Literature DB >> 1254552

Change in quantity of lipids and cell size during intracytoplasmic membrane formation in Gluconobacter oxydans.

D L Heefner, G W Claus.   

Abstract

Electron microscopy previously revealed that Gluconobacter oxydans differentiates by forming quantities of intracytoplasmic membranes at the end of exponential growth. It was also shown that the formation of these membranes appears concurrently with an increased rate of polyol oxidation. In the present study, exponential-phase cells devoid of intracytoplasmic membranes were harvested and the quantity of free lipid was determined. This quantity was compared with that extracted from cells harvested 4 and 16 h into the stationary phase that contained intracytoplasmic membranes. Cells harvested 4 and 16 h into the stationary phase contained 58 and 43% more free lipid per 100 mg of cell weight than found in undifferentiated exponential-phase cells. These same cultures were used to compare the quantity of lipid extracted per cell. This analysis revealed 89 and 142% more lipid per cell in 4 and 16 h stationary-phase cells. Further study demonstrated that cells increased in length and decreased in density with time after they entered the stationary phase. We estimated, however, that intracytoplasmic membrane development in G. oxydans is accompanied by a 57 to 62% increase in free-lipid that cannot be attributed to a change in cell size. These results suggest that the traditional expression of extracted lipid per milligram of cellular dry weight should not be used for comparative purposes during differentiation in gram-negative bacteria, unless it is first established that both cell size and cell density remain constant throughout differentiation.

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Year:  1976        PMID: 1254552      PMCID: PMC236196          DOI: 10.1128/jb.125.3.1163-1171.1976

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


  23 in total

1.  Fine structural changes of Acetobacter suboxydans during growth in a defined medium.

Authors:  B L Batzing; G W Claus
Journal:  J Bacteriol       Date:  1973-03       Impact factor: 3.490

2.  Quantitative analysis of the phospholipids of some marine bioluminescent bacteria.

Authors:  A Eberhard; G Rouser
Journal:  Lipids       Date:  1971-06       Impact factor: 1.880

3.  [Quantitative determination of the fatty acids of Rhodospirillum rubrum and Rhodopseudomonas capsulata during the morphogenesis of thylakoids].

Authors:  J Schröder; G Drews
Journal:  Arch Mikrobiol       Date:  1968

4.  The ultrastructures of autotrophically and heterotrophically grown Thiobacillus novellus.

Authors:  L Van Caeseele; H Lees
Journal:  Can J Microbiol       Date:  1969-07       Impact factor: 2.419

5.  Lipids of Salmonella typhimurium and Escherichia coli: structure and metabolism.

Authors:  G F Ames
Journal:  J Bacteriol       Date:  1968-03       Impact factor: 3.490

6.  Indentification and localization of the fatty acids in Haemophilus parainfluenzae.

Authors:  D C White; R H Cox
Journal:  J Bacteriol       Date:  1967-03       Impact factor: 3.490

7.  Isocitrate dehydrogenase and glutamate synthesis in Acetobacter suboxydans.

Authors:  S Greenfield; G W Claus
Journal:  J Bacteriol       Date:  1969-12       Impact factor: 3.490

8.  LIPIDS OF SARCINA LUTEA. I. FATTY ACID COMPOSITION OF THE EXTRACTABLE LIPIDS.

Authors:  C K HUSTON; P W ALBRO
Journal:  J Bacteriol       Date:  1964-08       Impact factor: 3.490

9.  Lipids of Bacteroides melaninogenicus.

Authors:  V Rizza; A N Tucker; D C White
Journal:  J Bacteriol       Date:  1970-01       Impact factor: 3.490

10.  NATURE OF THE LIPIDS OF SOME LACTIC ACID BACTERIA.

Authors:  M IKAWA
Journal:  J Bacteriol       Date:  1963-04       Impact factor: 3.490

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  4 in total

1.  Effects of arginine density on the membrane-bound structure of a cationic antimicrobial peptide from solid-state NMR.

Authors:  Ming Tang; Alan J Waring; Mei Hong
Journal:  Biochim Biophys Acta       Date:  2008-11-14

2.  Effect of intracytoplasmic membrane development on oxidation of sorbitol and other polyols by Gluconobacter oxydans.

Authors:  S A White; G W Claus
Journal:  J Bacteriol       Date:  1982-05       Impact factor: 3.490

3.  Lipid and fatty acid composition of Gluconobacter oxydans before and after intracytoplasmic membrane formation.

Authors:  D L Heefner; G W Claus
Journal:  J Bacteriol       Date:  1978-04       Impact factor: 3.490

4.  Proteomic analysis of Ketogulonicigenium vulgare under glutathione reveals high demand for thiamin transport and antioxidant protection.

Authors:  Qian Ma; Weiwen Zhang; Lu Zhang; Bin Qiao; Chensong Pan; Hong Yi; Lili Wang; Ying-jin Yuan
Journal:  PLoS One       Date:  2012-02-22       Impact factor: 3.240

  4 in total

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