ライフサイエンスコーパス: mannanase

1 firming functionality of chloroplast-derived mannanase.

2 ents from pinewood than the cocktail without mannanase.

3 proposal based on comparing alpha- and beta-mannanases.

4 lti-enzymatic system containing (U/gds) beta-mannanase (1021), endo-xylanase (1 9 1), alpha-galactosi

5 he 25 enzymes, 10 cellulases, 4 xylanases, 3 mannanases, 2 xyloglucanases, 2 arabinofuranosidases, 2

6 Mannanase A (MANA) from Pseudomonas fluorescens, a membe

7 apparent loss of carboxymethyl cellulase and mannanase activities.

8 Man5B exhibited endo-1,4-beta-mannanase activity and little endo-1,4-beta-glucanase ac

9 strongly suggesting that dual endoglucanase-mannanase activity is widespread in this family.

10 Endo-beta-mannanase activity was present in discharged pollen, whi

11 s, the highest mRNA expression and endo-beta-mannanase activity were detected during late stages of a

12 LeMAN2 mRNA accumulation and mannanase activity were induced by gibberellin in gibber

13 i-mannanase antibody and exhibited endo-beta-mannanase activity, confirming the identity of the gene.

14 plants, charophytes possess high trans-B-1,4-mannanase activity, suggesting that land plants' algal a

15 ase, beta-D-mannosidase, endo-(1-->4)-beta-D-mannanase, alpha-D-xylosidase, beta-D-galactosidase, alp

16 des containing mannan requires endo-1,4-beta-mannanase and 1,4-beta-mannosidase activities.

17 perties and crystal structures of both a GH5 mannanase and a GH26 mannanase and describe the contribu

18 tructures of both a GH5 mannanase and a GH26 mannanase and describe the contributions to substrate sp

19 he Man5A derivatives displayed endo-1,4-beta-mannanase and endo-1,4-beta-glucanase activities and hyd

20 We conclude that trans-B-mannanase and trans-B-xylanase activities are present an

21 city to enhance the activity of GH5 and GH26 mannanases and CE2 esterases against intact plant cell w

22 Cellulases, hemicellulases including mannanases and other accessory enzymes are required for

23 bitors, their binding to GH99 endo-alpha-1,2-mannanases, and their structural analysis by X-ray cryst

24 ncoded by LeMAN2 cDNA was recognized by anti-mannanase antibody and exhibited endo-beta-mannanase act

25 n, however, was fully accessible to the GH26 mannanase appended to a cellulose binding CBM.

26 A, FBPase, limEH, Chitinase, rgl, rgh, rgaE, mannanase, ara) and nitrogen (ureC, nasA, narB, narG, ni

27 ferent electrophoretic isoforms of endo-beta-mannanase are expressed sequentially in different parts

28 Distinct mannanases are involved in germination and post-germinat

29 Endo-arabinanase- and endo-mannanase-assisted extraction is an effective method of

30 restricted by galactose side-groups than the mannanase BoMan26A of the same locus.

31 ydrolyzed into mainly mannobiose by the beta-mannanase BoMan26A.

32 wo glycoside hydrolase family 26 (GH26) beta-mannanases, BoMan26A and BoMan26B, and a GH36 alpha-gala

33 1 subsites, while the GH26 Bacillus subtilis mannanase, BsMan26A, displays tight specificity for mann

34 it can be hypothesized that the evaluated B-mannanase can degrade the enclosing matrix of encapsulat

35 Microbial mannanases can be used to break down mannan rich agro-re

36 beta-mannanase catalyzes endo-hydrolysis of the mannan backbo

37 r domains in the following order: a putative mannanase-cellulase catalytic domain, cellulose binding

38 ous studies on the Cellvibrio japonicus GH26 mannanases CjMan26A and CjMan26C reveals that the tighte

39 quential enzyme treatments with an endo-beta-mannanase confirmed the presence of cryptic epitopes and

40 that, high purity endo-arabinanase and endo-mannanase could be useful in the isolation of pectin of

41 interact with mannopentaose are conserved in mannanase-derived CBM35s, which will guide specificity p

42 n I with the catalytic core domain of a beta-mannanase (EC 3.2.1.78 or Man5A) from Trichoderma reesei

