» Articles » PMID: 3907571

The Functional Significance of Glucose Dehydrogenase in Klebsiella Aerogenes

Overview
Journal Arch Microbiol
Specialty Microbiology
Date 1985 Nov 1
PMID 3907571
Citations 18
Authors
Affiliations
Soon will be listed here.
Abstract

In order to assess the functional significance of the quinoprotein glucose dehydrogenase recently found to be present in K+ -limited Klebsiella aerogenes, a broad study was made of the influence of specific environmental conditions on the cellular content of this enzyme. Whereas high activities were manifest in cells from glucose containing chemostat cultures that were either potassium- or phosphate-limited, only low activities were apparent in cells from similar cultures that were either glucose-, sulphate- or ammonia-limited. With these latter two cultures, a marked increase in glucose dehydrogenase activity was observed when 2,4-dinitrophenol (1 mM end concentration) was added to the growth medium. These results suggested that the synthesis of glucose dehydrogenase is not regulated by the level of glucose in the growth medium, but possibly by conditions that imposed an energetic stress upon the cells. This conclusion was further supported by a subsequent finding that K+ -limited cells that were growing on glycerol also synthesized substantial amounts of glucose dehydrogenase. The enzyme was found to be membrane associated, and preliminary evidence has been obtained that it is located on the periplasmic side of the cytoplasmic membrane and functionally linked to the respiratory chain. This structural and functional orientation is consistent with glucose dehydrogenase serving as a low impedance energy generating system.

Citing Articles

Importance of twitching and surface-associated motility in the virulence of .

Corral J, Perez-Varela M, Sanchez-Osuna M, Cortes P, Barbe J, Aranda J Virulence. 2021; 12(1):2201-2213.

PMID: 34515614 PMC: 8451467. DOI: 10.1080/21505594.2021.1950268.


Tools for successful proliferation: diverse strategies of nutrient acquisition by a benthic cyanobacterium.

Tee H, Waite D, Payne L, Middleditch M, Wood S, Handley K ISME J. 2020; 14(8):2164-2178.

PMID: 32424245 PMC: 7367855. DOI: 10.1038/s41396-020-0676-5.


Comparative genome analysis reveals niche-specific genome expansion in Acinetobacter baumannii strains.

Yakkala H, Samantarrai D, Gribskov M, Siddavattam D PLoS One. 2019; 14(6):e0218204.

PMID: 31194814 PMC: 6563999. DOI: 10.1371/journal.pone.0218204.


Regulation of Pyrroloquinoline Quinone-Dependent Glucose Dehydrogenase Activity in the Model Rhizosphere-Dwelling Bacterium Pseudomonas putida KT2440.

An R, Moe L Appl Environ Microbiol. 2016; 82(16):4955-64.

PMID: 27287323 PMC: 4968544. DOI: 10.1128/AEM.00813-16.


Purification and characterization of the membrane-bound quinoprotein glucose dehydrogenase of Gluconacetobacter diazotrophicus PAL 5.

Sara-Paez M, Contreras-Zentella M, Gomez-Manzo S, Gonzalez-Valdez A, Gasca-Licea R, Mendoza-Hernandez G Protein J. 2015; 34(1):48-59.

PMID: 25576305 DOI: 10.1007/s10930-014-9596-4.


References
1.
van Schie B, Hellingwerf K, van Dijken J, Elferink M, van Dijl J, Kuenen J . Energy transduction by electron transfer via a pyrrolo-quinoline quinone-dependent glucose dehydrogenase in Escherichia coli, Pseudomonas aeruginosa, and Acinetobacter calcoaceticus (var. lwoffi). J Bacteriol. 1985; 163(2):493-9. PMC: 219149. DOI: 10.1128/jb.163.2.493-499.1985. View

2.
LANNING M, COHEN S . The detection and estimation of 2-ketohexonic acids. J Biol Chem. 1951; 189(1):109-14. View

3.
Altendorf K, Staehelin L . Orientation of membrane vesicles from Escherichia coli as detected by freeze-cleave electron microscopy. J Bacteriol. 1974; 117(2):888-99. PMC: 285586. DOI: 10.1128/jb.117.2.888-899.1974. View

4.
OBrien R, Neijssel O, Tempest D . Glucose phosphoenolpyruvate phosphotransferase activity and glucose uptake rate of Klebsiella aerogenes growing in chemostat culture. J Gen Microbiol. 1980; 116(2):305-14. DOI: 10.1099/00221287-116-2-305. View

5.
Whiting P, Midgley M, DAWES E . The role of glucose limitation in the regulation of the transport of glucose, gluconate and 2-oxogluconate, and of glucose metabolism in Pseudomonas aeruginosa. J Gen Microbiol. 1976; 92(2):304-10. DOI: 10.1099/00221287-92-2-304. View