THE ACCUMULATION OF α-KETOGLUTARATE BY SUSPENSIONS OF PSEUDOMONAS AERUGINOSA

1966 ◽  
Vol 12 (5) ◽  
pp. 1005-1013 ◽  
Author(s):  
Margaret von Tigerstrom ◽  
J. J. R. Campbell

Pyruvic and α-ketoglutaric acids accumulated during the oxidation of glucose by washed cell suspensions of Pseudomonas aeruginosa harvested from a glucose medium. The addition of ammonium salts had been shown to prevent the accumulation of the α-ketoglutaric acid in such suspensions. A similar situation was shown to exist with growing cultures. The accumulation of α-ketoglutaric acid was not due to inability of the cells to synthesize enzymes required for the oxidation of this compound. Cells harvested from a glucose medium required an induction period before oxidizing α-ketoglutaric acid but this was apparently due to the lack of a permease required for the transport of the substrate across the cell membrane. A comparison of the enzyme levels of cell extracts prepared from cells grown on a glucose medium with those grown on an α-ketoglutaric acid medium revealed that the latter had a higher level of the individual apoenzymes required for α-ketoglutaric acid oxidation. However, the apoenzyme level of the extracts of glucose-grown cells appeared adequate to prevent the accumulation of α-ketoglutaric acid during glucose oxidation.It is concluded that during growth in the presence of an excess of ammonium salts α-ketoglutarate never escapes from the internal metabolic pool of the cells and therefore the permease for α-ketoglutarate is not synthesized. During glucose oxidation by washed suspensions of glucose-grown cells, α-ketoglutarate is perhaps excreted from the cell either because the cells are deficient in the coenzymes necessary for α-ketoglutarate oxidation or because the avidity of the enzymes for substrate is such that, at low levels of substrate, the enzymes of α-ketoglutarate oxidation act so slowly that the intermediate accumulates.

1951 ◽  
Vol 29 (2) ◽  
pp. 143-146 ◽  
Author(s):  
Roger H. Warburton ◽  
B. A. Eagles ◽  
J. J. R. Campbell

Pyruvate has been determined at 16, 28, and 40 hr. in a culture of Pseudomonas aeruginosa when growing in a glucose medium. Throughout this interval the organism was shown to possess the enzyme system capable of rapidly oxidizing pyruvate. It was concluded that pyruvate is being formed and dissimilated continuously and that it is therefore to be considered an intermediate in the oxidation of glucose. It was found that glucose oxidation was not inhibited by 0.02 M fluoride and that pyruvate formation and utilization continued unimpaired in the presence of the inhibitor. This would indicate that enolase is not essential to the formation of pyruvate by P. aeruginosa and may be taken as further evidence supporting the contention that this organism does not dissimilate glucose by way of the conventional Embden–Meyerhof scheme.


1956 ◽  
Vol 2 (3) ◽  
pp. 304-309 ◽  
Author(s):  
J. J. R. Campbell ◽  
T. Ramakrishnan ◽  
A. G. Linnes ◽  
B. A. Eagles

Cell extracts of Pseudomonas aeruginosa were shown to oxidize glucose with the accumulation of 2-ketogluconate. The theoretical amount of oxygen was taken up during the reaction and no added hydrogen acceptors were necessary. With glucose as substrate these extracts did not form high energy phosphate nor did they reduce diphosphopyridine nucleotide or triphosphopyridine nucleotide. Almost identical amounts of growth were obtained when limiting equimolar amounts of glucose, gluconate, or 2-ketogluconate were compared as sole sources of carbon. It was concluded that P. aeruginosa 9027 does not gain energy during the oxidative steps glucose –→ gluconate –→ 2-ketogluconate.


