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Evolution of energy metabolism and its compartmentation in Kinetoplastida.

Kinetoplastida are protozoan organisms that probably diverged early in evolution from other eukaryotes. They are characterized by a number of unique features with respect to their energy and carbohydrate metabolism. These organisms possess peculiar peroxisomes, called glycosomes, which play a central role in this metabolism; the organelles harbour enzymes of several catabolic and anabolic routes, including major parts of the glycolytic and pentosephosphate pathways. The kinetoplastid mitochondrion is also unusual with regard to both its structural and functional properties.In this review, we describe the unique compartmentation of metabolism in Kinetoplastida and the metabolic properties resulting from this compartmentation. We discuss the evidence for our recently proposed hypothesis that a common ancestor of Kinetoplastida and Euglenida acquired a photosynthetic alga as an endosymbiont, contrary to the earlier notion that this event occurred at a later stage of evolution, in the Euglenida lineage alone. The endosymbiont was subsequently lost from the kinetoplastid lineage but, during that process, some of its pathways of energy and carbohydrate metabolism were sequestered in the kinetoplastid peroxisomes, which consequently became glycosomes. The evolution of the kinetoplastid glycosomes and the possible selective advantages of these organelles for Kinetoplastida are discussed. We propose that the possession of glycosomes provided metabolic flexibility that has been important for the organisms to adapt easily to changing environmental conditions. It is likely that metabolic flexibility has been an important selective advantage for many kinetoplastid species during their evolution into the highly successful parasites today found in many divergent taxonomic groups.Also addressed is the evolution of the kinetoplastid mitochondrion, from a supposedly pluripotent organelle, attributed to a single endosymbiotic event that resulted in all mitochondria and hydrogenosomes of extant eukaryotes. Furthermore, indications are presented that Kinetoplastida may have acquired other enzymes of energy and carbohydrate metabolism by various lateral gene transfer events different from those that involved the algal- and alpha-proteobacterial-like endosymbionts responsible for the respective formation of the glycosomes and mitochondria.

Journal Article↗

Prevention of incipient diabetic nephropathy by high-dose thiamine and benfotiamine.

Accumulation of triosephosphates arising from high cytosolic glucose concentrations in hyperglycemia is the trigger for biochemical dysfunction leading to the development of diabetic nephropathy-a common complication of diabetes associated with a high risk of cardiovascular disease and mortality. Here we report that stimulation of the reductive pentosephosphate pathway by high-dose therapy with thiamine and the thiamine monophosphate derivative benfotiamine countered the accumulation of triosephosphates in experimental diabetes and inhibited the development of incipient nephropathy. High-dose thiamine and benfotiamine therapy increased transketolase expression in renal glomeruli, increased the conversion of triosephosphates to ribose-5-phosphate, and strongly inhibited the development of microalbuminuria. This was associated with decreased activation of protein kinase C and decreased protein glycation and oxidative stress-three major pathways of biochemical dysfunction in hyperglycemia. Benfotiamine also inhibited diabetes-induced hyperfiltration. This was achieved without change in elevated plasma glucose concentration and glycated hemoglobin in the diabetic state. High-dose thiamine and benfotiamine therapy is a potential novel strategy for the prevention of clinical diabetic nephropathy.

Albuminuria↗

Syndromes with increased red cell glutathione (GSH).

GSH, the most abundant erythrocyte thiol, is synthesized from its constituent amino acids by two ATP-dependent enzymes present in the mature red cell. Its unusual gamma-glutamyl linkage precludes degradation by any known red cell peptidase. The erythrocyte lacks a complete "gamma-glutamyl cycle" as described by Meister. GSH has important enzymatic and non-enzymatic roles in oxidoreduction reactions. As the specific co-factor of glutathione peroxidase, it participates in the reduction of harmful organoperoxides. Oxidized glutathione is reconverted to GSH via NADPH-dependent, glutathione reductase. NADPH in the red cell is generated solely by the two dehydrogenases of the pentosephosphate shunt. Increased GSH concentrations are normally present in neonatal erythrocytes. For reasons not clear, they are an epiphenomenon in inherited pyrimidine 5'-nucleotidase deficiency. Many syndromes of heterogeneous etiology having in common dyserythropoietic anemia and ineffective erythropoiesis despite a cellular bone marrow also exhibit abnormally high concentrations of red cell GSH as one component of a constellation of metabolic abnormalities. In a single patient with the Lesch-Nyhan syndrome studied by us, erythrocyte GSH was increased. A kindred with dominantly transmitted (or possibly x-chromosome linked) hereditary hemolytic anemia in which the only thus far detected abnormality is increased red cell GSH has also been documented. The fundamental molecular lesion in this syndrome is unknown.

