Growth of spiroplasmas in the presence of various nutrients and metabolic inhibitors

1987 ◽  
Vol 33 (6) ◽  
pp. 555-562 ◽  
Author(s):  
C. J. Chang ◽  
Meredith G. Garrett
Keyword(s):  
Citric Acid Cycle ◽  
Defined Medium ◽  
Sodium Cyanide ◽  
Metabolic Inhibitors ◽  
Chemically Defined Medium ◽  
Limited Growth ◽  
Acid Cycle ◽  
Keto Acids ◽  
Glycolytic Intermediates ◽  
Spiroplasma Melliferum

Glycolytic intermediates replaced glucose as carbohydrate sources in a chemically defined medium CC-494N, whereas keto acids of citric acid cycle intermediates and glyoxylate were supplemented with 10 mM glucose. Glucose-6-phosphate, fructose-1,6-diphosphate, 3-phosphoglyceraldehyde, and pyruvate supported limited growth for Spiroplasma floricola (23-6), whereas only pyruvate supported SR 3 spiroplasma and Spiroplasma melliferum (AS 576). Oxalacetate and glyoxylate inhibited growth at 10 mM or greater. Hematin, 2,4-dinitrophenol, sodium fluoride, and arsenite were dramatically inhibitory, whereas acetic anhydride, tricarballylate, acetylene dicarboxylate, and sodium cyanide were mildly inhibitory at 10 mM or lower. Malonate at 50 mM was not inhibitory.

Inorganic salts and the growth of spiroplasmas

1986 ◽  
Vol 32 (11) ◽  
pp. 861-866 ◽  
Author(s):  
C. J. Chang
Keyword(s):  
Defined Medium ◽  
Optimal Concentration ◽  
Inorganic Salts ◽  
Chemically Defined Medium ◽  
Potassium Salts ◽  
Limited Growth ◽  
Spiroplasma Melliferum

A chemically defined medium (CC-494M) was used to study the effect of inorganic salts on the growth of three spiroplasmas representing three distinct serogroups: Spiroplasma melliferum (AS 576), Spiroplasma floricola (23–6), and SR 3 spiroplasma. KH2PO4 or NaH2PO4∙H2O was required. KH2PO4 supported faster growth and higher yield for spiroplasmas than NaH2PO4∙H2O. The optimal concentration of KH2PO4 for S. melliferum, S. floricola, and SR 3 spiroplasma was 0.5, 0.5, and 0.25 mM, respectively, whereas that of NaH2PO4∙H2O was 0.5, 0.05, and 2.5 mM. When supplemented with NaH2PO4∙H2O, KCl promoted growth comparable with that obtained from KH2PO4-supplemented medium and RbCl supported limited growth, whereas NaCl, LiCl, CsCl, CaCl2, and MgSO4∙7H2O were inhibitory. Spiroplasma growth decreased as the concentration of LiCl and CsCl increased. At 200 mM LiCl totally inhibited the growth of S. melliferum and SR 3 spiroplasma, whereas limited growth was obtained for S. floricola. CsCl at 150 mM totally inhibited the growth of S. floricola, while limited growth was observed for S. melliferum and SR 3 spiroplasma. RbCl supported limited growth when supplemented with NaH2PO4∙H2O, whereas it was inhibitory when added in KH2PO4-supplemented medium. All the 10 potassium salts (KCH2COOH, KBr, K2CO3, KHSO4, KCl, KOH, Kl, KNO3, KH2PO4, and K2HPO4) at concentrations of 20 mM promoted growth when supplemented with NaH2PO4∙H2O.

scholarly journals Unique Host Iron Utilization Mechanisms of Helicobacter pylori Revealed with Iron-Deficient Chemically Defined Media

