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  Afr. J. Biotechnol.

  Vol. 8 No. 22

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  Simoes MLG
  Tapia TDM

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African Journal of Biotechnology Vol. 8 (22), pp. 6317-6326, 16 November 2009

ISSN 1684-5315  © 2009 Academic Journals  

 

 

Full Length Research Paper

 

Screening of culture condition for xylanase production by filamentous fungi

 

Maria Lúcia Garcia Simőes1*, Samia Maria Tauk-Tornisielo2 and Daniel Mario Tapia Tapia1

 

1Universidade Estadual do Sudoeste da Bahia, Km 4, Vitória da Conquista, Bahia, CEP 45050-020, Brazil.

2Centro de Estudos Ambientais, Universidade Estadual Paulista, Avenida 24-A, 1515, Bairro Bela Vista, Rio Claro, SP 13506-900, Brazil.

 

*Corresponding author. E-mail: marialuciags@ig.com.br. Tel: (55) 77-3424-6513.

 

Accepted 25 June, 2008

 

   Abstract

 

The objective of this research was to investigate xylanase production by filamentous fungi (Trichoderma viride) to determine the best cultivation conditions in the process, aiming toward optimization of enzyme production. The best temperature, as well as the best carbon source, for biomass production was determined through an automated turbidimetric method (Bioscreen-C). The enzyme activity of this fungus was separately evaluated in two solid substrates (wheat and soybean bran) and in Vogel medium, pure and by adding other carbon sources. Temperature effects, cultivation time, and spore concentrations were also tested. The best temperature and carbon source for enzyme and biomass production was 25°C and sorbitol, respectively. Maximum xylanase activity was achieved when the fungus was cultivated in wheat bran along with sorbitol (1%, w/v), using a spore concentration of 2 x 106 spores.mL-1, pH 5.0, for 144 h cultivation. The study demonstrated not only the importance of the nature of the substrate in obtaining a system resistant to catabolic repression, but also the importance of the culture conditions for biosynthesis of this enzyme. T. viride showed a high potential for xylanase production under the conditions presented in these assays.

 

Key words: Trichoderma viride, xylanase activity, enzyme optimization.

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