ライフサイエンスコーパス: butanediol

1 accumulation of by-products acetoin and 2,3-butanediol.

2 ethylene, succinic acid, isobutanol, and 1,4-butanediol.

3 cluding the growth promoting VOC (2R,3R)-(-)-butanediol.

4 ansesterification of divinyl adipate and 1,4-butanediol.

5 ers were prepared from (2R,3R)- and meso-2,3-butanediol.

6 ntation or indirectly via the dehydration of butanediols.

7 to the synthetic building block chemical 1,3 butanediol (1,3-BDO).

8 rings were constructed from substituted 1,4-butanediol, 1,5-pentanediol, and 1,6-hexanediol, and ste

9 luding ethylene glycol, 1,3-propanediol, 1,4-butanediol, 1,5-petanediol, and 1,6-hexanediol.

10 , allylative oxidative lactonizations of 1,4-butanediol (10(6) tons/yr) are described that occur with

11 on of a Mars-specific rocket propellant, 2,3-butanediol (2,3-BDO), from CO(2), sunlight and water on

12 commercial vitamin D and enantiomers of 1,3-butanediol (23 and 24).

13 Here we systematically developed the 2,3-butanediol (23BD) biosynthetic pathway in Synechococcus

14 n (DHF), a monomer made in one step from 1,4-butanediol, a bioalcohol already produced on the plant s

15 2-3 Butanediol, a by-product of sugar-fermenting microbial m

16 s enhanced due to its ability to produce 2,3-butanediol, a neutral fermentation end product, and supp

17 l alcohols, acetaldehyde, ethyl acetate, 2,3-butanediol, acetoin and 2,3-butanedione.

18 Metabolomic analyses revealed that only 2,3-butanediol, acetoin, diacetyl and formate vary with the

19 , while metabolites such as dodecane and 2,3-butanediol always decreased.

20 Three compounds: ethanol, 2,3-butanediol and 2-ethyl-1-hexanol were selected based on

21 icators were 2,3,5,6-tetramethylpyrazine,2,3-butanediol and 4-ethylguaiacol, beta-linalool, 2-,3-dime

22 subtilis that emitted reduced levels of 2,3-butanediol and acetoin conferred reduced Arabidopsis pro

23 wth whereas bacterial mutants blocked in 2,3-butanediol and acetoin synthesis were devoid in this gro

24 In particular, the volatile components 2,3-butanediol and acetoin were released exclusively from tw

25 he known plant growth-promoting volatile 2,3-butanediol and acetoin.

26 we afford to optimize the production of 1,4-butanediol and demonstrate the de novo production of 1,5

27 nt regulation by the federal government, 1,4-butanediol and gamma-butyrolactone, another precursor of

28 droxybutyrate and a history of ingesting 1,4-butanediol and patients discovered through public health

29 brid glycoboehmite (GB) synthesized from 1,4-butanediol and potassium hydroxide mineralizer.

30 of toxic effects due to the ingestion of 1,4-butanediol and reviewed the related health risks.

31 , were identified as key contributors to 2,3-butanediol and/or mixed acid fermentation as the major m

32 rted to diols including 1,3-propanediol, 1,4-butanediol, and 1,5-pentanediol.

33 on of a metabolic sink, such as sucrose, 2,3-butanediol, and 2-phenyl ethanol, in cyanobacteria impro

34 olic pathway, 3) a catabolic pathway for 2,3-butanediol, and 4) an antimicrobial resistance to ampici

35 o generate strain designs for succinate, 2,3-butanediol, and ethanol overproduction in yeast, which p

36 anol and ethyl propanoate; peak 3, (R,R)-2,3-butanediol, and peak 4, nonanoic acid.