Anemia, Hemolytic↗

Purification and properties of glucose 6-phosphate dehydrogenase from Aspergillus aculeatus.

Glucose 6-phosphate dehydrogenase (EC 1.1.1.49) was purified from Aspergillus aculeatus, a filamentous fungus previously isolated from infected tongue of a patient. The enzyme, apparently homogeneous, had a specific activity of 220 units mg(-1), a molecular weight of 105,000 +/- 5,000 Dal by gel filtration and subunit size of 52,000 +/- 1,100 Dal by sodium dodecyl sulphate-polyacrylamide gel electrophoresis. The substrate specificity was extremely strict, with glucose 6-phosphate (G6P) being oxidized by nicotinamide adenine dinucleotide phosphate (NADP) only. At assay pH of 7.5, the enzyme had K(m) values of 6 microM and 75 microM for NADP and G6P respectively. The k(cat) was 83 s(-1). Steady-state kinetics at pH 7.5 produced converging linear Lineweaver-Burk plots as expected for ternary-complex mechanism. The patterns of product and dead-end inhibition suggested that the enzyme can bind NADP and G6P separately to form a binary complex, indicating a random-order mechanism. The enzyme was irreversibly inactivated by heat in a linear fashion, with G6P providing a degree of protection. Phosphoenolpyruvate (PEP), adenosinetriphosphate (ATP), and fructose 6-phosphate (F6P), in decreasing order, are effective inhibitors. Zinc and Cobalt ions were effective inhibitors although cobalt ion was more potent; the two divalent metals were competitive inhibitors with respect to G6P, with Ki values of 6.6 microM and 4.7 microM respectively. It is proposed that inhibition by divalent metal ions, at low NADPH /NADP ratio, is another means of controlling pentosephosphate pathway.

Aspergillus↗

[Characteristics of carbohydrate metabolism of R-, S- i M-dissociants of Pseudomonas aeruginosa].

R and S dissociants of the hydrocarbon-oxidizing strain Pseudomonas aeruginosa K-2 differed but little in their growth in a minimal defined medium with glucose as the source of carbon and energy. At the same time, the number of cells of M dissociant in the late exponential phase was five orders of magnitude less than that of R and S dissociants. The growth of M dissociant was accompanied by the accumulation of formate in the culture liquid and a concurrent decrease in pH. All three dissociants contained the key enzymes of the Entner-Doudoroff pathway of glucose oxidation; however, the activities of these enzymes, especially 6-phosphogluconate dehydrogenase, were low in M dissociant. Conversely, the activity of formate dehydrogenase in cells of M dissociant was higher than in other dissociants. The activity of 6-phosphogluconate dehydrogenase, a key enzyme of the pentosephosphate pathway of glucose oxidation, was detected only in S dissociant. The peculiarities of the carbohydrate metabolism of M dissociant are probably responsible for its poor growth on glucose and determine the more pronounced anaerobic type of its metabolism.

Carbohydrate Metabolism↗

[The biochemical mechanisms of the metabolic disorders in gestosis].

The paper is concerned with disturbances in major metabolic routes of bodily energy supply in patients with gestoses, such as glycolysis, gluconeogenesis, and pentosephosphate route of production of nicotinamide coenzymes. Dysfunctional breakages in the mechanisms of homeostasis maintenance, first of all, of adaptation systems in the obstetric pathology under consideration are multiform and interrelated. In addition, pathogenetical specificity of gestoses necessitates a specific correction of intracellular metabolism in order that complications might be prevented. Thus, promoting artificial activation of the patient's body detoxifying systems and optimization of blood functions by ways similar to physiological mechanisms of regulation of homeostasis is, according to the published literature, ozonohemotherapy as an efferent method of detoxification.

Adaptation, Physiological↗

[Aqueous dynamics and ciliary epithelium enzyme systems (author's transl)].

