1. Carboxylase synonyms, Carboxylase pronunciation, Carboxylase translation, English dictionary definition of Carboxylase

2. 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.

3. Acetyl CoA Carboxylase has three important features

4. There is a noted implication in Pyruvate Carboxylase …

5. Cyclohexane derivatives as inhibitors of acetyl-coa carboxylase (acc)

6. Acetyl-CoA Carboxylase (ACC) is a complex multifunctional enzyme system

7. Example sentences from the Web for carboxylase With regard to the relation of Carboxylase to the process of alcoholic fermentation, nothing definite is yet known

8. Preferred Names Ribulose bisphosphate Carboxylase (small chain) family protein NP_001031981.1

9. Definition of Carboxylase : an enzyme that catalyzes decarboxylation or carboxylation Examples of Carboxylase in a Sentence Recent Examples on the Web The problem lies with an enzyme known as …

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

11. Acetyl-coenzyme a carboxylase 2 as a target in fat regulation and insulin action

12. Acetyl-CoA Carboxylase (ACC) is a biotin-dependent enzyme that catalyzes the irreversible carboxylation of acetyl-CoA to produce malonyl-CoA through its two catalytic activities, biotin Carboxylase (BC) and carboxyltransferase (CT)

13. Acetyl-CoA Carboxylase (ACC) catalyzes the carboxylation of acetyl-CoA to malonyl-CoA (1)

14. Acetyl-CoA Carboxylase (ACC) catalyzes the carboxylation of acetyl-CoA to malonyl-CoA (1)

15. The enzyme that carries out the carboxylation of glutamic acid is gamma-glutamyl carboxylase.

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

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

18. Carboxylase an enzyme that assists in the CARBOXYLATION or decarboxylation of a SUBSTRATE (3)

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

20. PEP Carboxylase is located in the mesophyll cells, on the leaf exterior near the stomata

21. Alcoholic Fermentation Arthur Harden A comparison of the conditions of action of Carboxylase and zymase has …

22. Ribulose bisphosphate Carboxylase (small chain) family protein; FUNCTIONS IN: ribulose-bisphosphate Carboxylase activity; INVOLVED IN: carbon fixation, response to blue light, response to red light, response to far red light; LOCATED IN: in 7 components; EXPRESSED IN: 12 …

23. Acetyl-CoA Carboxylase (ACC) catalyzes the biotin-dependent carboxylation of acetyl-CoA to produce malonyl-CoA

24. 17 rows  · Multiple Carboxylase deficiency (MCD) is a term used to describe inborn …

25. Biotin works with carboxylase enzymes, ATP, and magnesium to use carbon dioxide to help make fatty acids

26. (1995) cloned and sequenced the cDNA coding for acetyl-CoA Carboxylase of the human HepG2 cell line

27. Ribulose 1,5-bisphosphate Carboxylase/oxygenase (Rubisco) is the cornerstone of atmospheric CO 2 fixation by the biosphere

28. In in vitro experiments, 2 μM concentrations of palmityl-CoA or oleoyl-CoA depressed acetyl-CoA carboxylase activity.

29. Other rare congenital defects are methylmalonic acidemia, a functional vitamin B12 deficiency, and biotin-responsive multiple carboxylase deficiency.

30. Carboxylase definition: any enzyme that catalyses the release of carbon dioxide from certain acids Meaning, pronunciation, translations and examples

31. ‘Phosphoenolpyruvate Carboxylase, which catalyses the carboxylation of phosphoenolpyruvate using HCO 3-to generate oxaloacetic acid, is an important enzyme in the primary metabolism of plants.’ ‘A reduction of oxaloacetate does seem likely because both phosphoenolpyruvate Carboxylase and total malate dehydrogenases were activated under

32. (1988) reported the structure of the coding sequence and the primary amino acid sequence of the rat acetyl-CoA Carboxylase

33. Ribulose-1,5-bisphosphate carboxylase/oxygenase (Rubisco) Catalyses the incorporation of inorganic CO 2 into the organic molecules of life

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

35. Acetyl-CoA Carboxylase (ACC) is a biotin-dependent enzyme that catalyzes the ATP-dependent carboxylation of acetyl-CoA to malonyl-CoA

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

37. CO2 entering the stomata is rapidly fixed by PEP Carboxylase into a 4-carbon compound, called malate, by attaching the CO2 to PEP.

