pyruvate in English

noun

salt or ester of pyruvic acid; ionized form of pyruvic acid

Use "pyruvate" in a sentence

1. Pyruvate Carboxylase (PC) catalyzes the biotin-dependent carboxylation of pyruvate to produce oxaloacetate

2. 2-Ketoaldonic acid is synthesized by aldolase condensation reaction involving pyruvate and an aldose acceptor in the presence of excess pyruvate.

3. There is a noted implication in Pyruvate Carboxylase …

4. Pyruvate Carboxylase is a nuclear-encoded mitochondrial enzyme that catalyzes the conversion of pyruvate to oxaloacetate.It is a key regulatory enzyme in gluconeogenesis, lipogenesis, and neurotransmitter synthesis

5. Abyssinians can develop a hereditary condition called pyruvate kinase deficiency; pyruvate kinase is a key regulatory enzyme required for energy metabolism in red blood cells

6. The liver absorbs Alanine from the blood and converts it into pyruvate.

7. Methods of producing 7-carbon chemicals via pyruvate and succinate semialdehyde aldol condensation

8. Pyruvate Carboxylase is a somewhat unique enzyme in that it is essentially inactive in …

9. Provided below are ELISA kits targeting pyruvate Carboxylase, a human protein encoded by PC

10. Measurement of lactate, pyruvate, ATP and CP demonstrated domination of aerobic metabolism.

11. After ammonia addition the levels of α-ketoglutarate and pyruvate fall in the medium.

12. The present invention relates to a recombinant microorganism with increased productivity of 2,3-butanediol, wherein a pathway for converting pyruvate to acetyl-CoA, a pathway for converting pyruvate to formic acid, or a pathway for converting pyruvate to lactate is inhibited in a microorganism having acetyl-CoA and lactate biosynthetic pathways.

13. Pyruvate Carboxylase is a biotin-requiring enzyme that is referred to as an ABC enzyme

14. As expected, more pyruvate was found in the tissues of Cysticerci incubated with this substrate.

15. First, glucose is released from glycogen stores suchlike lactate and pyruvate, probably due to preceeding anoxia.

16. Pyruvate Carboxylase (PC) catalyzes an important 2-step reaction - (i) ATP-dependent carboxylation of covalently attached biotin (ii) transfer of carboxyl group to pyruvate, and this interconversion is essential for replenishment of TCA/citric acid cycle intermediates (anaplerosis).

17. Bacteria that can grow on this medium produce an enzyme, Citrate-permease, capable of converting Citrate to pyruvate.

18. Similar activities of glyceraldehyde-3-phosphate dehydrogenase were found in cells grown in pyruvate and glucose mediums.

19. The concentrations of glucose, lactate, pyruvate, ammonia and urea were estimated in the medium during 150 min.

20. However, this reaction is not completely specific for Creatinine since other reducing substances such as glucose, pyruvate, ascorbic

21. 29 There were no significant differences in the serum lactate, pyruvate, or alkaline phosphatase concentrations between the treatment groups.

22. Pyruvate Carboxylase deficiency is an inherited disorder that causes lactic acid and other potentially toxic compounds to accumulate in the blood

23. Pyruvate Carboxylase (PC) deficiency is characterized in most affected individuals by failure to thrive, developmental delay, recurrent seizures, and metabolic acidosis

24. Blastocoel is a cavity filled with fluid containing high concentrations of lactate and specific amino acids and lower concentrations of glucose and pyruvate

25. Note that Alanine is the α-amino acid analog of the α-keto acid pyruvate, an intermediate in sugar metabolism.

26. Pyruvate Carboxylase deficiency results in malfunction of the citric acid cycle and gluconeogenesis, thereby depriving the body of energy; the former biochemical process derives

27. 19 Consequently, these mutant cells rely exclusively on glycolysis for their energy requirements and require exogenous pyruvate and pyrimidines for growth.

28. Abyssinians have hereditary health issue called pyruvate kinase deficiency that can be a concern, especially if you aren’t cautious about who you buy from

29. Pyruvate Carboxylase deficiency (PCD) is a rare disorder that can cause developmental delay and failure to thrive starting in the neonatal or early infantile period

30. Plant Cytoplasm Symbiosome Membrane Sugars Bacteroid Membrane Organic Acids Photosynthesis Citric Acid Cycle 4Hs Electron Bacteroid Succinate Malate Fumarate Pyruvate Proton Motive Transport

31. Abstract Multiple Carboxylase deficiency has previously been characterized by deficient activity of three biotin-dependent enzymes: propionyl CoA Carboxylase, pyruvate Carboxylase and beta-methylcrotonyl CoA Carboxylase.

