ライフサイエンスコーパス: galacturonic acid

1 ent of WSP is about 95.5% including 34.4% of Galacturonic acid.

2 ts in the synthesis of xyloglucan that lacks galacturonic acid.

3 cids, lacks phosphate, and contains a single galacturonic acid.

4 g a polymer of 2,3-diacetamido-2,3-dideoxy-l-galacturonic acid.

5 tle leaves and cell walls of leaves had less galacturonic acid.

6 ulosonic acid (Kdo), mannose, galactose, and galacturonic acid.

7 lpha-d-galacturonic acid (d-GalA) to alpha-d-galacturonic acid-1-phosphate (GalA-1-P).

8 unique Arabidopsis gene encoding an alpha-d-galacturonic acid-1-phosphate kinase (GalAK) and compare

9 Glucose, galacturonic acid, alpha-ketoglutarate, pyruvate, acetoi

10 omponent, with low levels of glucosamine and galacturonic acid also present.

11 soluble fibre (SDF) was composed of glucose, galacturonic acid and arabinose; for amaranth, xylose wa

12 precursor UDP-2,3-diacetamido-2,3-dideoxy-l-galacturonic acid and illustrate the usefulness of struc

13 The DASS fraction contained less galacturonic acid and more neutral sugars than ChSS.

14 ex free oligosaccharides, composed mainly of galacturonic acid and N-acetylgalactosamine, were charac

15 After hydrolysis, the contents of galacturonic acid and neutral sugars were measured by HP

16 from the atgatl5-1 mutant demonstrated that galacturonic acid and rhamnose contents are decreased si

17 alleles, a tight proportionality of xylose, galacturonic acid, and rhamnose was evidenced, except fo

18 m quinoa and amaranth was mainly composed of galacturonic acid, arabinose, galactose, xylose and gluc

19 turonan, indicating that the carboxylates of galacturonic acid are key specificity determinants.

20 network with mannose (Man), myoinositol, and galacturonic acid as principal entry points.

21 d cannot utilize UDP-glucuronic acid and UDP-galacturonic acid as substrates.

22 e galactosyl residue, another that lacks the galacturonic acid attached to O-5 of Kdo, and a third th

23 mogalacturonan component of pectin, exposing galacturonic acids, can occur processively or non-proces

24 ng doses of a bacteria-derived weak agonist, galacturonic acid-containing glycosphingolipid, or a syn

25 oglucan that is composed of both neutral and galacturonic acid-containing subunits, the latter contai

26 ression of At1g63450 led to the synthesis of galacturonic acid-containing xyloglucan in these tissues

27 Pectins isolated from MHF were higher in galacturonic acid content (52-59% w/w) and weight-averag

28 the yield, degree of methoxylation (DM) and galacturonic acid content (GA) of pectins extracted from

29 lter the chemical structure of WSP, in which Galacturonic acid content and yield are 34.4% and 4.33%,

30 yzes the ATP-dependent conversion of alpha-d-galacturonic acid (d-GalA) to alpha-d-galacturonic acid-

31 educing (distal) GlcpN3N, and one residue of galacturonic acid (d-GalpA) alpha-(1-->1)-linked to the

32 inase activity toward sugars as diverse as d-galacturonic acid, d-talose, l-altrose, and l-glucose, a

33 The ChSS pectin consisted mainly of galacturonic acid followed by arabinose and galactose.

34 on graph for determination of non-esterified galacturonic acid (GalA) content in pectin solutions wit

35 Extraction yield, galacturonic acid (GalA) content, average molecular weig

36 Galacturonic acid (GalA) is a major component of plant c

37 aride, the inner core is modified with three galacturonic acid (GalA) moieties, two on the distal 3-d

38 eguminosarum lipopolysaccharide contain four galacturonic acid (GalA) residues.

39 haride (LPS) contains four terminally linked galacturonic acid (GalA) residues; one attached to the l

40 ld, protein, ash, non-starch polysaccharide, galacturonic acid (GalA), neutral sugar composition, mol

41 d plant cell wall polysaccharides containing galacturonic acid (GalA).

42 r, they are derivatized with an alpha-linked galacturonic acid group at position 4', as shown by nucl

43 This mutant phenotype and the absence of galacturonic acid in the root xyloglucan are complemente

44 of the proximal glucosamine 1-phosphate, and galacturonic acid instead of the 4'-phosphate.

45 or sucrose was normal, growth on galactose, galacturonic acid, maltose, or xylose was somewhat reduc

46 the presence of an unusual C28 acyl chain, a galacturonic acid moiety at position 4', and an acylated

47 hydrolysis of pectin, starch and xyloglucan; galacturonic acid oligomers, glucose oligomers (e.g., ma

48 rs to be predominant in leaf tissue, but a D-galacturonic acid pathway operates in developing fruits.

49 Eighty-nine percent of the galacturonic acid present in the segment membranes was r

50 cleaves at a single position of the 4-linked galacturonic acid producing an unsaturated sugar product

51 reproducibility and allowed for glucose and galacturonic acid quantification.

52 ied the Arabinose/Galactose and the Rhamnose/Galacturonic acid ratios in Canada Judio and Albatana te

53 ised of a diacylated glucosamine moiety with galacturonic acid residue at position 4' and a secondary

54 A lacks phosphate groups, but it contains a galacturonic acid residue at the 4'-position and an amin

55 upled to the anomeric carbon of the reducing galacturonic acid residue by a hydrazone linkage.

56 with a backbone of alternating rhamnose and galacturonic acid residues and side chains that include

57 We established that more than seven galacturonic acid residues in the HG chain are required

58 he hydrolysis of methylester groups from the galacturonic acid residues of homogalacturonan chains, t

59 the OGA mobility relies on the charge of the galacturonic acid residues.

60 saccharides, followed by arabinose, glucose, galacturonic acid, rhamnose, mannose, xylose and traces

61 f all land plants and encompasses a range of galacturonic acid-rich polysaccharides.

62 '-phosphate groups but is derivatized with a galacturonic acid substituent at position 4'.

63 ro-D-galactose, 6-O-methyl-D-galactose, or D-galacturonic acid, suggesting that the C-6 OH is an esse

64 UDP-D-galacturonic acid, the key building block of pectins, is

65 opolygalacturonase treatment to mono- and di-galacturonic acid, thereby showing that GalAT synthesize

66 onate dehydrogenase (At Udh) that oxidizes D-galacturonic acid to D-galactarolactone.

67 we also engineered E. coli to synthesize UDP-galacturonic acid (UDP-GalA) and UDP-galactose (UDP-Gal)

68 olgi apparatus, where it is converted to UDP-galacturonic acid (UDP-GalA), UDP-arabinose, and UDP-xyl

69 -D-glucuronic acid (UDP-GlcA) to UDP-alpha-D-galacturonic acid (UDP-GalA).

70 ion/hydrogenolysis caused by the presence of galacturonic acid were overcome by protecting the acid w

71 ligogalacturonides (oligomers of alpha-1,4-D-galacturonic acid) with degrees of polymerization (DP) b

72 The yield of galacturonic acid (YGA), which took into account both th