2010 ◽  
Vol 78 (5) ◽  
pp. 1841-1849 ◽  
Author(s):  
Olga Senkovich ◽  
Shantelle Ceaser ◽  
David J. McGee ◽  
Traci L. Testerman
Keyword(s):  
Helicobacter Pylori ◽  
Defined Medium ◽  
Normal Serum ◽  
Chemically Defined Medium ◽  
Limited Growth ◽  
Defined Media ◽  
Iron Deficient ◽  
Novel Strategy ◽  
H Pylori

ABSTRACT Helicobacter pylori chronically infects the gastric mucosa, where it can be found free in mucus, attached to cells, and intracellularly. H. pylori requires iron for growth, but the sources of iron used in vivo are unclear. In previous studies, the inability to culture H. pylori without serum made it difficult to determine which host iron sources might be used by H. pylori. Using iron-deficient, chemically defined medium, we determined that H. pylori can bind and extract iron from hemoglobin, transferrin, and lactoferrin. H. pylori can use both bovine and human versions of both lactoferrin and transferrin, contrary to previous reports. Unlike other pathogens, H. pylori preferentially binds the iron-free forms of transferrin and lactoferrin, which limits its ability to extract iron from normal serum, which is not iron saturated. This novel strategy may have evolved to permit limited growth in host tissue during persistent colonization while excessive injury or iron depletion is prevented.

Lactate Reverses Insulin-Induced Hypoglycemic Stupor in Suckling—Weanling Mice: Biochemical Correlates in Blood, Liver, and Brain

1983 ◽  
Vol 3 (4) ◽  
pp. 498-506 ◽  
Author(s):  
Jean Holowach Thurston ◽  
Richard E. Hauhart ◽  
James A. Schiro
Keyword(s):  
Amino Acids ◽  
Citric Acid ◽  
Energy Metabolism ◽  
Citric Acid Cycle ◽  
Plasma Lactate ◽  
Brain Glucose ◽  
Acid Cycle ◽  
Glucose Levels ◽  
Glycolytic Intermediates ◽  
Lactate Levels

The recovery of weanling mice from insulin-induced hypoglycemic stupor–coma after injection of sodium -l(+)-lactate (18 mmol/kg) was as rapid (10 min) as in litter-mates treated with glucose (9 mmol/kg). Stimulated by this dramatic action, we studied the effects of lactate injection on brain carbohydrate and energy metabolism in normal and hypoglycemic mice; blood and liver tissue were also studied. Ten minutes after lactate injection in normal mice, plasma lactate levels increased by 15 mmol/L; plasma glucose levels were unchanged, but the β-hydroxybutyrate concentration fell 59%. In the brains of these animals, glucose levels increased 2.3-fold, and there were significant increases in brain glycogen (10%), glucose-6-phosphate (27%), lactate (68%), pyruvate (37%), citrate (12%), and malate (19%); the increase in α-ketoglutarate (32%) was not significant. Lactate injection reduced the cerebral glucose-use rate 40%. These changes were not due to lactate-induced increases in blood [HCO−3] and pH (examined by injection of 15 mmol/kg sodium bicarbonate). Although lactate injection of hypoglycemic mice doubled levels of glucose in plasma and brain (not significant) and most of the cerebral glycolytic intermediates, values were far below normal (still in the range seen in hypoglycemic animals). By contrast, citrate and α-ketoglutarate levels returned to normal; the large increase in malate was not significant. Reduced glutamate levels increased to normal, and elevated aspartate levels fell below normal. Thus, recovery from hypoglycemic stupor does not necessarily depend on normal levels of plasma and/or brain glucose (or glycolytic intermediates). Near normal levels of the Krebs citric acid cycle intermediates suggest that changes in these metabolites, amino acids, or derived substrates relate to the dramatic recovery of hypoglycemic mice after lactate injection.