Aqueous humour is produced by ultrafiltration (30%) and active ion transport (70%) predominantly achieved by nonpigmented ciliary epithelial cells. They need chemical energy supplied by intracellular metabolisms. Suspensions of isolated ciliary epithelial cells and ciliary cell layers prepared from single rabbit eyes have been assayed for activities of glucose-6-phosphate-dehydrogenase, lactate dehydrogenase, malate dehydrogenase, NAD- and NADP-depending isocitrate dehydrogenase. Levels of enzyme activity were found to be higher in the nonpigmented cell type. Enzyme activity of cell layers exceeded those of isolated cells for technical reasons. By comparing ciliary epithelial enzyme patterns to those of different tissues it may be deduced that ciliary epithelium draws its energy chiefly from pentosephosphate and citric cycle. High levels of lactate dehydrogenase activity suggest special functions of this in enzyme in aqueous formation.

Aqueous Humor↗

[Effect of inoculum parameters on the specificity of secondary synthesis in cultures producing novobiocin and mycoheptin].

The impact of the vegetative inoculum parameters on specificity of the secondary synthesis in the cultures producing novobiocin and mycoheptin was studied. During the study the fermentation conditions were varied by using the vegetative inoculum differing in the respiration rate after its transfer to the fermentation medium. To show the decisive role of the inoculum parameters in regulation of the specificity of the secondary synthesis, the dynamics of accumulation of certain metabolites forming from glucose along with the main antibiotic and the activity of the key enzymes of the carbohydrate metabolism during the culture growth in the fermentation media were studied. It was found that the specificity of the secondary synthesis with respect to certain metabolites was defined by the intensity of carbohydrate metabolism, i. e. the ratio of the activity of enzymes of glycolysis and the pentosephosphate pathway. In this regard, the inoculum with the maximum respiration rate in an amount of 10 to 20 per cent promoted the highest productivity of the mycelium by the synthesis of novobiocin and mycoheptin while the rate of accumulation of fatty acids, carbohydrates and phenol compounds (for Streptomyces spheroides) and mycopentene (for Streptoverticillium mycoheptinicum) decreased.

Anti-Bacterial Agents↗

[Enzymes protecting the erythrocyte membrane during the combined exposure to an antioxidant complex and acute irradiation].

The data are presented concerning the effect of ionizing radiation on the hemolytic process and the influence of an antioxidant vitamin complex on the pentosephosphate metabolism and glutathione reductase activity after gamma-irradiation. The antioxidant vitamin complex has been shown to produce a favourable effect on the erythrocyte membrane stability in correcting the radiation-induced changes.

Animals↗

[Effect of nitrobenzoic acid on methemoglobin content in blood and activity of antioxidative enzymes in erythrocytes].

Intraperitoneal administration of meta-nitrobenzoic, 3,5-dinitrobenzoic, 2,4,6-trinitrobenzoic and 3,5-dinitro-4-methylbenzoic acids to the white mice in a dose equal to LD50 has induced an increase in the methaemoglobin content in their blood. Total activity of dehydrogenases of pentosephosphate pathway, content of 2,3-diphosphoglycerate increase in response to the intoxication evoked by the mentioned acids. The acute intoxication does not practically change the activity of the key enzymes of antioxidant protection: superoxide-dismutase, catalase and glutathione peroxidase.

2,3-Diphosphoglycerate↗

[Impact of stress on hepatic lipid and carbohydrate metabolism, prevention].

An oligomer proantocyanidine complex (OPCC) isolated from the aqueous-and-alcoholic extract Kalifen and a polyphenol complex (PPC) isolated from the eleutherococcus extract were tested for their effects on carbohydrate and lipid metabolism in the rat liver under acute stress caused by hanging up of the animals by the cervical fold for 22 hours. This acute stress was accompanied by decreases in aerobic glycolysis and pentose cycle and by an increase in lipolysis. Hepatic etherifying function impaired. Lipids became predominant energy substrates. The administration of OPCC and PPC during stress promoted the preservation of carbohydrate metabolic reactions (gluconeogenesis, pentosephosphate pathway, Krebs cycle) and to the decrease of lipolysis. OPCC was shown to have stress-protective properties and to be able to diminish adrenal hypertrophy, to increase the production of oxidized equivalents (NAD+), and to enhance the activity of G-6-PDH in the rat liver. The complex is superior to the well-known antistress agent eleutherococcus, which makes it possible to regard these drugs as possible promising drugs in preventive and rehabilitative medicine.

Animals↗

[Changes in carbohydrate metabolism in hens experimentally infected with Pasteurella multocida kokoshki].

Studied were the concentration of blood sugar, the activity of glucose-6-phosphatase and glucose-6-phosphatedehydrogenase, and the level of glycogen in the liver of P. multocida infected chickens. An abrupt decrease of the liver glycogen was found as well as a negligible rise of the blood sugar. The activity of glucose-6-phosphatase remained unchanged, and that of glucose-6-dehydrogenase was twice as high. It is concluded that the intense exhaustion of liver glycogen is in connection with the activation of the pentosephosphate pathway.

