Literature DB >> 2317193

Study of the mode of action and site-specificity of the endo-(1----4)-beta-D-glucanases of the fungus Penicillium pinophilum with normal, 1-3H-labelled, reduced and chromogenic cello-oligosaccharides.

K M Bhat1, A J Hay, M Claeyssens, T M Wood.   

Abstract

The modes of action of the five major endo-(1----4)-beta-D-glucanases (I, II, III, IV and V) purified from Penicillium pinophilum cellulase were compared by h.p.l.c. analysis, with normal, 1-3H-labelled and reduced cello-oligosaccharides and 4-methylumbelliferyl glycosides as substrates. Significant differences were observed in the preferred site of cleavage even when substrates with the same number of glycosidic bonds were compared. Thus, although endoglucanase I was unable to attack normal cello-oligosaccharides shorter than degree of polymerization 6, it hydrolysed reduced cellopentaose to yield cellotriose and cellobi-itol, and it produced cellotriose and 4-methylumbelliferyl glucoside from 4-methylumbelliferyl cellotetraoside. Endoglucanase IV hydrolysed [1-3H]cellotriose but did not attack either cellotri-itol or 4-methylumbelliferyl cellobioside. These and other anomalous results indicated clearly that modification of the reducing glycosyl residue on the cello-oligosaccharides induces in an apparent change in the mode of action of the endoglucanases. It is suggested that, although cello-oligosaccharide derivatives are useful for differentiating and classifying endoglucanases, conclusions on the mechanism of cellulase action resulting from these measurements should be treated cautiously. Unequivocal information on the mode of endoglucanase action on cello-oligosaccharides was obtained with radiolabelled cello-oligosaccharides of degree of polymerization 3 to 5. Indications that transglycosylation was a property of the endoglucanases were particularly evident with the 4-methylumbelliferyl cello-oligosaccharides. Turnover numbers for hydrolysis of the umbelliferyl cello-oligosaccharides were calculated, and these, along with the other analytical data collected on the products of hydrolysis of the normal, reduced and radiolabelled cello-oligosaccharides, suggested that the various endoglucanases had different roles to play in the overall hydrolysis of cellulose to sugars small enough to be transported through the cell membrane.

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Year:  1990        PMID: 2317193      PMCID: PMC1131141          DOI: 10.1042/bj2660371

Source DB:  PubMed          Journal:  Biochem J        ISSN: 0264-6021            Impact factor:   3.857


  10 in total

1.  Extracellular enzyme system utilized by the fungus Sporotrichum pulverulentum (Chrysosporium lignorum) for the breakdown of cellulose. 1. Separation, purification and physico-chemical characterization of five endo-1,4-beta-glucanases.

Authors:  K E Eriksson; B Pettersson
Journal:  Eur J Biochem       Date:  1975-02-03

2.  The action pattern of Penicillium lilacinum dextranase.

Authors:  G J Walker; M D Dewar
Journal:  Carbohydr Res       Date:  1975-02       Impact factor: 2.104

3.  Two alternative HPLC separation methods for reduced and normal cellooligosaccharides.

Authors:  E K Gum; R D Brown
Journal:  Anal Biochem       Date:  1977-10       Impact factor: 3.365

4.  Isolation and characterization of the 1,4-beta-D-glucan glucanohydrolases of Talaromyces emersonii.

Authors:  A P Moloney; S I McCrae; T M Wood; M P Coughlan
Journal:  Biochem J       Date:  1985-01-15       Impact factor: 3.857

5.  Cellobiase from Trichoderma viride: purification, properties, kinetics, and mechanism.

Authors:  C S Gong; M R Ladisch; G T Tsao
Journal:  Biotechnol Bioeng       Date:  1977-07       Impact factor: 4.530

6.  Properties of cellulolytic enzyme systems.

Authors:  T M Wood
Journal:  Biochem Soc Trans       Date:  1985-04       Impact factor: 5.407

7.  The cellulase of Trichoderma koningii. Purification and properties of some endoglucanase components with special reference to their action on cellulose when acting alone and in synergism with the cellobiohydrolase.

