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Biochemical
characterization of digestive amylase of wheat bug,
Eurygaster maura (Hemiptera: Scutelleridae)
Sultan Ravan1,
Mohammad Mehrabadi2 and Ali R. Bandani2*
1Plant
Protection Department, Faculty of Agriculture, University of
Zabol, Zabol, Iran.
2Insect
Physiology and Molecular Biology Lab. Insect Physiology and
Molecular biology Laboratory
Plant
Protection Department, School of Plant Protection and
Horticultural Sciences, University of Tehran, Karaj, Iran.
*Corresponding author. E-mail:
abandani@ut.ac.ir.
Tel: +98- 261- 2818705.
Fax: +98-261- 2238529.
Accepted
27 March, 2009 |
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Biochemical
characterization of α-amylase in the midgut and salivary
glands of Eurygaster maura was conducted. Results
showed that α-amylase activities were present in the
salivary glands and gut. The activity of α-amylase in the
midgut and in the salivary glands was 0.098 and 0.057 U/ml,
respectively. The pH of salivary glands and the gut
was determined to be in the range of 5- 5.5 (for the
salivary glands) and in the range of 6-6.5 (for the gut),
using staining indicator. The optimum pH and temperature for
salivary glands and midgut amylase activity was 6-7 and
35-40ºC, respectively. The stability of amylase was highest
in the acidic pH (4-5). Ethylenediamine tetraacetic acid (EDTA),
urea, sodium dodecyl sulfate (SDS) and Mg2+
inhibited the enzyme activity but, NaCl and KCl enhanced
enzyme activity. Based on linear regression analysis of
reciprocal starch concentration versus reciprocal amylase
activity Km and Vmax were 0.11% and
0.04 mM maltose/min for midgut amylase and 0.298% and 0.071
mM maltose/min for salivary amylase, respectively. Sodium
dodecyl sulfate electrophoresis (SDS-PAGE) showed that both
midgut and salivary glands contain isozymes.
Key
words:
Eurygaster maura,
digestive amylase,
biochemical characterization, kinetic study. |