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

39. These herbicides inhibit the enzyme acetyl-CoA Carboxylase (ACCase), which catalyzes the first step in fatty acid synthesis and is important for membrane synthesis

40. These results demonstrate that inhibition of ACC2 acetyl-CoA carboxylase could be used to regulate fat oxidation and accumulation for purposes of weight control.

41. 3-Methylcrotonyl-CoA Carboxylase (3-MCC) deficiency is an inherited (genetic) condition that prevents your baby’s body from breaking down certain proteins properly

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

43. 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

44. Light-dependent control of FAS is partially achieved by regulation of acetyl-coenzyme A Carboxylase (ACCase; EC.6.4.1.2) which catalyzes the first committed step in …

45. 3-methylcrotonyl-CoA Carboxylase deficiency (also known as 3-MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins properly

46. 3-methylcrotonyl-CoA Carboxylase deficiency (also known as 3-MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins properly

47. 3-methylcrotonyl-CoA Carboxylase deficiency (also known as 3-MCC deficiency) is an inherited disorder in which the body is unable to process certain proteins properly.

48. This disorder is classified as a multiple Carboxylase deficiency, which is a group of disorders characterized by impaired activity of certain enzymes that depend on biotin.

49. Malate Carboxylase (the malolactic enzyme) is the enzyme which carries out the malolactic conversion: a direct decarboxylation of l (−)-malic acid into l (+)-lactic acid (Fig

50. Each, isovaleric acidemia and 3-methylcrotonyl-CoA carboxylase deficiency were found in four individuals, which may indicate a considerably higher incidence of these diseases than previously reported.

51. 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

52. Propionic acidemia is caused by a gene defect leading to malfunction of the enzyme propionyl–CoA carboxylase (PCC) and in turn to a pathologic accumulation of propionic acid.

53. Acetyl-CoA-carboxylase activities were measured in adipose tissues of pigs during a breeding experiment for a low-fat line, and of rats and obese mice under different nutritional conditions.

54. Acetyl-CoA Carboxylase (ACC) catalyses the formation of malonyl-CoA, an essential substrate for fatty acid synthesis in lipogenic tissues and a key regulatory molecule in muscle, brain and other tissues

55. Reversion to a balanced diet for 12 h resulted in a normalization of in vivo EPI lipogenesis, and in a restoration of acetyl-CoA carboxylase activity to levels that did not differ significantly from control values.

56. Propionic acidemia (PA) is a rare autosomal recessive disorder resulting from deficiency of the biotin-dependent enzyme propionyl-CoA carboxylase, which is necessary for the catabolism of branched chain amino acids and odd-chain fatty acids.

57. A number of rare metabolic disorders exist in which an individual's metabolism of biotin is abnormal, such as deficiency in the holocarboxylase synthetase enzyme which covalently links biotin onto the carboxylase, where the biotin acts as a cofactor.

58. 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.

59. Correlation with body fat under a variety of experimental conditions confirms the rate-limiting character of acetyl-CoA-carboxylase, not only for the biosynthesis of fatty acids, but obviously also for their esterification and for triglyceride deposition.

60. 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).

61. 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.

62. Acetyl-CoA carboxylase, malic enzyme and glucose-6-phosphate dehydrogenase are more active in the inner layer, while 6-phosphogluconate and isocitrate dehydrogenases are distinguishable in the two layers of adipose tissue as well if age, sex, and breeding lines are taken into consideration.

63. 3-Methylcrotonyl-CoA Carboxylase Deficiency Disorder (3-MCC Deficiency Disorder) is an inherited condition in which the body is unable to breakdown the amino acid, leucine (a building block of protein) 3-MCC Deficiency Disorder is caused by changes (mutations) in MCCC1 or MCCC2 gene and is inherited in an autosomal recessive manner

64. More particularly, the present invention relates to a Pseudomonas aeruginosa transformed to an expression vector including a nucleotide coding acetyl-CoA carboxylase carboxyltransferase subunit alpha and/or a nucleotide coding malonyl-CoA-[acyl carrier protein]transacylasetransacylase of Pseudomonas aeruginosa, and/or a nucleotide coding acyl (acyl carrier protein) thioesterase of Streptococcus pyogenes, and a method of manufacturing the Pseudomonas aeruginosa.