SciELO - Scientific Electronic Library Online

 
vol.32 issue2Production of pectin lyase by Penicillium griseoroseum in bioreactors in the absence of inducerCharacterization of Aujeszky's disease virus isolates from South and Southeast Brazil by RFLP analysis author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

Share


Brazilian Journal of Microbiology

Print version ISSN 1517-8382On-line version ISSN 1678-4405

Braz. J. Microbiol. vol.32 no.2 São Paulo Apr./June 2001

http://dx.doi.org/10.1590/S1517-83822001000200014 

PRODUCTION OF  XYLAN-DEGRADING ENZYMES BY A TRICHODERMA HARZIANUM STRAIN

 

André O.Guerreiro Cacais; Fabiane Q. de Paula Silveira; Edivaldo Ximenes Ferreira Filho*

Laboratório de Enzimologia, Departamento de Biologia Celular, Universidade de Brasília, DF, Brasil

Submitted: January 19, 2001; Approved: May 28, 2001

 

 


SHORT COMMUNICATION


ABSTRACT

Trichoderma harzianum strain 4 produced extracellular xylan-degrading enzymes, namely b-xylanase, b-xylosidase and a-arabinofuranosidase, when grown in liquid medium cultures containing oat spelt xylan as inducer. Cellulase activity was not detected. The pattern of xylan-degrading enzymes induction was influenced by the form of xylan present in the medium. They were detected in different incubation periods. Electrophoretic separation of the proteins from liquid culture filtrates by SDS-PAGE showed a variety of bands with high and low molecular weights.

Key words: xylan, T. harzianum, xylanolytic activity


 

 

Xylans, the most abundant hemicelluloses, are comprised of D-xylopyranose units connected by b-1,4 linkages which may be linear or branched. Depending on the origin of the wood species, their degree of polymerization varies from 70 to 130 (softwood xylans) and 150 to 200 (hardwood xylans) (15). O-Acetyl-4-O-methylglucuronoxylan and arabino-4-O-metheylglucuronoxylan are the main hemicelluloses in hardwood and softwood, respectively. The latter one comprises about one-third of the total hemicelluloses (15). Xylans vary in solubility and may be isolated into water-soluble or –insoluble fractions (8). b-D-Xylanase and b-D-xylosidase are involved in the breaking down of xylan backbone to xylooligosaccharides (1,6). Additional enzymes, such as acetyl xylan esterase and a-L-arabinofuranosidase, are required to remove side-chain substituents that are attached at various points on xylan, creating more sites for subsequent enzymic hydrolysis (2,6).

Selected strains from the soft-rot fungus Trichoderma have been shown to be efficient producers of xylan-degrading enzyme activity (13,17). In this work, we report the production of xylan-degrading enzymes obtained from liquid state cultures of Trichoderma harzianum strain 4 when grown on medium containing xylans from oat spelt as substrates.

T. harzianum strain 4 was kindly provided by I. S. Melo (National Research Center for Monitoring and Environmental Impact Assessment - Brazil). For xylan-degrading enzyme production, spore suspension from 7 days routine subculture was used to inoculate a liquid medium containing 0.5% xylan suplemented with KH2PO4, 0.7%; K2HPO4, 0.2%; MgSO4.7H2O, 0.05%; (NH4)2SO4, 0.1% and yeast extract, 0.06% at pH 7.0. The cultivation was carried out for 5 days in 1000 ml Erlenmeyer flasks at 28ºC and 100 rpm. Aliquots were harvested every 6 h during 5 days, and used to estimate xylan-degrading enzyme activities. Soluble and insoluble xylan fractions from oat spelt were prepared as described elsewhere (5). All results represent the mean of three separate experiments. Cellulase, b-xylanase, b-xylosidase and a-arabinofuranosidase activities were determined as reported elsewhere (13). Sodium dodecyl sulphate polyacrylamide gel electrophoresis (SDS-PAGE) was performed on a 10% acrylamide gel (10). After electrophoresis, protein bands were revealed by silver staining (3). Molecular weight standards from Sigma (USA) were used as size markers.