37 hesis of butadiene from ethanol, butanol and butanediols, and (iii) the catalytic synthesis of HMF an

38 The health risks of 1,4-butanediol are similar to those of its counterparts, gam

39 ic acid derivative Bis-O-dihydroferuloyl-1,4-butanediol (BDF) was used as an active additive (up to 4

40 lls) to biofuels like isopropanol (IPA), 2,3-butanediol (BDO), C(11)-C(15) methyl ketones (MKs), and

41 DNA-DNA cross-links, 1,4-bis-(guan-7-yl)-2,3-butanediol (bis-N7G-BD) and 1-(guan-7-yl)-4-(aden-1-yl)-

42 which can then form 1,4-bis-(guan-7-yl)-2,3-butanediol (bis-N7G-BD) lesions.

43 DNA conjugates, e.g. 1,4-bis-(guan-7-yl)-2,3-butanediol (bis-N7G-BD), 1-(guan-7-yl)-4-(aden-1-yl)-2,3

44 , EgO(2), 1; 1,2-propanediol, PrO(2), 2; 1,2-butanediol, BuO(2), 3; 1,2-pentanediol, PeO(2), 4; glyce

45 ), thus increasing glucose conversion to 2,3-butanediol by more than 600-fold.

46 inor pathway to an industrial precursor (2,3-butanediol) can thus be designed.

47 er system; the addition of water reduces the butanediol concentration, inducing the formation of a di

48 the 1,4-bis(2'-deoxyadenosin-N(6)-yl)-2R,3R-butanediol cross-link arising from N(6)-dA alkylation of

49 etics of formate dehydrogenase (FDH) and 2,3-butanediol dehydrogenase (BDH) through the use of time-c

50 determine whether the ketone ester, R, S-1,3-butanediol diacetoacetate (BD-AcAc(2)), increases energy

51 Dietary R, S-1,3-butanediol diacetoacetate reduces body weight and adipos

52 zirconia particles and cross-linked with 1,4-butanediol diglycidyl ether (BUDGE).

53 ane (HAM) by chemical crosslinking using 1,4-butanediol diglycidyl ether for the effective treatment

54 radiolytic markers and isomerisation of 2,3-butanediol during irradiation of food.

55 hermore, pharmacological applications of 2,3-butanediol enhanced plant growth whereas bacterial mutan

56 (including tyrosol, phenylethyl alcohol, 2,3-butanediol, erythritol, tryptophol, putrescine, cadaveri

57 Peak area RSDs were 2-7% for 2, 3-butanediol, ethanol, glycerol, erythritol, rhamnose, ara

58 cohol esters, namely 3-methyl-1-butanol, 2,3-butanediol, ethyl lactate, 3-methyl-1-butyl acetate, 2-p

59 dicated that B. subtilis grows by mixed acid-butanediol fermentation but that no formate is produced.

60 ma-hydroxybutyrate; gamma-butyrolactone, 1,4-butanediol, flunitrazepam, ketamine, and nitrites.

61 ionally produced pseudo-enantiomerism in 1,3-butanediol generates a chiral response in the frontier e

62 Novel compounds, 2,3-butanediol glycosides, were identified in almond milk.

63 cis-1,2-cyclopentanediol > 2,3-dimethyl-2,3-butanediol > 1,2-propanediol.

64 norbornene-2,2-dimethanol > 3,3-dimethyl-1,2-butanediol > cis-1,2-cyclopentanediol > 2,3-dimethyl-2,3

65 configurational enantiomers of 1,3- and 2,3-butanediols has been examined with a focus on the large

66 Multivariate data analyses revealed that 2,3-butanediol, hexanal, hexanol and cinnamaldehyde contribu

67 ble these enzymes to produce stereo-pure 2,3-butanediol in cell-free systems and in Escherichia coli,

68 del, we explore conversion of glucose to 2,3-butanediol in extracts from flux-enhanced Saccharomyces

69 yst, does not explain the dehydration of 1,4-butanediol in HTW without catalyst.