43 Endo-beta-mannanase (EC 3.2.1.78) is involved in cell wall disasse

44 Endo-beta-mannanase (EC 3.2.1.78) is involved in hydrolysis of the

45 Aspergillus quadrilineatus endo-beta-mannanase effectively degraded konjac glucomannan (66.09

46 Aspergillus quadrilineatus endo-B-mannanase effectively degraded konjac glucomannan (66.09

47 age-specific antisera and an endo-alpha1,6-D-mannanase (endoM) were used to quantitate the amount of

48 Endo-beta(1 -> 4)-mannanases (endomannanases) catalyse degradation of beta

49 Endo-beta-mannanase expression levels reached up to 25 units per g

50 Expression of endo-beta-mannanase for the first time in plants facilitated its c

51 nding domain components of the highly active mannanase from the thermophile Thermoanaerobacterium pol

52 (PaMan5A) and GH26 (PaMan26A) endo-beta-1,4-mannanases from the coprophilic ascomycete Podospora ans

53 beta-Mannanases from the glycoside hydrolase 26 (GH26) family

54 A novel endo-beta-mannanase gene (termed LeMAN5) was found in the tomato g

55 eing an extremely active enzyme, is the only mannanase gene cloned which shows this domain structure.

56 The 5'-upstream region of this endo-beta-mannanase gene contained four copies of the pollen-speci

57 As a result, a mannanase gene, manA, has been found downstream of engL.

58 Endo-beta-mannanase genes are expressed in tomato (Lycopersicon es

59 d using a recombinantly expressed endo-alpha-mannanase (GH76) from Salegentibacter sp. Hel_I_6.

60 Chloroplast-derived mannanase had higher temperature stability (40 degrees C

61 alpha-Mannosidases and alpha-mannanases have attracted attention for the insight they

62 Hydrolytic enzymes such as endo-beta-1,4-mannanases have recently been involved in a wide range o

63 labeling of newly formed reducing ends of B-mannanase-hydrolyzed polysaccharides after the native re

64 These data suggest that the mannanase hydrolyzes mannooligosaccharides by a double-d

65 ymatic fingerprinting method using endo-beta-mannanase, in addition to being used to differentiate be

66 The mechanism of endo-beta-mannanase induction by GA was also investigated using is

67 results demonstrate that chloroplast-derived mannanase is an important component of enzymatic cocktai

68 These data suggest that the LeMAN5 endo-beta-mannanase is associated with anther and pollen developme

69 The known endosperm cap enzyme endo-beta-mannanase is induced by gibberellin (GA), which is thoug

70 It was revealed that B-mannanase is not only active at the cell wall but also a

71 on of Man- and Glc-configured sugars by beta-mannanases is discussed.

72 ce similarity with a post-germinative tomato mannanase (LeMAN1).

73 beta-Mannanases, located in glycoside hydrolase (GH) families

74 biochemical properties of two endo-beta-1,4-mannanases (Man5A and Man5B) from Caldanaerobius polysac

75 rived from the Cellvibrio japonicus beta-1,4-mannanase Man5C.

76 xgS, several endoglucanases of family 9, the mannanase ManA, and the hydrophobic protein HbpA contain

77 do-alpha-1,2-mannosidases and endo-alpha-1,2-mannanases, members of glycoside hydrolase family 99 (GH

78 Saccharophagus degradans produces an endo-B-mannanase of glycoside hydrolase family 5 subfamily 8 wi

79 In order to unravel the effect of B-mannanase on soybean meal's cell structure, a novel imag

80 Of the two beta-mannanases, only BoMan26B hydrolyzed galactoglucomannan.

81 HhMAN1 encodes a mannanase, representing a class of glycosyl hydrolases t

82 Gel diffusion assay for endo-beta-mannanase showed the zone of clearance confirming functi

83 rmational itinerary of the family GH76 alpha-mannanases studied through structural analysis of the Mi

84 d shows high sequence similarity with fungal mannanases, such as Agaricus bisporus Cel4 (17.3% identi

85 supplementation of exogenous enzymes, like B-mannanase, to soybean-based diets is beneficial to impro

86 Although the action of the GH5 mannanase was independent of the context of mannan in to

87 In this study, the man1 gene encoding beta-mannanase was isolated from Trichoderma reesei and expre

88 cal properties of the two characterized beta-mannanases, we propose a scheme of sequential action by

89 In this study, P. anserina mannanases were further subjected to detailed comparativ

90 Chloroplast-derived mannanase when added to the enzyme cocktail containing a

91 isualizing the spatial activity pattern of B-mannanase with high sensitivity by fluorescence microsco