A comparison was made of the activity of xylan-degrading enzymes from T. harzianum strain 4 during growth on different xylan preparations (results not shown). The carbon sources included oat spelt xylan and its soluble and insoluble fractions. The fungus did not produce cellulase activity, suggesting that the production of cellulolytic and xylanolytic enzymes is under separate regulatory control (2). The inductive effect of xylan substrates it seems to depend on their chemical composition and structure (12). The induction profile after growth on insoluble fraction of oat spelt xylan showed that the b-xylanase activity increased without a lag and was detected from the first hour to the end of cultivation period. The basal synthesis of b-xylanase suggests the production of a soluble fragment from xylan which penetrated the mycellium and effected induction of xylan-degrading enzymes (9). On the other hand, the time lag for induction of b-xylanase by both oat spelt xylans and its soluble fraction was about 10 h and thereafter the activity increased steadily and reached the highest value at 106 h of cultivation. Since the degree of substitution in xylan is directly proportional to solubility (8), this result suggest that the arabinose side-chains should be a obstacle for induction of b-xylanase activity. In this case, the synergistic action of a-arabinofuranosidase was required for the removal of arabinosyl groups from xylan (16). A low level of a-arabinofuranosidase activity was found since the early period of growth, reaching a maximum induction at 76 h of cultivation.

The growth profile on all xylan preparations was accompanied by more than two peaks of xylanase activity (results not shown). The multiplicity of forms is commonly described for b-xylanases from fungi and bacteria as result of differential mRNA processing and posttranslational modifications (4,14). Since all xylosidic linkages are not equivalent and equally accessible in xylan molecule, its catalytic cleavage requires the action of multiple forms of xylan-degrading enzyme systems (4). b-Xylosidase activity was only expressed at 52 h of cultivation in all xylan-containing media. Xylan was probably converted into small xylooligosaccharides by b-xylanases which were then further hydrolysed by b-xylosidase into xylose units (7).

SDS-PAGE analysis was performed on the crude extracts from inducing media. Fig. 1 shows the results of SDS-PAGE of the crude extract from oat spelt xylan medium. The number of protein bands suggests the effects of the inducers on the synthesis of multiple forms of xylan-degrading enzymes. The zymogram technique (11) will be necessary for identification and preliminary characterization of the multiple forms of xylanase activity. Proteins bands began to be detected at 34 h of cultivation period. A strong protein band with molecular weight value of about 24 kDa was observed at the incubation range of 46-118 h. After 34 h of cultivation was visualized a protein band with high molecular weight size. In the above culture, a xylanase activity peak was found at cultivation period of 10-34 h. The same result was found for the inducing medium containing soluble xylan fraction. In this case, protein bands were detected after 22 h of cultivation. In contrast to the above results, protein bands from crude extract of growth culture containing insoluble xylan fraction as carbon source were detected in the early stage of growth. It is noteworthy that the above 24 kDa protein band was also strongly detected at 70 h of cultivation. A protein band with high molecular weight size was also revealed at the same period.

 

 

In conclusion, T. harzianum strain 4 secretes a very active xylanolytic system with no cellulase activity when grown in liquid media containing different xylan forms as the carbon source. This is advantageous considering exploitation of the above fungus in biopulping and preparation of modified hemicellulose (14). Further work will be required to determine the role of these various forms of xylan-degrading activities on the mechanisms of hydrolysis of the substrate.

 

ACKNOWLEDGEMENTS

This work was supported by research grants PADCT III (Brazil) and FAPDF (Brazil). E.X.F.F. acknowledges receipt of a research fellowship from CNPq (Brazil).

 

 

RESUMO

Produção de enzimas xilanolíticas por uma cepa de Trichoderma harzianum

O fungo Trichoderma harzianum linhagem 4 produziu, enzimas xilanolíticas quando crescido em meios de cultura líquido contendo xilana como indutor. Atividade celulolítica não foi detectada. O tipo de xilana presente no meio de cultura influenciou a indução das enzimas xilanolíticas. As enzimas foram detectadas em diferentes períodos de incubação. SDS-PAGE de amostras de meios de cultura apresentou uma variedade de bandas protéicas com alto e baixo pesos moleculares.

