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Production of cellulolytic and xylanolytic enzymes by a
phytopathogenic Myrothecium roridum and some
avirulent fungal isolates from water hyacinth
Wahab Oluwanisola Okunowo1*, George Olabode
Gbenle1, Akinniyi Adediran Osuntoki1,
Adedotun Adeyinka Adekunle2 and Sikiru Abiola
Ojokuku1
1Department
of Biochemistry, College of Medicine, University of Lagos,
Lagos State, Nigeria.
2Botany
and Microbiology Department, University of Lagos, Akoka,
Lagos State, Nigeria.
*Corresponding author. E-mail:
modelprof@yahoo.com
Accepted 18 January, 2010 |
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The
cellulolytic and xylanolytic activity of a pathogenic
Myrothecium roridum Tode (IMI 394934) and non-pathogenic
Fusarium solani and Curvularia pallescence
Boedjin isolates from water hyacinth were investigated. The
mycelial plugs of each isolate was grown in submerged
cultures of Czapeck Dox broth containing the appropriate
carbon source (carboxymethylcellulose, sawdust and
homogenized dry water hyacinth leaf) at 25°C for 16 days.
The enzyme activity assay was carried out on the culture
filtrates obtained. This was measured as micromole sugar
released per min. The result obtained showed that the enzyme
activity (U/ml) for
b-1,4-exoglucanase,
b-1,4-endoglucanase
and xylanase was maximum 3.70
±
0.43, 0.95
±
0.03 and 2.32
± 0.10, respectively, in C. pallescens Boedjin grown on
carboxymethylcellulose and minimum 0.12 ± 0.02, 0.13 ± 0.03
and 0.34 ± 0.01 respectively, in M. roridum grown on
homogenized dry water hyacinth leaf. The
b-glucosidase
activity (U/ml) was highest, 1.74
±
0.06 in M. roridum grown on sawdust and least, 0.08 ±
0.00 in C. pallescens Boedjin grown on
homogenized water hyacinth leaf broth. The maximum (324.00 ±
19.51
mg/ml) and minimum (130.00 ± 5.83
mg/ml)
total extracellular protein was produced in M. roridum
grown on homogenized dry water hyacinth leaf and
carboxymethylcellulose, respectively. This study showed that
the phytopathogenic strain of M. roridum is capable
of producing cellulases and xylanase enzyme in submerged
cultures but to a lesser degree compared to F. solani
and C. pallescence Boedjin.
Key
words:
Cellulase enzymes, Curvularia pallescence Boedjin,
Fusarium solani, Myrothecium roridum, Phytopathogens. |