  J Bacteriol       Date:  1971-03       Impact factor: 3.490

4.  Three-dimensional reconstruction of whole cells of Streptococcus faecalis from thin sections of cells.

Authors:  M L Higgins
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

5.  Septation deficiency and phosphilipid perturbation in Escherichia coli genetically constitutive for the beta oxidation pathway.

Authors:  E Vanderwinkel; M De Vlieghere; M Fontaine; D Charles; F Denamur; D Vandevoorde; D De Kegel
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

Review 6.  Procaryotic cell division with respect to wall and membranes.

Authors:  M L Higgins; G D Shockman
Journal:  CRC Crit Rev Microbiol       Date:  1971-05

7.  Organization of mesosomes in fixed and unfixed cells.

Authors:  M L Higgins; H C Tsien; L Daneo-Moore
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

8.  Study of cycle of cell wall assembly in Streptococcus faecalis by three-dimensional reconstructions of thin sections of cells.

Authors:  M L Higgins; G D Shockman
Journal:  J Bacteriol       Date:  1976-09       Impact factor: 3.490

9.  Inhibition of wall autolysis in Streptococcus faecalis by lipoteichoic acid and lipids.

Authors:  R F Cleveland; A J Wicken; L Daneo-Moore; G D Shockman
Journal:  J Bacteriol       Date:  1976-04       Impact factor: 3.490

10.  Model for cell wall growth of Streptococcus faecalis.

Authors:  M L Higgins; G D Shockman
Journal:  J Bacteriol       Date:  1970-02       Impact factor: 3.490

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.