ライフサイエンスコーパス: erythritol

1 or catabolism of d-threitol, l-threitol, and erythritol.

2 btained from bacteria grown on (13)C-labeled erythritol.

3 (250 mm) without concomitant accumulation of erythritol.

4 ), promoting threitol synthesis over that of erythritol.

5 evalonate and deuterium-labeled 2-C-methyl-D-erythritol.

6 lar weight non-electrolytes (malonamide-14C, erythritol-14C, D-arabinose-14C, and D-mannitol-14C) are

7 erythritol 4-phosphate (MEP) to 2-C-methyl-d-erythritol 2,4-cyclodiphosphate (cMEDP) in the MEP entry

8 The enzyme 2-C-methyl-D-erythritol 2,4-cyclodiphosphate (MECDP) synthase catalyz

9 yl-D-erythritol 2-phosphate into 2C-methyl-D-erythritol 2,4-cyclodiphosphate at catalytic rates of 19

10 hritol) and third (synthesis of 2-C-methyl-d-erythritol 2,4-cyclodiphosphate) steps.

11 onversion of 4-diphosphocytidyl-2-C-methyl-D-erythritol 2-phosphate (CDP-ME2P) to MECDP, a highly unu

12 own genes of the non-mevalonate 2-C-methyl-D-erythritol 2-phosphate (MEP) pathway for synthesis of is

13 conversion of 4-diphosphocytidyl-2C-methyl-D-erythritol 2-phosphate into 2C-methyl-D-erythritol 2,4-c

14 linic acid, 1,3-dipetroselinin, 2-C-methyl-d-erythritol, 2-C-methyl-d-erythritol 4-O-beta-d-glucopyra

15 d on addition of the substrate, 2-C-methyl-D-erythritol-2, 4-cyclo-diphosphate.

16 he IspG-catalyzed conversion of 2-C-methyl-D-erythritol-2,4-cyclo-diphosphate into (E)-1-hydroxy-2-me

17 e synthase (GcpE/IspG) converts 2-C-methyl-D-erythritol-2,4-cyclodiphosphate (MEcPP) into (E)-4-hydro

18 es not catalyze the formation of 2C-methyl-D-erythritol 3,4-cyclophosphate from 4-diphosphocytidyl-2C

19 linin, 2-C-methyl-d-erythritol, 2-C-methyl-d-erythritol 4-O-beta-d-glucopyranoside and linalool.

20 hyl-D-erythritol is formed from 2-C-methyl-D-erythritol 4-phosphate (MEP) and CTP in a reaction catal

21 pD) catalyzes the conversion of 2-C-methyl-D-erythritol 4-phosphate (MEP) and cytidine triphosphate (

22 yzes the conversion of DXP into 2-C-methyl-D-erythritol 4-phosphate (MEP) by consecutive isomerizatio

23 nhibitor of the MVA-independent 2-C-methyl-D-erythritol 4-phosphate (MEP) isoprenoid pathway, unexpec

24 Most bacteria use the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway for the synthesis o

25 ounds are synthesized using the 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway in many gram-negati

26 The 2-C-methyl-D-erythritol 4-phosphate (MEP) pathway leads to the biosyn

27 xy-D-xylulose 5-phosphate (DXP)/2-C-methyl-D-erythritol 4-phosphate (MEP) pathway of isoprenoid synth

28 hesised in chloroplasts via the 2-C-methyl-d-erythritol 4-phosphate (MEP) pathway.

29 supply of precursors through the 2C-methyl-D-erythritol 4-phosphate (MEP) pathway.

30 pathway and the plastid-associated 2C-methyl erythritol 4-phosphate (MEP) pathway.

31 sm of the reaction catalyzed by 2-C-methyl-d-erythritol 4-phosphate (MEP) synthase from Escherichia c

32 eductoisomerase (DXR, also known as methyl-d-erythritol 4-phosphate (MEP) synthase) is a NADPH-depend

33 The conversion of 2-C-methyl-d-erythritol 4-phosphate (MEP) to 2-C-methyl-d-erythritol

34 osphorylation of enzymes in the 2-C-methyl-d-erythritol 4-phosphate (MEP)/terpenoid and shikimate/phe

35 2-C-Methyl-D-erythritol 4-phosphate (MEP, 2) and 4-diphosphocytidyl-2

36 ctively, and plants, utilize the 2C-methyl-D-erythritol 4-phosphate (MEP, 5) pathway for the biosynth

37 rpene, monoterpene, triterpene, 2-C-methyl-D-erythritol 4-phosphate and mevalonate pathways.

38 deoxy-d-xylulose 5-phosphate to 2-C-methyl-d-erythritol 4-phosphate in the presence of NADPH.