The effects of imidazole-4-acetic acid on cerebral carbohydrate metaboifsm

1982 ◽  
Vol 60 (12) ◽  
pp. 1610-1617
Author(s):  
M. Bovell ◽  
T. Chung ◽  
V. MacMillan ◽  
R. Shankaran
Keyword(s):  
Acetic Acid ◽  
Citric Acid ◽  
Cerebral Hemisphere ◽  
Citric Acid Cycle ◽  
High Energy ◽  
High Energy Phosphate ◽  
Acid Cycle ◽  
Glycolytic Intermediates ◽  
Tissue Contents ◽  
Eeg Pattern

The effects of intravenous administration of 50–400 mg/kg imidazole-4-acetic acid (IMA) on the carbohydrate metabolism of the rat brain were assessed by measurement of the cerebral hemisphere contents of energy phosphates and glycolytic – citric acid cycle metabolites. IMA (100–400 mg/kg) produced a spectrum of electroencephalographic (EEG) change ranging from desynchronization to electrical suppression which was associated with unchanged tissue contents of ATP, ADP, and AMP, increasing levels of phosphocreatine, glucose, and aspartate, and decreasing levels of pyruvate, lactate, α-ketoglutaratc, and malate. The changes in glycolytic intermediates were present within 5 min of injecting IMA (200 mg/kg) and the pattern suggested a suppression of glycolysis. The EEG stage of electrical suppression with episodic spiking (400 mg/kg) was associated with a 30% reduction of cortical high-energy phosphate use. The lowest dose of IMA (50 mg/kg) resulted in episodic EEG desynchronization which was associated with no significant changes of the measured metabolites. The results indicate that IMA is associated with metabolite changes that are compatible with a state of cerebral depression and that the desynchronous EEG pattern is without a biochemical con-elate of increased neuronal activity.

UTILIZATION OF CARBOHYDRATES AND AMINO ACIDS BY MICROCOCCUS RADIODURANS

1960 ◽  
Vol 6 (3) ◽  
pp. 289-298 ◽  
Author(s):  
Harkison D. Raj ◽  
Frances L. Duryee ◽  
Anne M. Deeney ◽  
Chih H. Wang ◽  
Arthur W. Anderson ◽  
...  
Keyword(s):  
Amino Acids ◽  
Amino Acid ◽  
Tricarboxylic Acid Cycle ◽  
Radioactive Tracer ◽  
Defined Medium ◽  
Tricarboxylic Acid ◽  
Chemically Defined Medium ◽  
Acid Cycle ◽  
Tracer Techniques ◽  
Simple Carbohydrates

The nutrition and metabolism of a recently isolated Micrococcus species resistant to closes of gamma radiation as high as 6 × 106 r.e.p. were studied by manometric and radioactive tracer techniques. Methionine, the only amino acid shown to be essential in a chemically defined medium, appears to be rapidly incorporated into the cells. DL-Glutamic acid is readily metabolized, the D isomer apparently after an initial lag. Among the simple carbohydrates, fructose, glucose, and glycerol are readily utilized. The operation of the tricarboxylic acid cycle is suggested by the oxidation of certain TCA intermediates. The prompt conversion of C-1 of gluconate to CO2, in the presence of glucose, may indicate that a C1–C5 cleavage pathway is operative for catabolism of glucose in this organism.

The Role of Lipid in Adult Development and Flight-Muscle Metabolism in Hyalophora Cecropia

1964 ◽  
Vol 41 (3) ◽  
pp. 573-590
Author(s):  
LAWRENCE A. DOMROESE ◽  
LAWRENCE I. GILBERT
Keyword(s):  
Fatty Acid ◽  
Citric Acid ◽  
Fatty Acid Oxidation ◽  
Adult Development ◽  
Citric Acid Cycle ◽  
Flight Muscle ◽  
Muscle Metabolism ◽  
Metabolic Inhibitors ◽  
Acid Oxidation ◽  
Acid Cycle