1960 ◽  
Vol 198 (4) ◽  
pp. 807-810 ◽  
Author(s):  
Irving B. Fritz

The metabolic fate of glucose in isolated muscle after addition of insulin was shown to be dependent upon the functional state of the tissue. While nonstimulated muscle responded primarily with an increased incorporation of glucose into glycogen, stimulated muscle showed predominantly an increased conversion of labeled glucose to CO2 following insulin addition. The oxidation of palmitic-1-C14 acid by muscle was not influenced by the presence of insulin. Ryanodine, used as a chemical agent for inducing contraction of diaphragm, resulted in stimulation of oxygen consumption, fatty acid oxidation and glucose oxidation to an extent comparable to that previously achieved with electrical stimulation of muscle. The conclusion was reached that insulin increased the oxidation of glucose but not of palmitate, and that the specific metabolic fate of intracellular glucose is not influenced by insulin. The data are discussed in relation to the prevailing theory that insulin acts by increasing permeability of muscle cell membranes to certain substrates.


1949 ◽  
Vol 27c (4) ◽  
pp. 165-171 ◽  
Author(s):  
Jack J. R. Campbell ◽  
Flora C. Norris ◽  
Margaret E. Norris

Acetic acid has been isolated as an intermediate compound in the oxidation of glucose or α-ketoglutaric acid by Pseudomonas aeruginosa. Cells of this organism produced under conditions of intense aeration were found to have lost the ability to oxidize acetic acid and this compound was found in large quantities in the growth medium. When these cells were used to carry out the oxidation of glucose, it was found that the oxygen consumed was the amount needed to convert glucose to acetic acid, thus confirming the role of acetate as an intermediate in glucose oxidation. In contrast to the above-mentioned criteria the technique of simultaneous adaptation ruled out acetic acid as a possible intermediate in the oxidation of either glucose or α-ketoglutaric acid. The status of the theory of simultaneous adaptation is discussed in relation to the data obtained.


1949 ◽  
Vol 27c (5) ◽  
pp. 253-261 ◽  
Author(s):  
Flora C. Norris ◽  
Jack J. R. Campbell

The technique of paper chromatography has been adapted to the identification of gluconic, 2-ketogluconic, and α-ketoglutaric acids. Combinations of methyl and ethyl alcohol were found to be the most suitable solvents and ammoniacal silver nitrate was found to give the most satisfactory reaction. When grown under normal physiological conditions where glucose was metabolized to carbon dioxide and water, Pseudomonas aeruginosa 9027 was shown to have oxidized glucose by way of gluconic and 2-ketogluconic acids. Since a strong system for oxidizing both gluconic and 2-ketogluconic acids was demonstrated, the presence of these acids over at least an eight hour period of growth is taken as evidence of their importance as intermediates in the oxidation of glucose by this organism.


1950 ◽  
Vol 28c (2) ◽  
pp. 203-212 ◽  
Author(s):  
Jack J. R. Campbell ◽  
Flora C. Norris

The acid soluble phosphorus fraction of cells of Pseudomonas aeruginosa harvested from a glucose medium was found to consist mainly of difficultly hydrolyzable compounds. None of the fractions contained reducing compounds even after 12 hr. hydrolysis with normal hydrochloric acid nor could fructose be detected. It could therefore be concluded that glucose-1-phosphate, glucose-6-phosphate, fructose-6-phosphate, and hexose diphosphate were absent. Analysis of a glucose solution that had been metabolized by cells of this organism under conditions of fluoride inhibition confirmed the analysis of the cellular material. The lack of normal intermediates of the Embden–Meyerhof scheme is discussed in relation to the gluconic acid, 2-ketogluconic acid pathway of glucose oxidation.