Animals↗

[Activity of cytoplasmic NADP-dependent dehydrogenase in rat liver during induction of cytochrome P-450 by phenobarbital].

Activity of oxidation enzymes of the pentosephosphate way (glucose-6-phosphate dehydrogenase (EC 1.1.1.49) and 6-phosphogluconate dehydrogenase (EC 1.1.1.44), cytoplasmic malate dehydrogenase (decarboxylating oxaloacetate) (NADP+) (EC 1.1.1.40) and isocitrate dehydrogenase (NADP+) (EC 1.1.1.42) as well as the content of microsomal cytochromes b5 and P-450 in the rat liver have been studied 24 hours after 1, 2, 3, 4 and 5 intraperitoneal administrations of phenobarbital (4 mg per 100 g of the body weight). It is shown that the cytochrome P-450 content increases after a single administration of phenobarbital and then it gradually grows reaching its maximum after 4 administrations and falls after 5 administrations (though it remains high as compared to the control animals). The content of cytochrome b5 increases only after 4 administrations of phenobarbital and after 5th one it returns to the initial level. The content of microsomal gangliosides calculated per 1 mg of microsomal protein decreases after a single administration of phenobarbital and 5 days later it returns to the initial level. Activity of glucose-6-phosphate dehydrogenase increases after a single administration of phenobarbital, that of malate dehydrogenase--after 3 administrations, 6--phosphogluconate-dehydrogenase--after 4 administrations of the preparation. The 5 administrations of phenobarbital makes activity of all the mentioned dehydrogenases return to the initial level. Activity of isocitrate dehydrogenase under given conditions of the experiment does not change.

Animals↗

Characterization of erythrocytic glucose-6-phosphate dehydrogenase in a mouse strain with reduced G6PD activity.

Erythrocytic glucose-6-phosphate dehydrogenase (G6PD) of a mutant mouse strain with X-linked G6PD-deficiency was purified and compared with the wildtype G6PD by biochemical and physiological characteristics. The red cell G6PD activity of the mutant was 20% of the wildtype. The Michaelis constant (Km) of the substrate glucose-6-phosphate (G6P) was higher (90 microM) for the mutant than for the wildtype (56 microM). The isoelectric focusing with a pH range from 3 to 10 showed one more enzymatically active band for the wildtype G6PD compared to the mutant enzyme. Other enzyme characteristics, however, such as Km for nicotinamide adenine dinucleotide phosphate (NADP), utilisation of 2-deoxy-glucose-6-phosphate (2dG6P) and deamino-NADP, heat stability, pH optimum, molecular weight, and glucose metabolisation via the pentosephosphate pathway were similar in mutant and wildtype enzyme.

Animals↗

[Changes in the intracellular glucose-6-phosphate dehydrogenase metabolism in the rat liver during thiamine deficiency].

Patterns of intracellular glucose-6-phosphate dehydrogenase turnover were studied in liver tissue of intact and thiamin-deficient rats using a new procedure for the enzyme purification. The alternations, found in the half-life period, in constant rates of synthesis and degradation of the key enzyme of the pentosephosphate pathway, correlated with a decrease of the glucose-6-phosphate dehydrogenase activity in vitamin B1 deficiency.

Animals↗

[Effect of thrombin and prostaglandins E and F on various indices of carbohydrate metabolism in human platelets].

After incubation of intact thrombocytes with prostaglandins E2 and F2 alpha stimulation of glucose-6-phosphate dehydrogenase and glutathione reductase activities as well as an increase in the rate of sedoheptulose-7-phosphate accumulation were found. Thrombin inhibited the glucose-6-phosphate dehydrogenase activity by 30% in these thrombocytes. Addition of thrombin, following the incubation of thrombocytes with prostaglandins, removed the activating effect of the prostaglandins on the pentosephosphate pathway reactions, inhibited glutathione reductase and lactate dehydrogenase.

Blood Platelets↗

[Energy metabolism in the kidney cortex of rats with alloxan diabetes].

Activity of lactate dehydrogenase was decreased in kidney cortex of rats with alloxane diabetes. The lactate dehydrogenase activity, catalyzing the lactate transformation into pyruvate, was increased. Activation of the pentosephosphate pathway enzymes was the characteristic property of metabolism impairments in kidney tissue under conditions of alloxane diabetes.

Animals↗