1. Changes in total lipid and R.Q. show that female pupae of H. cecropia begin to catabolize lipid early in adult development. In males there is a conservation of lipid during adult development resulting in the male moth having about three times the lipid content of the female. In the adult moth both sexes utilize lipid as the major energy source. 2. Lipid is the available substrate as well as the preferred substrate in flight-muscle metabolism in male moths. 3. Flight-muscle homogenates show greater oxidative activity with fatty acids and citric acid cycle intermediates than with glucose or glycolytic intermediates, indicating that carbohydrate pathways are not prominent. 4. A fatty acid oxidizing system has been identified in flight muscle which requires ATP, magnesium and a citric acid cycle intermediate for optimum activity. 5. Experiments with radiotracers and metabolic inhibitors reveal that fatty acid oxidation in flight muscle proceeds via the citric acid cycle and the cytochrome chain. 6. Active fatty acid activating enzymes are present in flight muscle, and fatty acid oxidation in H. cecropia is discussed in relation to vertebrate and other invertebrate systems.

The Action of an Aniline Derivative (AN 162) on Blood Coagulation and on Platelets

1971 ◽  
Vol 26 (01) ◽  
pp. 145-166
Author(s):  
E Deutsch ◽  
K Lechner ◽  
K Moser ◽  
L Stockinger
Keyword(s):  
Blood Coagulation ◽  
Citric Acid Cycle ◽  
Second Phase ◽  
Aniline Derivative ◽  
Acid Cycle ◽  
Enhancing Effect ◽  
Low Concentrations ◽  
Dual Action ◽  
High Concentrations ◽  
Induced Aggregation

Summary1. The aniline derivative AN 162, Donau Pharmazie, Linz, Austria, has a dual action on the blood coagulation: an anticoagulant and an coagulation enhancing effect.2. The anticoagulant action may only be demonstrated with high concentrations (over 1 X 10”3 M related to plasma) preferentially in PPP. It is partially caused by an inhibition of the endogenous way of generation of the prothrombin converting principle. In addition it is suggested that it interferes with the fibrinogen-fibrin reaction in a manner not yet understood.3. The coagulant action is caused by a greater availability of platelet constituents at low concentrations of AN 162 (over 1 × 10-4 M) and by the induction of a release reaction at higher concentrations. The platelet factors 3 and 4, serotonin, adenine, and acid phosphatase are released.4. AN 162 inhibits platelet aggregation. This inhibition can be demonstrated by the PAT of Breddin and in the stirred aggregation test of Born. It is more effective to inhibit the collagen-induced and the second phase of the adrenaline-induced aggregation than the ADP induced one. The platelet retention (test of Hellem) is also reduced.5. The action of AN 162 on the platelets is caused by a damage of the platelet membrane which becomes permeabel for both, soluble platelet constitutents and granula.6. AN 162 interferes with the energy metabolism of the platelets. It causes a loss of ATP, and inhibits the key-enzymes of glycolysis, citric acid cycle, fatty acid oxydation and glutathione reduction.7. AN 162 inhibits the growth of fibroblasts without influence on mitosis.

EFFECT OF SERUM GONADOTROPHIN ON DEHYDROGENASES OF THE CITRIC ACID CYCLE IN THE OVARY OF THE RAT

1963 ◽  
Vol 42 (4) ◽  
pp. 480-484 ◽  
Author(s):  
B. Eckstein ◽  
R. Landsberg
Keyword(s):  
Citric Acid ◽  
Citric Acid Cycle ◽  
Age Groups ◽  
Succinic Dehydrogenase ◽  
Immature Rat ◽  
Acid Cycle ◽  
Immature Rats ◽  
Rat Ovary

ABSTRACT The succinic, malic and isocitric dehydrogenases in the ovary of immature and mature, normal and serum gonadotrophin injected rats were examined. The Qo2 of these enzymes were markedly enhanced in the gonadotrophin injected rats of both age groups, except in the case of succinic dehydrogenase in the ovary of the immature rats, where a slight non-significant decrease was noted. It is concluded that in the mature rat ovary, gonadotrophin administration stimulates the activity of all the examined dehydrogenases of the citric acid cycle, whereas in the immature rat ovary, at least the isocitric- and malic dehydrogenases are thus stimulated.

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