32. Mechanistically, p53 activation represses the expression of the mitochondrial enzyme pyruvate Carboxylase (PC), resulting in diminished production of the TCA cycle intermediates oxaloacetate and

33. In aerobic conditions, the process converts one molecule of glucose into two molecules of pyruvate (pyruvic acid), generating energy in the form of two net molecules of ATP.

34. Central venous blood samples were collected every 30 minutes and analysed for free fatty acids, glycerol, β-hydroxybutyrate, acetoacetate, glucose, lactate, pyruvate, cortisol and growth hormone concentrations.

35. Itaconate dissimilation in Mtb involves the Bifunctional enzyme Rv2498c, which cleaves (S)-citramalyl-CoA producing Ac-CoA and pyruvate, effectively using a host-derived antibacterial molecule as a nutrient source.

36. The purpose of the present study was to compare Arterialized venous and arterial pH, PCO2, K+, lactate, pyruvate, and epinephrine during the constantly changing circumstances of an incremental exercise test.

37. Plasma levels of lactate pyruvate, “excess lactate”, lactat-dehydrogenase (LDH), leucin-aminopeptidase (LAP) as well as lysosomal acid phosphatase and beta-glucuronidase have been investigated in haemorrhagic shock.

38. The ability of carbohydrate fuels (lactate, pyruvate, glucose) and the ketone bodies (acetoacetate, β-hydroxybutyrate) to compete with fatty acids as fuels of respiration in the isolated Langendorf-perfused heart was studied.

39. Coenzyme A (CoA, CoASH, or HSCoA) is a Coenzyme, well known for it's role in the synthesis and oxidation of fatty acids, and the oxidation of pyruvate in the citric acid cycle

40. 3 Cadaverine + 4 pyruvate -> 17-oxosparteine + 4 L-alanine + H+ + 3 H2O PlantCyc Cadaverine, Cadaverine, Cadaverine, Cadaverine, Cadaverine, Cadaverine: L-lysine + H+ -> CO2 + Cadaverine PlantCyc Cadaverine, Cadaverine, Cadaverine, Cadaverine, Cadaverine, Cadaverine, Cadaverine

41. Citrate in milk originates from the Citrate formed in the mammary secretory cell where it is a central intermediate in the citric acid cycle, used for oxidation of fatty acids, acetic acid, and pyruvate

42. The Cysticerci from medium containing only labeled pyruvate as a food source were depleted in glycogen, glucose, and lactate as compared with those for which glucose had been made available in the media

43. ‘In Aerobes with sufficient oxygen, pyruvate is transported to the mitochondrion to undergo further transformations in the Krebs cycle.’ ‘By contrast, only 1 or 2 types of Gram-positive organisms are generally cultured in osteomyelitis, almost universally Aerobes.’

44. Murashige and Skoog basal nutrient (half strength) medium, supplemented with 6-benzylaminopurine (BAP), 2,4-dichlorophenoxyacetic acid (2,4-D), and pyruvate was selected for the in vitro co-culture of C. equisetifolia callus explants, G. mosseae, and Frankia.

45. Pyruvate Carboxylase deficiency (PC deficiency) is a rare genetic disorder present at birth characterized by failure to thrive, developmental delay, recurrent seizures and a failure of the body to produce the necessary fuels for energy and neurotransmitters important for brain function.

46. Pyruvate Carboxylase deficiency is an inherited disorder that causes lactic acid and other potentially toxic compounds to accumulate in the blood. High levels of these substances can damage the body's organs and tissues, particularly in the nervous system.

47. L-Alanine + 5-oxooctanal <--> 8-aminooctan-4-one + pyruvate PlantCyc L-ALPHA-Alanine: L-cysteine + MoO2-molybdopterin cofactor + a reduced electron acceptor -> L-Alanine + thio-molybdenum cofactor + an oxidized electron acceptor + H2O PlantCyc L-ALPHA-Alanine:

48. What type of enzyme Catalyses this reaction? CH-CC-0 + CO, Pyruvate -CH, Oxaloacetate EC 5: isomerases EC 3: hydrolases EC 4: lyases EC 6: ligases EC 2: transferases EC 1: oxidoreductases / dehydrogenases What type of enzyme Catalyses this reaction?

49. Although fat is a common way of storing energy, in vertebrates such as humans the fatty acids in these stores cannot be converted to glucose through gluconeogenesis as these organisms cannot convert acetyl-CoA into pyruvate; plants do, but animals do not, have the necessary enzymatic machinery.

50. Alanine transaminase (ALT) is a transaminase enzyme (EC 2.6.1.2).It is also called Alanine aminotransferase (ALT or ALAT) and was formerly called serum glutamate-pyruvate transaminase or serum glutamic-pyruvic transaminase (SGPT) and was first characterized in the mid-1950s by Arthur Karmen and colleagues