39 o catalyze the transformation of 2C-methyl-D-erythritol 4-phosphate into 4-diphosphocytidyl-2C-methyl

40 biosynthesis, the conversion of 2C-methyl-d-erythritol 4-phosphate into its cyclic diphosphate proce

41 2-C-methyl-D-erythritol 4-phosphate is the first committed intermedia

42 hloroplastic methylerythritol 2-C-methyl-D: -erythritol 4-phosphate isoprenoid pathway.

43 ncoding enzymes involved in the 2-C-methyl-d-erythritol 4-phosphate pathway and the biosynthesis of s

44 ase in transcript levels of the 2-C-methyl-D-erythritol 4-phosphate pathway enzyme 1-deoxy-D-xylulose

45 hosphoantigens derived from the 2-C-methyl-d-erythritol 4-phosphate pathway of isoprenoid synthesis.

46 xenobiotics; methanogenesis; and 2-methyl-d-erythritol 4-phosphate pathway-mediated biosynthesis of

47 o be the key step in regulating 2-C-methyl-D-erythritol 4-phosphate substrate flux in kiwifruit.

48 sphite dianion, d-glycerol 3-phosphate and d-erythritol 4-phosphate.

49 izes the immediate precursor of 2-C-methyl-D-erythritol 4-phosphate.

50 nthesized via the chloroplastic 2-C-methyl-d-erythritol 4-phosphate/1-deoxy-d-xylulose 5-phosphate pa

51 We synthesized five D-MEP analogues-D-erythritol-4-phosphate (EP), D-3-methylthrietol-4-phosph

52 ipt levels of several plastidic 2-C-methyl-d-erythritol-4-phosphate (MEP) pathway genes, geranylgeran

53 The plastidic 2-C-methyl-D-erythritol-4-phosphate (MEP) pathway is one of the most

54 tol metabolism involves phosphorylation to L-erythritol-4-phosphate by the kinase EryA and oxidation

55 e inhibitors of Plasmodium spp. 2-C-methyl-D-erythritol-4-phosphate cytidyltransferase (IspD), the th

56 Escherichia coli 2-C-methyl-D-erythritol-4-phosphate cytidyltransferase (YgbP or IspD)

57 (HMBPP), an intermediate in the 2-C-methyl-d-erythritol-4-phosphate pathway used by microbes, and iso

58 2-C-Methyl-D-erythritol-4-phosphate synthase (MEP synthase) catalyzes

59 A pathway, and in plastids from 2-C-methyl-d-erythritol-4-phosphate through the MEP pathway.

60 een applied to a new synthesis of 2-methyl-D-erythritol, a branched five-carbon sugar of importance t

61 hosphate from 4-diphosphocytidyl-2C-methyl-D-erythritol, a side reaction catalyzed in vitro by the Is

62 tudies of sugar alcohols mannitol, sorbitol, erythritol, adonitol, arabitol, galactitol, and xylitol

63 ther by the type of growth on Casamino Acids-erythritol-albumin agar and by micromorphological differ

64 The combination of erythritol and chlorhexidine displayed stronger antimicr

65 this study, a new formulation consisting of erythritol and chlorhexidine is compared with the standa

66 nient method for the synthesis of 2-methyl-D-erythritol and is expected to be useful for generating i

67 se may contribute to the association between erythritol and obesity observed in young adults.

68 One group was negative for I-erythritol and ribitol and included all the isolates bel

69 e remaining three groups were positive for I-erythritol and ribitol and were grouped within Nocardia

70 ructose-1,6-bisphosphatases grew normally on erythritol and that EryC, which was assumed to be a dehy

71 hosphate into 4-diphosphocytidyl-2C-methyl-D-erythritol and the conversion of 4-diphosphocytidyl-2C-m

72 synthesis of 4-diphosphocytidyl-2-C-methyl d-erythritol) and third (synthesis of 2-C-methyl-d-erythri

73 glycoside) to 725.6 mg/100 g dm (puree with erythritol), and the content of these compounds strongly

74 by glycerol-like osmolytes such as xylitol, erythritol, and propanediol.

75 sucrose), four polyols (glycerol, mannitol, erythritol, and sorbitol), five amino acids (glycine, al

76 was detected, as well as elevated amounts of erythritol, arabitol, and ribitol in the plasma of affec

77 Elevated urinary excretion of erythritol, arabitol, ribitol, and pent(ul)ose-5-phospha

78 We now have to recognize erythritol as a candidate for food allergen, and to be c

79 jelly product for diet supplement containing erythritol as a major component.