70 The doses of 1,4-butanediol ingested ranged from 5.4 to 20 g in the patie

71 we identified cases of toxic effects of 1,4-butanediol involving patients who presented to our emerg

72 1,4-Butanediol is an industrial solvent that, when ingested,

73 cals such as n-butanol, 1,3-propanediol, 1,3-butanediol, isopropanol, and butyrate.

74 -furanacrylic acids (monomer II), with a 1,4-butanediol linker.

75 caused by metabolites such as glycerol, 2,3-butanediol, malic acid, alpha/beta-glucose and phenolic

76 eucine, isoleucine and alanine, and also 2,3-butanediol, methanol, glycerol and isotopic variables we

77 arch, palm oil, or R-3-hydroxybutyrate-R-1,3-butanediol monoester (3HB-BD ester).

78 ially available beta-hydroxybutyrate-(R)-1,3-butanediol monoester (DeltaG; KE-2) diet.

79 ercially available B-hydroxybutyrate-(R)-1,3-butanediol monoester (DeltaG; KE-2) diet.

80 diet in which D-beta-hydroxybutyrate-(R)-1,3 butanediol monoester [ketone ester (KE)] replaced equica

81 The dietary R-3-hydroxybutyrate- R-1,3-butanediol monoester increases resting energy expenditur

82 engineering to produce chemicals such as 2,3-butanediol, N-acetylneuraminic acid, and n-butanol using

83 bis-N7G-BD), 1-(guan-7-yl)-4-(aden-1-yl)-2,3-butanediol (N7G-N1A-BD), and 1,N(6)-(1-hydroxymethyl-2-h

84 -N7G-BD) and 1-(guan-7-yl)-4-(aden-1-yl)-2,3-butanediol (N7G-N1A-BD).

85 omatography-mass spectrometry to measure 1,4-butanediol or its metabolite, gamma-hydroxybutyrate, in

86 e dehydrogenase, pyruvate formate-lyase, and butanediol pathways.

87 e regulation enables carbon fixation and 2,3-butanediol production in the absence of light.

88 -butene-1,2-diol metabolism to 3,4-epoxy-1,2-butanediol, rather than from 1,2;3,4-diepoxybutane.

89 fects in eight patients who had ingested 1,4-butanediol recreationally, to enhance bodybuilding, or t

90 Optimized cyclic ketogenic diet and 1,3-butanediol supplementation regimens enhance the efficacy

91 An N16961 mutant (SSY01) defective in 2,3-butanediol synthesis showed the same defect in growth th

92 tion environment significantly increases 2,3-butanediol titers and volumetric productivities, reachin

93 the chemocatalytic conversion of ethanol and butanediols to butadiene, including thermodynamics and k

94 -2-butene-1,4-diol to form n-butanol and 1,4-butanediol, to quantify the concentration of solvated H(

95 hanism of tetrahydrofuran synthesis from 1,4-butanediol via dehydration in high-temperature liquid wa

96 emic mixture of (RR) and (SS) isomers of 2,3-butanediol was found to trigger ISR and transgenic lines

97 The L(3) phase was the monoolein/butanediol/water system; the addition of water reduces t

98 (R,R) and (S,S)-2,3-butanediol were detected in samples irradiated at 8 kGy,

99 ycerol, tartaric acid, succinic acid and 2,3-butanediol were greater in December, while proline and l

100 cyclic dimer [AA-BD](2) (AA:adipic acid, BD:butanediol), were detected only by APGC-MS.

101 nd glucose, and produces 12.6 g l(-1) of 2,3-butanediol with a rate of 1.1 g l(-1) d(-1) under contin

102 to the phosphorus atom and obtained from d,l-butanediol, with hexafluoroacetone (CCl4, -40 degrees C)

103 treatment (25 g D-B-hydroxybutyrate-(R)-1,3-butanediol x 4 daily) and isocaloric and isovolumic plac

104 -propanediol, 1,3-propanediol, glycerol, 1,4-butanediol, xylitol, and sorbitol), furanoids (furfural