ライフサイエンスコーパス: assimilatory

1 Assimilatory 3'-phosphoadenosine 5'-phosphosulfate (PAPS

2 DOS originates from assimilatory and bacterial dissimilatory S reduction (BD

3 Assimilatory and dissimilatory biomass utilisation was i

4 uman health, taxonomy of nitrate reductases, assimilatory and dissimilatory nitrate reduction, cellul

5 ruvate is located at a metabolic junction of assimilatory and dissimilatory pathways and represents a

6 bacteria metabolize nitrogen oxides through assimilatory and dissimilatory pathways.

7 inked formaldehyde oxidation pathway and the assimilatory and dissimilatory ribulose monophosphate cy

8 cluded gene transcripts associated with both assimilatory and dissimilatory single-carbon compound ut

9 owth, hydrogen sulphide is a product of both assimilatory and dissimilatory sulphate reduction.

10 Assimilatory and dissimilatory utilisation of autotroph

11 net 80% higher protein abundance for carbon assimilatory and glycolytic pathways leading to fatty ac

12 s was confirmed by demonstrating the loss of assimilatory and respiratory nitrate reductase activity

13 e results suggest that the dissimilatory and assimilatory APS reductases evolved convergently.

14 However, only the assimilatory branch of the denitrification pathway was e

15 sR-type regulator, is the major regulator of assimilatory C1 metabolism in Methylobacterium extorquen

16 Assimilatory carbon enters the ethylmalonyl-CoA pathway

17 icture of the flhDC master operon as a major assimilatory checkpoint in Proteus mirabilis and other G

18 The binding of GS, the principal ammonia assimilatory enzyme, to the conserved C-terminal domain

19 ulfur (S), we examined the activity of key S assimilatory enzymes ATP sulfurylase (ATPS), APS reducta

20 ammonium or dinitrogen through the action of assimilatory enzymes.

21 ssimilation, despite having normal levels of assimilatory enzymes.

22 nd (18)epsilon) for nitrate reduction by two assimilatory eukaryotic nitrate reductase (eukNR) enzyme

23 m previously characterized dissimilatory and assimilatory Fe(III) reductases in its molecular composi

24 erates as a linear pathway carrying the full assimilatory flux to produce glyoxylate, malate, and suc

25 synthesis pathway through formate dominates assimilatory flux.

26 g that the levels of mRNA for plant nitrogen assimilatory genes such as glutamine synthetase (GLN) an

27 Fungal transcripts for putative S assimilatory genes were identified, indicating the prese

28 and NLP7, which act as activators of nitrate assimilatory genes, bind to adjacent sites in the upstre

29 with increased expression of several nitrate assimilatory genes.

30 te in turn regulates the expression of key N-assimilatory genes.

31 e biomass pathways, MtdA plays a key role in assimilatory metabolism.

32 ns to convert formate to methylene H(4)F for assimilatory metabolism.

33 in methylotrophy-specific dissimilatory and assimilatory modules suggested that methylamine use via

34 regressions were in agreement with predicted assimilatory N-uptake based on additional metabolic data

35 Assimilatory NADPH-sulfite reductase (SiR) from Escheric

36 is converted through nitrite to ammonium by assimilatory nitrate and nitrite reductase, respectively

37 tion pathways were absent, as were genes for assimilatory nitrate and sulfate reduction and vitamin B

38 It is well established that assimilatory nitrate reductase (ANR) activity in soil is

39 the inhibitory effect of ammonium (NH4+) on assimilatory nitrate reductase (ANR) activity in soil is

40 ap), respiratory nitrate reductase (Nar) and assimilatory nitrate reductase (Nas), they are defined b

41 Eukaryotic assimilatory nitrate reductase (NR) is a multi-domain pr

42 es the oxidized sites in sulfite oxidase and assimilatory nitrate reductase as deduced from crystallo

43 g the nitrate/proton symporter NasA from the assimilatory nitrate reductase pathway, support that Nar

44 e nasDE genes, together with nasBC (encoding assimilatory nitrate reductase) and nasF (required for n

45 catalytic subunit of R. solanacearum's sole assimilatory nitrate reductase, did not grow on nitrate

46 trate stimulated expression of some genes in assimilatory nitrate reduction and denitrification pathw

47 The assimilatory nitrate transporter NasA of Bacillus subtil

48 Diverse species of bacteria that have an assimilatory nitrate/nitrite reductase system (NAS) can

49 6 km2) revealed a strong correlation between assimilatory NO3- uptake and growth primary production (

50 Percentage daily assimilatory NO3- uptake peaked at 47.4% of the daily NO

51 Mean yearly assimilatory NO3- uptake rates (Ua) were 7.4 times highe

52 multiparameter sensor measurements to relate assimilatory NO3- uptake to metabolic rates and calculat

53 ire watershed, whereas the percentage yearly assimilatory NO3- uptake was 9.0% of nitrogen loading to

54 The percentage yearly assimilatory NO3- uptake was lower in the forest-dominat

55 APSK evolved after bifurcation of the sulfur assimilatory pathway in the green plant lineage and that

56 es, containing a blockage in the primary CO2 assimilatory pathway, derepress the synthesis of compone

57 by either an increased Se flux through the S assimilatory pathway, generated by the biosynthesis of t

58 coli dependent on the low-affinity ammonium-assimilatory pathway, we determined that biosynthetic gl

59 primary and secondary branches of the sulfur assimilatory pathway; however, the biochemical regulatio

60 Carbon assimilatory pathways in castor were compared with previ

61 imilatory pathways was higher than those for assimilatory pathways.

62 y provide a link between carbon and nitrogen assimilatory pathways.

63 eeds is directed toward transforming primary assimilatory products (sugars and amino acids) into seed

64 tant strains with lesions affecting ammonium-assimilatory proteins.

65 alent cations might serve other, potentially assimilatory, purposes.

66 r of NH4+ assimilation by microorganisms, on assimilatory reduction of nitrate (NO3-) in aerated soil

67 tion serves as an intermediate enzyme in the assimilatory reduction of sulfate.

68 bundance of functional genes associated with assimilatory sulfate reduction was higher than those inv

69 ic to the aerobic phase were responsible for assimilatory sulfate reduction, genetic information proc

70 Assimilatory sulfur metabolism, i.e. reactions used for

71 alphaproteobacterial clade are deficient in assimilatory sulphate reduction genes.

72 All aerobic marine bacteria are known to use assimilatory sulphate reduction to supply sulphur for bi

73 ously thought to occur only as a cofactor in assimilatory sulphite/nitrite reductases.

74 ates that the structural genes of the carbon assimilatory system are unusually arranged and possess a

75 ional analyses identify CTR1 and CTR2 as the assimilatory transporters of Chlamydomonas based on loca

76 no structural or sequence homology with the assimilatory-type APS reductase reported here.