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

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

6 apparent loss of carboxymethyl cellulase and mannanase activities.

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

24 Distinct mannanases are involved in germination and post-germinat

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

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

27 1 subsites, while the GH26 Bacillus subtilis mannanase, BsMan26A, displays tight specificity for mann

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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

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