Authors:  T M Wood; S I McCrae
Journal:  Biochem J       Date:  1978-04-01       Impact factor: 3.857

8.  The cellulase of Penicillium pinophilum. Synergism between enzyme components in solubilizing cellulose with special reference to the involvement of two immunologically distinct cellobiohydrolases.

Authors:  T M Wood; S I McCrae
Journal:  Biochem J       Date:  1986-02-15       Impact factor: 3.857

9.  Enzymic activities of endo-1,4-beta-D-glucanases purified from Trichoderma viride.

Authors:  S P Shoemaker; R D Brown
Journal:  Biochim Biophys Acta       Date:  1978-03-14

10.  EGIII, a new endoglucanase from Trichoderma reesei: the characterization of both gene and enzyme.

Authors:  M Saloheimo; P Lehtovaara; M Penttilä; T T Teeri; J Ståhlberg; G Johansson; G Pettersson; M Claeyssens; P Tomme; J K Knowles
Journal:  Gene       Date:  1988       Impact factor: 3.688

  10 in total
  9 in total

1.  Specificity mapping of cellulolytic enzymes: classification into families of structurally related proteins confirmed by biochemical analysis.

Authors:  M Claeyssens; B Henrissat
Journal:  Protein Sci       Date:  1992-10       Impact factor: 6.725

2.  Purification and characterization of an endoglucanase from Streptomyces lividans 66 and DNA sequence of the gene.

Authors:  M Théberge; P Lacaze; F Shareck; R Morosoli; D Kluepfel
Journal:  Appl Environ Microbiol       Date:  1992-03       Impact factor: 4.792

3.  Studies of the cellulolytic system of the filamentous fungus Trichoderma reesei QM 9414. Substrate specificity and transfer activity of endoglucanase I.

Authors:  M Claeyssens; H van Tilbeurgh; J P Kamerling; J Berg; M Vrsanska; P Biely
Journal:  Biochem J       Date:  1990-08-15       Impact factor: 3.857

4.  Characterization of CenC, an enzyme from Cellulomonas fimi with both endo- and exoglucanase activities.

Authors:  P Tomme; E Kwan; N R Gilkes; D G Kilburn; R A Warren
Journal:  J Bacteriol       Date:  1996-07       Impact factor: 3.490

5.  Biochemical characterization and mechanism of action of a thermostable beta-glucosidase purified from Thermoascus aurantiacus.

Authors:  N J Parry; D E Beever; E Owen; I Vandenberghe; J Van Beeumen ; M K Bhat
Journal:  Biochem J       Date:  2001-01-01       Impact factor: 3.857

6.  Purification, characterization, and molecular analysis of thermostable cellulases CelA and CelB from Thermotoga neapolitana.

Authors:  J D Bok; D A Yernool; D E Eveleigh
Journal:  Appl Environ Microbiol       Date:  1998-12       Impact factor: 4.792

7.  Mode of action of endoglucanase III from Trichoderma reesei.

Authors:  R Macarrón; C Acebal; M P Castillón; J M Domínguez; I de la Mata; G Pettersson; P Tomme; M Claeyssens
Journal:  Biochem J       Date:  1993-02-01       Impact factor: 3.857

8.  Mode of action, kinetic properties and physicochemical characterization of two different domains of a bifunctional (1-->4)-beta-D-xylanase from Ruminococcus flavefaciens expressed separately in Escherichia coli.

Authors:  V Garcia-Campayo; S I McCrae; J X Zhang; H J Flint; T M Wood
Journal:  Biochem J       Date:  1993-11-15       Impact factor: 3.857

9.  A novel automatable enzyme-coupled colorimetric assay for endo-1,4-β-glucanase (cellulase).

Authors:  David Mangan; Claudio Cornaggia; Vincent McKie; Tadas Kargelis; Barry V McCleary
Journal:  Anal Bioanal Chem       Date:  2016-04-06       Impact factor: 4.142

  9 in total

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