Palavras-chave: xilana, T. harzianum, atividade xilanolítica

 

 

REFERENCES

1. Bajpai, P. Microbial xylanolytic enzyme system: properties and applications. Adv. Appl. Microbiol., 43:141-194, 1997.         [ Links ]

2. Biely, P. Biochemical aspects of the production of microbial hemicellulases. In: Coughlan, M.P.; Hazlewood, G.P. (Eds). Hemicellulose and hemicellulases, Portland Press, London, 1993, p.127-143.         [ Links ]

3. Blum, H.; Beier, H.; Gross, B. Improved silver staining of plant proteins, RNA, and DNA in polyacrylamide gels. Electrophoresis, 8:93-99, 1987.         [ Links ]

4. Breccia, J.D.; Sineriz, F.; Baigorí, M.D.; Castro, G.R.; Hatti-Kaul, R. Purification and characterization of a thermostable xylanase from Bacillus amyloliquefaciens. Enzyme Microb. Technol., 22:42-49, 1998.         [ Links ]

5. Filho, E.X.F.; Puls, J.; Coughlan, M.P. Biochemical characteristics of two endo-b-1,4-xylanases produced by Penicillium capsulatum. J. Ind. Microbiol., 11:171-180, 1993.         [ Links ]

6. Filho, E.X.F. The xylan-degrading enzyme suystem. Brazilian J. Med. Biol. Res., 27:1093-1109, 1994.         [ Links ]

7. Ghosh, M.; Das, A.; Mishra, A.K.; Nanda, G. Aspergillus sydowii MG 49 is a strong producer of thermostable xylanolytic enzymes. Enzyme Microb. Technol., 15:703-709, 1993.         [ Links ]

8. He, L.; Bickerstaff, G.F.; Paterson, A.; Buswell, J.A. Evaluation of catalytic activity and synergism between two xylanase isoenzymes in enzymic hydrolysis of two separate xylans in different states of solubility. Enzyme Microb. Technol., 16:696-702, 1994.         [ Links ]

9. Kyu, K.L.; Ratanakhanokchai, K.; Uttapap, D.; Tanticharoen, M. Induction of xylanase in Bacillus circulans B6. Biores. Technol., 48:163-167, 1994.         [ Links ]

10. Laemmli, U.K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature, 227:680-685, 1970.         [ Links ]

11. Lee, Y-E.; Lowe, S.E.; Zeikus, J.G. Regulation and characterization of xylanolytic enzymes of Thermoanaerobacterium saccharolyticum B6A-RI. Appl. Environ. Microbiol., 59:763-771, 1993.         [ Links ]

12. Saraswat, V.; Bisaria, V. Biosynthesis of xylanolytic and xylan-debranching enzymes in Melanocarpus albomyces IIS 68. J. Ferment. Bioeng., 83:352-357, 1997.         [ Links ]

13. Silveira, F.Q.P.; Melo, I.S.; Filho, E.X.F. Carbohydrate -hydrolysing enzyme activity production by solid-state cultures of Trichoderma harzianum strains. Rev. Microbiol., 28:1-5, 1997.         [ Links ]

14. Tuohy, M.G.; Coughlan, M.P. Production of thermostable xylan-degrading enzymes by Talaromyces emersonii. Biores. Technol., 39:131-137, 1992.         [ Links ]

15. Viikari, L.; Kantelinen, A.; Sundquist, J.; Linko, M. Xylanases in bleaching: From an idea to the industry. FEMS Microbiol. Rev., 13:335-350, 1994.         [ Links ]

16. Ximenes, F.A.; Sousa, M.V.; Puls, J.; Silva-Jr., F.G., Filho, E.X.F. Purification and characterization of a low-molecular weight xylanase produced by Acrophialophora nainiana. Curr. Microbiol., 38:18-21, 1999.         [ Links ]

17. Wong, K.Y.; Saddler, J.N. Trichoderma xylanases, their properties and applications. In: Visser, J.V.; Beldman, G., Kusters-Van-Someren, M.A.; Voragen, A.G.J. Xylan and xylanases, Elsevier Science Publishers, Amsterdam, 1992, p.171-186.         [ Links ]

 

 

* Corresponding author. Mailing address: Laboratório de Enzimologia, Departamento de Biologia Celular, Universidade de Brasília,. 70910-900, Brasília, DF, Brasil. Fax: (+5561) 273-4608. E-mail: eximenes@unb.br

Creative Commons License All the contents of this journal, except where otherwise noted, is licensed under a Creative Commons Attribution License