Production of chitinolytic enzymes with Trichoderma longibrachiatum IMI 92027 in solid substrate fermentation |
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Authors: | Krisztina Kovacs Gyorgy Szakacs Tunde Pusztahelyi Ashok Pandey |
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Affiliation: | (1) Department of Agricultural Chemical Technology, Budapest University of Technology and Economics, Gellert ter 4, 1111 Budapest, Hungary;(2) Department of Microbiology & Biotechnology, Faculty of Science, University of Debrecen, Egyetem ter 1, 4010 Debrecen, Hungary;(3) Biotechnology Division, Regional Research Laboratory, CSIR, 695 019 Trivandrum, India |
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Abstract: | Thirty Trichoderma strains representing 15 species within the genus were screened for extracellular production of chitinolytic enzymes in solid substrate fermentation. Trichoderma longibrachiatum IMI 92027 (ATCC 36838) gave the highest yield (5.0 IU/g of dry matter of substrate) after 3 d of fermentation on wheat bran-crude chitin (9:1 mixture) medium. The optimal moisture content (66.7%), chitin content (20%), initial pH of the medium (2.0–5.0), and time course (5 d) of solid substrate fermentation were determined for strain IMI 92027. Cellulase, xylanase, α-amylase, and β-xylosidase activities were also detected. The pH and temperature optima of the chitinase complex of T. longibrachiatum IMI 92027 were 4.5 and 55°C, respectively. The enzyme totally lost its activity at 70°C in 5 min in the absence of the substrate but retained about 15% of its initial activity even at 70°C after a 60-min incubation in the presence of solid substrate fermentation solids. Purification of protein extract from the solid substrate fermentation material revealed high chitinolytic activities between pI 5.9 and 4.8, where N-acetyl-β-d-hexosaminidase and chitinase peaks have been found in the same pI range. Two chitinases of 43.5 and 30 kDa were purified at acidic pI. |
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Keywords: | Chitinase chitinolytic enzymes N-acetyl-β - font-variant:small-caps" >d-hexosaminidase solid substrate fermentation solid-state fermentation Trichoderma longibrachiatum |
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