Literature DB >> 7068538

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

S A White, G W Claus.   

Abstract

By using membrane-bound dehydrogenases, Gluconobacter oxydans characteristically accomplishes single-step oxidation of many polyols and quantitative release of the oxidation product into the medium. These cells typically differentiate by forming intracytoplasmic membranes (ICM) after exponential growth on glycerol. Earlier experiments demonstrated that glycerol-grown cells containing ICM oxidized glycerol more rapidly than cells which were harvested during exponential growth and lacked ICM (Claus et al., J. Bacteriol. 123:1169-1183). This report demonstrates that ICM are also formed after growth on sorbitol. Sorbitol-grown, ICM-containing maximum stationary-phase (MSP) cells showed from 50 to 300% greater oxidation (respiration) rates on mannitol, glycerol, glucose, meso-erythritol, and meso-inositol than did exponential-phase (EXP) cells which lacked ICM. Both EXP and MSP cells exhibited maximum sorbitol oxidation at pH 5.0, 38 degrees C, and 5% (wt/vol) sorbitol. When assayed under these optimum conditions, ICM-containing MSP cells demonstrated a 72% increase in respiration on sorbitol compared with that of EXP cells lacking ICM (oxygen quotients of 3,100 and 1,800, respectively). Gas chromatographic studies showed that sorbose was the only detectable product released from cells during oxygen quotient analysis. The specific activity of particulate-bound sorbitol dehydrogenase from ICM-containing MSP cells was twice that obtained from particulate fractions prepared from EXP cells lacking ICM. These results show that neither ICM formation after exponential growth nor increased respiration of other polyols is dependent upon the polyol used to grow cells. Our results suggest that increased respiratory activity of MSP cells is caused both by ICM formation and by increased synthesis (or activity) of the polyol dehydrogenases found in these membranes.

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Year:  1982        PMID: 7068538      PMCID: PMC216447          DOI: 10.1128/jb.150.2.934-943.1982

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


  26 in total

1.  Oxidative phosphorylation in Acetobacter suboxydans.

Authors:  L KLUNGSOYR; T E KING; V H CHELDELIN
Journal:  J Biol Chem       Date:  1957-07       Impact factor: 5.157

2.  Growth of acetobacter suboxydans and the oxidation of aldoses, related carboxylic acids, and aldehydes.

Authors:  J A FEWSTER
Journal:  Biochem J       Date:  1958-08       Impact factor: 3.857

3.  [Effects of culture on oxidation of sorbitol by Acetobacter suboxydans].

Authors:  Z G RAZUMOVSKAIA; S M ZHDAN-PUSHKINA
Journal:  Mikrobiologiia       Date:  1956 Jan-Feb

4.  Sources of energy and the dinitrophenol effect in the growth of Acetobacter suboxydans.

Authors:  T E KING; V H CHELDELIN
Journal:  J Bacteriol       Date:  1953-11       Impact factor: 3.490

5.  The enzyme system of Bact. suboxydans: Variation of aerobic activity with age of culture.

Authors:  K R Butlin
Journal:  Biochem J       Date:  1938-03       Impact factor: 3.857

6.  Internal membrane control in Azotobacter vinelandii.

Authors:  J L Pate; V K Shah; W J Brill
Journal:  J Bacteriol       Date:  1973-06       Impact factor: 3.490

7.  Incomplete tricarboxylic acid cycle in a type I methylotroph, Methylococcus capsulatus.

Authors:  R Patel; L Hoare; D S Hoare; B F Taylor
Journal:  J Bacteriol       Date:  1975-07       Impact factor: 3.490

8.  Ultrastruct of Methylosinus trichosporium as revealed by freeze etching.

Authors:  T L Weaver; P R Dugan
Journal:  J Bacteriol       Date:  1975-02       Impact factor: 3.490

9.  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

10.  Correlation of ultrastructure in Azotobacter vinelandii with nitrogen source for growth.

Authors:  J Oppenheim; L Marcus
Journal:  J Bacteriol       Date:  1970-01       Impact factor: 3.490

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  1 in total

1.  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

  1 in total

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