2015 ◽  
Vol 36 (6) ◽  
pp. 658-663 ◽  
Author(s):  
Greg S. Whiteley ◽  
Chris Derry ◽  
Trevor Glasbey ◽  
Paul Fahey

OBJECTIVETo investigate the reliability of commercial ATP bioluminometers and to document precision and variability measurements using known and quantitated standard materials.METHODSFour commercially branded ATP bioluminometers and their consumables were subjected to a series of controlled studies with quantitated materials in multiple repetitions of dilution series. The individual dilutions were applied directly to ATP swabs. To assess precision and reproducibility, each dilution step was tested in triplicate or quadruplicate and the RLU reading from each test point was recorded. Results across the multiple dilution series were normalized using the coefficient of variation.RESULTSThe results for pure ATP and bacterial ATP from suspensions ofStaphylococcus epidermidisandPseudomonas aeruginosaare presented graphically. The data indicate that precision and reproducibility are poor across all brands tested. Standard deviation was as high as 50% of the mean for all brands, and in the field users are not provided any indication of this level of imprecision.CONCLUSIONSThe variability of commercial ATP bioluminometers and their consumables is unacceptably high with the current technical configuration. The advantage of speed of response is undermined by instrument imprecision expressed in the numerical scale of relative light units (RLU).Infect Control Hosp Epidemiol2015;00(0):1–6


1991 ◽  
Vol 3 (5) ◽  
pp. 571 ◽  
Author(s):  
JG Thompson ◽  
AC Simpson ◽  
PA Pugh ◽  
RW Wright ◽  
HR Tervit

Embryos were collected from superovulated donors at various intervals from onset of oestrus, ranging from Day 1.5 to Day 6. In addition, blastocysts obtained from the culture of 1-cell embryos collected in vivo or of oocytes matured and fertilized in vitro were used to assess the effects of in vitro manipulation and culture on glucose utilization. Glycolytic activity was determined by the conversion of [5-3H]glucose to 3H2O, and oxidation of glucose was determined by the conversion of [U-14C]glucose to 14CO2. Glucose utilization increases significantly from the 8-cell stage and during compaction and blastulation. Glucose oxidation was at a relatively low level (5-12% of total utilization) compared with glycolysis. No difference was observed between the glycolytic activity of blastocysts derived from in vivo or in vitro sources. However, glucose oxidation was lower (P less than 0.05) in blastocysts derived from the culture of 1-cell embryos or from oocytes matured and fertilized in vitro. Exogenous tricarboxylic acid cycle substrates (i.e. pyruvate and lactate supplied in the medium) affected the level of glucose oxidation.


Author(s):  
Sebastian Franz ◽  
Nataliya D. Shcherban ◽  
Igor Bezverkhyy ◽  
Sergii A. Sergiienko ◽  
Irina L. Simakova ◽  
...  

AbstractOxidation of a mixture of glucose and arabinose over Au particles deposited on porous carbons, N-doped carbons and carbon nitrides was investigated at 70 °C, under constant pH of 8, and oxygen partial pressure 0.125 atm. In particular, Au deposited on nitrogen-containing carbon-based mesoporous structures demonstrated activity in the oxidation of the sugars to the corresponding aldonic acids higher than gold deposited on undoped carbon supports (conversion of glucose up to ca. 60%, arabinose–ca. 30% after 200 min). The results can be explained by the basic nature of the supports leading to an increase in the polarity of the carbon surface and the oxygen activation. Glucuronic acid (with selectivity ca. 10–93.5%) together with gluconic acid was formed as a result of glucose oxidation, while arabinose was selectively oxidized to arabinonic acid.


1956 ◽  
Vol 2 (4) ◽  
pp. 433-440 ◽  
Author(s):  
Jack J. R. Campbell ◽  
Roberts A. Smith

It was demonstrated that Pseudomonas aeruginosa possesses all the enzymes necessary for the oxidation of pyruvate to CO2 and water without passing through the conventional intermediates oxalosuccinate and α-ketoglutarate. These intermediates are bypassed by the action of the enzyme isocitratase which splits d-isocitrate to succinate plus glyoxylate. This reaction was shown to be readily reversible. The malic acid dehydrogenase content was low and in addition this enzyme required a high pH for optimum activity. In fresh cell extracts at pH 7.4 its activity was only 10% that of the other enzymes of the cycle. The malic and isocitric dehydrogenases were TPN specific. The organism was also shown to possess all the enzymes necessary for the operation of the conventional tricarboxylic acid cycle.


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