80 Accordingly, growth on erythritol as the sole C source should require aldolase

81 and compared to the corresponding bis(diol), erythritol, as well as the corresponding mono(alpha-hydo

82 vide clues to the preferential metabolism of erythritol by Brucella and its role in pathogenicity.

83 Efficient erythritol catabolism under conditions that promote thre

84 (MEP, 2) and 4-diphosphocytidyl-2-C-methyl-D-erythritol (CDPME, 3) are metabolites in the MEP pathway

85 anium disks and air polished with glycine or erythritol-chlorhexidine powders.

86 Air polishing with erythritol-chlorhexidine seems to be a viable alternativ

87 Canalicular bile flow, as measured by [14C]erythritol clearance after functional nephrectomy, was s

88 21-fold (95% CI: 19.84, 21.41) higher blood erythritol compared with participants with lower HbA1c (

89 ce interval (CI): 13.27, 16.25] higher blood erythritol compared with participants with stable adipos

90 Glycerophosphocholines, erythritol, creatinine, hexadecanoic acid, and glutamine

91 idial retrograde signaling metabolite methyl-erythritol cyclodiphosphate (MEcPP) and the defense horm

92 Based on utilization of I-erythritol, D-glucitol, i-myo-inositol, D-mannitol, and

93 agine, L-Aspartic Acid, L- Glutamic Acid, m- Erythritol, D-Melezitose, D-Sorbitol) triggered the fung

94 of the bovine reproductive tract are rich in erythritol during the latter stages of pregnancy, and th

95 Therefore, endogenous production of erythritol from glucose may contribute to the associatio

96 eoxyribonic acid; 3,4-dihydroxybutyric acid; erythritol; gluconic acid; and ribose were validated in

97 ation of the growth medium with 2-C-methyl-D-erythritol has been shown to complement disruptions in t

98 formation of 4-diphosphocytidyl-2-C-methyl-D-erythritol in the presence of MEP and CTP.

99 oral challenge test in the hospital, 3 g of erythritol induced remarkable coughing, urticaria, edema

100 that prevented the transport of 2-C-methyl-D-erythritol into the cell.

101 Erythritol is a natural sugar alcohol, with the molecula

102 Erythritol is an important nutrient for several alpha-2

103 MEP pathway, 4-diphosphocytidyl-2-C-methyl-D-erythritol is formed from 2-C-methyl-D-erythritol 4-phos

104 of pregnancy, and the ability to metabolize erythritol is thought to be important to the virulence o

105 prolylhydroxyproline) is a dipeptide, and 1 (erythritol) is a sugar alcohol.

106 Erythritol metabolism involves phosphorylation to L-eryt

107 zed in isoprenoid biosynthesis, 2-C-methyl-D-erythritol must be phosphorylated.

108 had statistically significantly higher blood erythritol [P < 0.001, false discovery rate (FDR) = 0.04

109 HMBPP) in the penultimate step of the methyl-erythritol phosphate (MEP) pathway for isoprene biosynth

110 hate, HDMAPP), an intermediate in the methyl erythritol phosphate pathway, and (E)-[4-(2)H]HDMAPP wer

111 thyl-2,3-O-isopropylidene-tartrate, and meso-erythritol, respectively.

112 2-7% for 2, 3-butanediol, ethanol, glycerol, erythritol, rhamnose, arabitol, sorbitol, galactitol, ma

113 ant by genetic complementation abolished the erythritol-specific growth defect exhibited by this stra

114 ctive effects of some additives (palm sugar, erythritol, steviol glycoside, xylitol and inulin) on th

115 ing 30% increase in the biliary clearance of erythritol suggested that the choleresis was primarily o

116 talyzed by a 4-diphosphocytidyl-2-C-methyl-D-erythritol synthase (IspD).

117 this strain was cultured in the presence of erythritol than that required when it was cultured in th

118 xperiments and through in vivo conversion of erythritol to erythronate in stable isotope-assisted dri

119 ated by the observation that the addition of erythritol to low-iron cultures of B. abortus 2308 stimu

120 display wild-type growth in the presence of erythritol under iron-limiting conditions is due to a de

121 tion and efficient growth in the presence of erythritol under low-iron conditions.

122 ortus 2308, when cultured in the presence of erythritol under low-iron conditions.

123 HBA production and growth in the presence of erythritol was further substantiated by the observation

124 Prick test with erythritol was negative even at 300 mg/ml, which was alm

125 Erythritol was shown to be synthesized endogenously from

126 ains of RMC26 unable to grow on 2-C-methyl-D-erythritol were incubated in buffer containing mevalonat

127 ent natural sweeteners (sucrose, palm sugar, erythritol, xylitol, steviol glycoside, Luo Han Kuo), an